anyone out there with auto-immune/chronic pain issues before dx?
Comments
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Kate - thinking about you today going to the doctor. Hope you get your questions answered and hope for nothing else bad. I too have high cholestrol. When I lost a lot of weight going through my divorce my cholestrol was great but now not so great. Sorry spell check isn't working. I'm not on any meds for it though.
Bevin, it was me who had Shingles. When my doctor was talking to me he just said when your immune system is not acting properly then you are more open to other diseases and cancer - isn't that lovely! I do agree I think stress probably hits us in more and in harder ways than typical people.
Also, Barb, re-read about how the sheet can hurt you - me too! I have that as well and sometimes just can't wear long sleeves as for me it is usually the lower part of my left arm.... so weird. No wonder my Mom thought I was a bit nuts growing up cause nerve pain is just so strange if you don't have it don't think you can understand how disturbing the pain is cause regular methods just don't touch it.
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Yep, it's a psychotic-like disease. You really feel like you're going crazy!!! They didn't recognize it as a legitimate disease until 1992.
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Hi Ladies - checking in with all of you. Wow, Kate, this is interesting. Wouldn't it be nice if this piece of the puzzle comes together and makes you feel a whole lot better?!
Hope you are each keeping the symptoms at bay.
XO,
Mary
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Mary- Great to hear from you. How have you been? How all is well!
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Hi Kate - well - I was found to be hypothyroid when I was 27 and I am now 46. I had fertility issues and it was found during screening. I have Hashimotos thyroid disease. I'd offer up to find an endocronologist that will work with you. Just being in normal range of TSH doesn't make everyone feel better. Mine keeps me a bit on the more hyperthyroid side with synthroid and I feel much better. If you have any friends with it, see who they go to. I dont see my primary for it as I feel a specialist should direct how my hormones work.
I also take spironolactone and dexamethasone as I have high levels of DHEAs and testosterone. These two meds lower these two androgenic hormones and have cleared up what was awful adult acne and hair loss. never had it as a teen, but got it as a 30 year old woman and to top it off was losing my hair... arghhh. I was pimple free within 4 months of these meds and my hair stopped falling out.
I will say, once I was treated for thyroid, I felt so much better. My mind got clearer and I was not so tired all the time. It was like night and day.
As for breast cancer, I was diagnosed August 2010.
Good luck with the thyroid. It's amazing how many woman have this. Let me know how you're doing and feel free to send a message with any questions.
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bevin- Thank you for all the information. After meeting with my GP today I realized I do need to find a specialist as it was obvious they didn't know that much about it. Just curious- what does your doctor say is "normal" for TSH? Every web site I get on seems to give a different figure. I am hoping once the meds kick in I will feel the same relief you did.
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I believe she aims to keep everyone around at a TSH around 2.0 , I have been at .81 for the past 10 years. I feel best there. If I recall, while the range may go to 2.0- 6.0 as "normal", she finds most women feel better on the lower end.
If you can find a women - I think that's even better. I think they listen more to the issues women have with hypothyroid problems.
p.s. - Your dog is adorable!!
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bevin- My GP told me today that my TSH level was 5.1. Guess that's why I've been feeling so crummy! I like your idea of finding a woman. Pretty much all of my Dr.'s are- GP, BS and PS. (BTW- My pup is a Yorki-poo named Piper. I also have her sister from the same litter whose name is Scout. I need a picture with both of them!)
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Oh my gosh - cutest dog ever. yes you'll need to post the sisters together.!!
Let me know how you do with the doctor search. It does take some time for the synthroid to build up in your system and to start to feel well again. And yes, 5.1 is on the high end. Most doctors will want to treat that for sure. If they don't , find another one!
I'd definately ask about the combined T3 (cytomel) and synthroid treatment combo. The theory is some women with hypothyroid don't conver the T4 ( synthroid) into the T3 so the cytomel helps. I really felt less groggy and mentally foggy when they added the cytomel.
