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Lyme Disease ForumsGeneral & SupportSymptoms: Can anyone describe their FOOT PAIN?
10/14/2010 06:06 PM
hopesalive
hopesalive
 
Posts: 1129
Senior Member

Hi. Me again. Tons of questions. Smile

I have read that foot pain and numbness is typical

in late stage Lyme disease, but I thought I read that

the foot pain is more of an achy pain or a shooting

pain? I ask, because for the last three to four days

I am getting horrible foot CRAMPS. Almost like a

"charlie horse" would feel. Started in the toes, and

tonight involves my entire foot. Hurts like hell.

Is this something anyone else has experienced? I maybe

need more calcium or to eat a banana? Hoping this is

NOT a new symptom.

Best Wishes,

Hope :)

"Hope is a good thing, maybe the best of things, and no good thing ever dies."
~~The Shawshank Redemption~~

Igenex IGG: Negative
**23-25 KDA IND
**31 KSD IND
**41 KDA ++
45 KDA +
58 KDA ++
66 KDA +

Igenex IGM: Positive
18 KDA ++
**31 KDA IND
**34 KDA ++
**39 KDA IND
**41 KDA +++
66 KDA +
Reply

10/14/2010 06:42 PM  Top
toothfairy55
toothfairy55
 
Posts: 3856
Senior Member

Hi hopesalive,

have an xray or mri done on foot. I have Bart and this is a symptom BUT I also had a Mortons neuroma inbetween toes and it caused nerve damage and now I have perm. neuropathy. Please get it checked out with a foot doc

Carol

I am NOT a doctor, anything I share is based on my experience & research. I encourage you to discuss any and all information that I share with a health care provider.

10/14/2010 06:55 PM  Top
TaraT
TaraT
 
Posts: 4164
VIP Member

Hope I too have those charlie horses that come sometimes and it seems its an all day struggle..The only thing that helps them for me is to try and stretch the toes up and toward my head...Stretch the foot out..

Sometimes I press my toes on the bedrail or something and put pressure on the foot in order to bed the toes upward...Sometimes upon release of that pressure they double over again with cramping..

STIFFNESS in entire foot..lots of pain in the ankle upon weight. My feet actually feel like they've been smashed or run over by a car or something..

The entire foot (both of them) ache even when at rest. It was much worse last year after taking doxy for another infection in my leg...Neuropathy flared at the same time..

It's much better now but I am getting shooting pains in my feet when I stand on them and with every step..feels like it's originating from the ankles..

*SHRUG*

With Him we "live" no matter the circumstances. At His feet peace of mind can be found. Peace that passes all understanding is my quest now and forever.

Numbers 6:24-26
"The LORD bless you and keep you;the LORD make his face shine upon you and be gracious to you; the LORD turn his face toward you and give you peace."

10/14/2010 07:23 PM  Top
VicMac
VicMac
 
Posts: 1649
Senior Member

Hope,

I have had a lot of weird symptoms involving my feet. Actually glad you mention it right now!

Early on I remember I used to get pain on the tops of my feet alot. Hurt to walk. Then had it on the bottoms and with a real bad burning one time that kept me from walking much for several days.

Cramps I agree with Tara about. All you have to do to stop those Charlie horse cramps in the toes, is bend all your toes up towards your face. It works for me. And yes, I get them more since having Lyme. Especially horrible RLS.

You are right about Calcium and bananas. If I don't keep up the calcium and potassium and magnesium, the RLS is unbearable. So it could really help your feet too.

Also early on, I had a huge dark spot that formed under my large toenail several times, but was not painful, and went away but came back.

Now the same large toe keeps having an infection under the nail that hurts so bad I can't even wear my shoes sometimes, or have the bed sheets over it. There is no dark spot under the nail now though. Just hurts like hell. But it is worrisome because nothing seems to work to clear it up. Not even all the oral antibiotics I have taken recently. So I am trying a poultice now for it.

Hope you feel better!!

