I'm new here and just found out I have hypothyroidism... I'ts helps that I am not alone...
Joy
I'm new here and just found out I have hypothyroidism... I'ts helps that I am not alone...
Joy
Welcome to the forum! Think that's the best point about present day technology-we know we are not alone and can talk about our problems and fears.
Keep reading and learning and always get into the habit of asking for blood results so you can post them on here for help and advice. The ranges are important as they diff from lab to lab.
ThyroidUk who run this forum for HU also have a site with useful info that would be helpful for you to read. Shout out if anything you don't understand. .
You are definitely not alone. ark sure you get vit D,b12, folate and ferritin tested as all can be very low with thyroid issues. Also antibodies to check for Hashinotos, very common.
T3 and RT3 levels are hugely important too. You're not likely to get tested on the NHS unless you are very lucky. If you still feel rottin on T4 mono therapy (Levo) then good to get tested as lots of have conversion problems and then need to add T3 or switch to NDT to feel well.
Isabella Wentz Hashimotos protocol is a good first read.
Mary Shomon books
Chris Kresser website
Amy Myers MD
You really need to educate yourself as the GP's don't tell you half you need to know. x
Welcome Joyandmirth,
I echo all that has already been said here. Always get your results and compare them each time and question anything and everything, which is your right to do so. Also keep in check tests for B12, vitamin D deficiency and anaemia, as they have similar symptoms and sometimes go hand in hand with thyroid conditions.
If not happy with a decision/opinion by a GP or medical professional, always seek a second one. I have come to realise over the years, it is merely an opinion they have and you don't want someone telling your how you feel and compared to others.
Everyone here will try to help and there are some good links and information.
I have always had a thyroid condition, was born with a partial non working gland, so have always been on medication. Mine is a long story, but lets just say, I have not got a lot of faith in the Professionals.
Take care and keep in touch.