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Femoral hernia
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Recent diagnosis & upcoming hysterectomy - what should I expect?
Hello, this is my first post and I am so thankful to have found this group 😄 In the last 5 months, I have experienced surgical menopause, been diagnosed with endo and adenomyosis; and am due to have a hysterectomy in just under a fortnight's time. I only discovered that I had endometriosis 5 months
Hello, this is my first post and I am so thankful to have found this group 😄 In the last 5 months, I have experienced surgical menopause, been diagnosed with endo and adenomyosis; and am due to have a hysterectomy in just under a fortnight's time. I only discovered that I had endometriosis 5 months
Hidden
in
Endometriosis UK
1 year ago
Tocilizumab
Hi. Has anyone had Tocilizumab injections for pmr? I've been looking at recent research which seems to suggest favourable outcomes for pmr sufferers who have problems tapering prednisolone.
Hi. Has anyone had Tocilizumab injections for pmr? I've been looking at recent research which seems to suggest favourable outcomes for pmr sufferers who have problems tapering prednisolone.
BlueMozart
in
PMRGCAuk
1 year ago
Surgical menopause - HRT and cutting patches
HeyI had a oophorectomy in June, struggled to get the right balance of estrogen. Finally put on the 100mg patches which have made a difference in terms of I'm not a complete emotional wreck and can function with life better. But I have gained so much weight, I've gone up nearly two dress sizes since
HeyI had a oophorectomy in June, struggled to get the right balance of estrogen. Finally put on the 100mg patches which have made a difference in terms of I'm not a complete emotional wreck and can function with life better. But I have gained so much weight, I've gone up nearly two dress sizes since
My_adventures
in
Endometriosis UK
1 year ago
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Very newly diagnosed PBC still undergoing testing
Hello all! I'm a 59 year old female living in the Florida Panhandle Haven't had any serious issues of note, arthritis and joint replacements aside. I began with an overall itch in Sept of 2021 and didn't worry too much until about a week later, when I was sleep deprived and torn up from scratching,
Hello all! I'm a 59 year old female living in the Florida Panhandle Haven't had any serious issues of note, arthritis and joint replacements aside. I began with an overall itch in Sept of 2021 and didn't worry too much until about a week later, when I was sleep deprived and torn up from scratching,
Hidden
in
PBCers Organization
1 year ago
FET with prolapse?
Hey ladies I want to do a FET in April and am working on losing weight and getting healthier before then to give myself the best chance. I’m 43. I did an ICSI cycle with a fresh transfer in December which was unsuccessful. I’ve had recurring UTI’s since late Nov and am trying to get on top of them
Hey ladies I want to do a FET in April and am working on losing weight and getting healthier before then to give myself the best chance. I’m 43. I did an ICSI cycle with a fresh transfer in December which was unsuccessful. I’ve had recurring UTI’s since late Nov and am trying to get on top of them
TeddyBear5
in
Fertility Network UK
1 year ago
length of time for biopsy results
Hi, had a partial lung lobectomy and lymph node removal, was told biopsy results would be back in 7-10 days. It’s now been 41 days and I’ve heard nothing. When I contact various people I’m just being told this length of timeframe is not uncommon.. this does not sound right to me… Anyone else had to wait
Hi, had a partial lung lobectomy and lymph node removal, was told biopsy results would be back in 7-10 days. It’s now been 41 days and I’ve heard nothing. When I contact various people I’m just being told this length of timeframe is not uncommon.. this does not sound right to me… Anyone else had to wait
Hidden
in
Lung Conditions Community Forum
1 year ago
Update on my previous post trapped nerve and PMR.
After an MRI on my spine I do not have a trapped nerve in my back and my pain is two vertebrae bones crumbling. I have come to the conclusion that the pain in my back and bottom area is mainly my PMR flare, it is so bad I can't move without pain while in bed. Tried increasing my pred dosage from 6mg
After an MRI on my spine I do not have a trapped nerve in my back and my pain is two vertebrae bones crumbling. I have come to the conclusion that the pain in my back and bottom area is mainly my PMR flare, it is so bad I can't move without pain while in bed. Tried increasing my pred dosage from 6mg
Washingup
in
PMRGCAuk
1 year ago
Letrozole(Femara) /joint pain threads continued.....
