I hear you Twink. I am on the absolute minimum for me. I tend to try them and if they don't benefit me I stop them. I take four for MS related symptoms but there have been many more from time to time because with the nature of MS the symptoms can come and go. It's important to evaluate our condition and if we're able, to get off the meds that no longer help.

Well done Twinkletoes - I hope that this continues to work out really well for you.

Kitty, good luck with your surgery - you won't know yourself when it is all over and done with - you will probably wonder why the heck you waited so long - I know I did.

Cheers

Lyn

Some benefit from meds, alas I didn't. In the beginning I tried Rebif, Novantrone and ADs (to help increase endorphins.) Besides making me be sick or feel sick nothing helped. So I just take Amantadine (learned I go from dead to half dead and that is an improvement). With Vesicare in AM and Oxybutin before bed(anti-pee meds) ,I sleep all night until 5 AM and have to pee, can get out of house for awhile. If I get a neuro - pain, I sometimes take Vicodin.

kicker, glad you reminded me about Amantadine's slight energy benefit -- I thought maybe I was nuts.

In Feb. a doc in TX at an urgent care facility and I disagreed about why another doc had originally Rxd Amantadine.

I tried to tell the TX doc that I thought it was to help with fatigue. He actually went to the trouble of printing out an info sheet about the drug to prove I was mistaken. I've wondered about it ever since!

Twink,
All my neuros have been MS neuro - some University of Maryland MS Center, Some Johns Hopkins. My current is running Cliniocal trial on
Fingolimod for PPMS. A past JH neuro guy, another MS Clinical trial. Every doctor has their own way. One put me on ADs and never followed up. My current poo-poos trying LDN but put me on bird poison (sorry, they call it ? and went from $31 to have generic compounded to Big Pharma's $1500.00 a month drug.(Fampridine?)

My current neuro and I agree, he can do nothing right now for PPMS me and MRIs are a waste of time right now. He treats symptoms and/or problems as they arise. He answers all e-mails within hours and I never abuse the privilege. Maybe that's as good as it gets.

Thanks for posting what's going on, Twink...and everyone else.

I feel like a medicine chest sometimes, I take so much...I can't go off my muscle relaxant, it barely works as it is...thyroid, I'd die (literally) if I quit it...bladder meds-I've cut out this occasionally since my Rx is expired and I'm running out and don't want to see the bladder guy...he wants to do more surgery and I don't wanna...

I occasionally get tired of daily injections of Copaxone...I have a 3 month oversupply in the refrigerator.

As for statins, if I go off, the numbers skyrocket...the others are vitamins/cranberry etc. I know for sure the B12 helped my numbers climb to normal...

And new meds for RLS and emotional overreacting...the new RLS med is really nipping the movement in the bud, but as for the emotional stuff...cry cry cry...I'm thinking of going off of it, even though I don't cry when I can't find my car any more

Pharmas make a bundle off of me!!

Maybe it's too early to tell.......Ive only been off the LDN two days .......
but my legs seem better. They don't move around at night and I seem to be walking better first thing rather than having to wait till my legs "kick in" to be able to walk. We'll see how this next week goes. I go in tomorrow for my surgery and hope to be at home tomorrow afternoon. I've stopped taking everything except the Prozac, Levothyroxine (thyroid) and Lisinopril (HBP). I won't take anything tomorrow until I get home. If I still feel good after the surgery - and without the LDN - I might just give it a break and see how it goes. My pocketbook will like that!