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» LymeNet Flash » Questions and Discussion » Medical Questions » Cumanda (sp?)

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Author Topic: Cumanda (sp?)
kam
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I was on the full Cowden PRotocol. I found that I had trouble with Cumanda. I would feel so bad I was not able to do simple things.

I have tried backing off and only taking a few drops of it.

Just wondering if others have had this problem and what they did.

Wondering if I can still use it or not and how to keep functioning.

Posts: 15927 | From Became too sick to work or do household chores in 2001. | Registered: Dec 2002  |  IP: Logged | Report this post to a Moderator
JudyEric
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My son had to back off Cumanda and start out with 1/4th of one drop for about a week and then increase it in quarter drop increments for months. He eventually got up to 20 drops 2X/day. He had the same experience with Samento.

--Judy

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kam
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tHANKS JUDY. I had not considered going that low. I will try that.

I had heard I might need to do so with samento but all went well with it.

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SForsgren
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It is the most powerful one in my experience and though I was able to do the full dose, it really made my symptoms flare as it seemed to cause a die-off reaction. It is a great product in my experience. Starting lower makes sense.

--------------------
Be well,
Scott

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beths
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What does cumanda hit-does it affect bart at all?
Posts: 1276 | From maryland | Registered: Jan 2009  |  IP: Logged | Report this post to a Moderator
kam
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Thanks Scott.

Good question Beth.

I know it does not help with bart as my lyme doc said the company is working at coming up with a product to help with bart.

it must be killing off something in me as the recommended dose puts me back in lala land and bedridden full time plus feeling lousy...even more than usual.

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disturbedme
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Cumanda was probably also the hardest for me of the Cowden herbs. The other herbs didn't really do anything at all for me... or at least nothing herx-wise, etc. Cumanda though gave me bad vertigo.

--------------------
One can never consent to creep when one feels an impulse to soar.
~ Helen Keller

My Lyme Story

Posts: 2965 | From Land of Confusion (bitten in KS, moved to PA, now living in MD) | Registered: Jun 2007  |  IP: Logged | Report this post to a Moderator
   

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