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Lupus ForumsGeneral & SupportVibration sensation in legs/Neuropathy?/Lupus?
11/04/2009 02:16 PM
Mommyof1
Mommyof1
 
Posts: 238
Member

So I have recently noticed intermittently I get this really light vibrating sensation in my legs and I think its my cell phone vibrating but when I check my cell its not. Does anyone get this sensation? Can it be from peripheral neuropathy and/or Lupus? -Brittanee
*LadyBug*- Epilepsy Dx: 2003 & UCTD w/SLE features Dx: 2009 SLE/Lupus Dx: May 12th 2011--Current Meds:
Plaquenil- 200mg 2x/day
Hydrocortisone- 10mg/am & 10mg/4pm
Methotrexate- 2.5mg 4pills 1x/week
Keppra- 750mg 2x/day
Daily Vitamin- 1x/day
Folic Acid- 1mg 2x/day
Protonix- 40mg 1x/day
Bentyl- 10mg 4x/day
Miralax- 17g 1x/day
Vit. D- 800IU's 1x/day
Lyrica- 75mg 1x/day
Flonase- 50mcg 2 sprays each 1x/day

Wanna know my story, just ask!

*Lord_Walters_Lady*
Reply

11/04/2009 02:20 PM  Top
Looopie
Posts: 1867
Senior Member

Vibration, pins & needles, burning, shooting pain = impaired sense of touch + pain receptors. Perhaps a peripheral neuropathic problem?

Marie

Post edited by: Looopie, at: 11/04/2009 02:43 PM


11/04/2009 04:24 PM  Top
goojman
goojman
 
Posts: 92
Member

I get the vibrations But i call it a cat purring in the bottom of my back all the time. My nurologist said it is from the nurapothy (SP?) My suggestion is to talk to your md, Nurologist or reumy whomever it may be. My nurologist is the one who dx me. There are several types of it. I was told it is linked to the lupus but also people with Fibro can have it too...

Previous discussions I participated in:
Head rash...
pains in my feet!

11/04/2009 06:06 PM  Top
heidiclouser
 
Posts: 1036
Member

Your doc might refer you to a neurologist for an EMG. I had the test and the treatment was a higher dose of cymbalta. I felt better overnight.

11/05/2009 07:28 AM  Top
lisanaylor2007
lisanaylor2007
 
Posts: 423
Member
I'm an Advocate

I have noticed when my legs get like that. I have rubbed my legs. I also take a hot bath with epsom salt. It seems to help a little. Of course most of the meds help alot.
Keep fighting. Fighting back is sometimes harder than being diagnosed. Each day is a new challenge. But you can over come what ever you put your mind to.

11/11/2009 10:35 AM  Top
Mommyof1
Mommyof1
 
Posts: 238
Member

I just got my skin biopsied on my left leg in 3 places monday for the small nerve fiber peripheral neuropathy. I will have the results in a few weeks but the woman who did the testing said my symptoms are typical of that type of neuropathy so I really think its whats going on. Im on neurontin 300mg once a day but its not helping a whole lot.
*LadyBug*- Epilepsy Dx: 2003 & UCTD w/SLE features Dx: 2009 SLE/Lupus Dx: May 12th 2011--Current Meds:
Plaquenil- 200mg 2x/day
Hydrocortisone- 10mg/am & 10mg/4pm
Methotrexate- 2.5mg 4pills 1x/week
Keppra- 750mg 2x/day
Daily Vitamin- 1x/day
Folic Acid- 1mg 2x/day
Protonix- 40mg 1x/day
Bentyl- 10mg 4x/day
Miralax- 17g 1x/day
Vit. D- 800IU's 1x/day
Lyrica- 75mg 1x/day
Flonase- 50mcg 2 sprays each 1x/day

Wanna know my story, just ask!

*Lord_Walters_Lady*

11/11/2009 11:09 AM  Top
Looopie
Posts: 1867
Senior Member

Hi Brittney. I am sorry to hear you are unwell. It's always a relief when we actually have a diagnosis so that we could receive proper treatment for our problem.

Neurontin 300mg/day is just a starting dose, and your doctor will increase until you have relief from the neuropathic pain. It takes more than a month for Neurontin to work as I have remembered when taking it. If you have new symptoms whilst taking Neurontin, then you should let your rheumatologist know so she could distinguish whether the symptoms are from lupus or side-effects from medications.

I hope you will feel better soon.

Marie Smile

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