I have been reading with interest the threads concerning Letrozole and the many side effects we all deal with. My history: DX May 2019 MBC to right femoral hip/thigh. IM nail procedure to stabilize. Started Letrozole/Ibrance. NED after 3 months of treatment! Tried the brand name of Letrozole - Femara
I have been reading with interest the threads concerning Letrozole and the many side effects we all deal with. My history: DX May 2019 MBC to right femoral hip/thigh. IM nail procedure to stabilize. Started Letrozole/Ibrance. NED after 3 months of treatment! Tried the brand name of Letrozole - Femara
OceanBreeze3
in
SHARE Metastatic Breast Cancer
2 years ago
Women, ADHD Surgical menopause and memory loss
Hello, New to the forum and looking to learn more about the subject listed above. It seems that among the medical professionals I've seen ADD is overlooked, as is the impact of the loss of estrogen. I am scared that this is my new normal. I'm wondering. 1. Have any of you experienced worsening ADD
Hello, New to the forum and looking to learn more about the subject listed above. It seems that among the medical professionals I've seen ADD is overlooked, as is the impact of the loss of estrogen. I am scared that this is my new normal. I'm wondering. 1. Have any of you experienced worsening ADD
Learning1975
in
CHADD's Adult ADHD Support
2 years ago
morning fellow hearties
have not posted for a while just been cruising along taking my meds and adding more health conditions to my list, arthritis, peripheral neuralgia and now a
femoral
hernia
which the surgeon has told me to decide if want the op or not I am struggling with that.I then got a letter from my cardiologist
have not posted for a while just been cruising along taking my meds and adding more health conditions to my list, arthritis, peripheral neuralgia and now a
femoral
hernia
which the surgeon has told me to decide if want the op or not I am struggling with that.I then got a letter from my cardiologist
Thanksnhs
in
British Heart Foundation
2 years ago
Fantastic Book for PMR and GCA
On one of my earlier posts, a poster referred me to a book about PMR and GCA. My husband, 73 has been diagnosed with PMR. She recommended this book and it has been fantastic and eye opening and in many ways a Godsend, particularly for asking questions of the rheumatologist and his proactive GP who
On one of my earlier posts, a poster referred me to a book about PMR and GCA. My husband, 73 has been diagnosed with PMR. She recommended this book and it has been fantastic and eye opening and in many ways a Godsend, particularly for asking questions of the rheumatologist and his proactive GP who
Andymegv
in
PMRGCAuk
1 year ago
Steroid sparing agents
Could anyone tell me more about Steroid sparing agents please? I have read about Methotrexate and Tocilizumab (?) but not really sure when or if I would go on them ( I was only diagnosed with GCA at the end of January) - also, side effects etc? I see my Rheumatologist next Monday and want to armed with
Could anyone tell me more about Steroid sparing agents please? I have read about Methotrexate and Tocilizumab (?) but not really sure when or if I would go on them ( I was only diagnosed with GCA at the end of January) - also, side effects etc? I see my Rheumatologist next Monday and want to armed with
Janeval
in
PMRGCAuk
1 year ago
SIBO and NHS
Hi all Quite a few years ago I had my Gallbladder removed, a few years later IBS diagnosed after colonoscopy and endoscopy negative results thankfully, the last 6 months maybe longer have been horrible with flare ups IBS-D then the other way, bloating cramps the usual suspects, I had a really bad weekend
Hi all Quite a few years ago I had my Gallbladder removed, a few years later IBS diagnosed after colonoscopy and endoscopy negative results thankfully, the last 6 months maybe longer have been horrible with flare ups IBS-D then the other way, bloating cramps the usual suspects, I had a really bad weekend
Jaluga
in
IBS Network
2 years ago
Oopherectomy or Hysterectomy?
