I have Hashimoto’s thyroiditis and have suffered serious adverse drug reactions for many, many years.
Battling with bullies in the medical profession has been, and still is a nightmare.
I found this link today and am going to print it off to show to all doctors/consultants that I see in future.
Hope all Hashimoto patients will find it useful.-------
Hormones Matter
Adverse Reactions, Hashimoto’s Thyroiditis, Gait, Balance and Tremors hormonesmatter.com/adverse-...
Thanks for posting this interesting article. The medical establishment is notorious for bullying; I too have been a victim several times. In my personal experience, this so-called profession protects some of the most dangerous predators I have ever encountered. The title "Dr" offers predators in the medical "profession" (read: industry) the same kind of protection as other types of predators (eg the Saville type) enjoy by virtue of the title Sir/Lord, etc.
Thank you, I could not have put it better.
I love this bit :
'In fact, I would consider thyroid testing, specifically for autoimmune thyroid disease like Hashimoto’s, as one of the first disease processes to rule out.'
If only!!! Yes, this is a good thing to take to your doctors. They might learn something useful!!!
Good article, bomap. Thanks for posting.
Hugs, Grey
Thank you
My health problems started acute,high Bp170/115 blood shot eye,tremors,nausea,headache ,severe tinnitus,pins & needles,anxiety,palpitations.I was taking eutroxsig 50 mcg tested thoroughly Thyroid tests ok .pharmacist told me I was thyroidtoxic cease meds.bp came down ,night episodes continued.6 mths later diagnosed with B12 deficiency with genetic mutation MTHFR .Local drs ignored my neuro symptons & b12level 290 which should be have been over 450 .Google Vitamin b12 deficiency treatment protocol & could it be B12 ? My lifesaving book.
Actually, the Japanese treat any B12 level Under 800! Mine was about 250 and the doctor said it was 'perfect'! I could hardly walk and would forget what I was saying mid-sentence. I had been taking several médications that I've read deplete your B12 and magnesium, but the doctor denied this - and even said that magnesium was unimportant! Second time I've heard a doc say this.
I started supplementing with B12, and some other things, and began to feel much better. But my supply began to dwindle, I ordered more but it didn't arrive!!! By the beginning of this week I was completely out of B12, and I felt as if I were going to die.
My B12 arrived yesterday and I immediately took 2000 mcg and began to feel better. Last night I had the best night's sleep I've had in ages.
They just don't understand the importance of these things. It's criminal!
thank you yes, I am convinced now that a lot of my symptoms are down low to B12. Since I stopped taking it this week in readiness for my blood test on Tuesday I have felt worse and worse. Sleeping very badly, clumsy, knocking into things completely exhausted.
how do you take yours? I have sub-lingual tablets as these seem to work better than regular supplements although if levels are really low and in pernicious anemia injections are better.
My aunt received the injections but i think they were only every few months.
Thank you Bomap thats a realy valuable piece of work. I'm sure people think I am completely mad when I am trying to explain my illness, especially the doctors! I posted this to FB and sent it to my family. Hoping that my children will never suffer with these problems but if they do at least I can pre warn them about what help they may need so they don't have to battle like we all have.
You are most welcome.
Patients with Hashimoto’s thyroiditis and negative thyroid antibodies have a milder form of the disease
Teva adverse reaction 
Lupron, Estradiol and the Mitochondria: A Pathway to Adverse Reactions
Hashimoto's - med decrease and feeling awfulSelenium supplementation for Hashimoto's thyroiditis: Cochrane Review
