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This charts a cycle over a weekend from London to Glasgow to raise money for the A-T Society. 33 hours of cycling ending in hypothermia !nnAction for A-T has recently been established to help children with the condition Ataxia-Telangiectasia (A-T). A-T is a rare neurodegenerative and progressive disease which starts in early childhood causing severe disability and premature death. There is no cure for the disease and nothing that can halt its progression. Babies are born ‘normal’ and then sl
⏲ 3 min 72 sec ✓ 09-Jun-2012
Immunology Animations for Medical Students Education - Complete Lectures on sqadia.comn▶️ https://www.sqadia.com/categories/sqanimationsnn----Description-------------------------------------------nnKnowing is half of the battle!nnAlthough Ataxia telangiectasia can neither be treated nor it has a specific therapy for the neurological problems associated with this disease. But knowing about this diseases can be helpful in many ways!nnAtaxia TelangiectasianAtaxia Telangiectasia (A-T) is an
⏲ 1 min 66 sec ✓ 22-May-2021
CACNA1A Awareness Day is celebrated on March 19th. This video highlights members of our community who are suffering from CACNA1A genetic mutations. Variants on the gene cause many neurological issues, including epilepsy, balance and coordination issues (ataxia), hemiplegic migraines, which are stroke-like episodes, intellectual disability, autism and cerebellar atrophy. The CACNA1A Foundation's mission is to find specific treatment options and a cure for CACNA1A patients by building a collaborat
⏲ 1 min 13 sec ✓ 19-Mar-2022
At age two, most kids are running around and playing, attending
⏲ 2 min 87 sec ✓ 07-May-2021
I am from DisABLED In Action. I suffer from SpinoCerebellar Ataxia, a rare neurological movement disorder which is progressive, and has no cure. One of the symptoms is imbalance while walking. This symptom is especially frustrating when eating dinner by yourself, and trying not to spill anything. I have used this inexpensive gadget (get it here:https://vimeo.com/320531652) many times, and have managed to retain my ReelAbility.
⏲ 25 sec ✓ 28-Feb-2019
This was one of my favorite videos to shoot and edit. We filmed FARA ambassador Kyle Bryant and meeting up with USF Health 's neurologist Dr. Theresa Zesiewicz to promote the Fara-USF Health Scientific Symposium. This is more than an event. It’s a gathering, a milestone and a symbol of hope for the community of patients and families living with Friedreich’s Ataxia.
⏲ 1 min 82 sec ✓ 07-Jul-2018
CycleAtaxia is a charity Cycle to raise funds to research a cure for Fredrich's Ataxia nAll info at http://www.cycleataxia.iennDirected by Anthony Downesn2nd Camera: Alan Rogers
⏲ 2 min 36 sec ✓ 08-Jun-2016
When she was 12, Kate was diagnosed with Friedreich’s ataxia — a rare, progressive neurogenetic condition that affects 4,000 individuals in the U.S. and 15,000 individuals worldwide. She’s now a third-year University of Arkansas student studying supply chain management and marketing, while also working toward a cure for FA as a marketing intern for the Friedreich’s Ataxia Research Alliance and the founder of a nonprofit, Make It Happen CureFA. Learn about Kate’s rare journey in her My
⏲ 1 min 80 sec ✓ 27-Mar-2024
Dushyant Verma Shillong - Ataxia is a neurological disorder that affects the body’s ability to coordinate movement. It can cause difficulty in walking, standing, and speaking. It can also affect the eyes and other parts of the body. The severity of ataxia varies from person to person and is usually caused by damage to the cerebellum or spinal cord. While there is no cure for ataxia, there are treatments that can help manage symptoms and improve quality of life. In this blog dushyant verma sout
⏲ 45 sec ✓ 15-Apr-2023
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