Does anyone's feet get ice cold that they feel frozen at times.
Posted by c3mom (Member # 16412) on :
Yes, all the time. However, it is a lot worse in the winter.
Posted by maureen2174 (Member # 11471) on :
I get this too, all the time, but worse in the winter.
just the other day i was looking for heated slippers or socks to wear around the house.
Posted by sutherngrl (Member # 16270) on :
Ice cold hands too!
Posted by Cold Feet (Member # 9882) on :
I did get cold hands and feet during the onset of my disease (hence, my screen name). I've been on the Marshall Protocol for 26 months, and now have very good circulation. I also take enzymes of different sorts on occasion (Rechts Regulat, Noni, etc.).
Hope this helps in some way. Feel free to PM me too.
Posted by Barby (Member # 18348) on :
My feet were one of my very first symptoms. They were frozen and blue. Now I get it every now and then. Usually at night and it get's worse when I am in cold weather or a/c.
Posted by Fordace (Member # 14874) on :
yep....frozen quite a bit, and my hand gets frozen from this damn mouse....lol
strange, the feet can be cold for a few hours, then sweating the next day....
Posted by crystalkk (Member # 17223) on :
My feet are cold all day, then at night they are red and hot.
Posted by crystalkk (Member # 17223) on :
My feet are cold all day, then at night they are red and hot.
Posted by Julia (Member # 18779) on :
I know how you feel. I deal with cold hand and feet too
Posted by wantabe (Member # 14703) on :
Look into Raynauds' There are many sites if you Google This is one of my 1st dx :3 years ago
I'm taking a calcium blocker(blood pressure medication)prescription and Nattkonaise as a supplement. This helps at high enough doses.
Hot baths and sauna are a daily must to help get rid of the bone cold feeling. (***** -5 high in Iowa today ****)
This can become serious if you start getting chilbains and ulcers so be careful to stay warm and decrease your blue, white, red episodes.
Let me know if you want more information... Wantabe warm!
Posted by bettyg (Member # 6147) on :
wantabe, yes our iowa weather is BETTER than international falls, minn's ACTUAL 35 BELOW ZERO AND 50 BELOW WINDCHILL!!!
yes, my hands/feet all the time too! i wear socks to bed and my sneakers in house when i'm on pc to give feet extra warmth.
wear my long sleeves robe alot on here to come down over the hands but leaving finger tips out to type! Posted by ByronSBell 2007 (Member # 11496) on :
That use to be a symptoms of mine, everynow and then it will return but I think it is from the bartonella since it is known for restricting blood flow.
Posted by crystalkk (Member # 17223) on :
Hey, I diidn't know bartonella reduces blood flow. thanks
Posted by crystalkk (Member # 17223) on :
up
Posted by bejoy (Member # 11129) on :
Have you all had your thyroids checked? A little T3 or Armour can do wonders.
Also, a systemic infection of the common household mold Mucor Racemosus reduces blood flow. It seems to be a common infection in lymies, due to stress and reduced immune function.
Posted by steve1906 (Member # 16206) on :
My whole body is cold all the time. I also get cold spots on my body to touch.
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