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What Is Wrong With Me


rube2112

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rube2112 Newbie

Hi, I'm new to this board.  I know your not doctors etc but I just want to hear what my symptoms sound like to you.  I'm desperate.  

Joint pain, serious gut problems, had c-diff, serious eye inflammation, strange rashes on a few of my fingers, some neuropathy in a few different places, positive rheumatoid factor test and positive anti-ccp test.  tingling in hands and forearms especially when I wake up.  weight gain especially in abdominal area, serious fatigue, strange mask like feeling across my forehead.....chronic sinus infection that won't go away no matter what.   .there are probably other symptoms but you get the idea...

 

I've had celiac antibody test and it was neg, plus I've had gut biopsy done and it was also negative......please help.....Thanks....Robb

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guest134 Apprentice

"Anti-CCP is a very useful test to order during the Open Original Shared Link of a person who may have rheumatoid arthritis. If present in such a patient at a moderate to high level, it not only confirms the diagnosis but also may indicate that the patient is at increased risk for damage to the joints. Low levels of this antibody are less significant. In the past, doctors relied on another antibody, the Open Original Shared Link to help confirm a diagnosis."

You had two positive tests that were very specific for Rheumatoid arthritis, it looks to me like that is your issue. Has your doctor diagnosed you with R.A? Here are the symptoms:


  • Stiffness: The joint does not move as well as it once did. Its Open Original Shared Link (the extent to which the appendage of the joint, such as the arm, leg, or finger, can move in different directions) may be reduced. Typically, stiffness is most noticeable in the morning and improves later in the day.
  • Inflammation: Redness, tenderness, and warmth are the hallmarks of inflammation.
  • Swelling: The area around the affected joint is swollen and puffy.
  • Nodules: These are hard bumps that appear on or near the joint. They often are found near the elbows. They are most noticeable on the part of the joint that juts out when the joint is flexed.
  • Pain: Pain in rheumatoid arthritis has several sources. Pain can come from inflammation or swelling of the joint and surrounding tissues or from working the joint too hard. The intensity of the pain varies among individuals

    If I were to guess I would say that you have both Hashimoto's thyroiditis (autoimmune hypothyroid) and Rheumatoid arthritis. You already have your diagnostic tests for RA so start with that treatment and get the following done for your thyroid:
    Thyroid peroxidase ab
    Thyroglobulin ab
    Free T4 
    Free T3
    TSH

    I had a friends father who had both hashimoto's and R.A and your symptoms are dead on with what he had. Luckily, both can be managed with medication and some lifestyle adjustments. With a negative Celiac blood panel and biopsy I think it is pretty safe to write off that being the issue, do you know which tests they ran? It would be helpful if you could post up all results of your autoimmune tests.
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Juliebove Rising Star

Agree that it could be thyroid.  Also could be diabetes.

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rube2112 Newbie

Hi there, thank you so much for the replies.  My rheumatoid factor I was told was only doubled which my doctor said wasn't that bad.  I don't have access yet to the anti ccp test....here are my thyroid labs...

 

Reverse T3, Serum070105 27.7 13.5-34.2 ng/dL
**Please note reference interval change**

TSH+T4F+T3Free
Date Collected: 10/25/2012 12:45:00 PM

Test Description Result Range Units
TSH004264 2.64 0.450-4.500 uIU/mL
Triiodothyronine,Free,Serum010389 2.4 2.0-4.4 pg/mL
T4,Free(Direct)019745 1.02 0.82-1.77 ng/dL

 

I'm not going to survive if this doesn't get figured out soon because it has taken away every reason for living that I had.  

I am being treated for the reheumatoid arthritis with 20 mg methotrexate per week and it has done absolutely nothing.  I will not let them give me more or give me a biological because of the c-diff.  My new doctore has put me on a diet of only cod, salmon, and leafy greens.  I've been on the diet for 5 days and I can't report anything positive yet.  I can't do anything for myself really because of the mailaise fatigue etc.....

Thanks, Robb

 

 

 

"Anti-CCP is a very useful test to order during the Open Original Shared Link of a person who may have rheumatoid arthritis. If present in such a patient at a moderate to high level, it not only confirms the diagnosis but also may indicate that the patient is at increased risk for damage to the joints. Low levels of this antibody are less significant. In the past, doctors relied on another antibody, the Open Original Shared Link to help confirm a diagnosis."

