oleblue
Status:
Mood:
Ok
Offline
- How many suffer from these? I have been having a few bad days with them. This morning had a bad one and tossed my coffee, I have been getting them in my hand and it happens at the wrist where my hand just jerks inwards, the painful ones where my...
- Nor sure if this is part of being secondary or not, On my left foot the 2 toes next to the big one and a patch around them on my foot has had not feeling and my neuro said he was sure that that was permanate, now on my right foot the 2 toes and a...
- I was wondering if when you move to a progressive like secondary is that where it stops because you are progressive? Or do you change to PPMS over time? Or is it still anyones guess? Sorry about all the questions and I'm sure I will have more.Dave
- Any thoughts on this test, I think it is the blood test that has been discussed latelyhttp://www.glycominds.com/Products.asp?medical=1190
- My neuro prescribed me Ambien to help me sleep because since my steroid infusion I can't seem to be able to sleep. A couple of night ago I went to bed at 1:30am and the next thing I knew I was standing outside in my driveway at 4:30am. I woke...
- What has helped with SPMS, as in diet, exercise, meds to control this miserable disease. Is there any one thing you do that makes the difference in making this tolerabe? one thing that if you change you will notice the difference
- How many years did it take to become SPMS or were you DX'd out of the gait with SPMS, and if you were how many years do you think you had some form of MS before the DX?
- I was surprised to read that the people with SPMS can still have relapse's and I wonder why it is that with relapse's they change the name to SPMS,So how many still have relapse's even if they are very small?
- I was just wondering what other people thought was the worst MS symptom to have. Personally I have to go with the fatigue as this seems to drag me down the most. Anyways just curious, so throw what you think is the worst MS symptom as I'm sure they...
- Today I went to see my neuro for my 6 month check and because of a Flare last week and he told me I was Secondary. He sure knows how to ruin a guys day. I guess I wish I knew more about MS before I went to see him as I just assumed that I was RRMS....
- Well I got through day one of steroids and it went good. I was worried about having a fever but that did'nt get in the way. I'm getting relief in my eyes, double vision and all my joints are'nt hurting as bad. The side effects are'nt to bad. A...
- I'm putting up a link to my facebook page with the pic's of the bon fire wwe had Saturday, a small group of just over 50 people came. Enjoy the pic's, hopefully the link takes you right to the pic's and my profile is public so no one has to friend...
- My neuro called and even things seem a bit less he wants IV steroids to clear up any flare as I was not symptom free today, never had that before and I can almost feel my blood pressure climb any adviceDave
- Just looking for some input and here is the place for that. Today I woke up with a horrible headache, started last night. I've had double vision for 2 days now that is not of the normal come and go type. My eyes are hurting really bad the pain is...
- Just a quick question, if I pop the disk with my MRI on it in my computer will I be able to see the pictures the MRI took as well as the lesions? Probally a beginners question but inquiring mind wants to know.Thanks a lotDave