Hashimoto's Thyroiditis

Posted by rainglogirl @rainglogirl, Jul 29, 2011

Since Fall 2010, I have been diagnosed with Hashimoto's Thyroiditis. So far I've been to several doctors. My original treatment plan was Levothyroxine and Levothyronine (thyroid hormone) along with other hormones and supplements. I was put on 10K of Vitamin D3, DHEA, testesterone, estrodial, etc. I am no longer on that much of a regime. Our family had aleady been to a nutritionist before the diagnosis and were well on our way to improving our general health & diet. I've read the book, "Thyroid Power" by Shames & Shames, which is a great resource (also a book called, "The Thyroid Diet", which has some good information). When I learned of the classic thyroid symptoms, I realized I have experienced many of them all my life. In the late 80's, I had a hysterectomy for "fibroids" & excessive bleeding/clotting/enemia. I wonder now if that condition was really undetected thyroid issues? I am 61, I have studied and practiced good nutrition (as it has evolved over the years) most of my adult life. I have had weight issues since my first child was born in 1968. I had a kidney infection with that pregnancy, and in about the 7th month had kidney XRay and had an allergic reaction to the contact dye I was given to drink beforehand. I never gave it much more thought.

I tried using iodine about a year ago, on the advice of a healing practioner, and had a funny, allergic reaction to it (1 drop in water!) and so discontinued . . . . (my face heated up, chest got all red and I felt sweaty and stressed) so I do have some kind of sensitivity to iodine. She suggested later that I might have been needing more iodine, not allergic to it but I have not explored it any further at this point!

Sometime in May 2011, I think, I switched from the synthetic Levothyroxine to Armour (natural harmone derived from pig thyroid). In June 2011, I had two incidents - first, I had a bad fall off of a porch step onto concrete (shocking) and about a week later, my first recognizable "Thyroid Storm" and experienced scary heart palpatations and ended up in the ER overnight for observation. My pulse went up to 126. . . normally for me it's around 94-100 (still high but not nearly as scary!). When I was first diagnosed with Hashomoto's Thyroiditis, my labwork showed that my antibodies were 59 (high). During the Thyroid Storm the bloodwork showed they were at 186. This shows that one's autimmune system is attacking the thyroid. The naturopath prescribed a Thyroid Tincture (combo of healing herbe) which I feel did a good job of reducing the pulse and quieting the antibody activity (though I don't at this point understand exactly how that works with the tincture?). I was grateful to have that to take 3x/day during the worst of the "storm".

I still am very new to this disorder and some of it is confusing to me. Would sure help to hear from others who are going thru similar issues with thyroid, especially those who have more experience with it than I and some suggestions or resources, and have things to share about the mainstream medical or alternative medical points of view. I feel I have some important decisions to make soon and need all the information I can gather.

Hopefully some of this will be helpful to others.

I want to point out the subject of being an overweight person most of my adult life, dealing with symptoms I didn't always understand (like edema, depression, weight gain, insomnia for instance), and the stress physically, and distress of feeling judged for my appearance when in fact I had a definite disorder. I was never a "yo-yo" dieter, but did try a few programs like Pritikin, Low Carb, but executed the plans with common sense, not overboard. In all honesty, my dietary habits (young working mom) were not always pristine and I've downed many a pizza/ice cream dinner in my lifetime . . . and let's not even go to chocolate!! 🙂 The truth is in recent years I have done a much better job with it all, but nothing seemed to really help.

"Thyroid Power" talks about how underlying thyroid conditions can influence other physical challenges, and go unnoticed by the medical profession for what it is. One good thing the cardiologist said to me was that the thyroid condition (in my case) is genetic and that my heart is an innocent bystander to what the thyroid is doing. He helped me see that I can't just sit back and pretend this doesn't exist. I would like to live out my life as healthily and happily as I possibly can.

Yesterday I went to a cardiologist for the first time, just as a followup to my recent hospital stay. He is increasing my Metropolol (blood pressure med) for now, to protect my heart, and recommends I see an endrocrinolgist. Talked to me about thyroid ablation (whew, scary!). I read on this site where beta blockers actually masque the symptoms of thyroid, so I don't know what that means to my body/heart overall. If increasing the meds gives my heart a break while I find other answers, then that is a good thing. To just increase the meds and do no more research would be to my detriment, espcially if the beta blockers are just masquing the symptoms (logical but of course I'm no doctor so don't really know for sure). One last bit of info, I've been maintaining a fasting glucose of about 99-105 in recent months, without medication. While not the best numbers, I'm fully aware that I'm heading for more medical problems without the proper guidance.