You had two positive tests that were very specific for Rheumatoid arthritis, it looks to me like that is your issue. Has your doctor diagnosed you with R.A? Here are the symptoms:


  • Stiffness: The joint does not move as well as it once did. Its Open Original Shared Link (the extent to which the appendage of the joint, such as the arm, leg, or finger, can move in different directions) may be reduced. Typically, stiffness is most noticeable in the morning and improves later in the day.
  • Inflammation: Redness, tenderness, and warmth are the hallmarks of inflammation.
  • Swelling: The area around the affected joint is swollen and puffy.
  • Nodules: These are hard bumps that appear on or near the joint. They often are found near the elbows. They are most noticeable on the part of the joint that juts out when the joint is flexed.
  • Pain: Pain in rheumatoid arthritis has several sources. Pain can come from inflammation or swelling of the joint and surrounding tissues or from working the joint too hard. The intensity of the pain varies among individuals

    If I were to guess I would say that you have both Hashimoto's thyroiditis (autoimmune hypothyroid) and Rheumatoid arthritis. You already have your diagnostic tests for RA so start with that treatment and get the following done for your thyroid:
    Thyroid peroxidase ab
    Thyroglobulin ab
    Free T4 
    Free T3
    TSH

    I had a friends father who had both hashimoto's and R.A and your symptoms are dead on with what he had. Luckily, both can be managed with medication and some lifestyle adjustments. With a negative Celiac blood panel and biopsy I think it is pretty safe to write off that being the issue, do you know which tests they ran? It would be helpful if you could post up all results of your autoimmune tests.
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guest134 Apprentice

Robb, I am really sorry to hear how poorly you feel, hopefully you can get to the bottom of it soon.

The thing with the gluten free diet is that it does not require a prescription.... You are free to do it on your own, so why not give it a try? Desperate times call for desperate measures and you can very well have NCGI. That being said I think it is important to not put too much weight into gluten intolerance as there are many other things that need to be evaluated. 

For your free levels of thyroid, your T4 feeds your T3 basically and your T3 is what your body uses. So the lack of proper binding of T3 from T4 is usually what will cause the symptoms. Now the thing is that they are just beginning to discover that having elevated thyroid antibodies (Thyroid peroxidase, Thyroglobulin) will also cause the symptoms. You have to remember, when an autoimmune disease begins it is not just one big attack and then the organ/gland is left completely useless, it takes time. So for all we know, without having the antibodies tested, is that you are in fact in the beginning stages of Hashimoto's.

Another red flag for me is that even though your thyroid levels are in the "normal" range they are getting pretty close to the bottom of the range, especially the T3. For those reasons I would recommend insisting on the antibody tests that I just listed. There is a poster on this forum that got a diagnosis when her blood tests were positive and if I recall correctly her thyroid hormones were still normal but in the very low normal. Her username is nvsmom, you should contact her to get some info as from what I read she has responded well to treatment. Ideally, you want your T4 to be around 50 percent of the range while your T3 is the upper 66-80 percent. Most patients feel best at these levels.

Also, have you had the ANA and other associated antibodies looked at? Your symptoms also ring the lupus bell to me.

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ravenwoodglass Mentor

Don't have much time so this will be brief. You have nothing to lose by giving the diet a good strict try for a couple of months once all celiac testing is over. You may have more than one thing going on but the diet may give you some relief. Going gluten free won't effect testing for other problems.

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rube2112 Newbie

Thanks for the reply........if I get a lupus diagnosis I will kill myself..........plain and simple.

I have tested negative for thyroid antibodies but I'm not sure which test it was.  I can't get any of my doctors to do anything for me or to run more tests and since I've been working on this for months, I just don't have to energy anymore to call new doctors, wait a month for open appointments, etc.  I'm just not sure how to proceed anymore....Robb

 

 

Robb, I am really sorry to hear how poorly you feel, hopefully you can get to the bottom of it soon.

The thing with the gluten free diet is that it does not require a prescription.... You are free to do it on your own, so why not give it a try? Desperate times call for desperate measures and you can very well have NCGI. That being said I think it is important to not put too much weight into gluten intolerance as there are many other things that need to be evaluated. 

