I may be wrong, but I was told by my neuro that they don't advise Solu-Medrol treatment for parathesias per se. During last months relapse I was actually falling because I had very little feeling in my feet and couldn't feel anything on the left side of my face.
Can you ask your doctor if this is true? Maybe he has a different oppinion about when to treat and that would be good for us all to know. No two doctors think alike as most of us have come to learn.
I hope your appointment goes well tomorrow and you doctor gets you back on track whatever treatment you both decide on.
Julie
Thanks Ladies,
I called the Neuro first thing this morn. I am going in tomorrow at 215. It is so amazing that I found a neuro that will do that for me. My original appt was the 18th of this month.
He was very quick to put me on the sol u med the first time.
Are there questions I can ask about alternatives first?
to shell:
No prob for the questions. It helps me think about the right things.
I have been taking Baclofen since my first symptoms and recently switched to zanaflex. It did help more at first but the neuro upped me from 2mg to 4 mg 3x a day. Until this last 2 weeks, it was helping. I think the max dose is 6mg 3x a day. I would hate to hit that mark though.
I did have to do a ton of walking in the hospital which attributed to my spasticity in my hip. I just wish it would subside. I am having new parasthesia now too and that is the part that has me thinking this is a flare up.
Well I am gonna chat with neuro tomorrow and pray that this is just a little stress. I did notice that taking a xanax helped my hip pain hhhmmmm??
Love you all
D
You have certainly had a couple of full plates this past month. I hope August will be kinder to you and your family.
When was the last time you saw or spoke with your neuro? Since it looks like you have made it through the weekend ok, then you might want to give his/her office a call tomorrow and talk with the nurse and see if you need to treat this. They know how to ask the right questions to see if what is happening is a bonafide flare or a pseudoflare.
I know you don't want to be on the IVSM, who does especially when you just had a treatment recently. See what you doctor has to say first.
Please let us know how you are doing.
Hugs,
Julie
Hey D,
Nice to see you. My, my this IS all so very stressful. It's totally understandable to hate the solumed.
Only thing I can think of is this - if it's not an attack, and just an uprising of symptoms (which you can have - due to these recent events and the bronchitis) you could very well simmer without going full blown (where you'd know it for sure), and have to get the treatment to control it.
Maybe the spasticity can be controlled with a med too. I'm on baclofen.
When do you go next week? How's the Rebif treating you?
(sorry for all the questions)
ttys,
shell