Hi. I am 37 to make who has developed a lot of twitching and muscle pain in the past few months. I herniated a disc in my lower back last December, so I have had lots of sciatic pain/leg and foot numbness and tingling from that.
I developed severe anxiety and started having panic attacks this...
I am going to share with you my father's current symptoms. I am a bit worried about him and would like to know your opinions
My dad was diagnosed with Parkinson's disease and treated with levodopa for 3 months. Since the drug was not very effective, they did a neural imagining test and...
Hello everyone. I have been recently been diagnosed with ALS through a second opinion. Obviously things are very confusing right now and have yet to set in. I am still extremely hopeful that this is a misdiagnosis and will be seeking a third opinion. A little history about my journey to this...
Guys, I've been reading a TON of articles about how so many people have been misdiagnosed with ALS but actually had Lyme Disease! Does anyone have any experience with this? Does anyone in Ontario know where to get tested for it properly? Apparently 50% of people bitten by a tick don't even...
Hi new to the forum my husband has been diagnosed with mnd and its been a confusing sad frustrating time we are to return to the neuro brain mind centre in two weeks for the formal diagnosis. I would like to ask ; my husbsnds symptoms stated 12months ago in right hand weak grip very limited use...
I've been putting off posting this as long as I could, just holding on to any hope of a misdiagnosis but after my third clinic visit yesterday, it's time to completely accept the fact that I have ALS. I've been lurking on the forums since my original post on DIHALS in May when I first heard...
Hello. My partner was diagnosed about three weeks ago. He went to Social Security to inquire about disability (for the future, not yet). They told him that benefits will cease if it turns out to be a misdiagnosis, which is sometimes the case. I doubt they see many people diagnosed with ALS. Yet...
I have a strong familial link on my mothers side to ALS/MND where several people have passed away from the disease.
My Aunt(mothers sister) has recently passed away from Parkinsons (apparently)
However,I suspect that this was a misdiagnosis as the disease from start to finish only lasted 2 years...
My name is Joe. Firstly, I would like to say that my heart and all of my love goes out to you all. The strength that it takes to be apart of any disease, especially this one, is beyond all measure!
Hmm I don't really know where to begin. I suppose I will start from the top of my...
Do you have Bulbar/ALS or Cervical Spondlyotic Myelopathy?
Dear Bulbar ALS patients, friends and family. The most helpful thing you can do is purchase a saliva pump machine like dentists have for under $100 for the person suffering from bulbar ALS. My mom used her saliva machine very frequently...
stem cell research