Kewanee
Active member
- Joined
- Jul 6, 2007
- Messages
- 35
- Reason
- CALS
- Country
- US
- State
- New England
- City
- Skowhegan
Work it's way towards your trunk? I've got non stop stomach abdominal and midriff spasms that won't quit unless I'm sleeping or maybe in certain positions.
I had an emg which the Doctor coldly barked at me was ALS. My reflexes were brisk.
Only my lower legs and lower arms showed increased activity of some sort. What ever they look for. He wouldn't listen to me about the years of other things I've been through with sensory neuropathy and stomach muscles that react to certain meds like pain killers and proton pump inhibitors, with spasms.
Or the fact that I have had parathesia's and cramping in my hands and feet for years and that years ago my torso pulled me into a fetal position a number of times upon wakening.
The MDA does not think it ALS but I was holding my own strengthwise. They had not received the emg report in it's entirety but for almost a year now no changes. I have dropped feet and unable to stand on toes or heels.
I did well until I got an attack of Polymyalgia Rheumatica and had to go on prednisone.
Then the weakness increased, although I'm still on my feet as much as I can be. Then the infused me with Reclast which means I must take calium.
Just wanted to know what you think.
I had an emg which the Doctor coldly barked at me was ALS. My reflexes were brisk.
Only my lower legs and lower arms showed increased activity of some sort. What ever they look for. He wouldn't listen to me about the years of other things I've been through with sensory neuropathy and stomach muscles that react to certain meds like pain killers and proton pump inhibitors, with spasms.
Or the fact that I have had parathesia's and cramping in my hands and feet for years and that years ago my torso pulled me into a fetal position a number of times upon wakening.
The MDA does not think it ALS but I was holding my own strengthwise. They had not received the emg report in it's entirety but for almost a year now no changes. I have dropped feet and unable to stand on toes or heels.
I did well until I got an attack of Polymyalgia Rheumatica and had to go on prednisone.
Then the weakness increased, although I'm still on my feet as much as I can be. Then the infused me with Reclast which means I must take calium.
Just wanted to know what you think.