Search
Search
About
Log in
Join
Experiences with
Estrogen Replacement Therapy
Posts
Communities
21,970 public posts
Filter results
Oxygen Therapy
Hi Everyone, A relative, who has MS, has suggested that I try oxygen therapy. It seems to really help them but I wondered if anyone here has had any experience of this and provide a suitable comment. Many thanks!
Hi Everyone, A relative, who has MS, has suggested that I try oxygen therapy. It seems to really help them but I wondered if anyone here has had any experience of this and provide a suitable comment. Many thanks!
RLSofManyYears
in
Restless Legs Syndrome
6 months ago
Private endo recommendation in Wales, please
Hi. I haven't posted for a while as I've moved from England to Wales. I used to see Dr SZ at Gatwick Spire, and am hoping someone could recommend an endo closer to Wales. I can't find anyone on the ThyroidUk list.On the Thyroid UK list, Dr GC ( who has Hashimoto's herself ), does video conferencing
Hi. I haven't posted for a while as I've moved from England to Wales. I used to see Dr SZ at Gatwick Spire, and am hoping someone could recommend an endo closer to Wales. I can't find anyone on the ThyroidUk list.On the Thyroid UK list, Dr GC ( who has Hashimoto's herself ), does video conferencing
strawberryflower
in
Thyroid UK
11 months ago
Thyroid menopause supplement no hrt
Hi. I've been feeling quite good for a while now but I've had to stop taking HRT.I'm now feeling not fabulous again. I'm looking at all the natural alternatives. Anyone got any suggestions which won't interfere with thyroxine or aggravate the thyroid? Thank you
Hi. I've been feeling quite good for a while now but I've had to stop taking HRT.I'm now feeling not fabulous again. I'm looking at all the natural alternatives. Anyone got any suggestions which won't interfere with thyroxine or aggravate the thyroid? Thank you
Foggyk
in
Thyroid UK
11 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Thin lining 6.1 mm before transfer -any success stories?
Hi everyone,I've been preparing for my 4th FET transfer and was looking for support and maybe success stories of someone in a similar situation. I wasn't told the correct medication protocol until I sent 4 messages to my clinic to clarify via portal and for several days took my estrogen tablets orally
Hi everyone,I've been preparing for my 4th FET transfer and was looking for support and maybe success stories of someone in a similar situation. I wasn't told the correct medication protocol until I sent 4 messages to my clinic to clarify via portal and for several days took my estrogen tablets orally
Meliana
in
Fertility Network UK
11 months ago
Follow up to my last post re SDR
It's now almost 4 weeks since Mark's knee replacement. He's doing well after a small setback at the weekend. He saw our Dr a week ago to ask if he could drive. Dr told him to ask the physio. She tested him on a step, checking the force he could use on his knee and gave permission for him to drive
It's now almost 4 weeks since Mark's knee replacement. He's doing well after a small setback at the weekend. He saw our Dr a week ago to ask if he could drive. Dr told him to ask the physio. She tested him on a step, checking the force he could use on his knee and gave permission for him to drive
IdasMum
in
PMRGCAuk
8 months ago
North of England Endo
Good evening I’m looking for private message replies please on your recommended Endo’s in the North of England. Yorkshire and North East. Not many seem to be listed on Thyroid U.K. list. Someone open to combined therapy. Thank you! Look forward to hearing from you :)
Good evening I’m looking for private message replies please on your recommended Endo’s in the North of England. Yorkshire and North East. Not many seem to be listed on Thyroid U.K. list. Someone open to combined therapy. Thank you! Look forward to hearing from you :)
Bollieforme
in
Thyroid UK
6 months ago
hip replacement advice
Has anyone had joint replacement after being diagnosed with MBC? If so, do you have any advice? I was diagnosed with MBC to the bones and liver July 2020. After radiation and several lines of drug treatment, I was diagnosed with severe osteoarthritis in my right hip a year ago. I had existing painful
Has anyone had joint replacement after being diagnosed with MBC? If so, do you have any advice? I was diagnosed with MBC to the bones and liver July 2020. After radiation and several lines of drug treatment, I was diagnosed with severe osteoarthritis in my right hip a year ago. I had existing painful
ClarenceO
in
SHARE Metastatic Breast Cancer
8 months ago
Let's enjoy some predictions: cell and gene therapy in 2024
because sometimes we must also have some positive but realistic dreams.... https://www.massgeneralbrigham.org/en/about/newsroom/articles/2024-predictions-about-gene-and-cell-therapy
because sometimes we must also have some positive but realistic dreams.... https://www.massgeneralbrigham.org/en/about/newsroom/articles/2024-predictions-about-gene-and-cell-therapy
Maxone73
in
Advanced Prostate Cancer
6 months ago
Why should ft4 be at a certain percentage through reference range (mid to upper) when on T4/T3 combination therapy when T4 is inactive?