For your free levels of thyroid, your T4 feeds your T3 basically and your T3 is what your body uses. So the lack of proper binding of T3 from T4 is usually what will cause the symptoms. Now the thing is that they are just beginning to discover that having elevated thyroid antibodies (Thyroid peroxidase, Thyroglobulin) will also cause the symptoms. You have to remember, when an autoimmune disease begins it is not just one big attack and then the organ/gland is left completely useless, it takes time. So for all we know, without having the antibodies tested, is that you are in fact in the beginning stages of Hashimoto's.

Another red flag for me is that even though your thyroid levels are in the "normal" range they are getting pretty close to the bottom of the range, especially the T3. For those reasons I would recommend insisting on the antibody tests that I just listed. There is a poster on this forum that got a diagnosis when her blood tests were positive and if I recall correctly her thyroid hormones were still normal but in the very low normal. Her username is nvsmom, you should contact her to get some info as from what I read she has responded well to treatment. Ideally, you want your T4 to be around 50 percent of the range while your T3 is the upper 66-80 percent. Most patients feel best at these levels.

Also, have you had the ANA and other associated antibodies looked at? Your symptoms also ring the lupus bell to me.

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GottaSki Mentor

Good Morning Robb-

 

You are right - we are not doctors - but personally I have way too much experience with Lupus and other AIs that often run together with Celiac Disease.

 

My daughter was diagnosed with Lupus at 13...she'll be turning 30 next month and is living a very full life...has it been easy? No.  

 

Here is the interesting thing -- none of my kids tested positive on the celiac antibody tests -- with the exception of my daughter's DGP - IgG at 25 years of age.  ALL of them and my grandkids have had some or complete improvement in all our miscellaneous autoimmune symptoms since we removed gluten four years ago.  Regardless of your celiac antibody tests...with your symptoms remove gluten for at least three months - six is better while you keep working with your doctors to diagnose possible other AIs.

 

All that said -- I would be remiss if I did not address the statement about killing yourself.  Many of us understand how frustrating and hopeless getting a diagnosis can far to often be -- but you can get better.  If you are seriously feeling like you can not go on - call 

 

Eight hundred - 273 - TALK

 

or visit their website of that of another agency -- there are people trained to help.

 

Open Original Shared Link

 

Take care and let us know if we can help walk you through your upcoming doctor appointments - preparing for these appts can really help empower you.

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rube2112 Newbie

Hi again, None of my doctors are even trying to run more tests.  I have begged and its just not going to happen.  They wouldn't believe that I had a gut infection and it took me driving 2 hours to a distant hospital and begging them to do a stool sample which confirmed c-diff.  Even then, after first round of abx, they wouldn't retest me.  Drove two hours again and confirmed c-diff again.  My rheumatologist keeps trying to get me to take nsaids and they set off my gerd so bad that I can't function.  If I persue any more treatment like biologicals etc, I will die of c-diff.  Robb

 

 

 

 

Good Morning Robb-

 

You are right - we are not doctors - but personally I have way too much experience with Lupus and other AIs that often run together with Celiac Disease.

 

My daughter was diagnosed with Lupus at 13...she'll be turning 30 next month and is living a very full life...has it been easy? No.  

 

Here is the interesting thing -- none of my kids tested positive on the celiac antibody tests -- with the exception of my daughter's DGP - IgG at 25 years of age.  ALL of them and my grandkids have had some or complete improvement in all our miscellaneous autoimmune symptoms since we removed gluten four years ago.  Regardless of your celiac antibody tests...with your symptoms remove gluten for at least three months - six is better while you keep working with your doctors to diagnose possible other AIs.

 

All that said -- I would be remiss if I did not address the statement about killing yourself.  Many of us understand how frustrating and hopeless getting a diagnosis can far to often be -- but you can get better.  If you are seriously feeling like you can not go on - call 

 

Eight hundred - 273 - TALK

 

or visit their website of that of another agency -- there are people trained to help.

 

Open Original Shared Link

 

Take care and let us know if we can help walk you through your upcoming doctor appointments - preparing for these appts can really help empower you.