Hi everyone, I have been recently diagnosed with endometriosis and adenomyosis. I saw a gynaecologist at my local hospital who said my choices for treatment are either oopherectomy or abdominal hysterectomy as I've had 2 c-sections. There was no mention of a laparoscopy. I also have hypermobility (EDS
Hi everyone, I have been recently diagnosed with endometriosis and adenomyosis. I saw a gynaecologist at my local hospital who said my choices for treatment are either oopherectomy or abdominal hysterectomy as I've had 2 c-sections. There was no mention of a laparoscopy. I also have hypermobility (EDS
BluePanda7
in
Endometriosis UK
2 years ago
Treat-to-target recommendations in giant cell arteritis and polymyalgia rheumatica - a very useful reference to show your doctor
https://ard.bmj.com/content/early/2023/02/23/ard-2022-223429 This is Open Access so everyone can read it. It is something I think we should all have a read of, some will be beyond most of us and some is just plain boring but there are points in it everyone will understand and can bring to the notice
https://ard.bmj.com/content/early/2023/02/23/ard-2022-223429 This is Open Access so everyone can read it. It is something I think we should all have a read of, some will be beyond most of us and some is just plain boring but there are points in it everyone will understand and can bring to the notice
PMRpro
Ambassador
in
PMRGCAuk
1 year ago
gallbladder removal
hi I wonder if anyone has had there gallbladder removed with compensated cirrhosis I’m worried that this could affect my liver and cause more damage. I had a definite diagnosis of cirrhosis 6 months ago after a biopsy only Fibroscan was 13.6kpa but mri showed cirrhosis this was done in June I also had
hi I wonder if anyone has had there gallbladder removed with compensated cirrhosis I’m worried that this could affect my liver and cause more damage. I had a definite diagnosis of cirrhosis 6 months ago after a biopsy only Fibroscan was 13.6kpa but mri showed cirrhosis this was done in June I also had
Janden12
in
British Liver Trust
2 years ago
Could Members With Experience of PBC Without A Gallbladder Feels Like , Is Treatment and Diagnosis done the same way? Thanks
I've got a number of Chronic Health Conditions . I had a gallbladder removal in 2014 but have had recurrent pancreatitis, liver and pancreas pain and liver symptoms since then that have recently got worse. The burning in the upper quadrant us constant. I also have GERD , Gut dysmotility because of Dysautonomia
I've got a number of Chronic Health Conditions . I had a gallbladder removal in 2014 but have had recurrent pancreatitis, liver and pancreas pain and liver symptoms since then that have recently got worse. The burning in the upper quadrant us constant. I also have GERD , Gut dysmotility because of Dysautonomia
Blearyeyed
in
PBCers Organization
2 years ago
Preventative ovary removal hereditary link
Just wondered if people on this site may have experience of family members deciding to have elective surgery for removal of their ovaries based on possible hereditary links of ovarian cancer. I myself have ovarian cancer, and my sister and cousin are considering surgery to reduce their risk. An aunt
Just wondered if people on this site may have experience of family members deciding to have elective surgery for removal of their ovaries based on possible hereditary links of ovarian cancer. I myself have ovarian cancer, and my sister and cousin are considering surgery to reduce their risk. An aunt
Mirrorplace
in
My Ovacome
2 years ago
Do natural supplements work to reduce high cholesterol?
While strictly not a PMR issue I know there are a few whose cholesterol has risen markedly since being diagnosed. I am one of them. I have always had high-ish cholesterol but my last fasting blood test showed everything else perfectly normal but my cholesterol was up. I haven't seen the results
While strictly not a PMR issue I know there are a few whose cholesterol has risen markedly since being diagnosed. I am one of them. I have always had high-ish cholesterol but my last fasting blood test showed everything else perfectly normal but my cholesterol was up. I haven't seen the results
Pr0jection
in
PMRGCAuk
1 year ago
A giant cell arteritis suffer
A giant cell arteritis suffer on methotrexate and prednisolone. Has anyone been on this combination as well? How long did it take you to get off the steroids as i'm still on 4mg as struggling to get off them as symptoms keep returning once I reduce down any further.
A giant cell arteritis suffer on methotrexate and prednisolone. Has anyone been on this combination as well? How long did it take you to get off the steroids as i'm still on 4mg as struggling to get off them as symptoms keep returning once I reduce down any further.
BM16
in
PMRGCAuk
1 year ago
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