HealingWell
Search Close Search
☰

Hand pain

Support Forums
>
Lyme Disease
✚ New Topic ✚ Reply
❬ ❬ Previous Thread |Next Thread ❭ ❭
Posted 3/1/2021 8:46 PM (GMT 0)
Hello, just wondering if anyone else has hand pain and if there is anything that helps it. Lately my hands have been feeling so sore and almost feel like there is too much fluid in them. Thank you!
Posted 3/1/2021 11:50 PM (GMT 0)
I don’t know but I’m dealing with the same thing. My hands have felt swollen and sore for several days now. I also started having UTI symptoms again, and have been feeling inflamed all over. May just be cytokines. I took SPM Active last night and Chinese skullcap and kudzu earlier today, but I can’t tell they helped much.

I had a headache most of the day, too, and finally took a migraine pill late this afternoon. Felt better and less inflamed after that and went for a walk. Felt pretty good starting out, but I think I overdid it. Just ate supper, and now I feel all inflamed again.
Posted 3/1/2021 11:55 PM (GMT 0)
BTW, I have had soreness in my palms, soles, and inside of elbows before when herxing. I told the doctor it felt like my blood vessels hurt. She said it was from toxins and to take binders. I think I backed off of treatment instead. Seems like I was taking treating parasites at the time.
Posted 3/2/2021 12:18 AM (GMT 0)
Thank you for that info WBF. I am sorry that you are dealing with this issue too. I believe my whole body is inflamed as well. Dose anyone know a good supplement for inflammation? I have been taking activated charcoal for awhile now but maybe I will try another binder. I have not been taking any other killing herbs for a few months. Let me know if you find anything that helps! I hope we both start feeling better soon!
Posted 3/4/2021 3:14 PM (GMT 0)
My hands, primarily the right one, has had pain in it vary for a year now. Sometimes it swells. All autoimmune tests have been negative. When I use my hands too much, it gets worse. And what you mentioned about "my whole body feels inflamed," can relate to that as well. It has been worse in last week or so.

Pain in body can also be allergen related. I'm not sure what part of the world you live in, but in Georgia the pollen is jumping up early this year, which may be impacting WBF? Just a thought.
Posted 3/4/2021 3:17 PM (GMT 0)
RW....i was thinking of you yesterday. I've been speaking to a woman w/ sjogrens who very much has your symptoms. She's got lots of joint pain, skin issues, and she complains of exactly the same tissue loss that you have. In fact that is her biggest complaint, and made me think of you. But she also has the dry eyes that sjogrens casues. Are your eyes or mouth every dry?

She is sero-negative on all autoimmune markers, except the Sjogrens Early Antigen panel came back positive. This is a new test that you may not have had.
Posted 3/4/2021 3:37 PM (GMT 0)
dcd - Thanks for that information. I have been tested for sjogrens a number of times, but not sure about the early antigen. Would that still show up after months if I were to be tested now?
Posted 3/4/2021 10:18 PM (GMT 0)
Yea it would. Thats just the name of the antibody, i think because it sometimes shows up first.
✚ New Topic ✚ Reply