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bevin- Thanks for all your help. I'm feeling like a (sluggish) fish out of water. I definitely need as much help as possible in the "mentally foggy" arena. (Already have a strike against me with the onset of menopause!) I need to find an endocrinologist but am wondering if I should see if my GP would prescribe the cytomel in the meantime. Guess it can't hurt to ask them. You've been dealing with it for a long time! I think I have, too, but they just kept telling me it was fibro. Thanks again for all the info!
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One of the theories of cancer is that it's chronic inflammation that causes it. Have any of you researched gluten? Just curious because the rheumatologist thought I had fibro, and when I went off dairy, gluten, soy and corn (the top 4 food intolerances, and the ones that my kids had) my never-ending back spasms went away, and my thumb pain and my knee pain. Gluten is a problem with many auto immune diseases (celiac, RA, IBS, hashimoto's/grave's thyroid, and probably others) and it's inflammatory.
Not sure where you all live, but you might want to get checked for Lyme Disease as well (from a good lab like Igenex) because it can have many of the same symptoms.
And magnesium glycinate can help with muscle spasms (many people are low and don't know it; I had a blood test, but you're usually really low if it shows up on a blood test).
Just some things to think about.
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HI KJ, I have researched Gluton, I read Dr Mark Harmons book, Its very good. Gluten free is easy to follow if you just eat clean foods, non processed. I still find it hard though. I didnt know though that it had a link to Hashimotos which is what I have.
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I ate only salad for 5 months. No carbs, ergo, no yeast, gluten, etc. Didn't make a penny of a difference in how I felt!
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I was reading something and unless you really have a gluten intolerence it won't change a thing. There is a test but can be mis-leading.
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I envision a future where you can just step into a "health tube" and it immediately tells you what is wrong with you and what will fix it. Now wouldn't that be nice? Anyone tired of being their own health detective? Try this for months, ok now try this, etc, etc, etc. I will be extremely grateful if the thyroid meds are the answer for what ails me but, at the same time, I will be extremely ticked off for feeling unnecessarily crappy for the past decade! I know we have to be our own advocates but sometimes it feels less like doctors are trying to figure out what is wrong and more like the goal is to see how many different prescriptions they can put you on.
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I was at my doc this morning for prescription renewals. I'm on a LOT of narcotics and every three months we try to figure out a way to get me down and we just can't. I can wean myself off them quite easily but the pain is just too unbearable. I did ask him today if he thought my issues could be adrenal or thyroid related. He paused and then shook his head. He knows I'm always trying to find another excuse besides FM.....sigh.
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Oh Kate- I couldn't agree more. I went gluten free for 6 months- nothing. No Beans for 6 months! (leptins. don't worry about it I think it's maybe total garbage) Nothing. Etc etc. Although being dairy free has been helpful for me. I hope the thyroid dx makes it easier for you and not harder- I know that it's something that's very treatable with diet if you want to try non-pill means...
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barbe- Sorry there's no easy answer to help you be pain free. It's so draining to be in constant pain and no one really understands it because it's not something they can see. It's amazing after all this time they haven't come up with better options to be pain free.
jessamine- Hey! How have you been? You haven't been on here in awhile. Hope that's a good sign! I will definitely be doing a lot of research about options for treatment for thyroid issues. The less drugs the better!
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Barbe - have you had a full thyroid panel recently? (tsh, Free T3, Free T4, TPO) Or have you ordered a salivary corisol test? (from canaryclub.org). These can help you determine if you have thyroid or adrenal issues. I am just now learning about all this. I got my thyroid taken care of about 4 years ago with a brilliant, out-of-the-box doctor after 6 consecutive docs told me my issue needed antidepressants. The thyroid meds (both T4 and T3 products) were quite helpful. Since my cancer surgeries, I've been extra tired and achey, and am now fairly sure there is an adrenal component. There is a book called "Adrenal Fatigue" by James Wilson, which I'm in the middle of reading. Very interesting and patient-friendly. I wish you the best. There is a wealth of info out there which our docs simply are unaware of.
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I'm going to self-administer iodine to see if it makes a difference. Any recommendations?
