Please don't get the bashing stick after me. I guess I just need to vent. So how much progress have we made since the first case of ALS was diagnosed? Let's see Lou died in 1941. He lasted 2 years post onset. Wow what progress we have made. Seems all the other illnesses have made advancements...
We have a long history of ALS in our family, dating back at least 4 generations (losses include my mother, grandfather, great grandfather, and many distant relatives). I was surprised to know that my family didn't have much documentation or research to pass along to me when I was diagnosed. My...
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One year ago, I noticed fasciculations in my calves, which then spread throughout my body! My legs would cramp up, I felt like I was getting weaker, would constantly search for atrophy, my anexity went through the roof, people close to me thought I was having a breakdown! I seen a bunch of...
15 weeks ago has noticed I slurred a few times. This when was I talking a word here and there. then again a few weeks later-not anymore that I recall . No one has mentioned it to me.
Then 10-11 weeks ago I began to have stiffness arms and calves.
It went away in a few weeks. I have felt off...
I know someone whose family is affected by FALS. They have a running team that raises money for ALS Research and are running a half this weekend in my father's memory. I keep wondering how I can I make a difference/feel like I'm doing something positive myself.
My running skills are really bad...
Well this week is big for me and my cals. We have been actors& dancers our whole lives so far and have no intentions of stopping just because of a little old " nightmare" .
We will be in tech& dress rehearsal all week for an up coming show called "Chally's Follies" at our theatre house. My...
wow, how awkward to make final arrangements for a spouse. Talk about the last thing I wanted to do in life. He is adamant that his body go to science, ALS research like his mother and grandfather before him. Dr. Pioro at the Cleveland Clinic took charge of his mother and now my husband. These...
I heard a shorter version of this in an interview with him a couple of years ago. This is more detailed. It is shared here with his permission
My name is Rick Bedlack. In the past decade I have seen more than 1500 patients here at Duke with ALS. Tonight I will tell you about one who left a...
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Greetings all you wise people, experienced people. I really don't know what to say, so long story short: My father was a victim of ALS and pass away in 2009.
I am a freelancer in IT as an Active Directory Consultant, or was until the morning of the 4th of August this year.
I had noticed that I...
Hi all,
My name is Olly and I lost my Dad to MND/ALS a few years ago. He was diagnosed when I was 7 and died when I was 14 so much of my childhood/teenage years was spent caring for him before then dealing with the bereavement.
I am now carrying out a PhD/doctoral study to investigate a way of...