HealingWell
Search Close Search
☰

Bone pain in both feet?

Support Forums
>
Lyme Disease
✚ New Topic ✚ Reply
❬ ❬ Previous Thread |Next Thread ❭ ❭
Posted 6/16/2020 1:37 PM (GMT 0)
Hello, I have been having a new symptoms for about a month now and i am just wondering if anyone else has bone pain in both of their feet? It feels like the bones in my feet are score to the touch so when this feeling happens I try to tip toe instead of putting my whole foot down. I have been using an infrared sauna everyday for the past few months could this be the problem? And is there anything that could help this feeling? I hope everyone is doing good. Thank you!

Post Edited (CalmLittleBuddha) : 6/17/2020 11:32:41 AM (GMT-6)

Posted 6/16/2020 1:49 PM (GMT 0)
My doc says this is Bartonella. Is it worse in the morning?

I bet you're right about the sauna mobilizing toxins and maybe causing some inflammation.
Posted 6/16/2020 2:01 PM (GMT 0)
Thank you saraeli! It is worse in the morning and at night after sitting for a long amount of tIme. I am taking curcumin for inflammation but is there any other supplements that you know of to try? I know my body is very toxic and I am taking Benonite Clay or activated charcoal at night but I'm sure it is not getting all of the bad stuff out. Thank you again, you always have such helpful information!

Post Edited (CalmLittleBuddha) : 6/16/2020 8:15:33 AM (GMT-6)

Posted 6/16/2020 2:27 PM (GMT 0)
Definitely Bart. I have it, it's usually only there in the morning then disappears. Feels like someone has taken a hammer to my feet.
Posted 6/16/2020 2:58 PM (GMT 0)
Sorry you deal with this too orbit, dose anything help the pain?
Posted 6/16/2020 3:53 PM (GMT 0)
I did have bone pain - the worst was my tailbone. It was weird because while I was sitting in the chair ...could be for hours...when I stood up - that's when my tailbone would hurt...as I was rising from the chair.

It went completely away with bartonella treatment.

No more sore feet anymore either.
Posted 6/16/2020 4:00 PM (GMT 0)
Thank you for the reply Girlie, I'm glad yours went away, It's such a weird feeling. How long did you treat Bart for?
Posted 6/16/2020 4:09 PM (GMT 0)
Oh, i treated Bart....and then treated it again.

First time was with my LLND - I think I treated it then for over a year.

Then a couple years later, I treated with my LLMD (after doing babesia treatment) for about 6 months....and now on maintenance bart treatment - been on that (abx for a few days each month) for over a year now.
Posted 6/16/2020 4:23 PM (GMT 0)
Uuuugh I had the tailbone thing! Never heard anyone else mention it.
Posted 6/16/2020 7:48 PM (GMT 0)

CalmLittleBuddha said...
Sorry you deal with this too orbit, dose anything help the pain?

Mine is pretty transitory, so I just deal with it, I don't take anything for it. I told my LLMD -- I can put up with a lot of pain, but headaches are the only thing I can't deal with.
Posted 6/17/2020 2:05 AM (GMT 0)
The sauna is likely bringing it out or making it worse. Everyone says foot pain is bart, but Shoemaker says its a CIRS/mold symptom. I have had increased foot pain due to gut pathogens (likely yeast or mold) and relief with antifungals/expulsion of gut pathogens.

I am having a bad flare of hand/foot, wrist/ankle, fingers/toes stiffness and pain as well as fatigue, and I am pretty sure it’s gut related.

I have had the foot pain really bad the last couple of weeks. I can hardly walk and hobble a lot. Walking a lot just seems to make it worse. For me, it feels like blood vessels are affected, not just bones, although I have had pure bone pain in the feet at one time that felt like the bones were going to collapse.

Post Edited (WalkingbyFaith) : 6/16/2020 8:09:58 PM (GMT-6)

Posted 6/17/2020 12:01 PM (GMT 0)
Thank you everyone for the replys! The weird thing is that I have had so many different syptoms but never this for longer then a day before so it popping up was a little concerning but like you all said the sauna is probably being it out. Does anyone know what issue depersonalization would go most with, bartanella, mold or yeast issues, that is my worst symptom? I hope your feet get feeling better WBF, I know how you feel hobbling around.
Posted 6/17/2020 12:22 PM (GMT 0)
I'm so glad you asked this as I have been having terrible foot pain in the last two weeks and I am in a Bartonella relapse, no idea it could be connected. Thought maybe I needed new arch supports in my sneakers or something. Makes a lot of sense.

I hope your resolves quickly!
Posted 6/17/2020 12:22 PM (GMT 0)
Last night I used topical CBD on my feet and it did help, I'm going to keep using it twice a day. Have you tried it?
Posted 6/17/2020 5:31 PM (GMT 0)
Hi sunny! Topical CBD oil is a great idea, I have used it on my back before but never my feet. Maybe the change in seasons and the arrival of more humid weather is affecting us. I hope you get feeling better. Thanks for your suggestion!
Posted 6/18/2020 1:34 AM (GMT 0)
Walkingbyfaith mentioned the “blood vessels” and I feel the same. They are a huge part of the problem. I had foot pain for years leading up to my full Lyme decline and formal Dx. My first hint of problems to come was foot pain. I noticed that I could not walk barefoot in my house. Our hardwood flooring was too painful. The foot pain progressed into PN of both feet and shins with a burning sensation. It was just one of many symptoms. Foot pain was the first to occur and the last to resolve. Now it is down to the 15 to 20% level. Strategies to improving circulation are very helpful. It does fit well in the BERT model.
Posted 6/19/2020 10:19 PM (GMT 0)
I have a numb finger - I believe it’s from bart.

Bart is really nasty when it’s comes to our nervous system
Posted 6/19/2020 10:27 PM (GMT 0)
Doesn't Dr. M call Bartonella "small vessel disease" or at least equate it to that?
Posted 6/22/2020 7:27 PM (GMT 0)
My feet have been hurting a lot lately too. Like I've said in other posts, I'm really not sure what to for the bartonella now. My rashes seem to get better when I just take vitamins and enzymes.
✚ New Topic ✚ Reply