I think your experience is the normal one :o)
Sorry you're dragging Tammy. During my one IVSM advnture i was the opposite. My GF was a little ascared a me :-)
You're so welcome, Tammy.
I did a quick search-no Entocort wouldn't help you. I get mixed up with my steroids. Too many auto-immune diseases.
Sheila
Thank you Sheila.
Hugs to you too! :)
Tammy
Hi, Tammy.
I feel terrible for you.
Oh, I take Entocort for Lymphcytic Colitis. I don't know if it would help you.
You are NOT whining. You're feeling miserable, and we are here for you.
You should read some of my posts from when I 1st joined in 2007.
And believe me, I still complain.
Just sleep-your body needs it.
(((HUGS)))
Sheila
Today, I am so exhausted I can barely keep my eyes open. Still, without the steroids, I would be stuck in my wheelchair.
Sheila, I have never heard if Entocort. I will ask my neuro about it on Friday. I wish my insurance covered Acthar gel.
Sorry, I just can't seem to stop whining...
Hi, Tammy.
I'm so glad that your symptoms are improving.
When I had the 3 day IVSM and the tapering down with oral prednisone, I had a lot of energy.
But, now I have been on Entocort, since mid-December for another medical issue, and I have found that I am feeling very fatigued.
I wonder if taking steroids long term makes the difference.
Sheila
It is definitely more common to be "revved up" on steroids, but I've experienced them like you--steroids wipe me out. I actually sleep really well while on the 3 day IV infusion. I don't take steroids for every new symptom but only for those that are really bothersome. As far as my MS symptoms go, the steroids work great for that. I always see an improvement. Maybe not a dramatic one, but an improvement nonetheless.
It's good that your symptoms are improving!