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

Let's Help The Fm People On Fibrohugs


Jonesy

Recommended Posts

Jonesy Apprentice

:D

I guess you might say I'm on a crusade tonight. I just came from the forum on Fibromyalgia. I registered over there some time ago because my DD has FM. I went there to learn more about it, and never went back.

Tonight I got to thinking I should check out the forum over there to see if they are aware of the link of FM to celiac disease. I read page after page of posts and it seems they are not talking about celiac disease at all, and celiac disease is not on the list there of Associated Diseases.

So I plunged in, introduced myself and suggested they check into it. I didn't post a link because I didn't know if it was allowed. But here it is allowed, so you can all go over to Fibrohugs, go to the forum and see for yourself. Sign up, tell them who you are and tell them about celiac disease. I know everyone with FM doesn't also have celiac disease, but they should know about it.

Open Original Shared Link

If the administrator gives me permission I will post a link there to our forum so they can read here all that is written by Fibro's about the link to celiac disease. Wouldn't it be great if we could help them feel better by the gluten-free diet.

Some of you seasoned posters would do a much better job than I did because you are more knowledgeable. My name over there is mejco and I just posted about 5 minutes ago in the "introduce yourselves" topic. You can read that if you want, but I'd like you to browse around and see that they haven't made the connection. Can't you just imagine how many of those FM's are fellow Celiacs?

I hope I did the right thing. It sure felt like the right thing to do - to tell them about it, and hope they take it seriously.

P.S. Scott, their site isn't nearly as fast loading as ours, nor as easy to navigate.

Good job, Scott.

Maryellen


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



Celiac.com Sponsor (A8-M):



Nanjee Rookie

Hi Mary Ellen :)

I have visited the site you mention - and there is not a whole lot of research type info there, I agree.

I am new to gluten intolerance, but not new to FM - have had it for 20 years.

It certainly was made worse by the gluten intolerance, and I am fighting every day to regain some of my strength - one day at a time ;)

There is a very good site that is filled with research, and celiac disease, as well as gluten sensitivity is talked about often. Lots of research from leading MD'sd in the FM world .... and a VERY active message board. The message board is very active - and messages are answered many times as fast as you post them.

LOT's of members with celiac and gluten issues.

You can do searches for medical research, as well as searches on the message board.

I don't know the rules here well enough yet ---- I hope it is alright that I post the web addy ????

www.immunesupport.com

May be helpful for those of you who also suffer from FM ???

I have referred many people from there to this site - they were so thankful for all of the wonderful research here at celiac.com :)

Hugs,

Nancy

jenvan Collaborator

thanks for that site. i will ck out--trying to figure out how to improve my own fibro...

Jonesy Apprentice

Thanks Nancy

That's great information! Appreciate it.

Can you tell me if it's allowed to post that link on Fibrohugs? Sound to me like you are saying that you did, since you referred them to the site, you must have posted the link.

Thanks for your prompt and helpful reply. :)

Maryellen

mouse Enthusiast

I was diagnosed around 25+ years ago with FM. Every pressure point was super sensitive and they tell me that I have a high pain tolerance. I sure did not feel that way at the time. Before we down sized (June), I had a special made pool and spa that really helped relieve the pain. I had weights, etc. that the physical therapist had instructed me to use. After I went gluten-free, my pain slowly diminished and the areas on my thighs are the only places that are still tender on a daily basis. I would say that being totally gluten-free took away about 80% of my pain, which was something I did not expect, but was certainly welcomed. I don't remember how long it took, but I would say about 9 months to a year.

