Omg my nhs endo prescribed T3!!!: I went for my... - Thyroid UK

Thyroid UK

141,246 members166,490 posts

Omg my nhs endo prescribed T3!!!

scottishkitty profile image
7 Replies

I went for my appointment today armed with my stuff from the private endo expecting to have to beg to get them to follow his advice .... after I explained his findings re conversion problem she apologised that I had had to go private to get a diagnosis and promptly told me to stop taking the T3 I had got online and that she would prescribe it for me!!

She also assured me that she would send a letter to my doctor telling her that under the fair share program or something that she must keep prescribing me T3.

She has also gave me a loading dose of 20,000iu Vitamin D for 2 weeks and an 800iu sustaining dose for 3 months.

I AM SOOOOO HAPPY!!!!!!

Written by
scottishkitty profile image
scottishkitty
To view profiles and participate in discussions please or .
Read more about...
7 Replies
shaws profile image
shawsAdministrator

You must have been so shocked, I am surprised you didn't faint! :) It was good of GP who will be able to see the other side of treatment.

Binkie profile image
Binkie

omg thats brilliant. My endo has been told to stop prescribing but he gives me a private prescription which i fill in france so its not expensive but its great to hear some drs are stepping up to the plate, well done xxx

Barb1949 profile image
Barb1949

Scottishkitty, well done (a) for getting the diagnosis and (b) for getting an appointment with an endo who is willing to prescribe T3.. Presuming you are also in Scotland , from your name, I am also in Scotland and see an endocrinologist I was recommended on this page. At my initial appointment he examined me took a complete blood test and told me that my thyroid had been attacked by antibodies for so long that it had now atrophied and essentially was not working. He was happy to prescribe T3 and initially I was given 20 mcg with a reduction in thyroxine. Over the next year or so this was gradually changed to 40mcg T3 and 50mcg thyroxine. I feel I could perhaps benefit from another small increase in T3 but have other health issues at present which may be having an effect on how I feel. ((I was recently diagnosed with Chronic Venous Insufficiency, which causes my body to swell up with lots of fluid).

I have not heard of the fair share programme, nor has it been mentioned in any letters but I did learn, this week from my new gp that the T3 I am taking is costing the NHS about £500 per month. I mentioned that this was probably much less than all the other meds I was taking to relieve my symptoms eg depression, IBS, constant pains etc, before I got T3, to which he agreed. He is also of the opinion that the NHS should source its drugs from different sources. :-)

LouiseRoberts profile image
LouiseRoberts

Email me please with the name of this endo - thanks! :D xx

thyr01d profile image
thyr01d

Hi Scottish Kitty

So, so pleased for you.

Please could you tell me something? Were you advised on food and T3, my Consultant told me to take it with food but on this site I keep seeing to leave time between eating and taking the T3.

vida_sana profile image
vida_sana

Congratulations on managing to get t3!! How is it working out for you?

My GP said she wasn't unable to prescribe it as it has to go through a board...instead she 'TRIED' to refer me to an endo and it got rejected. So I literally have no other option but to go to a private endo...which I can't really afford.

I'm intrigues how your GP could prescribe T3 though as mine said she categorically could not prescribe it herself as a GP.

scottishkitty profile image
scottishkitty in reply tovida_sana

It's working out great. Feel like I have a new lease of life 😁

I had 1 private appt which cost me £230 and worth any penny.

I took his results back to my endo who said she would arrange to get it prescribed via the NHS.

I think doctors can be more tied down with regards to prescribing T3 due to the high monthly cost (approx £280 per month)

I think I was very lucky and honestly did not think I could get it on free prescription. Think my endo felt guilty that they couldn't get to the bottom of it for 6 years!

I would def advise to try to go private even just for the initial consultation.

Good luck xx

Not what you're looking for?

You may also like...

My nhs Endo has prescribed T3 trial

I’ve just had a phone consultation follow up with my nhs Endo. My first appointment was in June...
Oakwood4321 profile image

obtaining T3 on NHS query

hi everyone, Me again! I just want to ask a question about why my GP surgery aren’t giving me T3...
Essexlil profile image

T3 prescribed

Hello lovely people. Just had appointment with private Endo who has prescribed T3, 5mcgs twice a...
Lottyplum profile image

Being prescribed T3

Wondering if I could have some advice/help please. Had my thyroid removed 17 years ago and been on...
LFE12 profile image

NHS endo ....

Brief history - hypo symptoms started 2018 but normal blood results. TSH started to rise 2019, but...
muppetme profile image

Moderation team

See all
PurpleNails profile image
PurpleNailsAdministrator
Jaydee1507 profile image
Jaydee1507Administrator
SlowDragon profile image
SlowDragonAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.