Joy Khakasa Lwangu
Chronically Rare
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Chronically Rare – Health, Wellness and Awareness
Chronically Rare – Health, Wellness and Awareness
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E-shop
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Nation Newspaper Story 1
Nation Newspaper Story 1
Interview with SPSRF 2021
Vimeo
Interview with SPSRF 2021
Without SPS awareness in the medical community in Kenya, a lack of access to reliable insurance, and her own reluctance early on to undergo multiple tests, Joy Lwangu’s SPS went undiagnosed for almost 15 years. As a result, she lost her voice and her ability to walk.
Nation Follow Up
Nation Follow Up
WhatsApp Catalogue
WhatsApp Catalogue
Instagram
Instagram
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PayPal
Mchanga Fundraiser
Mchanga Fundraiser
Together, we can make it happen. Please donate and share the current Joy SPS Fund Every contribution brings us closer. Thank you for standing with Joy!
Stiff Person Syndrome Research Foundation
Stiff Person Syndrome Research Foundation
Learn About Stiff Person Syndrome
Learn About Stiff Person Syndrome
Learn about Stiff Person Syndrome, including symptoms, causes, and treatments. If you or a loved one is affected by this condition, visit NORD to find
Syringomyelia Fact Sheet | National Institute of Neurological Disorders and Stroke
Syringomyelia Fact Sheet | National Institute of Neurological Disorders and Stroke
Syringomyelia is a neurological disorder in which a fluid-filled cyst (syrinx) forms within the spinal cord. The syrinx can get big enough to damage the spinal cord and compress and injure the nerve fibers that carry information to and from the brain to the body.
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