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» LymeNet Flash » Questions and Discussion » Medical Questions » muscle twitches

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Author Topic: muscle twitches
Stephanie
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To anyone who has widespread muscle twitches (fasiculations) due to LD or Mycoplasma fermentens...is there anyone who has had the twitches completely go away? If so, what AB's did you take and how long until the twitching stopped? Thanks!!
Posts: 62 | From NY | Registered: Jul 2004  |  IP: Logged | Report this post to a Moderator
achey
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My muscle twitching is signifigantly decreasing after 7 wks of iv zith.

I still have some backsiding with herxing, but there is a signifigantly comfortable change.

Since this is a symptom that I have had for way to many years...30 yrs un-dxed..I am glad for the change


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Beverly
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Hi Stephanie,

My muscle twitching is also getting better. I used to have it all the time now it gets bad for a few days and then clears up for a few days. Hang in there, I hope it gets better for you too.


Posts: 6641 | From Michigan | Registered: Jun 2001  |  IP: Logged | Report this post to a Moderator
klcst
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Stephanie-

I head up a support group and it has been my experience those that are on oral abx for 2-3 years instead of IV do better. IV should only be used for the most severe cases initially and then when symptoms get better they should switch to orals. I know of several cases including my own where this is the case. A few of the Lyme patients are ahead of me in their treatment and they have hit the symptom free level. I must tell you that most do not turn the corner, where they feel well most of the time until the 18 month mark.
All of these patients are taking 100mg of Doxy BID for a month or two, and then they start taking Biaxin 500mg BID (do not take XL, which is time released)along with the Doxy. The Doxy works on the Lyme in the bloodstream and the Biaxin works deeper in tissues and can penetrate the brain barrier.

Hang in ther, Stephanie. When you finally reach the point where the twitches get better or go away completely you won't believe how different you feel. It is very tiring and debilitating to have those. Mine were so bad that weekly the muscles would twitch to the point that I would have a huge lump which was a huge spasm and it would cut my blood vessels so bad that they would burst from the pressure of the spasm. It was very painful and the bruses were huge. Of course Cleveland Clinic was convinced my husband was beating me. WHat a bunch of idiots.

Lisa


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klcst
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Stephanie-

I forgot to tell you, you have to be treated for any coinfections first before you get treatment for Lyme. I hope your doctor checked for these.

Lisa


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BJG
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Hi
I too have twitching.
I believe Magnesium reduced them.

Rifampon has been the only antibiotic that I know helped the twitching and burning.

Good luck
BJG


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cindy_leigh
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Thse came on with my first herx, then gradually faded away. When they come back, it's an early warning for me that i need to go back on abx. They are usually followed by other sx, such as the numbness and "vibrating" feeling in different areas, headaches, fatigue, etc. I use magnesium, and when the twitches come back, I add more. I usually take mag with my vits and supps in the morning, but add a nighttime dose, with more calcium, and a B-complex vit, at bed time.
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lymelady
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Hi Stephanie,
After a month of mepron and clindy/artesminin, my muscle twitches finally stopped. Had lots of them in early days of taking meds. Stomach vibrations were the worst, plus arm and leg. Only symptom that so far has responded to meds. Also a tickling feeling in my abdomen, which I have had for two years, also went away.

Has your lab work ever turned up babs? I know you took mepron but could this be a lingering babs symptom. I still have it because I am still herxing on artesminin, but something has kicked it I think to some degree.

Let's talk soon. After months of ignoring my holistic doc, I ordered and am reading Lab 271, which I thought would be BS, but it is well researched and fascinating. Amazon for around $5 amd well worth the read.

Regards,
Frances

[This message has been edited by lymelady (edited 06 January 2005).]


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Mathias
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Has your doctor started you on a Fluoroquinolone antibiotic yet?

You need one on board to get rid of m. fermentans.

Clindamycin and Telithromycin are also effective against it.

It is resistant to Biaxin and Zithromax.


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Stephanie
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I am still waiting for the Babesia results and am still on Biaxin/Penicilin. I will see my dr on mon to possibly change the Biaxin. Matthias-have you been re-tested to see if you still have Mycoplasma? Is it a reliable test? Thank you all for your responses!!!
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WildCondor
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Magnesium is VERY important for muscle twitching. Make sure you are taking Mag Tab SR daily and if needed, magnesium shots. It helps the twitching. Make sure you are also on a good quality multi vitamin.

------------------
Lyme Disease Help
http://www.wildcondor.com


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Mathias
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I have not been retested yet. The mycoplasma was only found in my spinal fluid so it would require another spinal tap. The plan is for me to have another one in the next 2-3 months to check levels.

PCR tests are extremely (virtually 100%) reliable.

I still have symptoms so I'm sure it has not been completely eradicated yet. Mycoplasma is difficult to get rid of. I'm in my 5th month of antibiotics specifically for this strain of mycoplasma and I still have symptoms, including muscle twitches.

Taking Biaxin for mycoplasma fermentans is a waste of time. The MIC is 64 ug/mL. It could even be making it more resistant to other antibiotics. For comparison, Levaquin and Cipro have MIC's of 0.125 ug/mL.

[This message has been edited by Mathias (edited 06 January 2005).]


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