Experiences with

Luteinizing hormone (LH) test

Hi everyone. I hope you are having a blessed day... I am hoping those with much more experience and research under their belt can share their thoughts or point to relevant reference material... I am currently adhering to 5day/week 18+hour of nightly fast. I eat last meal around 5-6 PM. In the morning

Hello, I’d appreciate a PM if anyone can recommend an Endo who specialises or is experienced in treating Graves’ disease in London or ideally SW London. I’ve been on NHS waitlist to see someone for three months and have only now started to get heart palpitations which are concerning so wanting to commence

Hi all, recently had a suspected TIA nearly 3 months ago. I got home one night and went to lock the door and I couldn’t get the key in the lock. I had no pain, no disorientation or confusion, no blurred vision, no pins and needles or numbness, no slurred speech, my left arm just felt a bit heavy. I immediately

I was diagnosed with Graves Disease last April 2023. Was treated with carbimazole. Quite quickly..3 mths .TSH ,FreeT3 and FreeT4 returned to be within normal range .This March endo suggested stopping meds in May and giving it till now to see what happened to hormone levels on basis that I had responded

Hello everyone! Finally got full testing including vitamins done. Results below. I think everything is ok with vitamins etc? Whats confusing me is the thyroid results. Higher TSH this time, but better results for my T4/T3. What is going on with this thyroid of mine?? I have an appointment booked

Hi everyone I have been on 50cm of Levo since June 3rd My first blood tests prior to taking medication were as follows TSH 110.64 ref range 0.35-6.5 T4 2.3 ref range 10.5-21 T3 1.2 ref range 3.5-6.5 after 7 weeks of medication I have had repeat bloods and I’m now at the following Same ranges

I know it's only been since last thursday since I got my results back to find I was overmedicating but still feeling very poorly, fatigue is awful, mentally confused, palps and the panic is awful. I can't do this, I just can't!!!!!!!!!! https://healthunlocked.com/thyroiduk/posts/150804459/please-help-so-very-frightened-right-now

hey all Just joined, just completed our first IVF round, we had 2 fertilised embryos (had to do frozen cycles), one in September which wasn’t successful and just had the news our final embryo didn’t develop as the pregnancy test was negative, we’re devastated obviously and I want to do another round

I take T4, alternating days with 100 and 125ug. Also T3 15ug each day. All in one go at 5am (I set an alarm). I know you guys have said consistency is key with T3, because it has a short half life. However quartering the tablets to get 15ug (3/4 of a tablet) is awkward. So I was thinking, cogitating

Hello again everyone, I now have the results of my Blue Horizon Gold test and would be grateful for your advice/comments please. Thanks. Sorry read out has decided to print itself above. Tried to move it down but can't.

Hello, I am new to the group and full of questions. My father had pernicious anemia so when I started feeling off after months of trying to figure out what was wrong...I had my labs drawn. My intrinsic factor was listed at 47.7. I can not find anything to indicate if this is what would be considered

Hello there ! Iam intolerant to nhs t3 and I have rash with Levothyroxine ( tried all brands years ago ) now iam self funding NTD and doing well on it ! (My current doctor ) is willing to prescribe me Armour thyroid but my currently endocrinologist doesn’t know where in Uk which hospitals ( endocrine

ok it's me again but my brain is so confused and foggy right now I just can't think straight in the best way to tweak my doses in light of my recent July test results shown in the linked post. https://healthunlocked.com/thyroiduk/posts/151062372/help-please I know I know I know a lot of you have been

just wondering if anyone else struggling with high levels on medication? been going on for years- since diagnosed in 2019. Takes forever to get back to relative normality each time. On carbimaxole and propanolol was 10mg BD but increased to 20mg as despite taking medication , t4 now 68.9, t3 25.4.

hi everyone, just wanting peoples thoughts or advice on the following: I had a B12 serum test done which showed my B12 was low at 188 on the 28th of august. This was repeated on September the 2nd and came out at 232 without treatment. My intrinsic factor was also negative. I have loads of B12 symptoms

Hi all, I am waiting for an endo appt in June to see if I need to go into Levo or T3. I get kidney pain in the morning after eating sugar/carbs the night before, which I am attempting to minimise. Can I ask if anyone has had the same thing, and if so, whether they have seen improvements after going

Hi lovely ladies ❤️I am on my first letrozole cycle (5 mg). On day 13 ultrasound scan, doctor saw 3 follicles and advised us to avoid intercourse because of the risk of multiples. Me and my husband are living in different cities, we did intercourse on day 13 and 14 but using condoms according to the

Hi lovely ladies ❤️I am on my first letrozole cycle (5 mg). On day 13 ultrasound scan, doctor saw 3 follicles and advised us to avoid intercourse because of the risk of multiples. Me and my husband are living in different cities, we did intercourse on day 13 and 14 but using condoms according to the

Further to my previous posts, after consultation with Roseway Labs last week the Pharmacist increased my t3 to 10ug daily (previously prescribed 5ug by Endo). I had reduced levo to 75ug from 100ug as last bloods showed T4 at very high end of the range even though I had been on T3 for the previous 10

Hi all, I’m looking for some advice about my blood test results and whether thyroid issues could be the cause of my symptoms. Also if anyone can recommend a doctor in Cardiff / South Wales I’d really appreciate it. I’ve spent years trying to manage and believing (being told) my symptoms are due to anxiety