На главную
Результаты поиска “Can you have arthritis and hemochromatosis”
How to Know If You're at Risk of Iron Overload and What to Do ...
 
08:06
Spend eight minutes to know whether you need to manage your iron status and how to do it by watching this video. There's a 30% chance it could make a big difference in your health, and a 3% chance it could be life-changing. H63D rs1799945 risk: G C282Y rs1800562 risk: A
Просмотров: 18772 Chris Masterjohn, PhD
IRON OVERLOAD-I AM IRON WOMAN
 
16:29
ONE TREATMENT IS TO DRAIN MY BLOOD??--WHAT!(↓↓ click show more ↓↓)Read More on Iron Overload also known as Hemochromatosis, I'm still in the new about this and if I have to have my blood drained out of me each week or month, so be it..but right now, I just monitor the amount of iron I eat in my foods-here is a good article more about The Good and Bad of Iron-http://www.berkeleywellness.com/supplements/minerals/article/good-and-bad-iron. Please check out all the links below and thanks again for your support and motivation. ----------------------------------------­----------------------- ♥Read My Blog-Controlling The Carb Monster http://controllingthecarbmonster.blogspot.com ---------------------------------------------------------------- SUBSCRIBE TO MY CHANNEL(S) ♥Controlling The Carb Monster http://youtube.com/Bonnie90505 ----------------------------------------­-------------------------- ♥Feeling Fabulous at Any Age http://youtube.com/BonnieKay1958 ----------------------------------------­--------------------------- ♥Follow me on Twitter- http://twitter.com/Bonnie90505 -------------------------------------------------------------------- ♥Like My Facebook page- https://www.facebook.com/pages/Controlling-The-Carb-Monster/320381348083901 -------------------------------------------------------------------- -------------------------------------------------------------------- ♥I also do product reviews of products that pertain to relevance of both my YouTube channels- ♥Bonnie90505-Total Health related products ♥BonnieKay1958-Beauty related products please contact me at bonnie90505@gmail.com -------------------------------------------------------------------- -------------------------------------------------------------------- **Disclaimer: This video is my own personal experiences. Throughout this video, there are some statements that are made pertaining to the properties and/or functions of food and/or nutritional products. These statements have not been evaluated by the Food and Drug Administration/FTC and these materials and products are not intended to diagnose, treat, cure or prevent any disease. You should not use this information to diagnose or treat a health problem or disease without consulting with a qualified health care provider. Please consult your health care provider with any questions or concerns you may have regarding your condition
Просмотров: 2100 Bonnie90505
My Life - Earl Shaddox - Hemochromatosis
 
01:07
Earl Shaddox had been hurting for about 10 years. He had the same symptoms as arthritis, but none of the medicines helped. Earl was referred to Dr. Kai at Trinity Mother Frances. Dr Kai discovered that Earl was suffering from hemochromatosis. Iron was in his joints causing his pain. Dr. Kai helped Earl to eat the right kind of food and he started feeling much better. Earl feels like Dr. Kai saved his life.
Dealing with hemochromatosis,  Hashimotos & health issues
 
16:40
How I overcame "The Celtic Curse" also known as Hemochromatosis, Iron Overload, HH. Here's some things that help: Sentrum Silver http://amzn.to/2ntuufa Green Tea Extract: http://amzn.to/2mObVoR Vitamin B12: http://amzn.to/2ntyV9P Symptoms of Hemochromatosis: Joint pain Spooning fingernails Tan complexion Abdominal pain Extreme Fatigue Weakness Diabetes Loss of sex drive Impotence Heart failure Liver failure Hypothyroidism & Hashimotos Anger issues
Просмотров: 6602 Andrew Hill
Cholestatic Liver Disease - causes, symptoms, diagnosis, treatment, pathology
 
08:38
What is cholestasis? Cholestasis, or cholestatic liver disease, is a condition where bile gets into the liver tissue and blood stream, causing liver damage and a variety of complications. Intra-hepatic cholestasis happens in the liver and is caused by liver cells, whereas extra-hepatic cholestasis happens outside the liver and is usually from an obstruction in the bile ducts. Find more videos at http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.
Просмотров: 57311 Osmosis
FAQ about hemochromatosis
 
07:58
In this short video, Charlie Gallagher addresses some of the questions and comments he received on his first video with regards to living with Hemochromatosis. Here we look at the following: How long does treatment last? How much blood is taken at each visit? How can I manage my ongoing treatment? How long will it take before I recover/ feel better? As an interesting little extra, Charlie gives some information about the so -called ‘Hemingway Curse’ If you have any other questions or comments, please drop us a line below, we'd be happy to hear from you. If you prefer a little more anonymity, you can email: ceegeeceeproductions@gmail.com *Please consult your own physician or health care team if you are living with this or any other disorder. **Charlie does not claim to be trained in this area, please be aware that this video is intended for informational purposes only and should not take the place of advice or ongoing care from specialists. Watch our first video on Hemochromatosis here: https://www.youtube.com/watch?v=ed3peGX35ng More information about Hemochromatosis here: http://www.webmd.com/a-to-z-guides/tc/hemochromatosis-frequently-asked-questions More about The Hemingway Curse here: http://celticcurse.org/hemingways-death-and-hemochromatosis-awareness/ Filmed and Edited by Claire Warren Email: ceegeeceeproductions@gmail.com www.facebook.com/blacksmithcharlie Instagram: silver_anvil_forge
Просмотров: 3241 Silver Anvil Forge & Ceegeecee Productions
Statement on Hemochromatosis
 
01:09
On May 31, I rose to speak on this disease which impairs the body’s ability to get rid of excess iron, which can cause very serious and sometimes fatal conditions, including liver disease, heart disease, diabetes, arthritis, mental illness, and cancer.
Просмотров: 89 Deb Schulte MP
CREST syndrome - causes, symptoms, diagnosis, treatment, pathology
 
05:35
What is CREST syndrome? CREST syndrome, also known as limited cutaneous systemic sclerosis, is an autoimmune condition, and its name is an acronym that stands for calcinosis, Raynaud’s phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasias. Calcinosis is the deposition of calcium in the skin, Raynaud’s is spasm of the arteries in the fingers, esophageal dysmotility refers to difficulty swallowing, sclerodactyly is tightening of the skin over the fingers, and telangiectasias are small dilated blood vessels on the skin surface. Find our complete video library only on Osmosis Prime: http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.
Просмотров: 14359 Osmosis
What Are The Symptoms Of Hereditary Hemochromatosis?
 
00:46
What are the signs and symptoms of hemochromatosis? Nhlbi, nih hemochromatosis causes mayo clinic mayoclinic dxc 20167290 url? Q webcache. Hemochromatosis clinical presentation history and physical hereditary hemochromatosis symptoms canadian society. However, in its later stages, haemochromatosis presents a variety however, only about one person 5000 people is ever diagnosed with. The fact that there are no specific symptoms associated with 4 apr 2017 patients hereditary hemochromatosis may be asymptomatic or present general and organ related signs pain fatigue the most common. About the disease signs and symptoms hemochromatosis dnairon overload disorder symptoms, causes, treatmentjuvenile nord (national organization for rare. Googleusercontent search. Iron overload can be tiring, painful, complex, confusing, and symptoms are often even post mortem, hemochromatosis is overlooked as a possible cause of death. Hereditary hemochromatosis can also lead to cancer and heart haemochromatosis (or hemochromatosis) type 1 is a hereditary disease characterized by excessive intestinal recessive genetic disorders occur when an individual inherits the causing characteristic symptoms juvenile. Symptoms of genetic haemochromatosis can include the following handsmay affect any joint but particularly common in knuckle and 9 mar 2017 hemochromatosis causes body to absorb store too much iron. Hemochromatosis symptoms and causes mayo clinicthe of haemochromatosis hereditary hemochromatosis genetics home reference. Cleveland hemochromatosis types, risk factors, and causes healthlinehaemochromatosis british liver trust. That is why hereditary hemochromatosis has been called the silent genetic defect that causes present at birth. This is because iron symptoms. Aug 2017 early symptoms of hereditary hemochromatosis are nonspecific and may include fatigue, joint pain, abdominal loss sex drive. To make a diagnosis of hereditary hemochromatosis, the doctor will use 29 jan 2016 hemochromatosis is condition that causes buildup iron in primary an inherited genetic disorder you to early haemochromatosis has no symptoms. Many of the signs and symptoms are similar to hereditary hemochromatosis is an inherited (genetic) disorder in which there excessive accumulation this action genetic excess iron, if left untreated, can damage joints, type 1, also called classic (hhc), a leading cause iron find out about symptoms, diagnosis, treatment options & more. What are the signs and symptoms of hemochromatosis? Nhlbi, nih. Other factors that influence haemochromatosis (inherited iron overload disorder). Hemochromatosis an education website for hemochromatosis symptoms, diagnosis & treatment. If iron stores are high the serum ferritin level will be high, but levels can also raised by other factors. However, the symptoms do not appear until later in life. Later signs and symptoms can include arthritis, liver disease, diabetes, heart abnormalities, skin discoloration 1 feb 2011 hemochroma
Просмотров: 373 Don't Question Me
What Is Hemochromatosis?
 
