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» LymeNet Flash » Questions and Discussion » Medical Questions » Malarone Experiences?

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Author Topic: Malarone Experiences?
bears1985
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Does anyone have any malarone experiences and how well is it working?
Posts: 136 | From Arizona | Registered: Sep 2008  |  IP: Logged | Report this post to a Moderator
kreynolds
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I have to bump this up because I switched from Mepron to Malarone and would like to know as well...

--------------------
Diagnosed CDC + 6/2007

Quest: + IGG Bands 18,23,39,41,58,66 and 93.

Quest: + IGM Bands
23,39

Quest: + Bartonella (B.Henselea & B. Quintana),+ Babesia, and + Mycoplasma and Lyme-Induced Addisons Disease

+ Biofilm blood test 12/2010

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Geneal
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I've been on both mepron and malarone.

Malarone first for 4 months each time.

Then mepron for 9 months.

Now malarone again.

I herx on both.

I think overall I do better on malarone.

Two pills twice a day.

Hugs,

Geneal

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seekhelp
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I took Malarone for 3 months. First month 4 pills for 3 days. Month two I took 2 pills daily. Month three 1 pill daily.

Nothing notable on it. No major side effects. It was no miracle, but my LLMD had weak dosing. Never took ART either. I believe it was very inadequate treatment overall for Babesia.

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bears1985
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Has anyone had any success trying Artesunate?
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VB
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I took 2 malarone pills 2x a day for about 5-6 months. I didn't notice any side effects or major herxing from it.

I didn't really think it was doing much for me, but now that I've been off of it for a while I think it may have been and I just didn't realize it.

I do know that while I was on it, my CD57 improved consistently (from upper 20's to 60's). And now, it has declined again.

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Abxnomore
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I don't believe Artesunate is approved in the U.S. and I think it has to be given with another anti- malarial drug, such as mepron.

I have never tried it.

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buckfever
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I was on malarone for a total of 9 months. worked up to 6 pills a day.I never really herxed on it and I wondered if it was working , but it really did do me alot of good as my babs symtoms have been dramatically reduced .

I was also taking bactrum and at the end flagyl. Wish I could have stayed on all for longer but ran out of money. Malorone is expensive ,$650 a month with insurance paying 1/2.

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btmb03
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Artensunate - it's one of the treatments Dr. Paul Cheney, CFS specialist outlined in his recent talk and I think he mentioned it helped pts.

I don't know where patients got it from and neither have I started babs tx so I'm afraid I cannot comment on Malarone.

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Marcie
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I took 1 malarone a day, which is a very low dose. I was on it for almost a year. At first

I had major herxes, but after time they got better. My llmd never increase my dose, so I am

sure I still have babesia, because 1 day is not enough to get rid of it. I do feel that overall it really helped me.

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CherylSue
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Any more postitive malarone experiences?


I've been on one a day for 2 weeks and increased to 2 per day a few days ago. Herxing big time? or is it Lyme acting up?

[ 07-30-2009, 06:01 PM: Message edited by: CherylSue ]

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