The Zanaflex does not make me sleepy in fact I can't sleep at night after taking it. I guess we are different.
Alex
Hi Alex-
HUGS, HUGS, & MORE HUGS TO YOU!!! I am so glad you are getting some help w/your pain, Dear.
Please keep us posted about you and keep looking UP!
Dee
Isn't it always an interesting trip to these people in the white coats....
makes you wish you could be a fly on the wall when they are in med
school to see what they are REALLY telling them and who is sleeping thru class......
Glad you're getting some pain relief anyway!
I know you must be relieved that the pain clinic appointment went better than you expected. I'm relieved for you too.
They are putting you on zanaflex 4 times a day? Wow, how do you stay awake, and more importantly, on your feet? Are you taking it for muscle spasms or spacicity?
I am taking it only at night because if I take it during the day it wipes me out and takes the spascicity away, something I need to be able to walk. I hope you are not having that affect.
I hope this PA was educated on MS especially PPMS. Hang in there lady and hope you make to your riding this week.
Hugs,
Julie
Yup, that makes perfect sense.
I have a coworker who had terrible headaches - he was treated with botox, which really helped. It did make his forehead rather cro-magnon like!
It sounds like you have found a good one, Hvac. The phone misunderstanding I guess can happen with a busy doctor.
The only thing I do know about PPMS is that it isn't relieved by the use of steroids. I have one brain lesion that they are not even sure if it is MS related but many on my spine and brain stem. I have Progressive Relapsing MS. Guess it is the neuro's call to give the type. None of the progressive types are easy for us. I feel for you, as I understand you cannot be treated with a DMD that stops the progression. That would be a hard blow to handle.
I am glad that at least you are receiving relief from your pain.
Sumana