This is topic muscle cramping / Lyme titre still high 5 yrs. post diagnosis in forum Seeking a Doctor at LymeNet Flash.


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Posted by Dee Dee (Member # 35108) on :
 
I had a lyme titre recently 6 yrs. post initial diagnosis. For the 6 months, I've been experiencing painful muscle cramping mostly in my lower extremities. The spasms/cramping/charlie horses (whatever you want to call them) come on mostly when I'm at rest.

I am beginning to wonder if the cramping is a manifestation of LD.

Has anyone experienced these symptoms?

I see a rheumatologist who wants to put me on Lyrica which I emphatically say NO! I haven't been able to find anyone knowledgeable LD physician in Rhode Island. I'm looking to find a LD physician in Boston. I have been given a diagnosis of Fibromyalgia by the way.
 
Posted by Robin123 (Member # 9197) on :
 
Hi - it would be best if you could repost this with a heading about looking for LLMD in Boston.

Then you can also post in Medical Questions for a medical discussion and folks will respond there.
 
Posted by Nancy2 (Member # 95) on :
 
PM Sent!
 
Posted by LymeGoAway (Member # 25041) on :
 
Hi Dee Dee,

Sorry to hear that you're going through this.

I had some pretty bad cramping and spasms in my legs before I was treated for Lyme initially. It definitely is a symptom of Lyme.

Until you can get into see an LLMD, you might want to try supplementing with magnesium. That can help a lot with muscle cramps, spasms and charlie horses.

I take the Mag-Tabs recommended by Dr. Burrascano, but others here have had success with other brands--if you search "magnesium" you'll find lots of information on it.

Try to avoid the magnesium oxide that is most commonly found in stores--it is not absorbed by the body very well.
 
Posted by Ann-OH (Member # 2020) on :
 
Another help for me is a small glass of tonic water with dinner. It has quinine and I haven't had leg cramps in a very long time since drinking it. Magnesium and potassium are good helps as well. And I take those, but quinine did the trick for me.

Of course, if you are on meds, no gin!

There is a diet version, too.

Ann - OH
 
Posted by TF (Member # 14183) on :
 
Fibromyalgia is generally lyme disease if it is more than a very mild case.
 
Posted by LaurenMiddleTN (Member # 35174) on :
 
Hi Dee Dee,
I had spasms too; arms, legs, fingers, feet, and head. Hot showers before bed and a heated matress pad on my bed seemed to help. I was treated with cymbalta for 2 months while we waited on my testing for lyme. Cymbalta had no effect; first 2 series of test neg., requested a Western Blot test I head about from my aunt,,, after 14 months I finally got my Positive Test result. Since my antibiotics have been in my system 5 weeks now, spasms/cramps have subsided by 80%. Hang in there.
 
Posted by Lymetoo (Member # 743) on :
 
Moving to Medical Questions.

DeeDee.. let us know if you need more names of doctors.
 


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