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  • A profile pic of Rashmi framed in teal and white representing colours of Scleroderma with the logo PatientsEngage
    Not Giving Up Helps Me Cope With Scleroderma
    Rashmi Bhasin,48 suffers from a rare autoimmune condition called Scleroderma, as well as a host of other issues. It hasn’t been easy for her, but she doesn’t like ‘giving up’, which keeps her going through difficult times. Who is Rashmi, the person Rashmi as a person is very outgoing, loves travelling, meeting people, loves baking and cooking, is a movie buff and loves online shopping. Ready to do anything for anyone. Loves children. Loves animals. Please tell us a bit about your condition…
  • Make Lupus Visible To Improve Awareness and Access To Healthcare
    On World Lupus Day, we ask Lupus patient advocates about their experience in Lupus management and what they think of the theme this year which focusses on "Let's make Lupus visible"   Vachasamrita 1.  What has been the last year like in terms of challenges in handling Lupus? I have been living with 8 years of Lupus, but since mine is a case of juvenile Lupus, it’s been aggressive with rare reactions and drug intolerances. Last year has been more about about handling the…
  • Battling Alone With An Invisible Chronic Illness Is Very Hard
    Annie Verghese, 53 has been fighting Sjogren’s Syndrome for 10 years now, along with a host of other issues. She talks about her difficult health journey, being a patient and a caregiver and the effect of her health on her life. EARLY HISTORY I was diagnosed with Sjogren's Syndrome in 2012, when I was around 43 years old. Around the same time I developed diabetes and also had high BP problems which led to a mini heart problem. After undergoing angiography, I was cleared with 'no problems'. As a…
  • Battling The Odds For A Better Life With Sjogrens
    Devika Phukan, currently a professor in Guwahati, not only battled Sjogren’s but also the trauma caused due to lack of understanding of her condition by medical practitioners (in far flung areas) and the social taboos and ostracization by loved ones. This article has been contributed by Sjogren’s India to highlight the need for early diagnosis and awareness among the medical community. “More than the physical harm from the disease, it was the emotional damage that was debilitating … the…
  • Courage And A Positive Attitude Help Fight Back Ankylosing Spondylitis
    Ramesh B. Choudhari, 64 from Nagpur was not only afflicted with Ankylosing Spondylitis from a young age, but was diagnosed very late which led to fusion of his joints and consequent surgeries. But that did not stop him from working, and leading a normal life to the best of his abilities. Please tell us a bit about your condition I have been suffering from Ankylosing Spondylitis (AS) since 1972 ( my age was 14 yrs then) , but I was only correctly diagnosed in as late as 1997. I have had multiple…
  • I Work My Way Around Fatigue and Pain Due To Ankylosing Spondylitis And Fibromyalgia
    Prachee Bhosle, 42, who was diagnosed with ankylosing spondylitis and fibromyalgia, two painful rheumatic disorders, shelved her career plans and chose to become a patient leader to raise awareness and advocate for better care and support. She is currently President of Ankylosing Spondylitis Welfare Society.  Please tell us a little bit about yourself, your background? I am a parent to 2 kids, a 14-year-old girl and a 10-year-old boy. Both my kids are homeschooled by me since 2017. After…
  • Profile pic of the author Shambhavi in a red dress framed in a blue and lavender background with a butterfly on the top left corner
    "I am okay if Lupus is in the body, I am just not okay if it is in the head"
    Shambhavi Chaudhary is a gutsy young lady living with Lupus who decided that life is too beautiful to allow a condition, however debilitating, to take control of her. Accordingly, she started pursuing a normal and active routine and also went vocal on social media to inspire her fellow Lupies. Is Lupus considered a rare condition? Or an autoimmune condition difficult to diagnose? Lupus, interestingly, is not a rare condition. According to the Lupus Foundation of America 1.5 million…
  • Upcoming Webinar: Lupus and Women's Health
    Knowing more about Lupus helps you make better informed choices and manage it well. Don't miss out on the webinar series on managing the various aspects of living with Lupus   Lupus is an autoimmune disease in which the immune system attacks its own tissues, causing widespread inflammation and tissue damage in the affected organs. It can affect the joints, skin, brain, lungs, kidneys, and blood vessels. With the support of Biocon Biologics, we bring a series of webinars with…
  • Living With A Rare Autoimmune Disorder
    Nishat Fatima, 28 from Hyderabad, India was diagnosed with ITP, Immune thrombocytopenic purpura, a rare autoimmune disorder that can lead to excessive bruising and bleeding. She shares her journey through diagnosis and the challenges of living with this condition and how it changed her from being an active and jolly person.  Initial symptoms In 2016, just a couple of days after my wedding, I was down with vomiting and dizziness. On one visit, my brother remarked that I looked yellow. The…
  • Upcoming Webinar: Impact of Rheumatic Diseases on Women
    This is Rheumatic Diseases Awareness Month. PatientsEngage brings together a panel of rheumatologists and patient leaders to talk about how rheumatic diseases affect women, the unique challenges women face and how their needs can be better addressed. Are women affected by rheumatic diseases more often than men? How do these differences play out? Especially for lesser known rheumatic conditions. We bring together a panel of doctors and patient leaders to discuss this issue and also suggest the…
This is an autoimmune disease. Please add this also.
I have a auto immune disease known as Phemphegus vulgaris
Scientists have successfully treated a patient with disfiguring sarcoidosis, a chronic disease that can affect multiple organs, with tofacitinib. a drug approved for rheumatoid arthritis. Sarcoidosis is an inflammatory…
Research shows that Iron deficiency, measured through the size variation of red blood cells, is correlated with increased fatigue in systemic lupus erythematosus (SLE) patients,. The association seems to be independent of age, ethnicity,…
Chandra Mohan, a Houston based Indian origin professor and his colleagues have received a private grant of USD 600,000 for their brilliant and pathbreaking research to develop a new…
what meds are good I'm looking into armour cause the synthetic ones don't do anything for me? also stem cell trails in the us, do anyone knows any?
diet for health
arthritis friendly kitchen ebook download
Hello Friends I am Pankaj Sethi Co-Founder of Y.T.A (Youth Thalassemic Alliance), I would like to Thanks to the team of Patient Engage to support us and give this platform, where we can be connected globally with all patients, parents, doctors and…
There is an increase in diagnosis of auto immune conditions in India -  Rheumatoid arthritis, Ankylosing spondylitis, Lupus, Thyroiditis (Hashimoto’s disease), Inflammatory bowel disease There was an article in…
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