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?

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.

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.

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.

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.

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

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

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.

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

I feel like I am on a one woman crusade in Scotland to get Hashimotos recognised for what it is an autoimmune disease, I now have four autoimmune diseases Hashimotos, Pernicious Anaemia, Coeliac disease, Hyperparathyroidism, and am being referred for testing for rheumatoid arthritis.

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

I have just found out the I have Hashimotos Disease and am going down the rabbit warren of Google trying to research what it is. How to live with it? What I can do to help myself? And generally get my head around the fact I have it.

I explained I no longer needed to as the endo and previous surgery were happy to prescribe it , they now want me to have a telephone review with the gp to see if they can increase my T4 instead of giving me T3 , 🤬 I explained I don't convert and have barely any thyroid left due to hashimotos disease

Is this high or very high, please, and has anyone with similar readings gone on to discover that they have hyperparathyroid disease plus Hashimotos?

Isn’t the serum C reactive protein meant to be raised when we have an autoimmune disease like hashimotos? mine isn’t 🤔 Or is it just the TPO that is raised? Thanks in advance for any help with this…

Right…another daft question, still trying to get my head around stuff: if you have hashis and hypothyroidism too, can an increase in symptoms at times sometimes be due to the hashimotos auto immune disease being more active rather than a problem with the hypo or levo dose?

Hi all, I am new to the forum and just looking for some clarity from someone who has more of an understanding from their own experience. After countless hours of googling trying to work out what’s going on with my mum’s recent diagnosis and worrying myself sick, I feel even more confused than ever

Hello everyone! I hope you are doing well. I wanted to post an update about my father's current situation. After PSA started to raise, the MO added Abiraterone 1000 mg. a day with 10 mg prednisolone to his treatment regimen with Zoladex (once every 3 month) and Zoledronic acid (once every month). Abiraterone