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Alendronic acid and rls
I have osteoporosis, Dr's want me to go on either Alendronic acid , IV Zolendronic acid, or Subcutaneous Denosumab Does anyone know if they make RLS worse please
I have osteoporosis, Dr's want me to go on either Alendronic acid , IV Zolendronic acid, or Subcutaneous Denosumab Does anyone know if they make RLS worse please
antelope99
in
Restless Legs Syndrome
5 months ago
stomach polyps
Hi all I’ve addressed a thyroid issue - Hashimotos, with the help from the thyroid site. I’m still experiencing fatigue. I am in meno/post menopausal stage. Symptoms do over lap, but have suspected B12 issue for some time. Tend to get low active B12 results. Lots of B12 symptoms. Dr not interested,
Hi all I’ve addressed a thyroid issue - Hashimotos, with the help from the thyroid site. I’m still experiencing fatigue. I am in meno/post menopausal stage. Symptoms do over lap, but have suspected B12 issue for some time. Tend to get low active B12 results. Lots of B12 symptoms. Dr not interested,
Bacca
in
Pernicious Anaemia Society
5 months ago
A cautionary tale
At short notice I accepted an invitation for a cryo ablation on last Monday. I have been on rivaroxaban and clopidogrel for a year. The ablation was straightforward and successful, however within minutes, while I was still very groggy from the local anaesthetic, I suffered a TIA (very minor stroke)
At short notice I accepted an invitation for a cryo ablation on last Monday. I have been on rivaroxaban and clopidogrel for a year. The ablation was straightforward and successful, however within minutes, while I was still very groggy from the local anaesthetic, I suffered a TIA (very minor stroke)
Pindarus
in
AF Association
1 year ago
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tinnitus
I’ve had tinnitus for 3 years now (covid infection caused it) ENT wasn’t helpful as ears and hearing test are good for age.. and don’t want to see me again Anybody know best next steps? I’ve been wondering about nerve damage being the cause 🤷♀️ want to see the gp with an idea of what needs doing
I’ve had tinnitus for 3 years now (covid infection caused it) ENT wasn’t helpful as ears and hearing test are good for age.. and don’t want to see me again Anybody know best next steps? I’ve been wondering about nerve damage being the cause 🤷♀️ want to see the gp with an idea of what needs doing
Molly108
in
Tinnitus UK
10 months ago
Brain metastasis on Ovarian Cancer
Hello everyone, I'm writing this post on behalf of my mother. My mother, aged 48, was diagnosed with OC back in Feb '21. Since then, she has undergone several surgeries and chemotherapy rounds. I know everyone here has either faced these challenges or witnessed a loved one going through them, so you
Hello everyone, I'm writing this post on behalf of my mother. My mother, aged 48, was diagnosed with OC back in Feb '21. Since then, she has undergone several surgeries and chemotherapy rounds. I know everyone here has either faced these challenges or witnessed a loved one going through them, so you
selosh16
in
My Ovacome
10 months ago
misdiagnosed ?
Hello. My name is Lynn. Eleven years ago, after 2 late miscarriages (17 weeks) and several stroke like episodes I was diagnosed with Primary Antiphospholipid Syndrome and have been on warfarin ever since with bridging doses of clexane when inr is not in range. I have continued to have some TIA like
Hello. My name is Lynn. Eleven years ago, after 2 late miscarriages (17 weeks) and several stroke like episodes I was diagnosed with Primary Antiphospholipid Syndrome and have been on warfarin ever since with bridging doses of clexane when inr is not in range. I have continued to have some TIA like
stillwaiting
in
Hughes Syndrome APS Forum
1 year ago
APS misdiagnosis???
Hello, this is my first post here. My name is Lynn. Eleven years ago, after 2 late miscarriages (17 weeks) and several stroke like episodes I was diagnosed with Primary Antiphospholipid Syndrome and have been on warfarin ever since with bridging doses of clexane when inr is not in range. I have continued
Hello, this is my first post here. My name is Lynn. Eleven years ago, after 2 late miscarriages (17 weeks) and several stroke like episodes I was diagnosed with Primary Antiphospholipid Syndrome and have been on warfarin ever since with bridging doses of clexane when inr is not in range. I have continued
stillwaiting
in
LUPUS UK
1 year ago
Hi, im on lercanidipine and olmesartan, does anyone get bone pain with these? My .
