To all Granuloma Annulare sufferers - what else is going on?

Posted , 91 users are following.

I have GA for 8 years - we all know that this skin disease itself is not painful however I want to know if other things are going on within your body? 

I, personally, have issues with toe and leg cramps and nerve pain. Is this related or something else all together?

If you could please share your personal experience, I believe we need all info to assist each other.

Thanks,

Carole

6 likes, 207 replies

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  • Posted

    ive had ga for about 4 years and now it hardly shows...i take boswella caps and i have cut nightshades out of my diet
  • Posted

    Hi everyone. Stumbled across this thread whilst trying to look for some clues about this stuff on my skin that's been present for about 3 months. Started as a small ring on my left elbow, now that ring is somewhat bigger, there is another next to it and also a small ring now formed by my knicker line (approx 1-2 months). Neither of these patches have been itchy. The colour changes though-sometimes skin coloured, other times purple..I'm not sure what flares it up (I think heat I.e getting out of a bath or shower?). I went to the doctors and was tested for dermatitis herpetiformis and a gluten intolerance. Blood tests came back clear. The doctor didn't mention GA at all, it is just my own theory and research which has led me to think it is GA. It doesn't bother me too much, although the fact it 'spread' to the top of my leg is of some concern as from reading online, when GA is generalised it could mean diabetes, which I see somebody of you have mentioned on here.

    I relative this is an old thread...has any one had any more updates from the remedies they have been trying?

    Thanks

    Hannah

    • Posted

      Also forgot to mention that I had fixed braces on my teeth for the last 5 months. A common occurance in this thread was also dental work maybe being a cause of GA..
    • Posted

      I had braces also. I feel it definitely can be associated with dental work but the Ga showed up before my fillings were removed and replaced. Mosquito bites/no see ums make it flare up and seem unmanageable. It's such a weird disease

    • Posted

      Did they do a biopsy of the spot?  I don't know if it can be diagnosed any other way.

      Mine was diagnosed by biopsy taken on my first appointment with a dermatologist after I started breaking out. I first went to my primary & she said, well it's not... - and then named several skin disorders and referred me to a dermatologist.

      Good luck!

      Patty

    • Posted

      I had braces on my teeth when I was in my early 40s.  I'm now in my 70s and did not get GA until I was in my late 60s so at least 25 years after the braces so I would say that for me, having braces did not contribute to getting GA.

       

    • Posted

      Thanks for the replies smile I haven't had a biopsy...just saw my GP and he said either DH/glucose intolterence, an insect bite reaction or friction?! I had a blood test for the DH/glucose which came back clear and heard nothing more...

      It seems no one really know but it's so good to hear people's thoughts and feelings on it. In all honesty, I think its down to stress-it can do all sorts of stuff to you can't it. I'll try and "De-stress", monitor these rings/patches on my skin and go with the flow I think

      Hannah

    • Posted

      The only thing that could have caused mine is the bad eating habits I had along with the fact I had diverticulitis. And the summer this started I had gotten eaten alive by hundreds of mosquitoes. I read somewhere back in 2014 that GA is a result of extra white bloods cells. I can no longer find that. It has slightly disappeared over the years after starting on the back of my elbow then to identical spots on each hip and identical spots on the backs of my legs and a spot on my belly. . However. I got pregnant end of may and since then it has for the most part disappeared.. however my diet has changed also. I eat way more home-cooked meals no fast food and barely restaurant food.
  • Posted

    I first started noticing a spot on my ankle around 2011. I wasn't formally diagnosed with GA until 2015 after requesting a biopsy. I have Type 1 Diabetes (diagnosed in 1995), hypothyroid (diagnosed in 2009), and alopecia areata (diagnosed in 2010). I received corticosteroid injections on my scalp to treat my alopecia, which cured it completely. I first noticed my GA sometime after my corticosteroid treatments. My first spot is on my right ankle. It was about the size of a dime when I noticed it and has since grown to an ellipse about 3 inches in diameter. I also have a spot on the side of my left foot about the size of a dime. I'm worried that one will grow as big as the first one. 

  • Posted

    Hi Carol, I have GA all over as well but as of late August I started getting leg cramping, tingling /numbing feeling in my hands and feet from knees down. I haven't found anything that works yet.

