advertisement
Reply
 
Thread Tools Display Modes
Old 05-16-2013, 09:52 AM #11
wingsscrub wingsscrub is offline
Junior Member
 
Join Date: Apr 2013
Location: metro Detroit
Posts: 43
10 yr Member
wingsscrub wingsscrub is offline
Junior Member
 
Join Date: Apr 2013
Location: metro Detroit
Posts: 43
10 yr Member
Default

Quote:
Originally Posted by Lynn View Post
Hello

I can't answer the question about the itching, but I am taking Topamax - mostly for nerve pain, and also to help me with getting scrambled neural messages to go to the right places (especially in my legs which like to shake and give out, causing me to fall).

Yes, I do get some tingling especially in my face, and some on my left side. It doesn't really bother me too much though, and has pretty much disappeared after I had been taking the drug for a few months. It still happens occasionally, but not badly.

Regards
I posted about topamax in the migraine/headache forum and another member mention that her neuro told her to eat kiwi for the tingling. It's super high in potassium and had ought to help. I took her advice (as I'm keen on the fruit) and it does seem to make a difference.

I haven't been on it long, but I'm...sceptical. I'll let you all know how it goes when it's been a few months.
wingsscrub is offline   Reply With QuoteReply With Quote

advertisement
Old 05-16-2013, 11:38 PM #12
Lynn's Avatar
Lynn Lynn is offline
Member
 
Join Date: Sep 2006
Location: Australia
Posts: 660
15 yr Member
Lynn Lynn is offline
Member
Lynn's Avatar
 
Join Date: Sep 2006
Location: Australia
Posts: 660
15 yr Member
Default

This is super interesting - I have recently tried Fampridine, and because of the tingling, dizziness (and a whole stack of other things too) had to stop. I later read that it is a potassium channel blocker. Seems to be a common thread with this symptom.

Thanks for the heads up

Cheers

Lyn
__________________
Lyn
.



Multiple Sclerosis Dx 2001 Craniotomy to clip brain aneurysm 2004. ITP 1993.
Lynn is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
SallyC (05-17-2013)
Old 05-17-2013, 10:56 AM #13
SallyC's Avatar
SallyC SallyC is offline
In Remembrance
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
SallyC SallyC is offline
In Remembrance
SallyC's Avatar
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
Default

My Neuro always gave me prescription potassium (vita K, I think?),
when giving me steroids, because she said it causes loss of
potassium. No other Neuro ever thought that was necessary, but,
that 1st time, was the only time, the steroid infusion worked for me.
Now I wonder if that was the reason. hmmmmm?
__________________
~Love, Sally
.





"The best way out is always through". Robert Frost



~If The World Didn't Suck, We Would All Fall Off~
SallyC is offline   Reply With QuoteReply With Quote
Old 05-17-2013, 03:59 PM #14
wingsscrub wingsscrub is offline
Junior Member
 
Join Date: Apr 2013
Location: metro Detroit
Posts: 43
10 yr Member
wingsscrub wingsscrub is offline
Junior Member
 
Join Date: Apr 2013
Location: metro Detroit
Posts: 43
10 yr Member
Default

Quote:
Originally Posted by SallyC View Post
My Neuro always gave me prescription potassium (vita K, I think?),
when giving me steroids, because she said it causes loss of
potassium. No other Neuro ever thought that was necessary, but,
that 1st time, was the only time, the steroid infusion worked for me.
Now I wonder if that was the reason. hmmmmm?
I find that when my tingling gets really bad, and mind you, I've only been on this Topamax for a week, eating a kiwi helps for a day or so. I've tried taking a K supplement, but the one I have only gives you 3% of your daily value and I'm thinking I need a whole lot more to overcome my symptoms.

All in all, kind of annoying. But if this helps in the long run, I'll take it.
wingsscrub is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
SallyC (05-17-2013)
Old 05-17-2013, 05:42 PM #15
SallyC's Avatar
SallyC SallyC is offline
In Remembrance
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
SallyC SallyC is offline
In Remembrance
SallyC's Avatar
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
Default

Bananas are also high in potassium.
__________________
~Love, Sally
.