Hi, im on lercanidipine and olmesartan, i was on irbesartan alone with no side effects for years but had to come off them as they were getting discontinued.does anyone get bone pan with these? I can barely put my arms behind my back.
Hi, im on lercanidipine and olmesartan, i was on irbesartan alone with no side effects for years but had to come off them as they were getting discontinued.does anyone get bone pan with these? I can barely put my arms behind my back.
Nannyvee
in
High Blood Pressure Support
10 months ago
SharonY
Wondering if anyone has had dental extraction while on Actemra. I was told by my dentist that it affects the jaw and I would need to see a specialist since an extraction would be problematic? I am in the UK and have weekly Actemra injections. Thx
Wondering if anyone has had dental extraction while on Actemra. I was told by my dentist that it affects the jaw and I would need to see a specialist since an extraction would be problematic? I am in the UK and have weekly Actemra injections. Thx
WaltzG
in
PMRGCAuk
1 year ago
Diverticulosis etc
interesting thread and a couple of anecdotes about having to rush off to the woods to do whatever the bears do there provoked some hollow laughter! I’ve been in them thar woods a couple of times myself. i don’t have coeliac but I do have diverticulitis flares and I do have severe sigmoid colon diverticular
interesting thread and a couple of anecdotes about having to rush off to the woods to do whatever the bears do there provoked some hollow laughter! I’ve been in them thar woods a couple of times myself. i don’t have coeliac but I do have diverticulitis flares and I do have severe sigmoid colon diverticular
Calceolaria
in
Thyroid UK
5 months ago
A&E AGAIN!!
So, not only have I enjoyed the delights of sampling A&E, Colchester a few weeks ago but I was also given the opportunity to sample Warwicks A&E offering on Sat night! Having almost reached the end of lots of investigations following my ambulance ride a few weeks ago, I found myself with yet
another
So, not only have I enjoyed the delights of sampling A&E, Colchester a few weeks ago but I was also given the opportunity to sample Warwicks A&E offering on Sat night! Having almost reached the end of lots of investigations following my ambulance ride a few weeks ago, I found myself with yet
another
Kendrew
in
PMRGCAuk
5 months ago
Two questions concerning RLS
1.For the past few months l have had horrendous bladder pain and l can no longer cope with that and the RLS. I am making an appointment to see my GP who knows nothing about RLS so l need some advice about treatment for the bladder pain which won’t worsen the RL S. l would be very grateful if anyone knows
1.For the past few months l have had horrendous bladder pain and l can no longer cope with that and the RLS. I am making an appointment to see my GP who knows nothing about RLS so l need some advice about treatment for the bladder pain which won’t worsen the RL S. l would be very grateful if anyone knows
bedith6
in
Restless Legs Syndrome
10 months ago
Gastroperesis + IBS C- thoughts
Hello ! My name is Jess and I have been dealing with Gastroperesis for over 25 years. I am SOOOO tired of it! I constantly get a distended bloated stomach, some from gas and some from the slow digestion and not be able to go. I also have IBS-C ( constipation) so this makes matters worse. I take
Hello ! My name is Jess and I have been dealing with Gastroperesis for over 25 years. I am SOOOO tired of it! I constantly get a distended bloated stomach, some from gas and some from the slow digestion and not be able to go. I also have IBS-C ( constipation) so this makes matters worse. I take
jr188
in
IBS Network
8 months ago
Dizziness
Sorry to ask another question, as you know I've seen ENT Consultant, had CT angiogram Aortic Arch, Carotid arteries and Intracranial, 2 weeks ago. Not heard anything back - my results don't get posted on my NHS account although my Hubs can access all his so I am going to ring tomorrow and try to get
Sorry to ask another question, as you know I've seen ENT Consultant, had CT angiogram Aortic Arch, Carotid arteries and Intracranial, 2 weeks ago. Not heard anything back - my results don't get posted on my NHS account although my Hubs can access all his so I am going to ring tomorrow and try to get
