This Is MS Multiple Sclerosis Community: Knowledge & Support

I have been very on off taking Avonex as of the side-effects which are hell if Im honest.

Not had one for 6 months and for some reason I decided I should really get back on it as it was my only hope.

Crashed spectacularly the next day, unable to walk and not been very mobile if at all, since. Gp said it is a relapse but coincidental that it happened the very night of the injection. Seems odd to me, felt ok and have been unable to straighten my back since as the pain is awful.

Not worked or done much for the last 5 days but starting to feel bit better.

spare me. glad you're starting to feel better now ww

thanks for your quick reply jimmylegs. from your reply am I right in thinking you dont think it a relapse.?

I have had relapses before but always 'knew' when they were coming. I have felt great for months and was good the day of the injection.

I always felt worse if I didn't take enough ibuprufen or paracetemol. I presume that you are taking these both before and after the injection? Having said that quite a few people seem to have quite bad reactions to the CRABS.

_________________
3 years antibiotics, 06/09 bilateral jug stents at C1, 05/11 ballooning of both jug valves, 07/12 stenting of renal vein, azygos & jug valve ballooning,

heya ww, i don't take pharma products but side effects are fact and i don't see why a doctor would blame a reaction on disease course when the dose and effect are so close in time.

I am not sure I believe in coincidences like that (especially if you had not had a relapse in a while) I think there is usually a cause and effect situation.

L

I am going with extreme reaction theory and hook or by crook I am going to try my hardest to get to work tom.

I aways take Ibruprofen 2hrs before and after but you may be right....this time I had none and took co-codamol.

Thank you all. GP thinks I should persevere with Avonex but I think I will quit it permanently now. It doesnt suit me and it never has.

Thank you all again for taking the time to write back.

Hi all again- still not returned to work and still not mobile. Had to have home-visit from GP and says I have Clonus which means my leg tremors when I put it to the floor making it very weak and it gives way.

Anyone know anything about this- I was told it is a waiting game and it will hopefully stop. I was doing ok until approx ten days ago and now its so different. I always resisted the idea of a wheelchair but I am going to get one in the next couple of days and stay in it whilst I feel like this. Trying to stand with my leg beating constantly on the floor is not working.

Any tips welcome for the clonus.

ww what are all the meds you are on, and what if anything do you take for a supplement regimen?

ww try lifting your foot and put your heel down first, mine does it in my chair but if i change the position of my foot on the rests it will stop.happens always when i change seats or get out of bed, more in my left leg than right.

_________________
Had ms for over 19 years now.

My husband had clonus in his left leg when he was diagnosed 2 years ago. He had IV solumedrol and it cleared up to 90% of prior function. He still gets spasms and pain in his calves, but is able to walk, bike ride, gets around pretty well.
How long have you had MS? Have you had clonus prior? Jimmylegs was asking about your nutritional/supplement routine. Do you have one?
Hang in there Westwood-
AC

_________________
Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
dual stents placed 5/09
CCSVI in MS

westwood -

Spatisity is my greatest nemisis with MS. Early on I had many instances of Colonus and at times I still do. Now my muscles stiffen. My leg muscles switch between hamstring dominant or quad dominant where my legs are fully extended and will not bend at the knee or the reverse where I cannot strainghten my legs. I also have the MS HUG where the diaphram and torso muscles are tightening.

I am diagonosed w/ PPMS. I stopped taking any the ABC drugs but I do take an anti-spasmatic. Baclophen is the prefered drug but it had no effect on me. Diazapam is a good drug but it can be addictive. I am using cyclobenzaprine a generic for Flexeril. There are about 10 drugs out here that are designed to reduced spastisity. You may want to discuss this w/ your Drs.

Peek a Boo

peek did u ever try magnesium for spasticity? might help a bit too

Hi Jimmylegs -

Yes and I have just started using the natural calm plus calcium supplement to help sleep reccommended from earlier threads. This product (natural calm plus) includes calcium, potassium, boron and D for better absorption.

sounds great! have you read about the ... less intended effects?