Good health to all!

A diet doctor I saw taught me this formula:

Carbs - fiber divided by 5 (because there are 5 carbs in every tsp of sugar)
This gives you the amount of sugar in anything you eat and a good guideline for planning one's daily menu. I think, by the way, that there are 10-12 tsps of sugar in ever serving of soda. My son with Downs has lost 45 lbs. this year and one of the main things he cut was steady drinking of soda. I'm just sayin' this is worth your conscious consideration.

Some additional information. I've had one knee replacement, Osteoarthritis symptoms, and weigh 296 as of my last step onto the scale. I am not proud of my weight, but it also shows how out of balance my body must be, especially when I've been following a sensible, low carb, organic, healthy diet. I'm working on improving sleep, and also exercise. I am usually fairly consistent with exercise (Curves and walking) but have been going slower since the Thyroid Storm. 20-30 minutes of walking seems really helpful and I'm starting back to Curves with a bit less exuberance until I know more about what is happeneing to me.

Well, that's part of my story anyway. My adult son also has thyroid issues. He was born with Down Syndrome. My neice was just diagnosed with Hashimoto's as well and I have a few other relatives I need to convince to go get testes. If you made if this far, thanks for staying with me while I told my basic story and please share your experience.


Interested in more discussions like this? Go to the Diabetes & Endocrine System Support Group.

@jmb73 - Welcome to Mayo Clinic Connect!
First thing to focus on is the nodule in your neck. You will have the ultrasound soon. Even if your PC went on maternity leave, she has someone who helps take care of her patients. The office staff knows and you should be able to talk to that doctor. You have an endocrinologist as well.
It is hard to lose weight when your hormones are unstable.
Also, if you continue on a 900 cal diet, the body will think it’s in starvation mode and you won’t lose weight because of that.
You have and have had multiple medical problems- it is overwhelming at times. I just think that you have to find out what the neck lump is as soon as possible.
Please correct me if I interpreted your wrong main concern.

REPLY
@astaingegerdm

@jmb73 - Welcome to Mayo Clinic Connect!
First thing to focus on is the nodule in your neck. You will have the ultrasound soon. Even if your PC went on maternity leave, she has someone who helps take care of her patients. The office staff knows and you should be able to talk to that doctor. You have an endocrinologist as well.
It is hard to lose weight when your hormones are unstable.
Also, if you continue on a 900 cal diet, the body will think it’s in starvation mode and you won’t lose weight because of that.
You have and have had multiple medical problems- it is overwhelming at times. I just think that you have to find out what the neck lump is as soon as possible.
Please correct me if I interpreted your wrong main concern.

Jump to this post

The lump is my main concern and it seems to be growing. My PC's office has said it's low thyroid and the nurse said she has it too. But my thyroid blood work came back normal! Thank you for your response. I guess I just have to wait until the ultrasound.
Joan

REPLY
@fatsfat

The information about PTU is about my daughter and I am trying to get advice on what she can do. I have thyroid, adrenal ,Fibro and lots of conditions and issues as a result of years of being mis-diagnosed and dismissed by doctors in variety of specialists. Severe depression and PTSD etc. as results of cortisol very high in am, DHEA levels extremely low for 10 plus years, serontonin, full menapause at 36 years old. Doctors just said I was stressed and the typical medication rabbit hole. Conditions and other blood levels off as a result and nobody can address or read labs right and pushed off to another doctor and about 20 doctors over last 10 yrs. No help anywhere.
I am trying to help my daughter before her conditions continue and she ends up with a yucky quality of life. please

Jump to this post

@fatsfat - Welcome to Mayo Clinic Connect!
I guess you see that others also have problems with their thyroid.
I agree that your daughter needs help before next possible appointment time. I’m not familiar with tapering of this medicine.
It would be best to see a doctor ASAP. The endocrinologist or an Internist.

REPLY
@astaingegerdm

@fatsfat - Welcome to Mayo Clinic Connect!
I guess you see that others also have problems with their thyroid.
I agree that your daughter needs help before next possible appointment time. I’m not familiar with tapering of this medicine.
It would be best to see a doctor ASAP. The endocrinologist or an Internist.