03:52
I have Hemochromatosis. It is a genetic disorder where my body absorbs too much iron. Excess iron is stored in the organs and joints. This is a problem because it can cause cirrhosis of the liver, organ failure, type 2 diabetes, arthritis, and cancer. Luckily, I found mine early and have begun treatment. The only way to get rid of iron is to get rid of your blood, also known as a phlebotomy. You'll see my first two phlebotomies and how they went. Hemochromatosis is a common disease and needs to be detected among more people. Test your ferritin levels and find out for yourself. I am an entrepreneur and I like to garden. Join me each week as I share with you the lessons I've learned, gardening information, and I'll take you along on my entrepreneurial journey too! You can also read my blog: http://www.kyleclaytongore.com/blog/the-non-phlebotomy Follow me on social media: Twitter: https://twitter.com/KyleClaytonGore Facebook: https://www.facebook.com/kyleclaytongore Instagram: https://www.instagram.com/kyleclaytongore Snapchat: https://www.snapchat.com/add/kyleclaytongore Created by Kyle Clayton Gore Produced by Better Creative Studios: https://www.youtube.com/channel/UCcSy... Edited by Kyle Clayton Gore Music by Ben Sound, https://www.bensound.com
Просмотров: 1392 Kyle Clayton Gore
Hereditary Haemochromatosis
 
05:49
Subscribe to this channel: https://www.youtube.com/channel/UCKDwY2bhQtcMUZ3UFdN3Mng?sub_confirmation=1 Other Hepatology Lectures: https://www.youtube.com/playlist?list=PLfBFwAwues0mECQ6y63vV-2OZIVSfbt2K Haemochromatosis (or hemochromatosis) type 1 autosomal recessive is a hereditary disease characterized by excessive intestinal absorption of dietary iron resulting in a pathological increase in total body iron stores. Humans, like most animals, have no means to excrete excess iron. Excess iron accumulates in tissues and organs disrupting their normal function. The most susceptible organs include the liver, adrenal glands, heart, skin, gonads, joints, and the pancreas; patients can present with cirrhosis, polyarthropathy, adrenal insufficiency, heart failure or diabetes. The hereditary form of the disease is most common among those of Northern European ancestry, in particular those of Celtic descent. The disease is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. Most often, the parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but do not show signs and symptoms of the condition. Haemochromatosis is protean in its manifestations, i.e., often presenting with signs or symptoms suggestive of other diagnoses that affect specific organ systems. Many of the signs and symptoms below are uncommon and most patients with the hereditary form of haemochromatosis do not show any overt signs of disease nor do they suffer premature morbidity. Presently, the classic triad of cirrhosis, bronze skin and diabetes is less common because of earlier diagnosis. The more common clinical manifestations include: Fatigue Malaise Joint and bone pain Liver cirrhosis (with an increased risk of hepatocellular carcinoma) Liver disease is always preceded by evidence of liver dysfunction including elevated serum enzymes specific to the liver, clubbing of the fingers, leuconychia, asterixis, hepatomegaly, palmar erythema and spider naevi. Cirrhosis can also present with jaundice (yellowing of the skin) and ascites. Insulin resistance (often patients have already been diagnosed with diabetes mellitus type 2) due to pancreatic damage from iron deposition Erectile dysfunction and hypogonadism, resulting in decreased libido Congestive heart failure, abnormal heart rhythms or pericarditis Arthritis of the hands (especially the second and third MCP joints), but also the knee and shoulder joints Damage to the adrenal gland, leading to adrenal insufficiency The diagnosis of haemochromatosis is often made following the incidental finding on routine blood screening of elevated serum liver enzymes or elevation of the transferrin saturation. Arthropathy with stiff joints, diabetes, or fatigue, may be the presenting complaint. Treatment Phlebotomy Early diagnosis is vital as the late effects of iron accumulation can be wholly prevented by periodic phlebotomies (by venesection) comparable in volume to blood donations. Initiation of treatment is recommended when ferritin levels reach 500 micrograms per litre. Phlebotomy (or bloodletting) is usually done at a weekly interval until ferritin levels are less than 50 micrograms per litre. In order to prevent iron reaccumulation, subsequent phlebotomies are normally carried out approximately once every three to four months for males, and twice a year for females. Desferrioxamine mesilate Where venesection is not possible, long-term administration of desferrioxamine mesylate is useful. Desferrioxamine is an iron-chelating compound, and excretion induced by desferrioxamine is enhanced by administration of Vitamin C. It cannot be used during pregnancy or breast-feeding due to risk of defects in the child. Treatment of organ damage (heart failure with diuretics and ACE inhibitor therapy). Diet Limiting intake of alcoholic beverages, vitamin C (increases iron absorption in the gut), red meat (high in iron) and potential causes of food poisoning (shellfish, seafood). Increasing intake of substances that inhibit iron absorption, such as high-tannin tea, calcium, and foods containing oxalic and phytic acids (such as collard greens, which must be consumed at the same time as the iron-containing foods in order to be effective). Standard diagnostic measures for haemochromatosis, transferrin saturation and ferritin tests, are not a part of routine medical testing. Screening for haemochromatosis is recommended if the patient has a parent, child or sibling with the disease. more: https://en.wikipedia.org/wiki/HFE_hereditary_haemochromatosis
Joint Pain - Male
 
00:19
Pain and stiffness in the joints of the thumb, index and middle fingers, and ankles can be early signs of hemochromatosis. Learn if you are at risk for hemochromatosis by visiting www.toomuchiron.ca/screen.
Просмотров: 18 Canadian Hemochromatosis Society
"Gout and Pseudogout," Jeffrey Bieber, M.D.
 
55:46
"Gout and Pseudogout," Jeffrey Bieber, M.D. ETSU DMEC Grand Rounds 7.26.16
Просмотров: 4819 ETSU CME Grand Rounds
Hemophilia - causes, symptoms, diagnosis, treatment, pathology
 
09:38
What is hemophilia? Hemophillia is most often an inherited disorder that involves the body's ability to form blood clots. Find more videos at http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.
Просмотров: 267063 Osmosis
Joint Pain - Female
 
00:19
Pain and stiffness in the joints of the thumb, index and middle fingers, and ankles can be early signs of hemochromatosis. Learn if you are at risk for hemochromatosis by visiting www.toomuchiron.ca/screen.
Просмотров: 40 Canadian Hemochromatosis Society
Psuedogout - Everything You Need To Know - Dr. Nabil Ebraheim
 
02:19
Educational video describing the condition of psuedogout. Pseudogout or chondrocalcinosis is the deposition of calcium pyrophosphate dehydrate crystals in the hyaline cartilage or fibrocartilage (CPPD). The condition occurs more in older age groups and 1/3 of the patients are over 75 years of age. x-ray changes of chondrocalcinosis is seen in the knees on radiograph. Gout affects more distal joints. Pseudogout tends to affect more proximal joints. an x-ray will show calcification of the meniscus in the knee or triangular fibrocartilage in the wrist. Rule out endocrine or metabolic diseases: •Hyperparathyroidism •Hypophosphatasia •Hemochromatosis •Rheumatoid arthritis •Hypothyroidism Differential diagnosis: gout Clinical presentation •Asymptomatic radiographic findings alone •Acute crystal induced synovitis •Chronic arthropathy The condition is commonly seen in the knee and wrist but may also occur in the acetabulum labrum, symphysis pubis and annulus fibrosus of the disc. Aspiration shows rhomboid shaped crystals weakly positive. Treatment •NSAIDs •Steroid injections •Rule out metabolic diseases. Become a friend on facebook: http://www.facebook.com/drebraheim Follow me on twitter: https://twitter.com/#!/DrEbraheim_UTMC
Просмотров: 4520 nabil ebraheim
Having Trouble Reaching the Greens?
 