I wish I had solutions for everybody here who is suffering, but I am still hunting for them myself and seem to be more of a student on this board than a teacher. All I have to offer is my experience, support, and prayers based on what I have learned in my recovery. I am not a physician.

10/16/2010 09:40 AM  Top
hopesalive
hopesalive
 
Posts: 1129
Senior Member

Thank you for your responses everyone.

I have not tried the stretching of the foot, but I actually try to push it down onto the floor as if I am going to stand up and it does relieve the cramping.

Just strange, because I never get these and here they come for four to five days in a row now.

I am afriad to ask, "What next?" ;P

Best Wishes,

Hope :)

"Hope is a good thing, maybe the best of things, and no good thing ever dies."
~~The Shawshank Redemption~~

Igenex IGG: Negative
**23-25 KDA IND
**31 KSD IND
**41 KDA ++
45 KDA +
58 KDA ++
66 KDA +

Igenex IGM: Positive
18 KDA ++
**31 KDA IND
**34 KDA ++
**39 KDA IND
**41 KDA +++
66 KDA +

10/16/2010 11:01 AM  Top
wlkthlne
wlkthlne
 
Posts: 1605
Senior Member

Yes, but I am careful with the stretch..I turned it in to a charlie-horse...yeee hawww!Sad

With me it is the "Bart". My Doc has got me on the Doxy and Rif protocal..

I find some releif at the foot end..but it is playing havoc on my eyes and head..

If I come on here and write nothing...

you know I just became brain dead..W00t Silly Unsure sorry, when it's bad I turn to awful humor...

I describe the foot pain..it starts at the arch and goes torward the heel...other times my foot feels like it is arching upward, no pain..but feel like I should be walkin' upside-down...LOL can't make it up!

Cool wlkthlne

Anything I post or respond to comes from a Lyme and Bart victim himself. I am NOT a doctor. I do my own research for ME...I may share my findings and will post them. They are for general talk and vent...If a group leader feels the info is worth saving somewhere, they are more than welcome to do with it as they like. Wlk=)

10/16/2010 05:34 PM  Top
walkersraven
walkersravenPosts: 412
Member

wlkthlne........Can I ask is the foot cramp specific to Bart? Last wk the arches on both feet would wake me up with bad charlie horse feeling. Also care to share what the eye issue is?

10/16/2010 06:19 PM  Top
zippysmom
zippysmom
 
Posts: 40
Member

The foot cramps seem to be common, I have them too. I also get sharp pain through my feet and just in the last 2 months So, this can do weird things. Hang in there!

10/16/2010 08:18 PM  Top
wlkthlne
wlkthlne
 
Posts: 1605
Senior Member

walkersraven, yes in my case the feet for sure seem to be the Bart. As for the eyes, been my biggest issue.

I get everything, uncontrolled twitchin' of eyes, blurry, hard to focus, tagpoles and when I take certain stuff before going to bed I wake up in the middle of a deep sleep with loss of vision..

It does come back and never happens during the day.

Due to that Lyme and many of it's co-friends can hide in the head...where it is most hard for the body to get rid of it and for abx to fight...

I may have more than just Bart effecting the eye's and head...It is a hard call...

At this momemnt I am on doxy and Rif...it has changed the symptoms to my feet,head and eyes in strange ways...

So I am going to stick with the "Bart" protocal and remind me to keep you posted...

Please keep me in the loop how you are doing...

As it has been said; "stranger things have happened"

Cool wlkthlne

Anything I post or respond to comes from a Lyme and Bart victim himself. I am NOT a doctor. I do my own research for ME...I may share my findings and will post them. They are for general talk and vent...If a group leader feels the info is worth saving somewhere, they are more than welcome to do with it as they like. Wlk=)

10/16/2010 08:38 PM  Top
Holly123
Holly123
 
Posts: 330
Member

Yes I have foot pain too I have to stop sometimes and bend my toes to stretch them.. and also have knee pain too.. I really really really hope it is not permanent.
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