Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Little Hard Blisters


Rebecca47

Recommended Posts

Rebecca47 Contributor

Does anyone know what these little hard blister like things are on a persons feet ? They are on bottom and next to my big toe. I also haven't had a migrain(wrong spelling) or a cold sore on my face since being gluten free. I assume being gluten free is also helping this? I have been gluten free since Aug, 2006 :huh:

Thanks

Rebecca


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Michi8 Contributor
Does anyone know what these little hard blister like things are on a persons feet ? They are on bottom and next to my big toe. I also haven't had a migrain(wrong spelling) or a cold sore on my face since being gluten free. I assume being gluten free is also helping this? I have been gluten free since Aug, 2006 :huh:

Thanks

Rebecca

Could it be plantar warts? Though gluten-free likely would have no affect on it.

Michelle

Sophiekins Rookie

They could just be callouses from your shoes - the way to check is to run your fingernail firmly (but not hard) across the bump. If it hurts and squishes, they are blisters. If it hurts and is hard, they are probably warts. If it doesn't hurt or squish, they are likely just callouses. If they are callouses, they are perfectly harmless, but if they bother you, you can sand them with an emery board when you get out of the shower and they will thin down. If they are warts, my best suggestion is to cut a hole in a potato roughly where the wart is in your foot and bury the potato in your garden - just as effective as nitrogen freezing, laser treatment or chemical burning the warts, and nowhere near as painful.

  • 2 weeks later...
angst2amity Rookie
If they are warts, my best suggestion is to cut a hole in a potato roughly where the wart is in your foot and bury the potato in your garden - just as effective as nitrogen freezing, laser treatment or chemical burning the warts, and nowhere near as painful.

Why exactly would that work?

ravenwoodglass Mentor
If they are warts, my best suggestion is to cut a hole in a potato roughly where the wart is in your foot and bury the potato in your garden - just as effective as nitrogen freezing, laser treatment or chemical burning the warts, and nowhere near as painful.

:lol::lol::lol: Actually this might work if you were very patient. Warts are caused by a virus and eventually the virus will leave your system. Thus if you bury the potato and wait long enough they will go away. If this wart is on the ball of your foot it could be plantars wart. Plantar warts grow in not out which is what makes them so painful. They do not appear on the toes though. You can tell a plantar wart by the fact that it is not raised and shows on the bottom of the foot as a whitish spot that is very sensitive to pressure. There are orthonics that can be attached to the bottom of your shoes that will take pressure off the wart and allow it to disapate. If the area on your foot is a lump near the toes it could also be a neuroma, don't let the name scare you it's not cancer but it is a growth on a nerve. Your best bet is to see a podiatrist for a firm diagnosis of what is going on.

Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to Ginger38's topic in Related Issues & Disorders
      1

      Shingles - Could It Be Related to Gluten/ Celiac

    2. - Ginger38 posted a topic in Related Issues & Disorders
      1

      Shingles - Could It Be Related to Gluten/ Celiac

    3. - Russ H commented on Scott Adams's article in Latest Research
      5

      Study Estimates the Costs of Delayed Celiac Disease Diagnosis (+Video)

    4. - Russ H posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Coeliac UK Research Conference 2025

    5. - Rejoicephd replied to Rejoicephd's topic in Related Issues & Disorders
      5

      Basic metabolic panel results - more flags


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,376
    • Most Online (within 30 mins)
      7,748

    Citydweller
    Newest Member
    Citydweller
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      I don't know of a connection. Lots of people who don't have celiac disease/gluten issues get shingles.
    • Ginger38
      I’m 43, just newly diagnosed with a horrible case of shingles last week . They are all over my face , around my eye, ear , all in my scalp. Lymph nodes are a mess. Ear is a mess. My eye is hurting and sensitive. Pain has been a 10/10+ daily. Taking Motrin and Tylenol around the clock. I AM MISERABLE. The pain is unrelenting. I just want to cry.   But Developing shingles has me a bit concerned about my immune system which also has me wondering about celiac and if there’s a connection to celiac / gluten and shingles; particularly since I haven't been 💯 gluten free because of all the confusing test results and doctors advice etc., is there a connection here? I’ve never had shingles and the gluten/ celiac  roller coaster has been ongoing for a while but I’ve had gluten off and on the last year bc of all the confusion  
    • Russ H
      There were some interesting talks, particularly Prof Ludvig Stollid's talk on therapeutics for coeliac disease.    https://www.youtube.com/playlist?list=PLRcl2mPE0WdigRtJPvylUJbkCx263KF_t
    • Rejoicephd
      Thank you @trents for letting me know you experience something similar thanks @knitty kitty for your response and resources.  I will be following up with my doctor about these results and I’ll read the articles you sent. Thanks - I really appreciate you all.
    • knitty kitty
      You're right, doctors usually only test Vitamin D and B12.  Both are really important, but they're not good indicators of deficiencies in the other B vitamins.  Our bodies are able to store Vitamin B12 and Vitamin D in the liver for up to a year or longer.  The other B vitamins can only be stored for much shorter periods of time.  Pyridoxine B 6 can be stored for several months, but the others only a month or two at the longest.  Thiamine stores can be depleted in as little as three days.  There's no correlation between B12 levels and the other B vitamins' levels.  Blood tests can't measure the amount of vitamins stored inside cells where they are used.  There's disagreement as to what optimal vitamin levels are.  The Recommended Daily Allowance is based on the minimum daily amount needed to prevent disease set back in the forties when people ate a totally different diet and gruesome experiments were done on people.  Folate  requirements had to be updated in the nineties after spina bifida increased and synthetic folic acid was mandated to be added to grain products.  Vitamin D requirements have been updated only in the past few years.   Doctors aren't required to take as many hours of nutritional education as in the past.  They're educated in learning institutions funded by pharmaceutical corporations.  Natural substances like vitamins can't be patented, so there's more money to be made prescribing pharmaceuticals than vitamins.   Also, look into the Autoimmune Protocol Diet, developed by Dr. Sarah Ballantyne, a Celiac herself.  Her book The Paleo Approach has been most helpful to me.  You're very welcome.  I'm glad I can help you around some stumbling blocks while on this journey.    Keep me posted on your progress!  Best wishes! P.S.  interesting reading: Thiamine, gastrointestinal beriberi and acetylcholine signaling https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.