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Tiredsean Explorer

May I ask Robb how long you've been struggling? Are you male/female and age? AI,s can vary from types that affect certain gender and age.Please feel free to keep posting but also please don't jump to conclusions.I know it's tuff with today's medical system to get help and rapid help, but don't do anything drastic .Lots of AI,s have treatements,remission and depending on the cause sometimes a cure

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rube2112 Newbie

I'm male 48 in Ohio.  The problem started 15 years ago.  First symptom, increased hunger, sinus infection that wouldn't go away then 6 months later, right shoulder was attacked, then left shoulder, then wrists. Robb

 

 

 

 

May I ask Robb how long you've been struggling? Are you male/female and age? AI,s can vary from types that affect certain gender and age.Please feel free to keep posting but also please don't jump to conclusions.I know it's tuff with today's medical system to get help and rapid help, but don't do anything drastic .Lots of AI,s have treatements,remission and depending on the cause sometimes a cure

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guest134 Apprentice

Ok, well Lupus at 48 is rather uncommon. Even if you did have Lupus, why would you end your life? Would you really want to succumb to this? You have to be stronger than that! My grandfathers brother had Lupus, guess what age he lived to? 92, no I am not kidding you NINETY-TWO. My grandfather who was perfectly healthy lived until 88. Lupus is known to often go into long periods of remission in which some people can even reach nearly a decade of symptom resolution. Would you rather not have it? Of course, everyone on this forum would like to be able to eat gluten without it destroying their intestines but you learn to cope and you become stronger because of it.

You sound like you are in awful shape right now, so it can only get better from here. If you get diagnosed with lupus, well guess what? You get treatment, and it will help push it into remission. At this point, it is only upwards for symptoms so don't give up and don't even think about ending your life because of it! There are a lot of people here that have multiple autoimmune diseases, they are all doing fine. 

Go look through my old threads about my panic about Celiac when I was first faced with it's probable reality, I look back on those posts and laugh now. I also had a childhood friend that was diagnosed with Lupus very early and he is as healthy as anyone else, in fact at this point I would say he is in much better shape than me and most of my friends. The anxiety and depression that come with being newly diagnosed are temporary, you are in a TEMPORARY state of mind right now so it is very important to not act out in any harsh way because of it. 

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rube2112 Newbie

Thanks, I just wish my stupid doctors would listen to me when I try to explain how bad I feel.  The methotrexate has done absolutely nothing.  In fact, I think it has made me worse.  I'm due to take it tomorrow and I think I'm going to stop it.  Its dangerous and isn't helping anyway.  Robb

Ok, well Lupus at 48 is rather uncommon. Even if you did have Lupus, why would you end your life? Would you really want to succumb to this? You have to be stronger than that! My grandfathers brother had Lupus, guess what age he lived to? 92, no I am not kidding you NINETY-TWO. My grandfather who was perfectly healthy lived until 88. Lupus is known to often go into long periods of remission in which some people can even reach nearly a decade of symptom resolution. Would you rather not have it? Of course, everyone on this forum would like to be able to eat gluten without it destroying their intestines but you learn to cope and you become stronger because of it.

You sound like you are in awful shape right now, so it can only get better from here. If you get diagnosed with lupus, well guess what? You get treatment, and it will help push it into remission. At this point, it is only upwards for symptoms so don't give up and don't even think about ending your life because of it! There are a lot of people here that have multiple autoimmune diseases, they are all doing fine. 

Go look through my old threads about my panic about Celiac when I was first faced with it's probable reality, I look back on those posts and laugh now. I also had a childhood friend that was diagnosed with Lupus very early and he is as healthy as anyone else, in fact at this point I would say he is in much better shape than me and most of my friends. The anxiety and depression that come with being newly diagnosed are temporary, you are in a TEMPORARY state of mind right now so it is very important to not act out in any harsh way because of it. 

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IrishHeart Veteran

Robb, you sound a lot like me and my friend Sherry (Dxed with c-diff in tandem with her celiac DX).

Do not give up. 

 

I was a mess before my DX. I even tried methotrexate (against my better judgement) upon the insistence of a snarky rheumatolgist. It made my gut worse and did nothing for the joint/bone pain. If a gut is impaired, meds can make us feel ten times worse. The meds are not absorbed. and may instead circulate in the body. I still can't tolerate medications at all. 

 

Your negative celiac tests are perplexing, but not uncommon. My celiac panel was negative, yet I have celiac.

And you could be gluten intolerant (not a celiac YET) and still have all the symptoms and AI diseases you have mentioned.

 

You need a better GI doctor. I wish you lived in NY...I'd walk you right into my guy in a heartbeat. You deserve to be taken seriously.

 

Please do not give up. I was in your boat for 3 years and I am a different person 2 years later. I have reclaimed my life and you can too.

