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» LymeNet Flash » Questions and Discussion » Medical Questions » cold hands

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Author Topic: cold hands
hezzer926
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why are my feet and hands so unbelievably cold all the time? (even if the rest of my body is warm)-- i have lyme,bart,babesia
Posts: 245 | From East Brunswick, NJ | Registered: Oct 2008  |  IP: Logged | Report this post to a Moderator
SForsgren
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I'd start looking at:

Hypothyroidism
Not enough salt in the diet

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

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carly
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Same thing here.

I suspect with treatment this symptom will ease up significantly.

I have lyme, erhlichia, babs, (bart?)

Thyroid normal. Salt intake normal.

Posts: 797 | From New York | Registered: Feb 2008  |  IP: Logged | Report this post to a Moderator
randibear
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i have this too, especially my feet. it got a lot better when i started walking a mile a day.

i still have cold spots all over my body tho. i stay like an iceberg.

--------------------
do not look back when the only course is forward

Posts: 12262 | From texas | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
Cold Feet
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Folks, this comes up a lot -- just search for cold hands or cold feet -- you'll find my replies too.

Since I have gotten better on the MP, and cleaned the bugs out of my blood, my excellent circulation has returned. Perhaps blood viscosity has a lot to do with it too -- think about the Hemex fibrinogen test, INR, etc.

--------------------
My biofilm film: www.whyamistillsick.com
2004 Mycoplasma Pneumonia
2006 Positive after 2 years of hell
2006-08 Marshall Protocol. Killed many bug species
2009 - Beating candida, doing better
Lahey Clinic in Mass: what a racquet!

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migs
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Are you on Flagyl?

Mine cleared up both times I went off Flagyl.

Posts: 410 | From Victoria BC, Canada | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
hezzer926
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not on flagyl... im on omnicef,zithromax,rifampin,malarone, and fluconazole
Posts: 245 | From East Brunswick, NJ | Registered: Oct 2008  |  IP: Logged | Report this post to a Moderator
bettyg
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me too; gives new meaning to being frigid!

then my cpap blows cold air on my face all night even though i get up 3-4 times a night to microwave the water for 3 minutes that lasts 10-15 min. only.

i'm on thyroid pills, and i get adequate salt with meals and my POPCORN! [Smile]

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map1131
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I too experienced with for years. I was hypothyroid prior to getting ill. All tests kept coming back as med levels good.

Finally I started Cymbalta for depression and guess what happened? Not only did it help depression but I also warmed up finally.

No longer had cold feet & hands. The medical people couldn't explain why to me, so I did my research.

Sure enough cymbalta contains serotonine, which happens to be something the body needs to regulate the body temperature. like a thermostat. So somebody(bad guys) must of consumed all my serotonine.

A few months ago I decided my Cymbalta wasn't working. I weened myself off of it easily. It only took two weeks for me to realize Cymbalta was working for me.

I'm back on it and made some new decisions such as, taking 2-30mg a day, instead of 60mg at one time. I thought this might help spread the serotonine around.

I certainly wouldn't advise anyone to take Cymbalta if not needed for depression. But there must be other ways of gettting serotonine in the body to regulate body temp.

Pam

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"Never, never, never, never, never give up" Winston Churchill

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hatsnscarfs
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My hands and feet were cold all the time while I was really sick with Lyme, I never went out without gloves. Even in summer my hands and feet would turn yellow and frozen.

After several years of antibiotics the problem went away. I am amazed that I can now go out in the cold for a few minutes without gloves and warm up quickly and easily.

For me it was a Lyme symptom. Keep warm.
hats

Posts: 956 | From MA | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
   

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