Experiences with

Bed rest

Last night I had to go to A&E because my heart was racing. Most unpleasant. I have experienced this before when I thought (or was told) it was down to anxiety. Long long time before diagnosis. Well yes I was certainly anxious because I do have a heart problem and experienced a heart attack twenty

Just read the info that Myo-inositol regulates the levels of TSH and FSH (follicle stimulating hormone), as well as insulin. It also reduces cholesterol. In the case of thyroid hormones, myo-inositol helps thyroid-hormone-producing cells become more efficient at building T4. Myo-inositol balances thyroid

Hi lovely people Any thoughts on my latest results please. Thankyou kindly in advance 🙏 TSH 3.0 [0.27-4.2] T3 5.1 [3.1-6.8] T4 <5.0 [12-22] B12 568 [180-1000.0] Ferritin 23 [10.0-300.0] Folate 3.3 [>4.0] Finally get to see Endo in 12 days. Will be interested to see if they are any use. I

Hi All, It's been a while since posting on here and having been diagnosed with Graves over a year ago. I was doing ok, in range and stable with alternating days on 5mg and 10 mg. After a series of issues with the endocrinology dept at the hospital, an inappropriate clinical secretary (long story),

wondering if anyone can take a look at my latest blood tests. Been on thyroxine now for 2 months .

Hello everyone. I would really appreciate any advice regarding my latest blood tests please. I didn't eat anything beforehand but wasn't able to go to the lab until 11am so it had been a bit longer that 24hrs after my last Levothyroxine (taken around 7am usually).Have been on 75mcg Levothyroxine since

hi, I’ve been doing really well on T3 only. I’ve been taking cytomel and sigma pharma which have been working really well and I finally feel well again :) Unfortunately it’s now impossible to get hold of cytomel due to shortages. I’m currently taking Tiromel but feel crap due to the lactose fillers.

I am continuing my experiment to wean off Metavive and switch to thyroxine only to find out if I can manage on levo alone and if I have adequate conversion of FT4 to FT3. Previously, my results taking Metavive Pro (100 mg) plus Metavive I (40 mg) were TSH <0.03 mu/L (0.35-4.94) FT3 5.7 pmol/L (

So my MO does frequent CMP, CBC, Diff, Testosterone, PSA as I'm doing chemo. Seeing my PCP soon and wondering about other lab tests to ask him to order. I was thinking Vit. D, B vits., lipids, A1C (done by MO when 1st saw her in April), Ferritin (as my hematocrit, hemoglobin & RBC count is slowly decreasing

Good morning everyone, I’m looking for both advice and help. Recently had blood tests (2 lots) a week apart both 4 hours after taking levo and liothyronine as recommended by Endo, always had tests in past prior to meds. I am on 75/50 alternate and 5mg lio x 2 per day 7/12 - TSH 0.20 (0.35-4.94) 1/

I am curious to see how I compare with others who suffer from bronchiectasis. So far, I have had pneumonia 3 X in an eight-month period. It seems like a lot. My last sputum test in June 2022 showed stenotrophonoma and aspergillus. I do lung clearance once daily and Ventolin 2X a day. Also, Breo Ellipta

I would like to hear from anyone who has experienced sudden hearing loss years after being diagnosed with hypothyroidism despite regular blood tests to check the thyroid. I was born with it (congenital) so have been on thyroxine since I was 3 months old. I have just had a sudden hearing loss

https://www.healthcentral.com/slideshow/thyroid-patients-and-t3

HiMy endocrinologist changed my dose this morning. I was taking 125 levo 10 lio for 3 months. These are my blood results T3 3.9 (2.4-6) t4 14.5 (8-19.1) Tsh 0.01 She has changed it to 100 levo 15 t3. I'd appreciate advice on how I go about changing. Do I just jump in and do it? I'm feeling pretty

Hi everyone, I have done my MMH results. I have been on 100mcg of accord for over 10 weeks with no breaks. My results look very strange as not only TSH is suppressed but also both FT3 and FT4 are out the scale high, but I actually felt as if I wasn’t on enough Levo as I am struggling so much with

I hope this hasn't already been posted, but well worth a read, though quite detailed and complex. A PATHWAY FOR T3 SIGNALING IN THE BRAIN TO IMPROVE THE VARIABLE EFFECTIVENESS OF THERAPY WITH L-T4 https://www.biorxiv.org/content/10.1101/2022.08.17.504300v1

Hi all, I’ve been posting a lot on here recently, I hope I’m not irritating anyone! I have a Q about long term damage from hypothyroidism. I developed hypothyroidism at 13, I am now 31. My initial symptoms were severe fatigue, bad depression and extreme anxiety and panic attacks. I was heavily medicated

Scenario just to make everyone aware of my mistake in being honest with GPLast year I was in seeing the nurse for my regular B12 injection I have PA & hashimotos. This was an afternoon appointment. The nurse pointed out I needed my thyroid bloods checked as they hadn't been done for some time ( well

After 20 years of Hashimotos I've had enough of GP's and Levothyroxine. I went to a private clinic and no suprise - I am very low on T3. She has prescribed slow release T3 5mcg but (maybe impatient) I feel no better. I've just discovered this site and read about NDT. Sounds like a better plan.

Hi all, I hope you are all keeping ok! My last bloods were in 14th Nov 2022 TSH as 0.70ml (range 0.27-4.4) Im on Levo Throxine 75 and Liothyronine 50mg I was put on Liothyronine as a request as I didn't feel Levo was doing anything. I really struggle with fatigue and weight gain even though I eat