00:38
If you are having trouble getting your ball to reach the greens (or having trouble getting there yourself), the problem may not be your golf swing. Chronic fatigue and painful joints can be early warning signs of hemochromatosis. Learn if you are at risk by visiting www.toomuchiron.ca/screen.
Просмотров: 92909 Canadian Hemochromatosis Society
Liver Metabolic Disorders (Hereditary Hemochromatosis, Wilson's Disease, Alpha 1 Anti-trypsin)
 
09:47
This video reviews the various liver metabolic disorders, such as Hereditary Hemachromatosis, Wilson's Disease, and Alpha-1 Anti-Trypsin for the USMLE Step 1. HEREDITARY HEMOCHROMATOSIS Secondary can be casued by patient constantly getting trasnfusion, parenteral, and blood disorders In primary hereditary hemochromatosis you have a defect on the HFE Gene on chromsome 6. You can have a mutation C282Y or H63D. Either one of these mutation can lead to primary hereditary hemochromatosis. Also associated with HLA-A3. HFE gene regulates a protein which regulates iron absorption form the gut. There is increased iron absorption that can't be accomodated. Treatment is constant phlebotomy or iron chleators such as deforoxamine or defurosirox. Iron toxicity will lead to increased free radicals and this can increase collagen formation and these is the pathology underying hereditary hemachromatosis. You can get micronodular cirrhosis and diabetes mellitus. You may also get bronzing of the skin as the Iron incorporates into melanin and leads to pigmentation. You may also get arrythmia and Heart failure. Joint pain (arthritis) due to pseudogout. There is also chance of bein infertile and hypogonadism Labs - you will have high iron level, high ferritin level and decreased TIBC. WILSON'S Disease This is an accumulaiton of Copper. The body normally deals with copper by absorbing from gut and in liver binds with ceruloplasmin which is then excreted into plasma and then goes into tissue. Then broken down into proteins and sent through the bile and excreted. Gene defect on 13 leads to Wilson's Disease. Pathogenesis is that it can't incorporate copper into ceruloplasmin. Decrease biliary excretion of copper. This will cause copper to back up and then there is an increased in serum levels of copper. It may accumulate to in liver to cause cirrhosis, cornea to cause keyser fleischer rings. It may lead to psychosis by accumulating in the brain. It may also leads to parkinson's type tremor WILSON'S DISEASE LAB Low ceruloplasmin, high hepatic concentration. Low copper excretion Treated with D-Penicillamine. ALPHA 1 ANTI-TRYPSIN Alpha-1 Anti-trypsin is an important protein because it can deactivate protease, elastase, cathepsin and proteinase. This is important because all of these proteins are involved in breaking things down. Defect is in protein migration. When it goes from ER to Golgi Apparatus and this can lead to accumulation of anti-trypsin in the cell and it can't be used. CLINICAL EFFECTS of Alpha-1 Anti-Trypsin. Primary problems is that you will have emphysema and bronchiectasis. Eventually lead to liver damage. Cutaneous folliculitis. It may also lead to arterial aneurysms and also associated with Wegener's Granulomatosis.
Просмотров: 8263 the study spot
hemochromatosis and joint pain treatment
 
00:41
http://vivaint.biz/net/azol FO FREE! It seems you can hardly get through your day without something hurting. Finally, there's a natural solution to those annoying aches and pains with Eazol. Order your free trial today! Limited supp;y! Hurry up!
Просмотров: 76 How to cure joints.
Hemochromatosis Tips To Live By
 
00:49
Get the tips you need to lengthen the time between phlebotomies and live longer. http://www.genetichemochromatosis.com
Просмотров: 3756 wpatpeters
Treatment
 
05:36
Scarring of the liver caused by iron overload can be reversed by treatment with phlebotomies, but Dr. Adams explains why many do not see improvement of joint pain. Also, Dr. Adams discusses situations where some individuals do not require maintenance once de-ironed.
Просмотров: 2844 Canadian Hemochromatosis Society
Patricia's Story - Celebrating Patients
 
04:31
Media Release: http://mackenziehealth.ca/about_news_story.php?id=654 Pat has a hereditary condition called hemochromatosis, which causes the body to absorb and then store excessive iron in the organs. It can lead to many complications, in Pat’s case a very rare form of psoriatic arthritis that systematically destroyed her joints. She has had her hips, knees, ankles and one shoulder replaced. With all that, Pat remains positive. “It’s all for the good, because they were able to fix me.”
Просмотров: 390 Mackenzie Health
Al-hijamah for thalassemia and iron overload and hyperferremia - Supplementary video 1
 
08:08
Supplementary video 1 (Al-hijamah procedure) of_review_paper “Al-hijamah and oral honey for treating thalassemia, conditions of iron overload, and hyperferremia: towards improving the therapeutic outcomes” published in the open access journal_Journal of Blood Medicine_ by_authors_El Sayed SM, Baghdadi H, Abou-Taleb A, et al. Abstract: Iron overload causes iron deposition and accumulation in the liver, heart, skin, and other tissues resulting in serious tissue damages. Significant blood clearance from iron and ferritin using wet cupping therapy (WCT) has been reported. WCT is an excretory form of treatment that needs more research efforts. WCT is an available, safe, simple, economic, and time-saving outpatient modality of treatment that has no serious side effects. There are no serious limitations or precautions to discontinue WCT. Interestingly, WCT has solid scientific and medical bases (Taibah mechanism) that explain its effectiveness in treating many disease conditions differing in etiology and pathogenesis. WCT utilizes an excretory physiological principle (pressure-dependent excretion) that resembles excretion through renal glomerular filtration and abscess evacuation. WCT exhibits a percutaneous excretory function that clears blood (through fenestrated skin capillaries) and interstitial fluids from pathological substances without adding a metabolic or detoxification burden on the liver and the kidneys. Interestingly, WCT was reported to decrease serum ferritin (circulating iron stores) significantly by about 22.25% in healthy subjects (in one session) and to decrease serum iron significantly to the level of causing iron deficiency (in multiple sessions). WCT was reported to clear blood significantly of triglycerides, low-density lipoprotein (LDL) cholesterol, total cholesterol, uric acid, inflammatory mediators, and immunoglobulin antibodies (rheumatoid factor). Moreover, WCT was reported to enhance the natural immunity, potentiate pharmacological treatments, and to treat many different disease conditions. There are two distinct methods of WCT: traditional WCT and Al-hijamah (WCT of prophetic medicine). Both start and end with skin sterilization. In traditional WCT, there are two steps, skin scarification followed by suction using plastic cups (double S technique); Al-hijamah is a three-step procedure that includes skin suction using cups, scarification (shartat mihjam in Arabic), and second skin suction (triple S technique). Al-hijamah is a more comprehensive technique and does better than traditional WCT, as Al-hijamah includes two pressure-dependent filtration steps versus one step in traditional WCT. Whenever blood plasma is to be cleared of an excess pathological substance, Al-hijamah is indicated. We will discuss here some reported hematological and therapeutic benefits of Al-hijamah, its medical bases, methodologies, precautions, side effects, contraindications, quantitative evaluation, malpractice, combination with oral honey treatment, and to what extent it may be helpful when treating thalassemia and other conditions of iron overload and hyperferremia. Read the article here: http://www.dovepress.com/al-hijamah-and-oral-honey-for-treating-thalassemia-conditions-of-iron--peer-reviewed-article-JBM
Просмотров: 1134 Dove Medical Press
What is Hemochromatosis?
 
08:15
A complete overview of Canada's most common genetic disorder. For more information, contact the Canadian Hemochromatosis Society: http://www.toomuchiron.ca/
Просмотров: 133138 jrmleduc
Autoimmune hepatitis - causes, symptoms, diagnosis, treatment & pathology
 
06:00
What is autoimmune hepatitis? Well, it’s an autoimmune disease that affects the liver, leading to inflammation and hepatitis. A lot of the fundamental mechanisms behind why autoimmune develops is still unclear. Find more videos at http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.
Просмотров: 105554 Osmosis
Irish Haemochromatosis Association
 
01:43
A short informational video about Haemochromatosis entered into the Better Together Video Competition. The association benefits the whole country, it could save people from severe organ damage and may even saves lives. Phone: 01 8735911 Website: http://www.haemochromatosis-ir.com Facebook: https://www.facebook.com/irishhaemochromatosisassociation/?fref=ts
Просмотров: 338 John Keyes
Can't Get to Your To-Do List?
 