As per the subject title, if ft4 is inactive, then why do some people on T4/T3 therapy only feel good if their ft4 level is at the mid/upper level despite the fact their ft3 (active form) may be at a optimal level? Or if they are not feeling well, why are they advised to increase their Levo dosage if
As per the subject title, if ft4 is inactive, then why do some people on T4/T3 therapy only feel good if their ft4 level is at the mid/upper level despite the fact their ft3 (active form) may be at a optimal level? Or if they are not feeling well, why are they advised to increase their Levo dosage if
RIGBY1978
in
Thyroid UK
6 months ago
sensitive update
Hi ladies, I hope this post isn’t difficult to read. I’ve always found reading people’s updates helped me to stay positive and feel that’s it’s possible for me. My last transfer was successful and I’ve reached the three month stage. Obviously there is still a long way to go but I wanted to post my
Hi ladies, I hope this post isn’t difficult to read. I’ve always found reading people’s updates helped me to stay positive and feel that’s it’s possible for me. My last transfer was successful and I’ve reached the three month stage. Obviously there is still a long way to go but I wanted to post my
Bed12
in
Fertility Network UK
11 months ago
anyone on estradiol?
My gp want to prescribe me estradiol internal tablets.. ( just to confirm...the ones that go up there!. Not patches cream or by mouth ) I'm 11 years post menopause. I hardly ever have relationships or sex because it's just impossible or agony.. Have tried ' yes ' lubricant get in the past.. With
My gp want to prescribe me estradiol internal tablets.. ( just to confirm...the ones that go up there!. Not patches cream or by mouth ) I'm 11 years post menopause. I hardly ever have relationships or sex because it's just impossible or agony.. Have tried ' yes ' lubricant get in the past.. With
MrsClanger
in
Thyroid UK
11 months ago
BCF after 9 years post proton therapy
My PSA had been increasing slowly since my nadir of .75 in 2017 reaching 1.19 in 2022. Both RO and Uro weren't terribly concerned. I wanted PSMA after 3rd consecutive increase but both recommended a wait and see approach, especially the RO who seems honor bound to wait for 2.0 over nadir. I skipped
My PSA had been increasing slowly since my nadir of .75 in 2017 reaching 1.19 in 2022. Both RO and Uro weren't terribly concerned. I wanted PSMA after 3rd consecutive increase but both recommended a wait and see approach, especially the RO who seems honor bound to wait for 2.0 over nadir. I skipped
hwrjr
in
Prostate Cancer Network
6 months ago
Update on Endo and WLAMS
Re the Endo who was determined to take away my T3 whilst all I wanted was a blood test to include T3. After an exchange of letters, he phoned this morning. He had back pedalled so far he was out of site. He agreed T3 was vital, he agreed testing the full TSH, T4 and T3 were needed to make a positive
Re the Endo who was determined to take away my T3 whilst all I wanted was a blood test to include T3. After an exchange of letters, he phoned this morning. He had back pedalled so far he was out of site. He agreed T3 was vital, he agreed testing the full TSH, T4 and T3 were needed to make a positive
serenfach
in
Thyroid UK
6 months ago
update Vanderbilt
just thought I would update and let y’all know that I have an appointment with a doctor at Vanderbilt university medical in Franklin Tennessee in April. Vanderbilt is a RLS quality care center and the closest to me. I actually had one of their Doctors call me and said that if there were any cancellations
just thought I would update and let y’all know that I have an appointment with a doctor at Vanderbilt university medical in Franklin Tennessee in April. Vanderbilt is a RLS quality care center and the closest to me. I actually had one of their Doctors call me and said that if there were any cancellations
6236
in
Restless Legs Syndrome
6 months ago
red light therapy
has anyone ever heard of or tried red light therapy? I’m sure that’s not the proper medical term but that’s what Dr Cooper called it. After the nerve induction test he said both my legs showed nerve weakness and the red light therapy is what he prescribed saying that it might possibly help the RLS.