Armetta :P

watkinson Apprentice

Hi Jonesy,

Thank you for taking the time to educate fibrohugs on celiac disease. I must say I am not shocked to find out that they seem to not know about the connection. I have suffered FM ect. for about 30 years (since Jr. high school). When I was diagnose a celiac I did my own research and found the connection. Since going gluten-free about one and a half years ago, my FM, restless leg, chronic fatigue, peripheral neuropothy, (nubbness and tingling) has nearly gone away! :D I believe that someone with Fm would benefit greatly from going gluten-free even if they are not a celiac. I will also visit the site and see what they have to say. :)

Again, thanks,

Wendy

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. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    2. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    3. - nanny marley replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      20

      Insomnia help

    4. - David Blake commented on Scott Adams's article in Product Labeling Regulations
      1

      FDA Moves to Improve Gluten Labeling—What It Means for People With Celiac Disease

    5. - nanny marley replied to wellthatsfun's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      nothing has changed

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,343
    • Most Online (within 30 mins)
      7,748

    emoryprose
    Newest Member
    emoryprose
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • asaT
      plant sources of calcium, such as spinach, have calcium bound to oxalates, which is not good. best source of calcium is unfortunately dairy, do you tolerate dairy? fermented dairy like kefir is good and or a little hard cheese. i do eat dairy, i can only take so much dietary restriction and gluten is hard enough! but i guess some people do have bad reactions to it, so different for everyone.  
    • asaT
      i take b12, folate, b2, b6, glycine, Nac, zinc, vk2 mk4, magnesium, coq10, pqq, tmg, creatine, omega 3, molybdnem (sp) and just started vit d. quite a list i know.  I have high homocysteine (last checked it was 19, but is always high and i finally decided to do something about it) and very low vitamin d, 10. have been opposed to this supp in the past, but going to try it at 5k units a day. having a pth test on friday, which is suspect will be high. my homocysteine has come down to around 9 with 3 weeks of these supplements and expect it to go down further. i also started on estrogen/progesterone. I have osteoporosis too, so that is why the hormones.  anyway, i think all celiacs should have homocysteine checked and treated if needed (easy enough with b vit, tmg). homocysteine very bad thing to be high for a whole host of reasons. all the bad ones, heart attack , stroke, alzi, cancer..... one of the most annoying things about celiacs (and there are so many!) is the weight gain. i guess i stayed thin all those years being undiagnosed because i was under absorbing everything including calories. going gluten-free and the weight gain has been terrible, 30#, but i'm sure a lot more went into that (hip replacement - and years of hip pain leading to inactivity when i was previously very active, probably all related to celiacs, menopause) yada yada. i seemed to lose appetite control, like there was low glp, or leptin or whatever all those hormones are that tell you that you are full and to stop eating. my appetite is immense and i'm never full. i guess decades or more ( i think i have had celiacs since at least my teens - was hospitalized for abdominal pain and diarrhea for which spastic colon was eventually diagnosed and had many episodes of diarrhea/abdominal pain through my 20's. but that symptom seemed to go away and i related it to dairy much more so than gluten. Also my growth was stunted, i'm the only shorty in my family. anyway, decades of malabsorption and maldigestion led to constant hunger, at least thats my theory. then when i started absorbing normally, wham!! FAT!!!    
    • nanny marley
      Great advise there I agree with the aniexty part, and the aura migraine has I suffer both, I've also read some great books that have helped I'm going too look the one you mentioned up too thankyou for that, I find a camomile tea just a small one and a gentle wind down before bed has helped me too, I suffer from restless leg syndrome and nerve pain hence I don't always sleep well at the best of times , racing mind catches up I have decorated my whole house in one night in my mind before 🤣 diet changes mindset really help , although I have to say it never just disappears, I find once I came to terms with who I am I managed a lot better  , a misconception is for many to change , that means to heal but that's not always the case , understanding and finding your coping mechanisms are vital tools , it's more productive to find that because there is no failure then no pressure to become something else , it's ok to be sad it's ok to not sleep , it's ok to worry , just try to see it has a journey not a task 🤗
    • nanny marley
      I agree there I've tryed this myself to prove I can't eat gluten or lactose and it sets me back for about a month till I have to go back to being very strict to settle again 
    • trents
      You may also need to supplement with B12 as this vitamin is also involved in iron assimilation and is often deficient in long-term undiagnosed celiac disease.
×
×
  • 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.