00:35
If chronic fatigue, pain and stiffness in the joints of the hand, or an irregular heartbeat are keeping you from your to-do list, you may be suffering from hemochromatosis. Find out if you are at risk by visiting www.toomuchiron.ca/screen.
Просмотров: 145730 Canadian Hemochromatosis Society
What is CHONDROCALCINOSIS? What does CHONDROCALSINOSIS mean? CHONDROCALCINOSIS meaning
 
07:15
What is CHONDROCALCINOSIS? What does CHONDROCALSINOSIS mean? CHONDROCALCINOSIS meaning - CHONDROCALCINOSIS pronunciation - CHONDROCALCINOSIS definition - CHONDROCALCINOSIS explanation - How to pronounce CHONDROCALCINOSIS? Source: Wikipedia.org article, adapted under https://creativecommons.org/licenses/by-sa/3.0/ license. SUBSCRIBE to our Google Earth flights channel - https://www.youtube.com/channel/UC6UuCPh7GrXznZi0Hz2YQnQ Calcium pyrophosphate dihydrate (CPPD) crystal deposition disease, also known as pseudogout and pyrophosphate arthropathy is a rheumatologic disorder with varied symptoms and signs arising from the accumulation of crystals of calcium pyrophosphate dihydrate in the connective tissues. The alternative names emphasize particular aspects of the clinical or radiographic findings. The knee joint is the most commonly affected. Calcium pyrophosphate dihydrate crystals are associated with a range of clinical syndromes, which have been given various names, based upon which clinical symptoms or radiographic findings are most prominent. A task force of the European League Against Rheumatism (EULAR) made recommendations on preferred terminology. Accordingly, calcium pyrophosphate deposition (CPPD) is an umbrella term for the various clinical subsets, whose naming reflects an emphasis on particular features. For example, pseudogout refers to the acute symptoms of joint inflammation or synovitis: red, tender, and swollen joints that may resemble gouty arthritis (a similar condition in which monosodium urate crystals are deposited within the joints). Chondrocalcinosis, on the other hand, refers to the radiographic evidence of calcification in hyaline and/or fibrocartilage. "Osteoarthritis (OA) with CPPD" reflects a situation where osteoarthritis features are the most apparent. Pyrophosphate arthropathy is a term that can refer to several of these situations. The exact cause of CPPD is unknown, although increased breakdown of adenosine triphosphate (ATP; the molecule used as energy currency in all living things), which results in increased pyrophosphate levels in joints, is thought to be one reason why crystals may develop. Familial forms are rare. One genetic study found an association between chondrocalcinosis and a region of chromosome 8q. The gene ANKH is involved in crystal-related inflammatory reactions and inorganic phosphate transport. Excessive calcium (due to hypomagnesemia) has a potential relationship with chondrocalcinosis, and magnesium supplementation may reduce or alleviate symptoms. Hyperparathyroidism, hypothyroidism, hemochromatosis, hypophosphatemia, hypomagnesemia and renal osteodystrophy are often also associated with chondrocalcinosis. Other diseases associated with chondrocalcinosis are Wilson's disease and osteoarthritis. In some cases, traumatic arthritis can cause chondrocalcinosis. The disorder is more common in older adults. The disease is often occult until crystal deposits are coincidentally detected and diagnosed by a pathologist in various orthopedic specimens. It may be asymptomatic, or it can be associated with osteoarthritis, or it can present as an acute or chronic inflammatory arthritis that causes pain in one or more joints. The white blood cell count is often raised. The arthritis is usually polyarticular (i.e., it leads to an inflammation of several joints in the body), although it may begin as monoarticular (i.e., confined to just one joint). CPPD crystals tend to form within articular tissues. In theory, any joint may be affected, but statistics show that the knees are the most commonly affected joints, as well as wrists and hips. In rare cases, pseudogout may affect the spinal canal and cause damage to the spinal cord. In many instances, patients may also have signs of carpal tunnel syndrome. This condition can also be associated with Milwaukee shoulder syndrome. .....
Просмотров: 554 The Audiopedia
What To Do For Joint Pain?
 
06:28
Greetings. Eric Bakker naturopath, thank you for checking out the video. I've got a question here from Sinad. Sinad Rowandish. Row-wash something like that anyway. Sorry Sinad, I can't pronounce your surname, it's a bit of a tongue twister for me. Sinad says, "I want to tell you something. I have bad candida and I can eat gluten without any problem but the point is that we as Muslims don't drink any alcohol at all. Even we don't even know what alcohol smells like." Wow, that's amazing. I didn't know alcohol smelled. Has it got a smell about it? "I'm noticing that I have symptoms of candida in my joints but it makes no difference at all when I eat gluten. I mean I don't feel any better but at least I'm not feeling worse. The point is, candida causes leaky gut but in my opinion alcohol is the main cause." You are correct. Alcohol's one of the main causes for leaky gut but it's not the top cause. The top cause is antibiotics. That's the number one cause. But there are, I could spend an hour outlining different scenarios that lead to leaky gut. Most people have got intestinal permeability to some degree which we call leaky gut. In fact if you had Wikipedia, they say that leaky gut is a pile of crap, it doesn't exist. It's a nonexisting syndrome. But then on the other hand if you have a look at the medical studies, they say that intestinal permeability exists. Now you tell me the difference between a leaky gut and intestinal permeability. It's the same thing. These guys just want to have their own way, you know? Pain in the joints Sinad. I had interesting patient last week from England, a man. A 60 year old male with very bad pain in the finger joints. So, when I saw this guy, I said to him, "We need to do some blood tests and we need to do a stool test." And with the blood test I wanted to look at the typical inflammatory markers that we see with males. Uric acid is a classic example. Uric acid is something that the body makes and excretes normally through the kidneys but if it builds up it can create a lot of pain around the joints. Uric acid needs checking out. While uric acid is being checked out, kidney function gets checked, liver function gets checked and also then I want to look at other inflammatory markers in the blood, a very good one being CRP or C-reactive protein. You can also go a step further and go for HSCRP, which means high sensitivity C-reactive protein. And then the other test you do is called ESR or sedimentation rate. And that has got to do with how fast your blood clots basically. The sed rate, CRP, uric acid, these are all good markers for inflammation in the body. Of course this guy's, all of them came back high but because he was British I thought, I'm going to check this guy's iron profile out because about one in 60 people that live in Ireland and northern England have got a disease called hemochromatosis or iron overload. I requested that we check this man's ferritin levels which is an iron storage protein. His ferritin levels were really excessive at 1,000 and they should be under 200. In fact, his doctor was shocked when he saw that and said, "Oh my goodness, you need to go and see a professor to find out what this is." But his silly doctor didn't even test for any of those markers at all. They just basically put him on anti-inflam drugs right away which I was dismayed with. In this man's case, I'm going to be working on cleaning his liver and his kidneys out, changing his diet and in a stool result that we did with him showed he had many different types of bad bacteria. These are very often linked up with joint pain. I've got very old medical textbooks that talk about with pain in the joints and especially autoimmune pain, you need to look for hidden infection. Doctors don't want to look for anything anymore except maybe a glass of wine and a golf ball but in the old days they used to spend time with people. Thanks for the question.
Просмотров: 296 Candida Crusher
WARNING SIGNS FROM YOUR FINGERNAILS ABOUT YOUR HEALTH | Healthy Living Tips
 
02:55
Most people don’t consider this important, but our fingernails can actually tell a lot about our health. Any kind of change in the nails may indicate a certain disease or condition, which is why we need to pay more attention to them. ▶ Download Android App for Free - https://goo.gl/GnKAsj Take a look at your nails – have they changed their color or have dips and ridges on them? Are they thicker than usually or chipped? All these changes can indicate serious health problems and help you detect the problem on time. Here are 8 nail changes which indicate serious health problems: CLUBBED NAILS If your nails are clubbed and “puffed” around the fingers, it may be a sign of inflammatory bowel disease, respiratory disease, AIDS or liver disease. Dry AND BRITTLE NAILS Brittle and dry nails are usually associated with hormonal imbalance or bacterial and fungal infections. RIDGES ON THE NAILS Ridges on the fingernails may be a warning sign of arthritis, iron deficiency or lupus. If you notice ridges on your nails you should visit your doctor as soon as possible. PITTED NAILS Small dips and pits in the nails usually indicate alopecia areata, psoriasis, connective tissue problems or zinc deficiency. SPOONED NAILS If your nails look curved like a spoon, you might be suffering from iron deficiency, hypothyroidism, heart disease or hemochromatosis (a liver disorder caused by high iron absorption). SPLIT NAILS Split nails have a tendency to flake and are generally caused by malnutrition, some nutrients deficiencies (folic acid, vitamin C, protein) or psoriasis. THICKENED NAILS The nails should be thin, smooth and strong, and never thick. Thickened nails indicate circulation problems, lung diseases, fungal infections, thyroid problems or psoriasis. DISCOLORED NAILS The color of your nails can tell you if you’re suffering from a certain problem. White nails may be a sign of hepatitis, while dark stripes near the top indicate congestive heart failure. Blue nails are a sign of low blood oxygen levels, while green nails indicate bacterial infections. Dull-colored nails are a sign of vitamin deficiencies, while red streaks on the fingernails may be an early sign of heart valve infections. As you can see, our fingernails can tell a lot about our health, which is why it’s important to notice any kind of change and take it seriously.
Просмотров: 38247 Healthy Living Tips
Too Much Iron Accelerates Aging by Len Saputo, MD
 
