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

Peripheral Neuropathy


Hungrylady

Recommended Posts

Hungrylady Rookie

As part of this disease I have peripheral neuropathy. I wear braces and edema gloves to bed every single night since I got pregnant (5 1/2 years ago). I can't talk on the phone or use the mouse very long, etc....horrible pain and nerve shots, falls asleep, it's a mess. I am showing a tiny bit of improvement already so I am excited. I was looking up things I might be able to do to improve things more and came across using a tens unit. My hubby has one in the basement he used for his back a million years ago. So it is actually something I can try. Before I do I was wondering if anyone else has used it and did it improve your hands and if so how?


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

Before you try this can you get a consult with a PT? They could advise you on whether it might be something that would help and make sure you know how and how long to use it.

Something else that may help is sublingual B12. I don't know if you have had the levels checked but often blood levels read higher than they really are. B12 is not a vitamin you can 'OD' on so if you are not taking it try some. Don't be scared off by the high amount but do make sure they are gluten free and the sublingual not the swallowed pills.

Glad to hear the diet is helping but it can take awhile when the nervous system is involved. I used to have to brace both legs at night myself and know how uncomfortable that can be. I had to do it because I would dislocate though. Once my edema went away I stopped dislocating as much so hopefully once you heal more things will improve for you also.

Hungrylady Rookie

wow, ouch. Glad it's better for you! Yes, I take DEVA B12 with folic acid&b6, sublingual, under tounge. I didn't think to ask my PT, havent seen her since she came up with the edema gloves under the braces. I can't wait to burn those braces, lol.

Takala Enthusiast

Used one for c spine injury - honestly the most useless, ridiculous thing, one is trying to get rid of the sensation of the nerves being impinged, so this 10s unit thing instead shoots you with the same sensation so it's even more annoying. Stick to the diet, supplements, try to keep busy so you don't think about the constant buzz, and it should eventually go away. Gentle yoga helps (no straining stuff) and meditation.

shadowicewolf Proficient

Have you tried water theraphy? I've heard that helps with nerve issues.

Hungrylady Rookie

Have you tried water theraphy? I've heard that helps with nerve issues.

No, but i'll look into water therapy, sounds nice. I am planning to swim to help regain strength when my son starts school in two weeks (thank goodness).

I guess the tens until would give me more of the same feelings. It doesn't actually heal the nerves huh? Somehow that's what I got in my head, lol.

Takala Enthusiast

No, it doesn't heal anything, it's the electrical equivalent of "white noise" which the theory is that by playing that, one does not hear the more annoying noises and it acts as a jamming/blocking device. If you want to heal, stick to the diet and take vitamins and exercise so your body can metabolize and use the nutrients properly.


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,544
    • Most Online (within 30 mins)
      7,748

    Jem68
    Newest Member
    Jem68
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.