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Posted 8/18/2019 3:58 AM (GMT 0)
Has anyone else here gotten raynaud's disease?

I think I have this. My hands and feet are constantly red and swollen with blood. If I exercise it gets worse. At night it gets worse. I was wondering if spirochetes could be blocking a blood vessel. I have an apt with a cardiologist in September. He'll probably just call my a hypochondriac, like they all do. Although I have pictures of feet and hands turning from bright red to purple. I also have chest pain quite frequently. My heart will have "cramps", similar to a leg cramp. Not sure if this is like a minor heart attack, or just a flare up.
Posted 8/18/2019 8:29 AM (GMT 0)
do you have livedo reticulitis?
bart in blood vessels does seem to calcify the biofilms . bee venom decimates borrelia biofims according to sapi. lumbrokinase on a empty , chanca piedra tincture and per d.m. msm water may help .
Posted 8/19/2019 1:22 AM (GMT 0)
I have Raynaud's, and for me it's not at all as your describe - hands turn white and lose circulation is response to cold and then feel very painful upon circulation returning. Your condition sounds different to me. Sorry not to be more helpful.
Posted 8/19/2019 7:09 AM (GMT 0)
ill make a separate thread soon but the biggest problem i have with syndromes or diseases named for the researcher/ doctor that found a set of symptoms that match a profile is that they then seemed content to forget the rest of the scientific method?! is hand foot and mouth disease a explanation for the pathogen causing the syptomology?is sclerosis anything other than a latin entitled fancy way of saying hardening or deterioration of tissues is present?! does hashimotos explain why the bodies immune system is attacking tissues in the thyroid?!
these "diagnosis"s are not the place to stop and accept but to question why is this pattern happening and what root causes are the symptoms pointing to . does the phrase post lyme disease syndrome anger u like it does me knowing that a persistent borrelia infection is the cause. now on to mcad and raynauds - allopathic medicine is great at explaining the what but not the why.... what is preventing circulation to extremeties should be the next question?! is it biofilm , a change in bp or endothelial resiliency? mineral deficiency or mitral valve prolapse or a bit of all the above ?! question the system please people if u value life just keep questioning .......? if u called a rose a stinkblossem it would still smell as sweet , just sayin

Post Edited (bluelyme) : 8/19/2019 1:16:08 AM (GMT-6)

Posted 8/19/2019 7:23 PM (GMT 0)
Hi gfields!-

I have Raynaud's. I have seen my finger tips turn blue. My feet are a lot worse. I have seen my toes turn completely white and very cold from having lack of blood flow.

When the blood flow returns to my toes, they turn purple/blue. Then turn bright red and burn very bad.

Last winter, my toes were swollen, bright red, severely itchy, and pealing a thin layer of skin. I found out that it was Chilblains.

If you are interested, here is a website about Lyme, Raynaud's, and Chilblains.

https://daretoselfcare.com/protect-yourself-from-extreme-cold-with-lyme/

I am so sorry to hear that you are dealing with chest pain also. That is such a scary symptom to have.

I hope that you are able to get some answers from your doctors appointment in September.

Best Wishes!
Posted 8/22/2019 10:54 PM (GMT 0)
I have raynaud’s, so does my father. Your hands fingers etc. extremities will turn white and blue when exposed to cold and or wearing tight clothing. My father gets that. For me it is more painful, cold extremities, and shaking and chills with overall lower body temp, etc. hands turn red and are painful before and when warming them I have to wear loose clothes, gloves etc., I heat my drinking water and I usually don’t drink cold drinks, and sometimes ac can bring it on. Running hands under warm water helps if affected. I also have hashimotos which causes lower body temps.
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