hollyrain
in
Tinnitus UK
10 months ago
Not sure what to do next
Hello. I suddenly developed loud tinnitus in my left ear 3 months ago and went to the doctors. It's a very high pitched ringing and varies between loud and very loud and sometimes has different pitches all at once like an orchestra. It's constant, 24/7. I'd had a very slight ringing for several months
Hello. I suddenly developed loud tinnitus in my left ear 3 months ago and went to the doctors. It's a very high pitched ringing and varies between loud and very loud and sometimes has different pitches all at once like an orchestra. It's constant, 24/7. I'd had a very slight ringing for several months
Sootymouse
in
Acoustic Neuroma Support
10 months ago
Bechets support pip
Hi I was wondering if anybody is on pip or had won there win appeal.I have severe problems with my mobility I keep getting flare up in my legs and feet they swell up and cause Me inflammation and I find it difficult to do anything as they hurt. And I cannot bare pain or do anything everything is a struggle
Hi I was wondering if anybody is on pip or had won there win appeal.I have severe problems with my mobility I keep getting flare up in my legs and feet they swell up and cause Me inflammation and I find it difficult to do anything as they hurt. And I cannot bare pain or do anything everything is a struggle
Tibz
in
Behçet's UK
5 months ago
how did your GI/gut symptoms start?
Hi All I hope everyone is doing well. looking for some insight - I’ve been diagnosed nearly 2 years. recently I have been having some minor gut issues and wondered if this was the beginning of SSC related gut problems and if there is anything I can do to prevent worse progression. I’ve found my
Hi All I hope everyone is doing well. looking for some insight - I’ve been diagnosed nearly 2 years. recently I have been having some minor gut issues and wondered if this was the beginning of SSC related gut problems and if there is anything I can do to prevent worse progression. I’ve found my
ruablue
in
Scleroderma & Raynaud's UK (SRUK)
5 months ago
All clear now for two years
Just sending a positive story. Diagnosed 2b HG clear cell, endometrioid 2020. Big op, chemo, diagnosed my own recurrence after 6 months. Another op, then RT. 2021. Last couple of scans have been clear. They are still going to check me every 6 months. I am taking alternative supplements and vitamins
Just sending a positive story. Diagnosed 2b HG clear cell, endometrioid 2020. Big op, chemo, diagnosed my own recurrence after 6 months. Another op, then RT. 2021. Last couple of scans have been clear. They are still going to check me every 6 months. I am taking alternative supplements and vitamins
candyapplegrey
in
My Ovacome
1 year ago
Advice for Hair Loss?
Anyone have a remedy for hair loss from liver disease? My hair is falling out a lot every day. I’ve been using collagen and keratin shampoo and I’ve tried rosemary oil but nothing works. I’m gonna be bald soon 😱 Does anything work? I read that the hair loss can be from lack of protein. I eat a lot
Anyone have a remedy for hair loss from liver disease? My hair is falling out a lot every day. I’ve been using collagen and keratin shampoo and I’ve tried rosemary oil but nothing works. I’m gonna be bald soon 😱 Does anything work? I read that the hair loss can be from lack of protein. I eat a lot
FlippinOut
in
British Liver Trust
10 months ago
Mebeverine
Hi all, just wondering about Mebeverine as my GP has prescribed this in the past, and I have it on repeat prescription. I do not take this regularly, as I seem to find that I can't take it before my evening meal as I have to take other meds then.Just wondering if anyone has taken the 2x a day slow release
Hi all, just wondering about Mebeverine as my GP has prescribed this in the past, and I have it on repeat prescription. I do not take this regularly, as I seem to find that I can't take it before my evening meal as I have to take other meds then.Just wondering if anyone has taken the 2x a day slow release
Pollyboo
in
IBS Network
1 year ago
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