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

Finger Joint Pain


KCG91

Recommended Posts

KCG91 Enthusiast

On and off over the years my right index finger has been a bit painful in the 'top' joint (nearest the nail). Over the last few months I've noticed it 'spreading' to the other joints in that finger and now into my wrist and middle finger. My wrist is just achy but the finger joints are a throbbing pain at times and a little stiff but not really hot or swollen that I can see. Tonight it feels like I've slammed my fingers in a car door :( not helped by three hours dialling phones at work. I feel stupid going to the doctor with a sore finger - any ideas here? In itself it isn't a particular problem but it's the spread in the painful area that's alarmed me a bit. 


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



Celiac.com Sponsor (A8-M):



IrishHeart Veteran

You may have osteoarthritis. I do. Sometimes, my fingers, and all my joints (esp, hips)  hurt quite a bit and sometimes, I do not notice them hurting at all. It depends on the weather, repetitive use, if I got glutened, that sort of thing.

 

I had OA develop long before my C D diagnosis,  but I am pretty sure C D came first. OA is a tag-along with celiac sometimes.

 

I take fish oil caps and collagen caps and off gluten, they feel a lot less ouchy. In fact, the OA is not that bad when managed and when I keep moving, "keep the joints lubed", so to speak. ^_^

 

Sorry you are hurting, but you may want to have a rheumatologist check you out. 

 

it's not as painful as RA, so i am told, but it is degenerative and I have had some disc degeneration. if I walk or swim daily, I can keep it under control. Just a suggestion, I may be wrong. 

GF Lover Rising Star

In my experience, When my immune system goes nuts my arthritic joints will flare (especially that coffee cup finger).  For me that means anything that surpresses the immune system: a cold virus, gluten, infection, allergies etc. will start a cascading effect of AI issues.  With me, my immune system is not very strong because of cancer and removed lymph nodes so any of those triggers will affect me for a good month.  If another trigger hits in that month I will continue with all of my symptoms.  Remember, if your immune system is attacking, you may experience any number of issues.  My list includes: joint, muscle and skin pain, sore throat, swollen neck and accompanying nodes, dry itchy eyes, migraines, constipation, mouth sores, dry red areas around my mouth, nausea, fatigue, loss of appetite, increase in lymphedema, increased sun sensitivity, increased thirst, mystery rashes and basically just feeling crappy...lol.

 

Hang in there and note that everything may not be a gluten hit but a different immune triggers.  I have only been glutened three times in the past 2 some years but have felt ill for much of that time due to other immune triggers.

 

Colleen

KCG91 Enthusiast

Thank you for the replies, guys. It's nice to have somewhere where 'oh no, my fingers hurts!' doesn't get totally side eyed ;) It's all still sore so I think I will get it checked. I also wondered about carpal tunnel syndrome as I do a lot of pole fitness, yoga, aerial acrobatics which puts stress on my wrist (but I can't spot a specific injury so hey who knows). 

That's an interesting point about the whole immune system effectively going on the attack as well... My doctor noticed that I always get thrush after a cold (TMI sorry!) which is the weirdest thing, but at least I'm prepared now. 
Irish you are so right about keeping moving. I've been doing a 20 day Bikram yoga challenge and even today when I just wanted to roll up in my mat and snooze through the rest of class it was worth it for how much better I felt afterwards! 

IrishHeart Veteran

 

Irish you are so right about keeping moving. I've been doing a 20 day Bikram yoga challenge and even today when I just wanted to roll up in my mat and snooze through the rest of class it was worth it for how much better I felt afterwards! 

 

Oh honey.. you're sweet.... but your "keep moving" and my "keep moving" are totally different. ^_^

 

I do yoga poses, not a Bikram challenge, I suspect  you are much younger and have never had a surgery yet. 

 

While my spirit is willing and I am flexible, my damaged body has different ideas.  :D

 

Don't kill yourself if you are still in healing mode. 

across Contributor

I also have had osteoarthritis in my finger joint. Going off gluten has made a world of difference in that, but so has fish oil. When I'm not taking it, the swelling and pain start back up.

Celiacandme Apprentice

I'm late to this thread. Let us know what the doctor says! Good luck!


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



Celiac.com Sponsor (A8-M):



KCG91 Enthusiast

Oh honey.. you're sweet.... but your "keep moving" and my "keep moving" are totally different. ^_^

 

I do yoga poses, not a Bikram challenge, I suspect  you are much younger and have never had a surgery yet. 

 

While my spirit is willing and I am flexible, my damaged body has different ideas.  :D

 

Don't kill yourself if you are still in healing mode. 

 

Haha! Yeah just after I got diagnosed I spent three months resting to recover. During this period my uncle admitted he was kind of intimidated about what I'd be like when I was 'more energetic'. I'm just grateful to have a body that works pretty well now and enjoy using it :)

I'll report back. I've had a few crazy weeks recently - I'm about to move home to England from Scotland so I've been, erm, making the most of my university city! Too much action, not enough sleep and I've just had to rush home from a street party with a thrush flare. So painful :( I will have to re-register with a new doctor at home and I'm really hoping that they just accept my blood tests/falling antibodies and aren't difficult about my non-biopsy diagnosis  - I can't stand a challenge but I have come to rely on my prescription basics. 

GottaSki Mentor

Thank you for the replies, guys. It's nice to have somewhere where 'oh no, my fingers hurts!' doesn't get totally side eyed ;) It's all still sore so I think I will get it checked. I also wondered about carpal tunnel syndrome as I do a lot of pole fitness, yoga, aerial acrobatics which puts stress on my wrist (but I can't spot a specific injury so hey who knows). 

That's an interesting point about the whole immune system effectively going on the attack as well... My doctor noticed that I always get thrush after a cold (TMI sorry!) which is the weirdest thing, but at least I'm prepared now. 

Irish you are so right about keeping moving. I've been doing a 20 day Bikram yoga challenge and even today when I just wanted to roll up in my mat and snooze through the rest of class it was worth it for how much better I felt afterwards! 

 

Oldest son had gotten thrush with cold bugs his entire life -- pre gluten removal -- now it is very rare -- can't remember the last time it happened to him...this month is his five year anniversary :)

 

In my experience -- no matter which decade I was living -- when joints are in pain it is time to take it easy on exercise...that doesn't mean stop...just meant I skied half day instead of whole (ok fuzzy math there...more like 6 hours instead of 8)...and rode my bike shorter distances...walked a little slower...you get the picture. 

 

Hang in there :)

KCG91 Enthusiast

GottaSki that's interesting that he had the same problem! Since March (when the doc made the link) I actually haven't had a problem (which is the longest break in ages). 

 

I think you may be in league with my knees...those tight runner's quads which sometimes cause knee pain have flared up so I'm taking the hint and scaling it back a bit :) My (wonderful!) new GP couldn't check for carpal tunnel symptoms as the pain is now gone but she's re-running all the usual coeliac bloods, including rheumatoid (not sure exactly what test) which should shed a bit more light. 

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,546
    • Most Online (within 30 mins)
      7,748

    KimberlyAnne76
    Newest Member
    KimberlyAnne76
    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.