
Certain genetic disorders can remain dormant in a person ‘s life till they present with a lethal manifestations. Diagnosis such diseases can be challenging due to lack of awareness. One such story is that of Ketan Goyal. . Ketan , a 21 year old, young B.tech student sudden weakness of right half of the body while at college.
The Vasculitis Society of India was founded with a clear and compelling purpose: to make a meaningful difference in the lives of individuals affected by vasculitis across India. Our journey began with a shared commitment to raise awareness, provide support, and advance research on this rare autoimmune disease that often goes undiagnosed and misunderstood. We are driven by the courage and resilience of patients, caregivers, and healthcare professionals who face the challenges of vasculitis every day. Our motivation stems from a deep desire to create a supportive and empowered community where individuals with vasculitis can find hope, understanding, and resources to live full and productive lives. We believe that by coming together, sharing our stories, and advocating for better care and treatments, we can make a significant impact and foster a brighter future for everyone affected by vasculitis in India. Join us in our mission to raise awareness, provide support, and advocate for change. Together, we can make a difference and inspire hope for a better tomorrow for those living with vasculitis
Our mission is to enhance the quality of life for people with vasculitis by promoting awareness, facilitating education, and fostering research initiatives.
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