Okay, I'll join in.
I did Avonex for a year. I had terrible flu-like symptoms that lasted longer than the MS doctor could explain. Each week I took it on Friday night and because I worked 40+ hours.

But on the weekend I was like a zombie. I had chills and fever, aches and pains until almost time for the next shot. We tried everything (dr) to pre-medicate, even one prednisone before and after each shot. Nada!

He always tested my blood every three months. My Liver enzymes went rather high and with the flu not leaving, he switched me to Copaxone, said no interferons for me.

I was having relapses 3 to 4 times a year on Avonex, getting residual damage. It did nothing for me, maybe made me worse.

On the Copaxone the shot was easy, and worked okay since I had no side effects. Then after 3 years I had terrible site reactions for 6 months. I also had a infection get passed the Copaxone surveillance system, and got really sick and almost septic. High temp. and allergic reaction. SS Pharma, did say they changed the ingredients in the "C" about that time. Hmm

I went to about 6 different doctors to clear the infection even though I stopped the "C".

I thought it helped after the first 6 months on it, but the MRI's showed enhancement in the brain and a new brainstem lesion while on the "C".

Perhaps one at C-2 or it might have been artifact on the MRI, that artifact showed up two more times, so it might be a lesion, not a ghost shot.

I went off all DMD's in late 2004-5, and in 2007 weaned off Neurontin. I still was having two attacks a year that were from heck.

I felt so much better taking control of my body and not doing any more drugs except Klonopin for my tremors and HRT since I was neutered young.

I was offered Ty, but said no. I wanted to clear out my system of drugs. By 2008 I was ready and decided to try LDN. I am very happy with it and have seen many improvements.

I still have the MS hug with more use of my arm, back muscles by about dinner times.

The burning feet, legs, still is bad, but I won't take anything for it, because I tried and lots of meds and nothing works for that for me. I deal with it.

Funny you can get used to pain, if you just try to ignore it. It is there hours two hours or less. LDN I think helps with pain because it lessens the pain, or it may be the higher endorphins blocking the pain, I don't know.

My fatigue is a big issue and I hate to nap, but that works for me. No med has helped that either. I plan to get the CCSVI sometime in the future, before I get too old for them to do it. I believe it plays a big part in my problems.

When exhausted, I get cog-fog, and I may limp and have my left foot swing out. Not foot drop just lack of energy when I do too much. Then all my issues haunt me until I nap right away.

That's when I feel so darn tired I could fall on my face. The nap helps recoup my energy. But then I go to bed late and sleep late, which I don't care for, oh well. Life is what it is.