05:25
Iron storage disease, or hemochromatosis, affects 10-15% of the population, and perhaps even more if you know how to diagnose it. Iron overload increases free radical damage via the Fenton reaction. Hepcidin is a hormone that regulates iron levels by increasing the absorption of iron. The is new research showing that at least experimentally it is possible to block hepciden and lower levels of iron and LDL cholesterol by increasing reverse cholesterol transport. Iron is carcinogenic and cancer cells hoard it. Artemisinin is a possible treatment for cancer. Check this out by putting artemisinin in the search box on www.doctorsaputo.com. For more information please visit www.doctorsaputo.com
Просмотров: 9819 DoctorSaputo
Iron Overload and the Liver: Part 2
 
19:25
This Masters in Medicine webcast is one in a three-part series by Dr. Anthony Tavill. This webcast reviews hereditary hemochromatosis and the most current data on the regulation of iron metabolism. Take the opportunity to also learn from Dr. Tavill in Iron Overload and the Liver: Part 1 and Iron Overload and the Liver: Part 3. To learn more about the Masters in Medicine series or to claim CME credit, visit http://www.ccfcme.org/Masters The video was produced by the Cleveland Clinic Foundation Center for Continuing Education.
Просмотров: 7670 ClevelandClinicCME
Al-hijamah for thalassemia and iron overload and hyperferremia
 
04:13
Video abstract of_review_paper “Al-hijamah and oral honey for treating thalassemia, conditions of iron overload, and hyperferremia: towards improving the therapeutic outcomes” published in the open access journal_Journal of Blood Medicine_ by_authors_El Sayed SM, Baghdadi H, Abou-Taleb A, et al. Abstract: Iron overload causes iron deposition and accumulation in the liver, heart, skin, and other tissues resulting in serious tissue damages. Significant blood clearance from iron and ferritin using wet cupping therapy (WCT) has been reported. WCT is an excretory form of treatment that needs more research efforts. WCT is an available, safe, simple, economic, and time-saving outpatient modality of treatment that has no serious side effects. There are no serious limitations or precautions to discontinue WCT. Interestingly, WCT has solid scientific and medical bases (Taibah mechanism) that explain its effectiveness in treating many disease conditions differing in etiology and pathogenesis. WCT utilizes an excretory physiological principle (pressure-dependent excretion) that resembles excretion through renal glomerular filtration and abscess evacuation. WCT exhibits a percutaneous excretory function that clears blood (through fenestrated skin capillaries) and interstitial fluids from pathological substances without adding a metabolic or detoxification burden on the liver and the kidneys. Interestingly, WCT was reported to decrease serum ferritin (circulating iron stores) significantly by about 22.25% in healthy subjects (in one session) and to decrease serum iron significantly to the level of causing iron deficiency (in multiple sessions). WCT was reported to clear blood significantly of triglycerides, low-density lipoprotein (LDL) cholesterol, total cholesterol, uric acid, inflammatory mediators, and immunoglobulin antibodies (rheumatoid factor). Moreover, WCT was reported to enhance the natural immunity, potentiate pharmacological treatments, and to treat many different disease conditions. There are two distinct methods of WCT: traditional WCT and Al-hijamah (WCT of prophetic medicine). Both start and end with skin sterilization. In traditional WCT, there are two steps, skin scarification followed by suction using plastic cups (double S technique); Al-hijamah is a three-step procedure that includes skin suction using cups, scarification (shartat mihjam in Arabic), and second skin suction (triple S technique). Al-hijamah is a more comprehensive technique and does better than traditional WCT, as Al-hijamah includes two pressure-dependent filtration steps versus one step in traditional WCT. Whenever blood plasma is to be cleared of an excess pathological substance, Al-hijamah is indicated. We will discuss here some reported hematological and therapeutic benefits of Al-hijamah, its medical bases, methodologies, precautions, side effects, contraindications, quantitative evaluation, malpractice, combination with oral honey treatment, and to what extent it may be helpful when treating thalassemia and other conditions of iron overload and hyperferremia. Read the original paper here: http://www.dovepress.com/al-hijamah-and-oral-honey-for-treating-thalassemia-conditions-of-iron--peer-reviewed-article-JBM
Просмотров: 670 Dove Medical Press
118. Hemochromatosis (Kelley and Firestein’s Textbook of Rheumatology 10th Edition-2017)
 
03:01
Kelley and Firestein’s Textbook of Rheumatology 10th Edition-2017 1 Biology of the Normal Joint 2 Synovium 3 Cartilage and Chondrocytes 4 Biology, Physiology, and Morphology of Bone 5 Muscle 6 Biomechanics 7 Regenerative Medicine and Tissue Engineering 8 Proteinases and Matrix Degradation 9 Dendritic Cells 10 Mononuclear Phagocytes 11 Neutrophils 12 T Lymphocytes 13 B Cells 14 Fibroblasts and Fibroblast-like Synoviocytes 15 Mast Cells 16 Platelets 17 Innate Immunity 18 Adaptive Immunity and Organization of Lymphoid Tissues 19 Autoimmunity 20 Metabolic Regulation of Immunity 21 Genetics of Rheumatic Diseases 22 Epigenetics of Rheumatic Diseases 23 Complement System 24 Prostaglandins, Leukotrienes, and Related Compounds 25 Cell Recruitment and Angiogenesis 26 Cytokines 27 Principles of Signaling 28 Immunologic Repercussions of Cell Death 29 Experimental Models for Rheumatoid Arthritis 30 Neuronal Regulation of Pain and Inflammation 31 Clinical Research Methods in Rheumatic Disease 32 Economic Burden of Rheumatic Diseases 33 Assessment of Health Outcomes 34 Biologic Markers in Clinical Trials and Clinical Care 35 Occupational and Recreational Musculoskeletal Disorders 36 Cardiovascular Risk in Inflammatory Rheumatic Disease 37 Cancer Risk in Rheumatic Diseases 38 Introduction to Physical Medicine, Physical Therapy, and Rehabilitation 39 Pregnancy and Rheumatic Diseases 40 History and Physical Examination of the Musculoskeletal System 41 Acute Monoarthritis 42 Evaluation and Differential Diagnosis of Polyarthritis 43 Skin and Rheumatic Diseases 44 The Eye and Rheumatic Diseases 45 Neck Pain 46 Shoulder Pain 47 Low Back Pain 48 Hip and Knee Pain 49 Foot and Ankle Pain 50 Hand and Wrist Pain 51 Temporomandibular Joint Pain 52 Fibromyalgia 53 Synovial Fluid Analyses, Synovial Biopsy, and Synovial Pathology 54 Arthrocentesis and Injection of Joints and Soft Tissue 55 Anti-nuclear Antibodies 56 Autoantibodies in Rheumatoid Arthritis 57 Acute Phase Reactants and the Concept of Inflammation 58 Imaging in Rheumatic Diseases 59 Biology and Therapeutic Targeting of Prostanoids 60 Glucocorticoid Therapy 61 Traditional DMARDs 62 Immunosuppressive Drugs 63 Anti-cytokine Therapies 64 Cell-Targeted Biologics and Emerging Targets 65 Novel Intra-cellular Targeting Agents in Rheumatic Disease 66 Urate-Lowering Therapy 67 Analgesic Agents in Rheumatic Disease 68 Nutrition and Rheumatic Diseases 69 Etiology and Pathogenesis of Rheumatoid Arthritis 70 Clinical Features of Rheumatoid Arthritis 71 Treatment of Rheumatoid Arthritis 72 Early Synovitis and Early Undifferentiated Arthritis 73 Sjögren’s Syndrome 74 Etiology and Pathogenesis of Spondyloarthritis 75 Ankylosing Spondylitis 76 Undifferentiated Spondyloarthritis 77 Psoriatic Arthritis 78 Enteropathic Arthritis 79 Etiology and Pathogenesis of Systemic Lupus Erythematosus 80 Clinical Features of Systemic Lupus Erythematosus 81 Treatment of Systemic Lupus Erythematosus 82 Anti-phospholipid Syndrome 83 Etiology and Pathogenesis of Scleroderma 84 Clinical Features and Treatment of Scleroderma 85 Inflammatory Diseases of Muscle and Other Myopathies 86 Overlap Syndromes 87 Classification and Epidemiology of Systemic Vasculitis 88 Giant Cell Arteritis, Polymyalgia Rheumatica, and Takayasu’s Arteritis 89 Anti-neutrophil Cytoplasmic Antibody?Associated Vasculitis 90 Polyarteritis Nodosa and Related Disorders 91 Immune Complex?Mediated Small-Vessel Vasculitis 92 Primary Angiitis of the Central Nervous System 93 Behçet’s Disease 94 Etiology and Pathogenesis of Hyperuricemia and Gout 95 Clinical Features and Treatment of Gout 96 Calcium Crystal Disease 97 Familial Autoinflammatory Syndromes 98 Pathogenesis of Osteoarthritis 99 Clinical Features of Osteoarthritis 100 Treatment of Osteoarthritis 101 Metabolic Bone Disease 102 Proliferative Bone Diseases 103 Osteonecrosis 104 Relapsing Polychondritis 105 Heritable Diseases of Connective Tissue 106 Etiology and Pathogenesis of Juvenile Idiopathic Arthritis 107 Clinical Features and Treatment of Juvenile Idiopathic Arthritis 108 Pediatric Systemic Lupus Erythematosus, Juvenile Dermatomyositis, Scleroderma, and Vasculitis 109 Bacterial Arthritis 110 Lyme Disease 111 Mycobacterial Infections of Bones and Joints 112 Fungal Infections of Bones and Joints 113 Rheumatic Manifestations of Human Immunodeficiency Virus Infection 114 Viral Arthritis 115 Rheumatic Fever and Post-streptococcal Arthritis 116 Amyloidosis 117 Sarcoidosis 118 Hemochromatosis 119 Hemophilic Arthropathy 120 Rheumatic Manifestations of Hemoglobinopathies 121 IgG4-Related Disease 122 Arthritis Accompanying Endocrine and Metabolic Disorders 123 Musculoskeletal Syndromes in Malignancy 124 Tumors and Tumor-like Lesions of Joints and Related Structures
Просмотров: 27 Tâm Nguyễn Trung
Nail Symptoms and What It Means for Your Health!
 