has anyone ever heard of or tried red light therapy? I’m sure that’s not the proper medical term but that’s what Dr Cooper called it. After the nerve induction test he said both my legs showed nerve weakness and the red light therapy is what he prescribed saying that it might possibly help the RLS.
6236
in
Restless Legs Syndrome
6 months ago
Sudden change in fT4 levels
I was diagnosed with autoimmune hypothyroidism in 1995 at age 19 and did well on levothyroxine alone for years. I always felt better with fT4 high in range, although this suppressed my TSH to almost undetectable levels. A few years ago, I started to get hypo symptoms again, and bloods showed that my
I was diagnosed with autoimmune hypothyroidism in 1995 at age 19 and did well on levothyroxine alone for years. I always felt better with fT4 high in range, although this suppressed my TSH to almost undetectable levels. A few years ago, I started to get hypo symptoms again, and bloods showed that my
hose1975
in
Thyroid UK
11 months ago
Hot flushes and night sweats
Hi everyone I would like some advice please. I had been in HRT for 22 years (implants) but when I moved 8 years ago I couldn’t find a gynaecologist to do implants so I decided to stop using HRT. All was fine for 4/5years then I suddenly start having flushes during the day and night sweats which have
Hi everyone I would like some advice please. I had been in HRT for 22 years (implants) but when I moved 8 years ago I couldn’t find a gynaecologist to do implants so I decided to stop using HRT. All was fine for 4/5years then I suddenly start having flushes during the day and night sweats which have
Allot
in
Menopause and Perimenopause Support
11 months ago
Secondary Cancers after CAR-T Cell Therapy
From New England Journal of Medicine dated 24th Jan 2024 (article is for subscribers only) This brief report states: [i]The demonstrated efficacy of the current generation of approved CAR-T products comes along with several well-described safety concerns, including risks of cytokine release syndrome
From New England Journal of Medicine dated 24th Jan 2024 (article is for subscribers only) This brief report states: [i]The demonstrated efficacy of the current generation of approved CAR-T products comes along with several well-described safety concerns, including risks of cytokine release syndrome
Jm954
Administrator
in
CLL Support
6 months ago
2nd frozen embryo transfer at 41yrs, endometriosis, under active thyroid, success stories needed!
Hi all, We’re about to have our 2nd FET at the beginning of September, I’ve had the Prostap injection and my first scan is tomorrow which afterwards I’ll start the estrogen tablets and then the progesterone pessaries. I had Endometriosis quite a few years ago and my pelvis was ‘frozen’ where all of
Hi all, We’re about to have our 2nd FET at the beginning of September, I’ve had the Prostap injection and my first scan is tomorrow which afterwards I’ll start the estrogen tablets and then the progesterone pessaries. I had Endometriosis quite a few years ago and my pelvis was ‘frozen’ where all of
LV2020
in
Fertility Network UK
11 months ago
Coping after hip replacement
Hi Everyone, Sorry its me again with yet more concerns about forthcoming hip replacement on 5th December. Despite my emphasising to the surgeon at my recent pre-op assessment that I was having excruciating pain in my right hip (which is what I had assumed would need replacing) BUT because the x-rays
Hi Everyone, Sorry its me again with yet more concerns about forthcoming hip replacement on 5th December. Despite my emphasising to the surgeon at my recent pre-op assessment that I was having excruciating pain in my right hip (which is what I had assumed would need replacing) BUT because the x-rays
Fib36
in
AF Association
8 months ago
1
...
59
60
61
...
100
Next page
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Advanced Prostate Cancer
4625 results
Thyroid UK
3084 results
Endometriosis UK
2190 results
View top 10 communities
Sort by
Most Relevant
Newest