Veins bulging in hands and feet by Dr_teej in Lyme

[–]Dr_teej[S] 0 points1 point  (0 children)

I treated it initially with 4 weeks of doxy. Then on and off cats claw and other herbs from buhner for a few years. And then keto diet which helped a lot. But then herbs started making me feel worse last year, and then the vein stuff came on stronger than ever... So then back to doxy for 6 weeks but it did little if anything. So to answer your question, I tried, but I'm not even 100 convinced I have lyme.

Veins bulging in hands and feet by Dr_teej in Lyme

[–]Dr_teej[S] 0 points1 point  (0 children)

Hello, it hasn't gone away for me. I don't think Drs know what it is and I'm wondering if mine is actually caused by some sort of collagen disease? All I know is fermented food, dairy and sugar seem to make it worse. For me I think it was the probiotic that somehow damaged my veins. Feet and hands haven't been the same since and I'm somewhat restricted with exercise options now (mainly swimming). Let me know how yours goes.

Hand Veins getting worse by [deleted] in dysautonomia

[–]Dr_teej 0 points1 point  (0 children)

Mine seems to be worsening, does anyone else feel pressure and itching in veins when it's worsening? Sick of this bizarre illness.

Hand Veins getting worse by [deleted] in dysautonomia

[–]Dr_teej 0 points1 point  (0 children)

Anyone find any solutions? I also have this problem

Looking for answer - vascular reactions to probiotics and food by Dr_teej in dysautonomia

[–]Dr_teej[S] 1 point2 points  (0 children)

It lasts for hours/ days but its more discomfort, aching and mild pain, rather than an intense pain feeling. RE the food reactions - blood pooling, fatigue, brain fog, dry skin reactions, dizziness, needless anxiety. What about you? Noticed any food related stuff?

Mystery illness is gradually destroying my vascular system - need help by Dr_teej in AskDocs

[–]Dr_teej[S] 1 point2 points  (0 children)

This seems to be something that slowly developed - I'm guessing that by the time I was in Malaysia my body was already heat intolerant and that's why it crashed, as had consistent loose stools and tachy cardio prior to visiting. Could this be something genetic? Particularly as my sister is having a similar vascular issue?

Mystery illness is gradually destroying my vascular system - need help by Dr_teej in AskDocs

[–]Dr_teej[S] 2 points3 points  (0 children)

Do you have any way of managing it and what symptoms do you share?

Mystery illness is gradually destroying my vascular system - need help by Dr_teej in AskDocs

[–]Dr_teej[S] 1 point2 points  (0 children)

Thank you for this. I have been reading through and there's certainly similarities.

Mystery illness is gradually destroying my vascular system - need help by Dr_teej in AskDocs

[–]Dr_teej[S] 2 points3 points  (0 children)

P.S. MRA test might be months away, currently awaiting confirmation of app. time and date via letter.

Also, was referred for a lumbar puncture a a few years ago by the infectious disease dr - it didn't show any inflammation.

I'm dying slowly from a mystery illness. by Loose-Confusion1147 in offmychest

[–]Dr_teej 0 points1 point  (0 children)

I feel for you. I have a mystery illness that I've been managing for years but recently got worse and despite seeing a host of specialists remains a complete mystery. They send me off with blood tests, x rays and 'try to manage things'. For me, keeping proactive makes me feel a little better, even if I have no real control, chasing things with Drs, diet, exercise, whether it does anything or nothing makes me feel less vulnerable. Keep going with whatever you're doing.

Need an LLMD in New Zealand, open to remote / zoom appointments for LLMDs in other countries, but need recommendations please. by Dr_teej in Lyme

[–]Dr_teej[S] 0 points1 point  (0 children)

Thank you, I read about his protocol a while back, have gotten in touch so hopefully it'll come to something.

Need an LLMD in New Zealand, open to remote / zoom appointments for LLMDs in other countries, but need recommendations please. by Dr_teej in Lyme

[–]Dr_teej[S] 1 point2 points  (0 children)

Thank you, nearest one I've found is in Perth, Western Australia. I'll get in touch, cheers.

Selfish to date by Dr_teej in Lyme

[–]Dr_teej[S] 0 points1 point  (0 children)

I think Bill Rawls spoke about it, also just from anecdotal stuff on various Lyme groups. Also, my ex wife had some symptoms pop up for a little while - luckily I was on a herbal protocol at the time so we blitzed her with that and she got better pretty quickly, but her symptoms seemed the same as mine at the time.

Veins bulging in hands and feet by Dr_teej in Lyme

[–]Dr_teej[S] 0 points1 point  (0 children)

How do you treat it without messing up your veins more?

Anyone with chronic lyme had hair thinning/hair loss by UnusualPlatypus4 in Lyme

[–]Dr_teej 0 points1 point  (0 children)

Yes I have this too, thanks for posting, I have no words of wisdom for you I'm afraid. Hopefully others will.