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» LymeNet Flash » Questions and Discussion » Medical Questions » botox for migraines

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Author Topic: botox for migraines
daffodil5924
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Member # 26207

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I was recently diagnosed with Lyme after being misdiagnosed for five years as having fibromyalgia/Chronic fatique Syndrome. I have debilitating migraines and recently saw a pain management dr who suggested botox for the migraines and headaches. I have a headache everyday and a migraine min. 3 times a week. Since I am new to Lyme, how it affects the body, what makes it worse/better, and have been treating for fibro for the last five years I have no idea if botox will exacerbate the Lyme. Has anyone ever had botox?? Is it safe for someone with Lyme??? Will it do more harm?? So far I am taking bactrim 800mg twice a day and had severe herx reaction. I have been treating for about a month. So far I have tested negative for co infections but I am waiting on a couple additional co infection results. Any information on botox and experiences would be greatly appreciated. I admire all of you on this site for your strength in fighting this disease....daffodil
Posts: 2 | From Toms River, New Jersey | Registered: May 2010  |  IP: Logged | Report this post to a Moderator
massman
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Drugs drugs drugs........

Seriously, any auto or other accidentsin the past ? There are other ways to treat migraines.

My ex averaged 14 per year. After we married I treated her for a month and she went to 1 per year.

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cactus
Frequent Contributor (1K+ posts)
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Odd. You are the second person to ask about botox in their very first post - in the last few days!

See this thread on cosmetic botox - I would say a lot of it applies:

http://flash.lymenet.org/ubb/ultimatebb.php/topic/1/95087

Also do a search on botox using the search function here.

Personally, with Lyme and co's... I would not consider injecting myself with a known neurotoxin.

I too suffer from migraines. Adequate Lyme and co-infection treatment has made a huge difference in their severity and frequency.

What does your LLMD (who is treating your Lyme, etc) say about the botox?

I would definitely explore other options first. Just my opinion.

--------------------
�Did you ever stop to think, and forget to start again?� - A.A. Milne

Posts: 1987 | From No. VA | Registered: May 2005  |  IP: Logged | Report this post to a Moderator
daffodil5924
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massman i had a car accident in 2001 and thaat is when my health started to decline...i havent been the same since. I just turned 34. I am going to call my LLMD tomorrow and see what he says
Posts: 2 | From Toms River, New Jersey | Registered: May 2010  |  IP: Logged | Report this post to a Moderator
JOLA
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My LD and ND said definitely NO to botox for

anyone with Lyme.

Posts: 146 | From Vancouver, BC | Registered: Dec 2009  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

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-
http://flash.lymenet.org/ubb/ultimatebb.php/topic/3/24039

Topic: Looking for long term pain management
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Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
massman
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daffodil you may want to try a practitioner that uses craniosacral therapy.

It is no force bodywork that concentrates on the skull and first neck bone. Some PTs, chiros, MTs excel in it.

No twisting or yanking. Google it.

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