Experiences with

Hormonin

Hi all, hope all are well and embracing this season of change - I LOVE autumn and cosy soup weather. I have recently turned 43 and just had our third round of IVF with PICSI - we took a break for Glastonbury to let off steam after 2 rounds, and to get (and implement) expert supplement and nutrition

Hello I’m doing my last ivf cycle , the last two rounds I couldn’t get any blast they were arresting in day 3 and 4th. So now trying the growth hormone , I would like to hear some feedback for the ones who has tried . Thanks in advance ♥️

Hi everyone, I used 225 Pergoveris in my first cycle, responded well, and had 5 mature eggs, 4 fertilised, which resulted in 3 good day 6 blasts. PGTA said they're all abnormal. I have switched to a new clinic as the doc just wanted to move me onto donor eggs. New doc (now in Greece, not Spain) uses

Has anyone had success with this? I took it for 10 days during my last stim cycle and ended up with 15 eggs retrieved (highest number yet) but no blasts. I'm about to start another cycle and the doc has prescribed saizen again, says its optional but helps with egg quality. Im not convinced as my previous

Unless I missed it, I haven't seen a post about the anticipated-this-fall results of the PATCH Study. I just noticed that it was reported out at the ESMO meeting a couple of weeks ago. They noted "key takeaways" to include: **Transdermal estradiol is as effective as LHRH agonist and there is no detriment

hi, I wonder if you have any thoughts please, I recently did a private thyroid blood test as was feeling quite rubbish with a long list of issues, ( have previously had parathyroid issue with high PTH and calcium leading to parathyroidectomy over 2 years ago) my thyroid results were normal except for

Hallo everyone, In last times I noticed that my level of PTH is rising despite the therapy. I use Cinacalcet + Osvaren every day and it worked good untill now. In my last numbers PTH is 919 picogramms/ml that is on 100 higher than 3 months ago. Maybe there is more powerful medications against PTH?

Trying to take a survey of transplant patients like me who have high pth and what their doctors recommended. It is not as high as when I was on dialysis but still runs above normal. My doctor has never recommended medication or surgery. I guess due to my blood tests for calcium and I have exhibited

this is more so for the real educated low dose naltrexone folks bc it involves biochemistry. I’m a woman and every time I’ve gone on LDN now it raises my testosterone due to its effects on the HPA axis (namely acth/cortisol and therefore the downstream hormones). Has anyone else experienced the same?

Hi I'm hypothyroid, currently on 112mcg levo which hasn't really hekped, plus Pernicious Anaemia which i self inject every othrr day B12. I had a cortisol test back in mid august as I suspected cushings, it was 86nmol/L so instead very likely Addisons /AI. This was via my private endo who was about

Hello 👋 We’re based in Shropshire and my partner has primary hyperparathyroidism . He has high calcium levels / PTH . We would be very very grateful of any private messages of any personal recommendations of surgeons who are very experienced in this type of surgery . Thank you 🙏 Kelly & John

hi, does anyone have any insight or experience with a natural modified ivf protocol? This is a cycle with low dose stimulation injections from day 7 to focus on collecting just a few eggs in hope they will be better quality. I can t find much information on this. I have had 6 cycles, short, long, luteal

Hello good people, The only available human growth hormone in my country is Genotropin by Pfizer. Has anyone ever used it as a HGH to improve egg quality in IVF?

Hello 👋 members , I just wanted to pop back and say thank you all for commenting on my posts regarding my John who has primary hyperparathyroidism . My goodness we didn’t have a very good experience today at local doctors 🙈 He wasn’t concerned with blood pressure and wasn’t going to do a referral

Once I started dialysis, we could not get the phosphorous to go down. Now mind you, before dialysis, it was always over 5 most times or even over 5.5 and was at 5.8 before I started dialysis. Neph put me on a binder, sevelamer, did nothing, except block me up completely. Then we tried Velphoro, and

My visit to Brightons Royal Sussex Hospital today has been exhausting but I have come away knowing the outcome of my short synacthen test and having delayed surgery on the pesky pituitary adenoma that was revealed (unexpectedly) by MRI in January. The good news is that my adrenal glands are capable

I ran into disability and it’s getting worse already for more than 2 years, Dutch doctors keep doing nothing and pinpointing me from one to another and not run even basic tests. Not hospitalizing, not trying to help. I got so many private doctors but financially I can’t afford a lot of tests. I could

I found Arty-fact's post on hyperparathyroidism enlightening, as I'd never heard of a connection between HPT and PD. Looking for studies on the subject, I was surprised to learn of a possible connection with restless leg syndrome too, and thought those with this affliction might want to read this paper

I did a Randox Female Hormone Test as NHS Endo refused to check Progesterone and Testosterone, and they don't believe in HRT. Until August 2022 I had been on HRT, Kliofem 2mg/ I mg , for more than 20 years. I was taken off it by my G.P. because of my age. I believe I have Pituitary Failure/ Central

After a year of being made to “wait and see” I am finally booked for surgery for hyperparathroidism I have really deteriorated in that time. I’ve developed osteoporosis, have severe hip pain, serious muscle weakness and worst of all have pretty much lost my sense of humor. I don’t know any more what