I am feeling rather depressed today. My PT, Shannon, pointed out some truths to me about my "lack of compliance" with my exercise routine. She sees right through me. She's good. And she isn't even a specialist with MS! Still, she certainly hit on my buttons, in a very kindly way, as we discussed the ebbs and flows that is MS. Why am I not doing my home exercises? I don't know. Because I don't believe that they will keep me from getting worse, I guess. In my heart of hearts I feel it is inevitable - getting worse. I have seen it - too much of it - it will happen to me, too. And I guess I feel that there's not anything I can do that will change that. So, I don't bother. I started out with high hopes, and I was getting stronger. . . THEN, I got that damned sinus infection which pretty much put me back where I was. I guess I'm feeling, "What's the point?" Of course, I know that if I continue the way I have been - not doing much of ...
Hi Webster,
ReplyDeleteDid not know you could adapt the dosage of baclofen, thought it had to be a standard dose.
Hope you have a good day despite the bloody spasms.
Love,
Herrad
I gave you a bunch of hugs, cuz it sounded like you needed some. Smile, we all have those days. DAR!
ReplyDeleteHerrad, I first started taking baclofen back in 1982, six months after my diagnosis. I took 60 mg. daily which at that time was considered the max you could take. Now, after all these years of experience with using the drug for different ills that cause spasticity, the maximum dosage is 120 mg. I rarely take that much, but my Rx is written for 100 daily. And I take it as needed rather than maintaining a blood level with it. Ask your doctor about a better way to use baclofen to manage your spacticity, since it's such an issue for you.
ReplyDeleteStuey - THANKS for all the hugs. With readers like you I may make it to 1000 by the end of the year! WooHoo!!
Spasms are good for now, BTW.
Hi Webster,
ReplyDeletePlease go to my blog and pick up your award.
Love,
Herrad