Jump to this post

The ENDO who put her on the meds, after a few months under her care and increasing the PTU MG's, and 3rd set of blood work and last on May 5,2021, said her blood work was all over the place and Said it was above her pay grade. Told her to see what the PCP can do. I can tell u, NOTHING but shoving her doctor to doctor and suck more money from with no regards for her financial status, plus the meds are expensive and making her worse. Same treatments I encountered for years. New endo is not available until mid July and many not taking new patients etc.etc.
I am connected with Dr.Lam and his site and other sites, and I need advise now and not watch a video and write stuff down with nerve damage in my own hand etc. Daughter does not have access to lots of media,cable etc. I am just needing direction and who can help sooner or guidance on the medication and rare but life threatening condition that I listed in initial post. Someone that knows how to address these things and get to the root, instead of wanting to cut thyroid out and not address if something else like adrenal etc is a problem Thanks.

REPLY
@fatsfat

The ENDO who put her on the meds, after a few months under her care and increasing the PTU MG's, and 3rd set of blood work and last on May 5,2021, said her blood work was all over the place and Said it was above her pay grade. Told her to see what the PCP can do. I can tell u, NOTHING but shoving her doctor to doctor and suck more money from with no regards for her financial status, plus the meds are expensive and making her worse. Same treatments I encountered for years. New endo is not available until mid July and many not taking new patients etc.etc.
I am connected with Dr.Lam and his site and other sites, and I need advise now and not watch a video and write stuff down with nerve damage in my own hand etc. Daughter does not have access to lots of media,cable etc. I am just needing direction and who can help sooner or guidance on the medication and rare but life threatening condition that I listed in initial post. Someone that knows how to address these things and get to the root, instead of wanting to cut thyroid out and not address if something else like adrenal etc is a problem Thanks.

Jump to this post

Yea, I see other post but they was from many years ago and maybe I cant see new stuff because had issue with my computer but good to go now. I also thought doctors looked at these to advise on conditions because not everyone is can get to them at the location in Jacksonville. Thx

REPLY

@fatsfat - I’m sorry to tell you that Connect does not have doctors to review health problems presented here. We are people who have been through similar problems as the posting members. We share information and offer advice, based on our experience.
I do agree that your daughter should see an endocrinologist or internist soon to manage the medication dosing.
During the past year many hospitals have opened Telehealth visits. Check your area hospitals if this is available. You might get help there in managing the PTU dose and side effects.

REPLY
@mfratt

I have Hoshimotos Thyroiditis and constantly have to have my levels checked almost every six or up to 12 weeks. I have just last month gone and trying to recover from hyperactive toxicosis. Prior to that my TSH was 6.99 since Oct of last year. This time my T3 and T4 were off possibly because of Zoloft, but recently changed to Lexapro. I have the Thyroid Diet book and The Thyroid Source book.
I know prednisone causes problems for my hoshimotos. If I have an MRI with IVP iodine I have to premedicate with prednisone since I’m allergic to the IVP iodine. It’s a constant rollercoaster. If you feel your levels aren’t right push the issue. None of this just have it checked just every six months like they prefer.

Jump to this post

interesting. didn't know that prednisone causes problems with Hashimoto. thank you for info and books !

REPLY

thank you very much. I knew about my TPOs for 10 years (over 1000). my tsh just now starting acting out. my free t4 is still in optimal zone. I also have clotting issues for long time, now on Xarelto for rest of my life. although endo md who I spoke to dismissed the idea that clotting is connected to thyroid issues. thank you for the books, I was told and still being told by Kaiser Permanente that nothing can be done about lowering TPOs. of course, I am aware about naturopathic mds but I want to try thyroid diet myself. naturopathic meds tend to be expensive and tends to want to take their tinctures .

REPLY

I was diagnosed with Hasimoto's in 2000. Went to a reputable endo in Philadelphia. He treated me with radioactive iodine to stop the thyroid from overreacting, hyperthyroidism. Did not suggest surgery. Then put me on Synthoid to treat the hypothyroidism. Even though I am now on Synthoid/levathyroxin for life but the Hasimoto's has been resolved. I don't know if that is still a treatment but it may be a possibility. Find an endo that specializes in autoimmune diseases, if possible.
Blessings 🙏

REPLY
Please sign in or register to post a reply.