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Bullous pemphigoid, a rare autoimmune skin disorder, primarily affecting older adults, characterized by large, fluid-filled blisters on flexural areas like the lower abdomen and thighs. Symptoms include intense itching and red or darkened skin around the blisters. It is caused by the immune system attacking the skin's basement membrane. 🔬 Diagnosis involves a skin biopsy and immunofluorescence tests. Treatment typically includes corticosteroids, immunosuppressants, and sometimes antibiotics. With appropriate management, the condition can be controlled, though it may require long-term treatment. 🌐 For more information or to get any kind of assistance regarding Autoimmune Blistering Diseases, visit our website www.aibdf.in. #aibdf #autoimmuneblisteringdisases #blisters #autoimmuneawareness #autoimmunediseasewarrior #autoimmunediseases #autoimmunediseaseawareness #autoimmunedisorder #friction #autoimmunefighter #blister #healthawareness #autoimmunedisorders #autoimmunewarriors #autoimmunecondition #raredisease #autoimmunewellness #autoimmunehealing #autoimmunedisease #health

World Hepatitis Day, observed on 28 July, raises awareness of viral hepatitis, an inflammation of the liver that causes severe liver disease and cancer. The theme for the year 2024 is: 𝐈𝐭'𝐬 𝐓𝐢𝐦𝐞 𝐟𝐨𝐫 𝐀𝐜𝐭𝐢𝐨𝐧, With a person dying every 30 seconds from a hepatitis-related illness, we must accelerate action on better prevention, diagnosis, and treatment to save lives and improve health outcomes. #WorldHepatitisDay #WHD #HepatitisCantWait #hepatitis #hepcantwait [Current Affairs, Important Days, General Knowledge, Facts, July 2024]

Today is Rare Disease Day which raises awareness about rare diseases and their impact. While epilepsy is common, there are types of epilepsy that are rare. Learn about Rare Disease Day at www.rarediseaseday.org and about epilepsy at www.bcepilepsy.com -- #rarediseaseday #rarediseases #raredisease #epilepsyawarenessmonth #purplemonth #purpleday #epilepsy #seizures #seizure #seizuredisorder #epilepsyawareness #epilepsyeducation #epilepsywarrior #epilepsylife #epilepsystrong #epilepsypositivity #epilepsyadvocate #endepilepsy #acceptepilepsy #epilepsycommunity #bcepilepsysociety #iamavoiceforepilepsyawareness

Guillain-Barré Syndrome (GBS) and Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) are rare disorders of the peripheral nerves that can often lead to paralysis. The aim of GBS|CIDP Awareness Month is to provide education and to advocate for better treatment and prevention options for these diseases. Find out how we help IV patients with GBS and CIDP at https://lnkd.in/e_Amvf5K. #GBSCIDPAwareness

Dystrophic #calcinosis is a frequently observed manifestation of systemic #sclerosis (18 to 49 % of the patients) that may result in #disability, and is associated with complications such as ulceration, infection, severe pain, and compression associated-outcomes. Ischemia, repeated trauma, and mechanical stress are considered as contributing factors for development of calcinosis, but also longer disease duration, older age, anti-centromere, anti-PM/Scl, and anti-RNA polymerase III antibody positivity, and a late capillaroscopic pattern. 🔗https://lnkd.in/dmQ6AEbf

Has your autoimmune disease led to a disability❓ The severity and manifestations of autoimmune diseases, such as severe fatigue, are crucial for determining NDIS eligibility. Conditions like severe rheumatoid arthritis can significantly challenge one's independence by affecting mobility and impacting fine motor skills, such as those needed for walking and using hands effectively. 👋 👣 Autoimmune disorders like lupus and multiple sclerosis may also qualify for NDIS support if they severely impact your everyday life. The NDIS assesses how these symptoms affect daily activities and work capability to determine the appropriate level of support.✅ May is Rheumatoid Arthritis Month. Explore the mobility tech options funded by the NDIS on our website!🔗 #invisibledisability #autoimmune #invisibleillness #autoimmunewarrior #hashimoto #autoimmunedisease

World Thyroid Day! This day is dedicated to promoting awareness and understanding of thyroid health and the advances made in treating thyroid diseases. It’s an essential reminder of the significant impact thyroid health has on our overall well-being. By focusing on education, early detection, and patient support, we can ensure a healthy life for all, particularly pregnant women, children, and senior citizens who are more vulnerable to thyroid disease risk factors and thyroid dysfunction. Let’s continue to raise awareness about thyroid health! 🦋🌟 #hypothyroidism #thyroid #hypothyroid #thyroidproblems #thyroidcancer #thyroiddisease #thyroidhealing #thyroidhealth #hashimotosthyroiditis #hypothyroidismweightloss #hyperthyroidism #thyroidwarrior #thyroidectomy #thyroidcancersurvivor #underactivethyroid #thyroidawareness #thyroidissues #hypothyroidmom #thyroidweightloss

Understanding MPGN Type II: A Rare KIDNEY Disease! OUTLINE: 00:00:00 A Rare Kidney Condition 00:01:00 What is MPGN Type II? 00:02:07 Diagnosing MPGN Type II 00:02:38 Recognizing the Signs 00:03:27 Understanding the Numbers 00:04:01 Living with MPGN Type II 00:04:36 A Message of Hope Kidneys are the unsung heroes of our bodies, silently filtering waste products and keeping our blood clean. But what happens when those filters malfunction? Membranoproliferative Glomerulonephritis type II (MPGN type II) is a rare autoimmune disease that throws a wrench into this vital process. Imagine your kidneys as intricate sieves, the glomeruli acting as tiny filters that remove toxins from your blood. In MPGN type II, the immune system gets confused and mistakenly attacks these filters, causing inflammation and scarring. This damage disrupts the delicate filtering process, leading to protein leaking into the urine and potentially waste products building up in the blood. While MPGN type II can affect people of all ages, it seems to have a particular fondness for young adults. The symptoms can be subtle at first, like fatigue, foamy urine, or high blood pressure. That's why early detection is crucial! Left untreated, MPGN type II can progress to kidney failure. The good news? Increased awareness can help identify cases earlier. Sharing this information can empower others to advocate for their health and seek timely diagnosis. Remember, even though MPGN type II is rare, knowledge is power. Let's keep the conversation going and empower the rare disease community! #MPGN #MembranoproliferativeGlomerulonephritis #RareKidneyDisease #AutoimmuneDisease #YoungAdults #KidneyHealth #KidneyFilters #EarlyDetection #StayInformed #ShareForAwareness #InvisibleIllness #ChronicIllness #MedicalMystery #ResearchNeeded #BeYourOwnHealthAdvocate #Strength #RareDiseaseCommunity #KidneyChampions

As a Certified Child Life Specialist, one of my favorite things is using visuals to help children understand their illness. The more they know in terms they can grasp, the more empowered they feel. In honor of Sickle Cell Awareness Month, here’s a quick video for parents and medical professionals. It features a child-friendly activity to explain sickle cell disease, along with some of my go-to coping strategies that have helped kids during pain crises. #childlifeteaching #sicklecelldisease #sicklecellawareness https://lnkd.in/gVP2q2tm

Take a listen as @NimGoldMD discusses the importance of collaboration, and the unique role of the neonatologist, in caring for neonates with Congenital Heart Disease.