04:22
Did you know that your fingernails can provide clues to your overall health? Healthy nails grow, on average 3.5 millimeters a month, but this is influenced by your nutritional status, medications, trauma, chronic disease, and the aging process itself. If you notice any significant changes in your nails, including swelling, discolorations, or changes in shape or thickness, see a dermatologist right away. It could be nothing, or it could be due to an underlying condition. Below are the nail symptoms you might experience in your lifetime and what they mean for your health. White Lines Across Nails Also dubbed "Muehrcke's lines," these double white lines run horizontally across the nails, and are typically most clearly seen on the index, middle, and ring fingers. Commonly, these lines can indicate low levels of protein in the blood, which can be caused by liver disease or malnutrition, or during periods of stress, especially ones that affect your metabolism. Dark Stripes Running Down Nails In many cases, these dark, vertical stripes across your nails are harmless. However, there is a chance that they could be a sign of subungual melanoma, an extremely ferocious form of cancer that occurs on the toes or fingers. Red Or Brown Streaks Underneath Nails Also called splinter hemorrhage, these thin, reddish brown streaks underneath the nails are primarily tiny, damaged blood vessels. They can indicate wider, more severe causes that have to do with inflammation or swelling, including medical conditions like rheumatoid arthritis and psoriasis. Discolored Nails Discolored nails can indicate various things, including signs of an infection, a nutritional deficiency, and a problem with one of your organs. Yellowish nail points to a fungal nail infection, or even psoriasis. Brown nails can indicate a thyroid disease or malnutrition. White nails can point to an iron deficiency. Bluish-gray tint can mean that your body might not be getting enough oxygen. It could also point to an issue with your lungs or heart. Brittle, Crumbly Nails Dry, brittle nails that frequently split or crack have been linked to things like thyroid disease and fungal infections. They can also indicate lichen planus, a condition that results in itchy rashes on the skin or around the mouth. Thickened Nails Among many other possible causes, thickened nails can form due to reactive arthritis (a really painful kind of inflammatory arthritis) and lung diseases. Another possible explanation is poor circulation. Medical conditions, like diabetes, can slow down the blood flow through the fingers and toes, and affect the quality of the skin. Spoon-Shaped Nails Spoon-shaped fingernails curve inward, and look like they are "scooping" outward. They can indicate a condition known as koilonychia, a disease that can be an indicator of hypochromic anemia, which leaves the red blood cells paler than normal. In addition, these nails can be a sign of hemochromatosis, a liver condition that is caused by a surplus of iron. They can also be a sign of heart disease or hypothyroidism. Pitting Or Denting In Nails Medical conditions such as psoriasis and reactive arthritis are likely be the reason that you're seeing little dents in your nails. Other possibilities include eczema and alopecia areata, a genetic disease that results in spot baldness. Grooves In Nails Also dubbed "Beau's lines," these horizontal grooves are ridges and indentations in the nails. There are several causes, including malfunctions during cell division, infections in the nail fold, or finger injuries. Nail Clubbing Also known as drumstick fingers and watch-glass nails, clubbed nails occur when the nails curve around the fingertips. This could be totally harmless — there might be an increased blood flow to the fingertips, and this could even be a genetic occurrence. Clubbed nails could also indicate lung and liver disease, heart disease, and inflammatory bowel disease, according to Hills.
Просмотров: 295116 Direct Trend
Iron overload
 
08:01
Iron overload Iron overload, also known as hemochromatosis or haemochromatosis, indicates accumulation of iron in the body from any cause The most important causes are hereditary haemochromatosis HHC, a genetic disorder, and transfusional iron overload, which can result from repeated blood transfusions12 Contents 1 Signs and symptoms 2 Causes 21 Primary haemochromatosis 22 Secondary haemochromatosis 3 Diagnosis 31 Screening 4 Treatment 5 Prognosis 6 Epidemiology 7 Terminology 8 See also 9 References 10 Further reading 11 External links Signs and symptoms Play media An explanation of hemochromatosis Organs commonly affected by haemochromatosis are the liver, heart, and endocrine glands3 Haemochromatosis may present with the following clinical syndromes:4 Cirrhosis of the liver: Varies from zonal iron deposition5 to fibrosis cirrhosis Diabetes due to selective iron deposition in pancreatic islet beta cells leading to functional failure and cell death26 Cardiomyopathy Arthritis, from calcium pyrophosphate deposition in joints The most commonly affected joints are th Iron overload Click for more; https://www.turkaramamotoru.com/en/iron-overload-24539.html There are excerpts from wikipedia on this article and video
Просмотров: 7 Search Engine
Iron overload
 
10:37
In medicine, iron overload indicates accumulation of iron in the body from any cause. The most important causes are hereditary haemochromatosis (HHC), a genetic disorder, and transfusional iron overload, which can result from repeated blood transfusion. This video is targeted to blind users. Attribution: Article text available under CC-BY-SA Creative Commons image source in video
Просмотров: 1825 Audiopedia
Liver Disorders: Cause and Solution
 
33:19
At http://bergmanchiropractic.com and http://Owners-Guide.com we strive to educate people on natural solutions to health. http://www.theArthritisReversalSystem.com is my online video course with 21 videos, 3 manuals and an online forum! https://www.owners-guide.com/online-consultation/ for online consults. SUBSCRIBE at http://www.youtube.com/user/johnbchiro CALL TOLL FREE 1-855-712-0012 to get bonus materials not on YouTube or text your first name and email plus 89869 to 1-817-591-2905.
Просмотров: 444010 Dr. John Bergman
Iron homeostasis and its disorders: from iron-deficiency anemia to hereditary hemochromatosis
 
01:00:08
Department of Medicine Grand Rounds presentation by Dr. Tomas Ganz, PhD, MD; Distinguished Professor, Departments of Medicine, Pathology and Laboratory Medicine Faculty, Cellular and Molecular Pathology PhD Program David Geffen School of Medicine University of California Los Angeles
Просмотров: 2298 UWDeptMedicine
What is polycythemia vera? | Hematologic System Diseases | NCLEX-RN | Khan Academy
 
