Experiences with

Hashimoto's disease

My doctor won't medicate me as she does not think I have hashimotos disease. So I am trying to get hold of amino after reading about the importance of this in my diet. Can anyone recommend a company for this?

Dear Mrs [ redacted name ] ,Dr [redacted doctor ] has looked at your letter and unfortunately your conditions Chronic Fatigue Syndrome, Fibromyalgia and Hashimotos Disease are not classed as immuno-suppressive conditions and he is therefore unable to do a letter to state this.

And I have since spoken to a Thyroid specialist who thinks that the symptoms may be due to my Hashimotos disease, so my levothyroxine has been increased.

I have osteoarthritis, osteoporosis, spondylithesis, hashimotos thyroid disease among other issues. I have had 3 surgeries in two years and know that with the bad arthritis I expect to have more. Looking to share ideas and support with others on how to manage the related pain.

I am not on any thyroid medication 2. 3 years ago I was diagnosed with hashimotos disease 3. I have been discharged and referred back to endocrologist twice in 2 years. Currently not with endocrologist. My current results: My free T3 and T4 were done in January 23.

I have been diagnosed with Hashimotos disease which my GP tells me is nit treatable until my levels get so bad it present as hypothyroidism.

If my thyroid temperator management is low (typical body temp 35c) could that explain my tendency for overactive immune system, ie b cells that can have consequence toward hashimotos, lymphoma, syrogens, Multiple sclerosis or other autimmune disease.

Hi I am new to the group.I am reaching out as I have a couple of questions.I have Hashimotos disease and on an alternating dose of 125mg to 150mg each other day of levothyroxin.

Does anyone with hashimotos thyroid disease take slippery elm? I want to try this but Im trying to work out how to stop it affecting absorption of thyroid meds (thyroxine and Liithyronine which I take on waking and at 9 pm. I usually take peptac at 11 pm.

Does anyone with hashimotos thyroid disease take slippery elm? I want to try this for gastritis but Im trying to work out how to stop it affecting absorption of thyroid meds (thyroxine and Liithyronine which I take on waking and at 9 pm. I usually take peptac also at 11 pm.Thanks

I pointed out that if I did that we would never know if it had been Graves disease or the Hashimotos going supanova due to the excess of vitamins. Where as -if by not taking the tablets my thyroid range increased again we could be sure of it being Graves disease.

Has anyone had a diagnosis of hashimotos disease and recieved any treatment or has anyone went private and been given levothyroxine or have any advice on how to get it? Thanks in advance

after a TSH of over 100 for months & a month long stay in hospital I have now been diagnosed with Addison’s disease as I already have hashimotos & underactive thyroid for the last 27 years can anyone give me any advice or patient to patient tips on living with this as I would like to do all I can to

Hi, My wife has been diagnosed with Hashimotos disease by her doctors in Egypt. Thyroid disease runs in her family, her mother has it, but she regulates it with medicine and has never been diagnosed with Hashimotos.

I only have one other health issue and that's hashimotos thyroid disease. Thank you

I also have hashimotos, addisons disease and sjogrens syndrome I was wondering if these autoimmune conditions could be causing nodules and just pray it's not cancer! Thanks for reading

Hello everyone, I am looking for your advice regarding the decision to proceed with prostate removal surgery. I was diagnosed with stage 4 P/ca in 2021 at the age of 70, and at that time, I had a metastasis on my hip bone. Surgery to remove the prostate was not an option then, so I began receiving

Have put myself on a vacation since I have some other issues which contribute to my increasing fatigue. Doing 6 months depot ADT for more than 4 years after radiation. PSA has been .01 every since. Was anxious to see my first PSA after 6 months. Still .01 and a little fatigue relief! Testosterone

Hi, these are my cortisol saliva test from last week. This was after being on 0.5mls of LDN for 4 weeks and 12.5mcg of T3 at 0300hrs (Paul Robinsons CT3M). Blood cortisol was also measure last week, 0730hrs, 350 nmol/L. Range: 73 - 507 My Dr has prescribed DHEA & Pregenonlone as well, but I have not

[u][i]Albumin[/i][/u] [i]This is a protein made in the liver. It is an indicator of how well the liver is functioning. This lab value will lower if liver function begins to deteriorate.[/i] [i]This lab value is part of your regularly drawn lab work - CMP. [/i] [i]3.4 to 5.4