 

I know that C-diff responds well to probiotics.  Lots of Pub Med journal articles on this, so please consider taking them.

Give the gluten-free/DF diet a strict trial for several months. Try to be patient (I know that is hard when you are in pain and feeling like total shyte, but please believe me, Lisa (Gotta Ski) and I GET IT. ) We share your painful symptoms,  but we have also improved drastically off gluten. We had a long road, but we're living proof healing happens. 

 

Dismissed by dozens of docs for many years, we know full well how frustrated you are.  But, you are not alone. 

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GottaSki Mentor

Robb, you sound a lot like me and my friend Sherry (Dxed with c-diff in tandem with her celiac DX).

Do not give up. 

 

I was a mess before my DX. I even tried methotrexate (against my better judgement) upon the insistence of a snarky rheumatolgist. It made my gut worse and did nothing for the joint/bone pain. If a gut is impaired, meds can make us feel ten times worse. The meds are not absorbed. and may instead circulate in the body. I still can't tolerate medications at all. 

 

Your negative celiac tests are perplexing, but not uncommon. My celiac panel was negative, yet I have celiac.

And you could be gluten intolerant (not a celiac YET) and still have all the symptoms and AI diseases you have mentioned.

 

You need a better GI doctor. I wish you lived in NY...I'd walk you right into my guy in a heartbeat. You deserve to be taken seriously.

 

Please do not give up. I was in your boat for 3 years and I am a different person 2 years later. I have reclaimed my life and you can too.

 

I know that C-diff responds well to probiotics.  Lots of Pub Med journal articles on this, so please consider taking them.

Give the gluten-free/DF diet a strict trial for several months. Try to be patient (I know that is hard when you are in pain and feeling like total shyte, but please believe me, Lisa (Gotta Ski) and I GET IT. We share your painful symptoms  but we have also improved drastically off gluten. We had a long road, but we're living proof healing happens. 

 

Could not have said it better myself - and yes IrishHeart and I both have walked in your painful - frustrated - sick to death of doctors dismissing our symptoms - shoes.

 

I still wake each morning in a great deal of pain -- a 15-20 minute soak in hot epsom salt bath gets me moving and then unless I run into a food from my no-no list I am generally full steam until evening -- it has been at least ten years since I could say that! 

 

If doctors have run ALL of your celiac antibody tests then remove gluten as soon as possible.  If you are unsure if everything has been run - post them here and we can help sort out if you need other tests -- then demand, don't ask for them -- our doctors work for us -- even though they often forget this ;)

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rube2112 Newbie

Hi, Thanks for everyone responding, I have had Prometheus celiac antibody test but not the genetic test.  I've been gluten free and dairy free for exactly 7 days.  My alternative MD has me on the following diet.  Wild caught cod, wild caught salmon, leafy greens, carrots.  Thats it.  I've been taking colostrum and it stopped the diarrhea, but I think it is also raising my immune system and make my whole gut ache a little worse every day.  I picked colostrum because of its track record with c-diff.  I'm thinking about trying to beg someone into ordering the cyrex gluten sensitivity test, but I serlously doubt that I will get it.  My lower back pain is getting worse for some reason and my eyes are constantly running.  There just seems to be no end.  Robb

 

 

 

Could not have said it better myself - and yes IrishHeart and I both have walked in your painful - frustrated - sick to death of doctors dismissing our symptoms - shoes.

 

I still wake each morning in a great deal of pain -- a 15-20 minute soak in hot epsom salt bath gets me moving and then unless I run into a food from my no-no list I am generally full steam until evening -- it has been at least ten years since I could say that! 

 

If doctors have run ALL of your celiac antibody tests then remove gluten as soon as possible.  If you are unsure if everything has been run - post them here and we can help sort out if you need other tests -- then demand, don't ask for them -- our doctors work for us -- even though they often forget this ;)

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kareng Grand Master

Sorry you are having so much trouble and feeling so down. Don't want you to waste your money, too!

Open Original Shared Link

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IrishHeart Veteran

As Karen has pointed out, there is no valid test for gluten sensitivity just yet. Save your cash.

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GottaSki Mentor

Hi Robb-

 

Has your pain increased on the diet you just listed?  If so, it is entirely possible it just is not the correct combo for you. For instance I consumed quite a bit of fresh spinach over the past few years -- thinking it was the best green for me -- WRONG -- it is high in histamine -- if you have severe damage in your small intestine - your body can't produce the enzyme necessary to regulate histamine.

