Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Other Hypermobiles Anything I Can Do?


ravenwoodglass

Recommended Posts

ravenwoodglass Mentor

Hi, I have posted before about benign hypermobility or Ehlers Danlos. I have the latter. I was glutened last week which causes my joints to swell with fluid. Anyway I have dislocated my feet and/or ankles every night this week. Night before last I had a hard time getting my ankle back in place so had a pretty miserable day yesterday. It finally snapped back late yesterday evening. Does anyone know of a way to prevent this other than the obvious avoidance of the demon gluten? Is there anything I can do to quicken the dispursal of this fluid. I am kind of grasping at straws here. I don't sleep well wrapped up like a mummy in ace bandages :(


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



Celiac.com Sponsor (A8-M):



sillymomx3 Newbie

Just posted to your other post about EDS. I have no connection that I have noticed to gluten & dislocating. However, my son has to wear smo & dafo braces to keep his knees from dislocating. I have been so used to it all my life I just pop myself back in & go. Best of luck & as I have to tell myself on many days... Don't get glutened!

Christi

nogluten- Newbie
  ravenwoodglass said:
Hi, I have posted before about benign hypermobility or Ehlers Danlos. I have the latter. I was glutened last week which causes my joints to swell with fluid. Anyway I have dislocated my feet and/or ankles every night this week. Night before last I had a hard time getting my ankle back in place so had a pretty miserable day yesterday. It finally snapped back late yesterday evening. Does anyone know of a way to prevent this other than the obvious avoidance of the demon gluten? Is there anything I can do to quicken the dispursal of this fluid. I am kind of grasping at straws here. I don't sleep well wrapped up like a mummy in ace bandages :(

Hi. Sorry you're having troubles. You might want to see a podiatrist to see if you would benefit from orthotics for your shoes. They really help keep everything supported. Once you're doing a little better it's important to have very good posture and to strengthen the muscles supporting your joints. I had physical therapy to show me the correct postures and exercises. You have to be careful about stretching, as I'm sure you've discovered. Good luck and get better soon. x

Guest Robbin

I'm sorry you have had such a bad time. I hope you are feeling better. I get a lot of fluid retention around my joints. I always thought it was from the fibromyalgia. Anyway, when it gets bad I guzzle iced tea or hot tea--maybe 4-5 glasses/cups ( or more depending on how bad it is) in the morning/afternoon and by evening after all the bathroom trips, it goes down. I know tea is a natural diuretic and if you're like me, you don't want anymore drugs than necessary. I hope that helps. I usually drink decaf or 1/2 and 1/2 to avoid too much caffeine.

tarnalberry Community Regular

edited 2/22/06 - deleted post because it was bad advice. ;-)

ravenwoodglass Mentor

Thank you all for your replies. Things are finally getting a bit better. I did up my fluid intake a bit it seems to help clear the toxin out a bit faster and keeps my pee from burning as much. I also decided to see if my orthonics people can make me soft braces to help keep my foot and ankle bones in place. I switched GP after my diagnosis and haven't seen him since I 'introduced' him to celiac (my gosh 3 years with no dr. visits!), can't wait to see his face when I ask for this referral. Guess I'll wear a dress so I can demonstrate the backward bending knees easier :D .

Thanks again everyone.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,605
    • Most Online (within 30 mins)
      7,748

    Horslvr123
    Newest Member
    Horslvr123
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • kopiq
      also my hands are always cold, freezing cold in the winter and even cold during hot summer days. its like i have a shield. i feel warm but its not penetrating inside, my teeth chatter as well and my left index finger goes dead white when im super hungry. all dr tests come back fine. im so hopeless.
    • kopiq
      thank you, ive asked my dr to test for vitamin deficiency and shes only said vitamin d (very low 26) and b12, she says all other vitamins are not included in her blood tests only the major ones, C, D, E, B12 etc. Ive been following the aip diet now and im going to stay on it very strict to see how it goes. im eating tons of food, romaine salads, mango, peaches, pears, cucumber, celery, zuccnini, sweet potator, plantains, ground turkey and beef and chicken.  i eat about 4 plate filling meals a day with two to three good size snacks a day including about 3 or 4 bananas. im still not absorbing nutrients, if i eat any sort of food with fat, I.e ground beef or fatty pork the taste of fat lingers in my...
    • Scott Adams
      The Trader Joe's GF hamburger buns are the best!
    • StuartJ
      Just ate some for lunch!  A really superb alternative to gluten-free bread and burger buns that all have the taste and consistency of compacted sawdust.  I bought two packs and now I'm down to one remaining muffin so need to get some more; the only thing is it's their own brand - they don't do mail or on line ordering and the nearest TJ's is in Charlottesville (a real nightmare to drive around) an hour away from me over the mountain.  😒
    • somethinglikeolivia
      When I underwent a scope three years ago, the GI told me I was negative for celiac because there was no intestinal damage (in spite of multiple strong positive labs). I went back to look at my biopsy report out of curiosity, and found this note: “Localized mild nodular mucosa was found in the duodenal bulb. Duodenum otherwise normal.” The pathology from this scope was negative. Does anyone have any insight into mild modular mucosa and what that could indicate or be a precursor to? I’ve read it can be a sign of celiac or other gut issues like h. Pylori, etc.  Thanks in advance! 
×
×
  • Create New...