"The best way out is always through". Robert Frost



~If The World Didn't Suck, We Would All Fall Off~
SallyC is offline   Reply With QuoteReply With Quote
Old 05-18-2013, 09:58 AM #16
new2net98's Avatar
new2net98 new2net98 is offline
Member
 
Join Date: Jan 2012
Location: Yooperland...somehow we all live in peace up here.
Posts: 171
10 yr Member
new2net98 new2net98 is offline
Member
new2net98's Avatar
 
Join Date: Jan 2012
Location: Yooperland...somehow we all live in peace up here.
Posts: 171
10 yr Member
Default

Quote:
Originally Posted by wingsscrub View Post
I hope you don't mind me posting here--I haven't been diagnosed with MS, but my symptoms are most like it.

Anyway--

For the itching-is it potentially all the time? (or most of it) Is there anything I can use besides benedryl? It's exhausting.

And the tremor-is it mostly an intention tremor? Or something else?

Thanks for the help. I might not know what's wrong with me, but I find this reassuring.
OMG...another person with this (not that I'm happy for you, lol)...my advice, keep your fingernails short. Other than that, you need to figure out what your triggers are. Mine started with tingling/itchiness around left side of face, ear, across left cheek bone & my nose & on left shoulder blade. It has eased somewhat, after trying Neurontin (I couldn't continue with it-I have weird reactions to some meds-genetic).

As for the tremor...does it happen all the time or just when you hold something? When leaning against something? They are positional tremors if so. Always good to check with a doctor on this kind of thing.

I hope you find either a med that helps or some natural rememdy. Keep at it & good luck!
__________________
It isn't a quest; it's the unknown reaction to the unaswered question. If you don't ask it, you'll never know. The journey, needs answers.
.
new2net98 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
wingsscrub (05-18-2013)
Old 05-18-2013, 04:06 PM #17
wingsscrub wingsscrub is offline
Junior Member
 
Join Date: Apr 2013
Location: metro Detroit
Posts: 43
10 yr Member
wingsscrub wingsscrub is offline
Junior Member
 
Join Date: Apr 2013
Location: metro Detroit
Posts: 43
10 yr Member
Default

Quote:
Originally Posted by new2net98 View Post
OMG...another person with this (not that I'm happy for you, lol)...my advice, keep your fingernails short. Other than that, you need to figure out what your triggers are. Mine started with tingling/itchiness around left side of face, ear, across left cheek bone & my nose & on left shoulder blade. It has eased somewhat, after trying Neurontin (I couldn't continue with it-I have weird reactions to some meds-genetic).

As for the tremor...does it happen all the time or just when you hold something? When leaning against something? They are positional tremors if so. Always good to check with a doctor on this kind of thing.

I hope you find either a med that helps or some natural rememdy. Keep at it & good luck!
My tremor is definitely an intention, but can also be positional/resting if I'm tired or done too much or whatever.

The itching is on my trunk a lot-especially the bottom of my shoulder blades on my back, right where I can barely reach. Just enough to drive me nuts.

The itching has either lessened in the past few days or I'm getting used to it. Either way, I can sleep through the night with just one dose of Benadryl, so I can't complain. The BF doesn't mind though-he hates to see me this uncomfortable (I try not to pout, but I def freaked out the other night).
wingsscrub is offline   Reply With QuoteReply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
A newly diagnosed friend - questions Suzanne13 Myasthenia Gravis 4 01-09-2013 11:42 PM
New not diagnosed but have questions mindyandy420 Trigeminal Neuralgia 1 11-20-2011 06:55 PM
Newly diagnosed, questions IVIG? susie54 Peripheral Neuropathy 4 08-09-2008 10:54 AM
Just diagnosed, have questions (of course) MorningBroken Fibromyalgia and Chronic Fatigue 2 04-25-2008 03:34 AM
Daughter just diagnosed. I have questions. Jessie Gluten Sensitivity / Celiac Disease 8 01-29-2007 11:38 AM


All times are GMT -5. The time now is 12:08 PM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.