 

Perhaps your body doesn't want that much fish?  Can you substitute chicken, beef or pork for a few days to see if it helps...

 

I completely understand the frustration that comes when you discover while eating seamingly perfect foods - they are not the right ones for your body.

 

Also, you are only at 7 days...your body could simply be detoxing -- I never really detoxed when I removed gluten -- but when I did a complete elimination diet -- it took my body about two or three weeks to detox.

 

PS>>> I agree -- don't waste your money on those tests.

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rube2112 Newbie

Hi, I honestly am so weary that I have no idea what try.  I've been unable to work since aug....My stomach hurts so bad today that I havn't eaten at all.  My latest ridiculous diagnosis is reactive hypoglycemia.  The only problem with that is that I've monitored my sugar for several days and it sits at 85 whether I eat or not.  The doctor that gave me that diagnosis argued with me and told me she was positive thats what my problem was.  She is wrong.  The dumb guesses these doctors are making isn't helping me at all.......Robb

 

 

 

 

Hi Robb-

 

Has your pain increased on the diet you just listed?  If so, it is entirely possible it just is not the correct combo for you. For instance I consumed quite a bit of fresh spinach over the past few years -- thinking it was the best green for me -- WRONG -- it is high in histamine -- if you have severe damage in your small intestine - your body can't produce the enzyme necessary to regulate histamine.

 

Perhaps your body doesn't want that much fish?  Can you substitute chicken, beef or pork for a few days to see if it helps...

 

I completely understand the frustration that comes when you discover while eating seamingly perfect foods - they are not the right ones for your body.

 

Also, you are only at 7 days...your body could simply be detoxing -- I never really detoxed when I removed gluten -- but when I did a complete elimination diet -- it took my body about two or three weeks to detox.

 

PS>>> I agree -- don't waste your money on those tests.

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rube2112 Newbie

Merry Christmas..........my C-Diff is back........Robb

 

 

 

Robb, you sound a lot like me and my friend Sherry (Dxed with c-diff in tandem with her celiac DX).

Do not give up. 

 

I was a mess before my DX. I even tried methotrexate (against my better judgement) upon the insistence of a snarky rheumatolgist. It made my gut worse and did nothing for the joint/bone pain. If a gut is impaired, meds can make us feel ten times worse. The meds are not absorbed. and may instead circulate in the body. I still can't tolerate medications at all. 

 

Your negative celiac tests are perplexing, but not uncommon. My celiac panel was negative, yet I have celiac.

And you could be gluten intolerant (not a celiac YET) and still have all the symptoms and AI diseases you have mentioned.

 

You need a better GI doctor. I wish you lived in NY...I'd walk you right into my guy in a heartbeat. You deserve to be taken seriously.

 

Please do not give up. I was in your boat for 3 years and I am a different person 2 years later. I have reclaimed my life and you can too.

 

I know that C-diff responds well to probiotics.  Lots of Pub Med journal articles on this, so please consider taking them.

Give the gluten-free/DF diet a strict trial for several months. Try to be patient (I know that is hard when you are in pain and feeling like total shyte, but please believe me, Lisa (Gotta Ski) and I GET IT. ) We share your painful symptoms,  but we have also improved drastically off gluten. We had a long road, but we're living proof healing happens. 

 

Dismissed by dozens of docs for many years, we know full well how frustrated you are.  But, you are not alone. 

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GottaSki Mentor

Merry Christmas..........my C-Diff is back........Robb

 

Hang in there....IrishHeart is spot on...you are not alone - many of us have been through similar frustrations.  It can get better.

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rube2112 Newbie

This is round three.  I honestly don't think its going to get better because of the inflammation in my gut.  I've had that same exact problem with my sinus infection for the last 15 years.....now its in my gut.  All of the vancomycin in the world isn't going to clear it up.  Robb

 

 

 

 

Hang in there....IrishHeart is spot on...you are not alone - many of us have been through similar frustrations.  It can get better.