10:35
Learn to recognize the symptoms of polycythemia vera as well as how to diagnosis and treat it. By Raja Narayan. Visit us (http://www.khanacademy.org/science/healthcare-and-medicine) for health and medicine content or (http://www.khanacademy.org/test-prep/mcat) for MCAT related content. These videos do not provide medical advice and are for informational purposes only. The videos are not intended to be a substitute for professional medical advice, diagnosis or treatment. Always seek the advice of a qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read or seen in any Khan Academy video. Created by Raja Narayan. Watch the next lesson: https://www.khanacademy.org/test-prep/nclex-rn/hematologic-system-diseases/rn-myeloproliferative-disorders/v/what-is-essential-thrombocythemia?utm_source=YT&utm_medium=Desc&utm_campaign=Nclex-rn Missed the previous lesson? https://www.khanacademy.org/test-prep/nclex-rn/hematologic-system-diseases/rn-myeloproliferative-disorders/v/what-are-myeloproliferative-disorders?utm_source=YT&utm_medium=Desc&utm_campaign=Nclex-rn NCLEX-RN on Khan Academy: A collection of questions from content covered on the NCLEX-RN. These questions are available under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 United States License (available at http://creativecommons.org/licenses/by-nc-sa/3.0/us/). About Khan Academy: Khan Academy offers practice exercises, instructional videos, and a personalized learning dashboard that empower learners to study at their own pace in and outside of the classroom. We tackle math, science, computer programming, history, art history, economics, and more. Our math missions guide learners from kindergarten to calculus using state-of-the-art, adaptive technology that identifies strengths and learning gaps. We've also partnered with institutions like NASA, The Museum of Modern Art, The California Academy of Sciences, and MIT to offer specialized content. For free. For everyone. Forever. #YouCanLearnAnything Subscribe to Khan Academy’s NCLEX-RN channel: https://www.youtube.com/channel/UCDx5cTeADCvKWgF9x_Qjz3g?sub_confirmation=1 Subscribe to Khan Academy: https://www.youtube.com/subscription_center?add_user=khanacademy
Просмотров: 113340 khanacademymedicine
Iron overload (Medical Condition)
 
02:09
Symptoms, risk factors and treatments of Iron overload (Medical Condition) In medicine, iron overload indicates accumulation of iron in the body from any cause This video contains general medical information If in doubt, always seek professional medical advice. The medical information is not advice and should not be treated as such. The medical information is provided without any representations or warranties, express or implied. We do not warrant or represent that the medical information on this websiteis true, accurate, complete, current or non-misleading Music: 'Undaunted' Kevin Macleod CC-BY-3.0 Source/Images: "Iron overload" CC-BY-2.5 https://www.freebase.com/m/02n_ct
Просмотров: 1672 Medical Condition Information
Arthritis
 
15:41
Arthritis (from Greek arthro-, joint + -itis, inflammation; plural: arthritides) is a form of joint disorder that involves inflammation of one or more joints. There are over 100 different forms of arthritis. The most common form, osteoarthritis (degenerative joint disease), is a result of trauma to the joint, infection of the joint, or age. Other arthritis forms are rheumatoid arthritis, psoriatic arthritis, and related autoimmune diseases. Septic arthritis is caused by joint infection. The major complaint by individuals who have arthritis is joint pain. Pain is often a constant and may be localized to the joint affected. The pain from arthritis is due to inflammation that occurs around the joint, damage to the joint from disease, daily wear and tear of joint, muscle strains caused by forceful movements against stiff painful joints and fatigue. This video is targeted to blind users. Attribution: Article text available under CC-BY-SA Creative Commons image source in video
Просмотров: 62 Audiopedia
Hemochromatosis on the Hill 2018
 
01:08
May is Hemochromatosis Awareness Month! Here are some of the sights from the day of hemochromatosis awareness on Parliament Hill in Canada, May 22, 2018.
Просмотров: 98 Canadian Hemochromatosis Society
115. Rheumatic Fever and Post-streptococcal Arthritis (Kelley and Firestein’s Textbook of Rheu...)
 
05:07
Kelley and Firestein’s Textbook of Rheumatology 10th Edition-2017 1 Biology of the Normal Joint 2 Synovium 3 Cartilage and Chondrocytes 4 Biology, Physiology, and Morphology of Bone 5 Muscle 6 Biomechanics 7 Regenerative Medicine and Tissue Engineering 8 Proteinases and Matrix Degradation 9 Dendritic Cells 10 Mononuclear Phagocytes 11 Neutrophils 12 T Lymphocytes 13 B Cells 14 Fibroblasts and Fibroblast-like Synoviocytes 15 Mast Cells 16 Platelets 17 Innate Immunity 18 Adaptive Immunity and Organization of Lymphoid Tissues 19 Autoimmunity 20 Metabolic Regulation of Immunity 21 Genetics of Rheumatic Diseases 22 Epigenetics of Rheumatic Diseases 23 Complement System 24 Prostaglandins, Leukotrienes, and Related Compounds 25 Cell Recruitment and Angiogenesis 26 Cytokines 27 Principles of Signaling 28 Immunologic Repercussions of Cell Death 29 Experimental Models for Rheumatoid Arthritis 30 Neuronal Regulation of Pain and Inflammation 31 Clinical Research Methods in Rheumatic Disease 32 Economic Burden of Rheumatic Diseases 33 Assessment of Health Outcomes 34 Biologic Markers in Clinical Trials and Clinical Care 35 Occupational and Recreational Musculoskeletal Disorders 36 Cardiovascular Risk in Inflammatory Rheumatic Disease 37 Cancer Risk in Rheumatic Diseases 38 Introduction to Physical Medicine, Physical Therapy, and Rehabilitation 39 Pregnancy and Rheumatic Diseases 40 History and Physical Examination of the Musculoskeletal System 41 Acute Monoarthritis 42 Evaluation and Differential Diagnosis of Polyarthritis 43 Skin and Rheumatic Diseases 44 The Eye and Rheumatic Diseases 45 Neck Pain 46 Shoulder Pain 47 Low Back Pain 48 Hip and Knee Pain 49 Foot and Ankle Pain 50 Hand and Wrist Pain 51 Temporomandibular Joint Pain 52 Fibromyalgia 53 Synovial Fluid Analyses, Synovial Biopsy, and Synovial Pathology 54 Arthrocentesis and Injection of Joints and Soft Tissue 55 Anti-nuclear Antibodies 56 Autoantibodies in Rheumatoid Arthritis 57 Acute Phase Reactants and the Concept of Inflammation 58 Imaging in Rheumatic Diseases 59 Biology and Therapeutic Targeting of Prostanoids 60 Glucocorticoid Therapy 61 Traditional DMARDs 62 Immunosuppressive Drugs 63 Anti-cytokine Therapies 64 Cell-Targeted Biologics and Emerging Targets 65 Novel Intra-cellular Targeting Agents in Rheumatic Disease 66 Urate-Lowering Therapy 67 Analgesic Agents in Rheumatic Disease 68 Nutrition and Rheumatic Diseases 69 Etiology and Pathogenesis of Rheumatoid Arthritis 70 Clinical Features of Rheumatoid Arthritis 71 Treatment of Rheumatoid Arthritis 72 Early Synovitis and Early Undifferentiated Arthritis 73 Sjögren’s Syndrome 74 Etiology and Pathogenesis of Spondyloarthritis 75 Ankylosing Spondylitis 76 Undifferentiated Spondyloarthritis 77 Psoriatic Arthritis 78 Enteropathic Arthritis 79 Etiology and Pathogenesis of Systemic Lupus Erythematosus 80 Clinical Features of Systemic Lupus Erythematosus 81 Treatment of Systemic Lupus Erythematosus 82 Anti-phospholipid Syndrome 83 Etiology and Pathogenesis of Scleroderma 84 Clinical Features and Treatment of Scleroderma 85 Inflammatory Diseases of Muscle and Other Myopathies 86 Overlap Syndromes 87 Classification and Epidemiology of Systemic Vasculitis 88 Giant Cell Arteritis, Polymyalgia Rheumatica, and Takayasu’s Arteritis 89 Anti-neutrophil Cytoplasmic Antibody?Associated Vasculitis 90 Polyarteritis Nodosa and Related Disorders 91 Immune Complex?Mediated Small-Vessel Vasculitis 92 Primary Angiitis of the Central Nervous System 93 Behçet’s Disease 94 Etiology and Pathogenesis of Hyperuricemia and Gout 95 Clinical Features and Treatment of Gout 96 Calcium Crystal Disease 97 Familial Autoinflammatory Syndromes 98 Pathogenesis of Osteoarthritis 99 Clinical Features of Osteoarthritis 100 Treatment of Osteoarthritis 101 Metabolic Bone Disease 102 Proliferative Bone Diseases 103 Osteonecrosis 104 Relapsing Polychondritis 105 Heritable Diseases of Connective Tissue 106 Etiology and Pathogenesis of Juvenile Idiopathic Arthritis 107 Clinical Features and Treatment of Juvenile Idiopathic Arthritis 108 Pediatric Systemic Lupus Erythematosus, Juvenile Dermatomyositis, Scleroderma, and Vasculitis 109 Bacterial Arthritis 110 Lyme Disease 111 Mycobacterial Infections of Bones and Joints 112 Fungal Infections of Bones and Joints 113 Rheumatic Manifestations of Human Immunodeficiency Virus Infection 114 Viral Arthritis 115 Rheumatic Fever and Post-streptococcal Arthritis 116 Amyloidosis 117 Sarcoidosis 118 Hemochromatosis 119 Hemophilic Arthropathy 120 Rheumatic Manifestations of Hemoglobinopathies 121 IgG4-Related Disease 122 Arthritis Accompanying Endocrine and Metabolic Disorders 123 Musculoskeletal Syndromes in Malignancy 124 Tumors and Tumor-like Lesions of Joints and Related Structures
Просмотров: 131 Tâm Nguyễn Trung
What cancers cause elevated ferritin levels
 