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Barbe, try seaweed so you have both iodine and selenium. It might help you get rid of toxins that may be causing your pain. Just check that you don't have thyroid disease already as it may be counter indicated. I would also tell your doc what you're doing. Because if toxins are causing your pain, they may have to watch for symptoms that the detox is straining vital organs.
we also have a ton of autoimmune diseases in the family. I have asthma, systemic lupus (in remission 20 years), Hashimoto's thyroiditis, hay fever, food allergies, and now bone mets only BC (NED 3 years). I don' take supplements myself because I'm popping too many pills already! But I don't have pain, other than femara pain, which has gotten a lot better over time. I exercise everyday, and if I don't do something today (running a fever with flu) it will be the first time since starting chemo. I did not have the swelling during rads so I guess that means the lupus is still in remission. -
i believe that what cancer needs is for you to detect it on time and be able to take treatment on time. Also you can check here www.themesotheliomaonlines.info for more details
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Sorry Gluten free didnt work for you. But, I dont think Dr Harmons book is just about Gluten. Actually few people have a real Gluten allregy. Its more about eliminating processed foods, eating whole natural foods they way our bodies were intended and really understanding the role all of the different things in our processed foods do and how they interact in our bodies.
I will say, once I started eating no processed foods , I lost alot of weight and it was easy. I also felt less tired , had more energy.
Talk soon.
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Yinka, we don't have that kind of cancer. Why are you guys here AGAIN??????
Bevin, I don't eat processed foods. I have a lot, a TON of salads, a tiny bit of pasta with tomato only sauce, grilled steak in nan bread, and cereal. That's about it.
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Barbe - I've been planning on adding iodine since I found out I had BC last summer. But then they found out I have an adrenal adenoma (benign tumor on my adrenal gland). So, my onc said after we finish chemo and rads you need to go to an endocrinologist and have this adenoma taken care of. I've been effin' around with endocrinologists for years and I can't get no satisfaction! So, after we take care of the adenoma thing, I'm sure he'll dismiss the rest of my concerns because everything will probably fall into the "normal" range. I already have a plan to take all this blood work they did last week (12 vials!) and go to a naturopath to help determine the correct dose of iodine and try to get ALL of my hormone levels balanced.
One endo I went to 2 years ago DID figure out something was wrong with my adrenal glands (he thought it must be adrenal fatigue - without some kind of scan you don't know you have an adrenal adenoma) and he said although my thyroid APPEARS like it's functioning normally (normal ranges and all), the adrenal glands were screwing it up. The endo I'm seeing now about the adrenal adenoma scoffed at that theory, so I have little faith - once again - in getting any satisfaction from the mainstream docs.
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barbe- Talk to MBJ about the iodine. I'm pretty sure she's taking it and has done a ton of research on it, too. I think it would definitely be worth checking out.
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Just found out there's a shortage of iodine in my area due to what's happening in Japan. There is a nuclear plant about 50 miles away, so people have been stocking up.....sigh. I was hoping that would be the ticket!!
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Barb - I used to take Iodine and it does change your thyroid - we experimented and finally being on the synthroid worked better for me. I think it can be hard to dose correctly but perhaps MJB can help you on that.
Does anyone take probiotics? I think I want to really research that and get some really good ones as from what I have read that can make a difference to a lot of things in your body.
Barb - I so understand you wanting to find an answer other than FM. Being in constant pain is just horrendous and knowing that you have so much going on I so admire your ability to find humor and have so many positive things to say.
My aunt is going to have surgery later this month for a cyst on one of her vertebrae. She can't lie down without pain on the side of her leg and her foot. Well hey wait! That is one of my biggest complaints and why sleeping has been so hard for me since 1990! Now wondering how to find a doctor who will order tests for me like that. She lives in another state so not helpful for me. But gosh sometimes pain can be caused by other things, My Doc keeps saying it is just MS but hey what if it isn't this time?
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barbe- Can you order the iodine online maybe? MBJ might have some sites she recommends.
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Hi Barbe- you eat really healthy , that's great. I just wish I could avoid the chocolate at holidays and then I'd be alot better off!!
Kate- when do you go to the endo?
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