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    • powerofpositivethinking
      I haven't been on this forum for a long time, but it was absolutely wonderful during the diagnostic process!  My path for celiac disease diagnosis was the following: -Had normal IgA level, and my only serology positive test was the DGP IgG -Deficiencies in both Vitamins D and K that did not increase at first despite massive supplementation -Diagnosis of fat malabsorption both total and neutral -Diagnosis of severe exocrine pancreatic insufficiency (EPI) -Testing was completed to rule out causes of EPI, and the only one not ruled out was celiac. -Both traditional endoscopy and pill capsule endoscopy yielded negative results for biopsy confirmation, but my GI doctor said that both procedures simply could have missed the damaged spots. -EPI and fat malabsorption resolved after taking Creon for 6 months since my EPI was caused by celiac -23 and Me said I don't have either of the two prominent genes for celiac disease   Remember that you might not have 'textbook' symptoms, but you still may have celiac disease.   Also, I am SO incredibly grateful for this site for all the learning it has allowed me to do. I have a senior dog, and these last few weeks with her were very scary! After two hospital stays, she finally received an IBD diagnosis after having gastroenteritis and pancreatitis. I know that celiac disease is not IBD, however, through reading this site, I learned more about it. I was relieved when I found out she had IBD and not cancer this past Wednesday. I know IBD can be managed thanks to what I've learned here!  So celiac.com, not only did you help me, but you helped my pup too! Thank you ❤️  
    • SuzanneL
      It was tTG IGG that was flagged high. I'm not sure about the other stuff. I'm still eating my normal stuff. 
    • cristiana
      Thank you for your post, @Nedast, and welcome to the forum. It is interesting to read of your experiences. Although I've not had TMJ, from time to time I have had a bit of mild pain in my jaw, sharp stabbing pains and tingling in my face which appears to have been caused by issues with my trigeminal nerve.  I read that sometimes a damaged trigeminal nerve in coeliacs can heal after adopting a gluten free diet.  I try to keep out of cold winds or wear a scarf over my face when it is cold and windy, those conditions tend to be my 'trigger' but I do think that staying clear of gluten has helped.  Also, sleeping with a rolled up towel under my neck is a tip I picked up online, again, that seems to bring benefits. Thank you again for your input - living with this sort of pain can be very hard, so it is good to be able to share advice.
    • Julie Riordan
      I am going to France in two weeks and then to Portugal in May   Thanks for your reply 
    • Nedast
      I made an account just to reply to this topic. My story resembles yours in so many ways that it is truly amazing. I also suddenly became lactose intolerant, went a little under 10 years attributing all my symtoms to different body parts, never thinking it was something systemic until much later. I had the same mental problems - anxiety, depression, fatigue, etc. In fact, the only real difference in our story is that I was never formally diagnosed. When I discovered that my myriad symtoms, that had been continuous and worsening for years, all rapidly subsided upon cessation of consuming gluten, I immediately took it upon myself to cut gluten out of my diet completely. I live in America, and had lost my health insurance within the year prior to my discovery, so I could not get tested, and I will never willingly or knowingly consume gluten again, which I would have to do in order to get tested now that I have insurance again. But that is not the point of this reply. I also had extreme TMJ pain that began within months of getting my wisdom teeth out at - you guessed it - 17 years old. I was in and out of doctors for my various symptoms for about 5 years before I gave up, but during that time I had also kept getting reffered to different kinds of doctors that had their own, different solutions to my TMJ issue, an issue which I only recently discovered was related to my other symptoms. I began with physical therapy, and the physical therapist eventually broke down at me after many months, raising her voice at me and saying that there was nothing she could do for me. After that saga, I saw a plastic surgeon at the request of my GP, who he knew personally. This palstic surgeon began using botox injections to stop my spasming jaw muscles, and he managed to get it covered by my insurace in 2011, which was harder to do back then. This helped the pain tremendously, but did not solve the underlying problem, and I had to get repeat injections every three months. After a couple of years, this began to lose effectiveness, and I needed treatments more often than my insurance would cover. The surgeon did a scan on the joint and saw slight damage to the tissues. He then got approved by insurance to do a small surgery on the massseter (jaw) muscle - making an incision, and then splicing tissue into the muscle to stop the spasming. It worked amazingly, but about three months later it had stopped working. I was on the verge of seeing the top oral surgeon in our city, but instead of operating on me, he referred me to a unique group of dentists who focus on the TMJ and its biomechanical relationship to teeth occlusion (i.e. how the teeth fit together). This is what your dentist did, and what he did to you was boderline if not outright malpractice. There is a dental field that specializes in doing this kind of dental work, and it takes many years of extra schooling (and a lot of money invested into education) to be able to modify teeth occusion in this