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    Financial support needed for PALS & family

    We can see that there are lots of local & international organizations which helps ALS/MND affected patients & families. Basically they focus on providing information about disease, suggesting you how to cope with life after ALS, complications in life after ALS etc. They conduct stress reducing...
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    Suspecting misdiagnosis after 10 years

    Hello Friends, I am Mahesh Thapa, 35, from Kathmandu, Nepal. I was diagnosed Motor Neuron Disease (ALS)on 2003. I have difficulty in walking, speaking (unclear & Nasal voice but I can communicate), gripping & having problems like: cramping, fasciculation on muscle & tongue. I can stand but need...
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