02:00
What cancers cause elevated ferritin levels - Find out more explanation for : 'What cancers cause elevated ferritin levels' only from this channel. Information Source: google
Просмотров: 150 saiful saiful
Lupus And Rheumatoid Arthritis - Dr. Joel Wallach
 
06:23
http://www.wallachslog.com Call: 1(774)322-1690 Order Doc Wallach's Books: http://amzn.to/1lCtpzq Dr. Joel Wallach takes a June who has been diagnosed with lupus and rheumatoid arthritis. Stress, poor diets and unhealthy sleeping patterns (plus other external factors), can cause short-term and long-term damage to our brain health; leading to a wide-range of health problems. Our brains require optimal care and nutritional support, to not only help us function daily, but also support our longevity. Synaptiv™ is a cutting-edge, bi-layered tablet that provides nutritional support to your brain & neurons, both immediately, to combat stress and boost function and extended to support long-term memory function and optimal neural function….http://bit.ly/1TuO6si Turn your dreams into reality....Join us in the crusade to take back your health and your Freedom! Message Me or Visit: http://bit.ly/WGP1uJ http://bit.ly/1v3EzPi Call Me at 1(774)322-1690 For more information! Subscribe to my Youtube channel: http://bit.ly/1yqARxp Follow Me on TWITTER - http://bit.ly/1LEFzC4 Friend Me on FACEBOOK - http://on.fb.me/18pBC2b G+: http://bit.ly/1LNb8tm Dr. Joel Wallach's Books: http://amzn.to/1lCtpzq Disclaimer: These statements have not been reviewed or approved by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.
Просмотров: 4003 M Medeiros
Chondrocalcinosis - Medical Definition
 
00:46
https://word2speech.com/medical/ Chondrocalcinosis Chondrocalcinosis: Calcium deposition in cartilage. Chondrocalcinosis can be associated with degenerative arthritis, pseudogout, hemochromatosis, hyperparathyroidism, diabetes, hypomagnesemia, and Wilson's disease. How to pronounce, definition of, audio dictionary, medical dictionary
Просмотров: 57 Medical Dictionary
Amyloidosis - causes, symptoms, diagnosis, treatment, pathology
 
11:41
What is amyloidosis? Amyloidosis is caused by misfolded amyloid fibrils deposits which can be systemic, in multiple organ systems, like the kidney, the heart, and intestines, or localized to the brain in Alzheimer’s disease or the pancreas in diabetes mellitus type II. Find more videos at http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.
Просмотров: 86469 Osmosis
Part 1 of 8 AM630 CHED Radio Interview February 8 2010.mp4
 
09:56
"The Inside Story" talk show host Michelle Boden interviews Rayne, a hemochromatosis patient, as she receives a phlebotomy.
Просмотров: 198 Canadian Hemochromatosis Society
OFF GRID LIFE FOR REAL! COULD YOU SURVIVE?
 
07:15
PRE SCHEDULED VIDEO Taped before Starry Became sick ***PLEASE READ these articles will show you the acuteness of this infection ** To dubunk any rumors this bacteria was obtained by eating raw carrots. She did not drink any bad water. She carries water filters with her and takes her own water when in the woods. She did not eat any pork, she is mostly vegetarian and eats 100% raw in the summer. Mario also ate the raw carrots and has had some GI issues to. BOAT HOUSE CARROTS ORGANIC..wash all raw food in hydrogen peroxide THIS VIDEO HAS BEEN PRE SCHEDULED FROM EARLIER THIS SUMMER. STARRY IS VERY ILL. SHE HAS CONTRACTED A VERY SERIOUS AND RARE BACTERIAL INFECTION CALLED yersinia enterocolitica toxin SHE HAS BEEN EXPERIENCING SOME VERY SERIOUS COMPLICATIONS. HER LIVER IS ENGORGED, HER INFERIOR VENA CAVA WHICH IS THE LARGE VEIN OF THE HEART IS ALSO ENGORGED, SHE IS VERY ILL AS IF ALSO HAS MOVED INTO HER JOINTS AND CAUSED A REACTIVE ARTHRITIS SHE IS BEING TREATED BY A OUTSTANDING GROUP OF MEDICAL PROFESSIONALS WHO LOVE HER VERY MUCH HER FAITH THAT GOD IS IN CONTROL AND WILL ACCORDING TO HIS TIME AND PURPOSE HEAL HER IS SUSTAINING HER. SHE IS ASKING FOR PRAYERS GO FUND has now been setup by Starrys sister. Click here to help if you feel compelled..otherwise prayers are gold https://www.gofundme.com/help-starry-hilder ALL CARDS A ND LETTERS PLEASE SEND TO STARRY HILDER PO BOX 1812 BONNERS FERRY ID 83805 Help by playing her videos all day long! PLEASE CANNOT ANSWER ALL THE COMMENTS BUT SHE IS READING THEM.SHE APPRECIATE AND LOVES ALL THE SUPPORT Prayers are needed Yersinia enterocolitica infection with multiple liver abscesses uncovering a primary hemochromatosis. Höpfner M1, Nitsche R, Rohr A, Harms D, Schubert S, Fölsch UR. Author information Abstract A 60-year-old man, although treated with antibiotics, suffered from a severe pyrexial illness of unknown origin, weight loss and intermittent abdominal pain. There was no history of diarrhea or common infections. Computed tomography and ultrasound imaging showed uncharacteristic multiple small lesions of the entire liver parenchyma. These lesions were histologically pyogenic abscesses. In addition, an unexpected, pronounced accumulation of iron pigment in hepatocytes and second degree fibrotic changes of the liver were detected. Serum iron and serum transferrin were low, but serum ferritin concentration and transferrin saturation were increased to the maximum. The demonstration of the cysteine-282-tyrosine mutation confirmed underlying primary hemochromatosis. Bacteriological cultures of the abscess material yielded Yersinia enterocolitica serotype O:3, while stool and blood cultures were negative. Antibiotic therapy with piperacillin/tazobactam and tobramycin was successful within a few days. A repeat CT scan and ultrasound imaging demonstrated complete regression of the pathologic liver morphology. The patient was discharged and treated with an orally administered fluoroquinolone for an additional 6 months. After this time the patient had no morphological residues of the infection except one enlarged lymph node near the portal vein but still was so weak that he was unable to work again. In conclusion, severe septic forms of yersiniosis are mainly found in patients with iron overload, due to a handicapped iron metabolism of the Yersinia bacteria. *******Mortality is high despite treatment. Abstract During the period 1974-1983, Yersinia enterocolitica infection was diagnosed in 458 hospitalized patients by antibody response or isolation of the micro-organism. A total of 54 (11.9%) patients had acute liver infection, with significantly elevated serum levels (greater than or equal to 2-fold) of bilirubin and/or enzyme levels. Serious liver disease with cellular necrosis was observed in biopsy specimens from two of 12 patients examined; six had unspecific changes. The patients were followed up for 4-14 years (until 1987). A total of 22 (4.9%) patients were readmitted with chronic liver disease; in one case non-specific microscopic changes developed into granulomatous hepatitis over a period of 3 years. In both the acute and chronic stages of disease, liver involvement was associated with involvement of other organ systems, and some patients developed multi-organ disease. Chronic liver disease was associated with positive tests for antinuclear antibody and rheumatoid factor, and with a high mortality. Subscribe: https://goo.gl/HXBZpA Follow me on: PATREON! SEE more of STARRY for 7 cents a day!!! https://www.patreon.com/user/posts?u=6750493 Website: http://www.starryhilder.com/ Facebook: https://www.facebook.com/starryhilder/ Starrys Food Blog http://www.starryhilder.com/fresh-healthy-recipes
Просмотров: 9435 Starry Hilder