I am a "Great Lakes" girl. Raised in London ON. I was single until I was 38 when I met a wonderful man who happens to have a Spinocerebellar Ataxia. This was not something I had ever heard of

Edto Group SDN Berhad emphasizes the acquisition of the world's fifth largest tower company by 2021. The company wants to complete at least two big acquisitions in this period. A collaborative organization

SORUCE UK Pilot Study to Evaluate Effects of Stem Cell Therapy in Friedreich’s Ataxia Patients **Klinik yararları kök hücre tedavisi Friedreich ataksisi hastaları olacak değerlendirildi küçük bir pilot

Arkadaşlar merhaba, ben Friedreich Ataksisi (FA) hastasıyım nörolojik bir hastalık denge kaybı, reflekslerde yavaşlama, konuşma bozukluğu, el ve kol dengesizliği oluyor. zamanla ilerleyen bir hastalık

"El modo de transmisión de la SCA7 es de tipo autosómico dominante. Esto quiere decir que es una enfermedad genética heredada y que la persona que la padece recibió el gen anormal de uno de los padres.

En sí misma, la ataxia no es una enfermedad sino más bien un síntoma que acompaña a un grupo de enfermedades heterogéneas y que puede ser adquirida o congénita, afectando en particular a una región del

Imagine usted que se encuentra ebrio y tiene problemas para poder caminar y coordinar sus movimientos (ataxia), además de que su visión empieza a ser doble o borrosa y tiene problemas para articular las

I have AOA2, aka Ataxia with Ocular Motor Apraxia Type 2. It is an very rare disease, affecting about 1 in 900k worldwide. I will be participating in a fundraiser in September and humbly ask for your support.

I bet you've never heard of Ataxia, or more specifically AOA2. I am blessed (sarcasm)with this rare neurological disease. So vote me up and raise some Steem for a cure. Thanks