  • Posted

    Ok. I'm turning 60 and was diagnosed with biopsy 7 years ago. It started on the back of my neck not long after too much sun and an almost burn (I do a lot of trail running). The dermatologist said, "Oh, it will go away in 1-2 years" but it has continued to spread on both sides around my neck and looks like it will meet on my throat in the next year. The derm thought that the sun exposure was unrelated but it was just weeks before this started.

    I started developing leg and foot cramps around the same time. Again, I'm a runner and for sure they're worse after long runs or after lay-offs but I rarely had them before I got GA. Could be coincidence. One of my sons has developed chronic urticaria and it makes me wonder if there is a genetic component to autoimmune skin conditions.

  • Posted

    Hi Carole, 

    I'm 59, live in Tennessee, and have had Annulare since 2011. It appeared a few months after I had brain surgery (I had a large benign tumor). After the surgery I stopped taking BC pills. But there was a trauma, which seems to be a pattern(?) I was under anesthesia, then on steroids for a few weeks.

    I fight fatigue, difficulty concentrating at times, and have more muscle aches than before, but it's too hard to sort out what causes what. I'm nearly 100% after my illness, though, so I thank God for that. The aches and pains could be age too. smile

    Have you ever heard of Morgellons or other possible environmental causes? I've wondered if there was a connection since that is a skin disorder as well. It definitely seems to be immune related. I give myself regular B12 shots and that helps a lot with the redness. Oregano oil helps a little too. Beefing up the immune system seems to be important. Has anyone tried a full on 'diet' cure - non-gmo, organic greens and berries etc..?

    Let me know what all you find out! I've got one on my tongue now(!) It feels almost like the beginnings of a cold sore.... and of course, it's ugly. sad

    Yvonne

  • Posted

    I have had GA for at least 35 years, it moves around, mostly on my feet and elbows, it never itches.  It is an autoimmune disorder. In addition I have hypothyroidsm which was diagnosed about 14 years ago and also lower than normal platelet count.  My sister's hypothyroidism has turned into Hashimoto's which is another autoimmune disorder. I suspect I may also have elevated candida in my body.  I do get toe cramps if I drink alcohol, but not leg cramps.  I also have hip pain (sacroiliac joint).  Recently I discovered that fluoride is bad for hypothyroidsm so I started drinking bottled water and am adding a reverse osmosis system on my tap water.  I've also eliminated soy and gluten from my diet and taking probiotics and L-Glutamine. My GA is slightly lighter already.  I will post future updates if I get any better.  I recommend searching the web for info on treating autoimmune disorders. Dermatologists are useless because you are treating the symptom and not the cause.

  • Posted

    I have had this 3 years now an argue with it daily!! Mine does itch sometimes but I control that w itch crime...  I have spent/dieted/ cried and all of the above...my Derm is one of the best but as was said by others there is no cure, only maintenance if u can find it..if it goes away as some do, it returns with a vengeance!!

    i am not crazy but my husband and I are convinced that it has its own brain and the game is to control me and fight ea thing I come up with! 

    I now am more in control than not but it gets quite angr and will turn almost purple..then get quiet!

    i use Tea Tree Oil multiple times a day without fail..I keep it upstairs downstairs in all 3 cars in my purse and travel bags!  When it's visible you will use it!! I mix it with Calendula Gel to give it adherence..TTO does dry out the skin and w Reg use you must hydrate about an hr or 2 later. I use 'Silver Gel (cvs) for cracking or splits..vasciline does not work because GA does not like to be covered, I was desperate.. I purchased recently a hand cream I used for years for winter cracking, 

    Camille Beckman Glycerin Hand Therapy...I am having GREAT results

    For your cramps..put a bar of any soap at your  feet between your sheets..this is a guarantee, if the cramp is very bad rub soap even had soap on the area..gone is seconds I promise..sounds nuts but a Dr told me that years ago, it works!

    my MD gave me a Lupus medicine when I had a MAJOR outbreak 'Hydroxychloquine', this really helped. Autoimmune medicines can had side effects but I had none! Good Luck and give this lots of attention.. I tried it ALL and am still in the works!  Also B12..D..E vitamins help!

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