manner. Just based on the way you describe your dentist doing this, I can tell he was not qualified to do this to you. Dentists who are qualified and engage in this practice take many measurments of your head, mouth, teeth, etc., they take laboratory molds of your teeth, and they then make a complete, life-size model of your skull and teeth to help them guide their work on you. They then have a lab construct, and give you what is called a "bite splint." It looks and feels like a retainer, but its function is entirely different. This is essentially a literal splint for the TMJ that situates on the teeth. The splint is progressively modified once or twice per week, over several months, in order to slowly move the joint to its correct position. The muscles spasm less, stress is taken off the joint, as the joint slowly moves back into its proper position. The pain reduces each month, each week, sometimes even each day you go in for a visit. The joint has to be moved in this manner with the splint BEFORE the modification to the teeth begins. They then add to your tooth structure with small bits of composite, to keep the joint in its proper place after it has been sucessfully repositioned. Subtracting from your teeth, by grinding down bits of your natural tooth structure, is done very conservatively, if they have to do it at all. This process worked for me - after six months, my face, jaw, neck all felt normal, and I had no more pain - a feeling I had not had in a long time. It also made my face look better. I had not realized the true extent that the spasming muscles and the joint derangement had effected the shape of my face. The pain began to return after a few months, but nowhere near where it had been before. This immense reduction in pain lasted for a little over two years. The treatment still ultimately failed, but it is not their fault, and it is still the treatment that has given me the most relief to this day. Later on, I even went about three years with very, very good pain reduction, before the joint severely destabilized again. This field of dentistry is the last line treatment for TMJ issues before oral surgery on the TMJ. There aren't as many denists around who practice this anymore, and the practice is currently shrinking due to dentists opting for less espensive, additional educations in things like professional whitening, which have a broader marketability. Getting this treatment is also very expensive if not covered by insurance (in America at least). My first time was covered by insurance, second time was not, though the dentist took pity on me due to the nature of my case and charged like a quarter of usual pricing. Most cases seen by these dentists are complete successes, and the patient never has to come back again. But occasionally they get a case that is not a success, and I was one of those cases. A little over a year ago, I began seeing the second dentist who keeps my TMJ stable in this manner. The first dentist retired, and then died sadly. A shame too, because he was a truly amazing, knowledgable guy who really wanted to help people. The new dentist began to get suspicious when my joint failed to stay stable after I was finished with the bite splint and his modifications, so he did another scan on me. This is ten years after the first scan (remember, I said the surgeon saw "slight" damage to the tissue on the first scan). This new scan revealed that I now no longer have cartilage in the joint, on both sides - complete degeneration of the soft tissues and some damage to the bone. The dentist sat me down and had a talk with me after these results came in, and said that when he sees damage like this in cases like mine, that the damage to the joint is most likely autoimmune, and that, in his experinece, it is usually autoimmune. He has sent patients with cases like mine to Mayo Clinic. He said he will continue to see me as long as the treatment continues to offer me relief, but also said that I will probably have to see a dentist for this type of treatment for the rest of my life. He is not currently recommending surgery due to my young age and the fact that the treatment he provides manages my symptoms pretty well. I still see this dentist today, and probably will see this kind of dental specialist for the rest of my life, since they have helped with this issue the most. I did not inform him that I am 100% sure that I have celiac disease (due to my complete symptom remission upon gluten cessation). I didn't inform him because I thought it would be inappropriate due to not having a formal diagnosis. I was disappointed, because I had believed I had caught it BEFORE it had done permanent damage to my body. I had never suspected that my TMJ issues may be related to my other symptoms, and that the damage would end up complete and permanent. Luckily, I caught it about 6 months after my other joints started hurting, and they stopped hurting right after I went gluten free, and haven't hurt since. I of course did the necessary research after the results of the second scan, and found out that the TMJ is the most commonly involved joint in autoimmune disease of the intestines, and if mutliple joints are effected, it is usually the first one effected. This makes complete sense, since the TMJ is the most closely related joint to the intestines, and literally controls the opening that allows food passage into your intestines. I am here to tell you, that if anyone says there is no potential relationship between TMJ issues and celiac disease, they are absolutely wrong. Just google TMJ and Celiac disease, and read the scientific articles you find. Research on issues regarding the TMJ is relatively sparse, but you will find the association you're looking for validated.
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