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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
5 months ago
CT Angio Test Results
First off, I’m so grateful for this forum and those listen to us and advise and support all of us on this unwanted journey we are on. I got the results of my chest, abdominal, and pelvis CT scan today. Chest: Ascending and descending aorta normal. Everything else normal. Abdominal Aorta: “No significant
First off, I’m so grateful for this forum and those listen to us and advise and support all of us on this unwanted journey we are on. I got the results of my chest, abdominal, and pelvis CT scan today. Chest: Ascending and descending aorta normal. Everything else normal. Abdominal Aorta: “No significant
Lenore58
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
5 months ago
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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
5 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
5 months 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
5 months ago
Can’t sleep
I was diagnosed in May of this year.. Started with double vision. I also have seizures, mostly controlled. I can’t sleep hardly at all. Tried several meds, nothing. Very frustrating. I get maybe 3, maybe 4 hours if lucky. There have been some nights I haven’t slept at all? Anyone else have
I was diagnosed in May of this year.. Started with double vision. I also have seizures, mostly controlled. I can’t sleep hardly at all. Tried several meds, nothing. Very frustrating. I get maybe 3, maybe 4 hours if lucky. There have been some nights I haven’t slept at all? Anyone else have
Cinjav
in
PSP Association
5 months ago
Laxido and acid reflux
I swear every time I take this stuff I end up with really bad regurgitation and heartburn. Coincidence? I am on other medications.
I swear every time I take this stuff I end up with really bad regurgitation and heartburn. Coincidence? I am on other medications.
Spaceboy_60
in
IBS Network
5 months ago
IAM having a moan,so I'm sorry.
My sister who has very bad arthritis, and was on methotrexate for years was taken off it, has had such a bad time having had sepsis and deep vein thrombosis and always in pain, hate to say even with my PMR I feel lucky I know what a comment to make as we all hate this illness. She had to fight to see
My sister who has very bad arthritis, and was on methotrexate for years was taken off it, has had such a bad time having had sepsis and deep vein thrombosis and always in pain, hate to say even with my PMR I feel lucky I know what a comment to make as we all hate this illness. She had to fight to see
Harrywogan
in
PMRGCAuk
5 months ago
piles and edoxoban
My poor hubby doesn’t seem to be able to catch a break at the moment, if you’ve read some of my previous posts concerning his stroke and AF. For the last five days he has bled after every bowel movement , he has had piles in the past but has not bled as much , I would say as much as a nosebleed ,
My poor hubby doesn’t seem to be able to catch a break at the moment, if you’ve read some of my previous posts concerning his stroke and AF. For the last five days he has bled after every bowel movement , he has had piles in the past but has not bled as much , I would say as much as a nosebleed ,
Jackiesmith7777
in
AF Association
5 months ago
Post op sleeping position
Hi everyone my husband is nearly 9 months post oesophagectomy with 2/3 of his stomach removed. He was diagnosed T4aN1M0 in September last year, had the op in March and is overall recovering really well. We’re so grateful that generally he’s sleeping well but currently using an OPA wedge but slipping
Hi everyone my husband is nearly 9 months post oesophagectomy with 2/3 of his stomach removed. He was diagnosed T4aN1M0 in September last year, had the op in March and is overall recovering really well. We’re so grateful that generally he’s sleeping well but currently using an OPA wedge but slipping
Tighan
in
Oesophageal & Gastric Cancer
5 months ago
Stopping Actemra
Good day all: Well, I called and canceled my Actemra infusion for today. I was recently diagnosed with something called MGRS (Monoclonal Gammopathy of renal Significance), It is related to Multiple Myeloma. I start chemotherapy for the MGRS next week, which is the same as the chemo for full
Good day all: Well, I called and canceled my Actemra infusion for today. I was recently diagnosed with something called MGRS (Monoclonal Gammopathy of renal Significance), It is related to Multiple Myeloma. I start chemotherapy for the MGRS next week, which is the same as the chemo for full
phebamom
in
PMRGCAuk
5 months ago
Very noisy ears and pressure
Hi - I have been diagnosed with TMJD - I have Tinnitus mostly in the right ear, but every so often I have ghastly whooshing in both ears very noisy and a feeling of pressure , is this possibly stress anxiety related? Or the TMJD effecting the ETs - I know it's a highly complex area, I have had this T
Hi - I have been diagnosed with TMJD - I have Tinnitus mostly in the right ear, but every so often I have ghastly whooshing in both ears very noisy and a feeling of pressure , is this possibly stress anxiety related? Or the TMJD effecting the ETs - I know it's a highly complex area, I have had this T
Seabob
in
Tinnitus UK
5 months ago
Waiting PMR Diagnosis
Started in September 2023 with stiff hips and buttocks, just woke up like that. Don't know if it was coincidence but this was 3 day's after a flu jab! Gradually over the next few weeks, hip's became stiffer, burning type pain at times down to the knees. Putting on lower half clothes and shoes became
Started in September 2023 with stiff hips and buttocks, just woke up like that. Don't know if it was coincidence but this was 3 day's after a flu jab! Gradually over the next few weeks, hip's became stiffer, burning type pain at times down to the knees. Putting on lower half clothes and shoes became
Grandmaziggy
in
PMRGCAuk
5 months ago
Sacroiliac joint fusion
After many painful years I'm on the NHS list for sacroiliac joint fusion. Of course there is a 12 month waiting list. Has any one had this operation done privately? Struggling to find a private consultant in Yorkshire.
After many painful years I'm on the NHS list for sacroiliac joint fusion. Of course there is a 12 month waiting list. Has any one had this operation done privately? Struggling to find a private consultant in Yorkshire.
eeeee
in
Pelvic Pain Support Network
5 months ago
Blepharitis
hi I have rheumatoid arthritis, herpes simplex in my right eye and acute glaucoma caused by the treatment for my eye. I’ve now got blepharitis in both my eyes which has just started on Monday after my infusion for my arthritis. I went to the doctor and they said just use baby shampoo but my eyes are
hi I have rheumatoid arthritis, herpes simplex in my right eye and acute glaucoma caused by the treatment for my eye. I’ve now got blepharitis in both my eyes which has just started on Monday after my infusion for my arthritis. I went to the doctor and they said just use baby shampoo but my eyes are
Golden87
in
Glaucoma UK
5 months ago
GCA flares and eyesight
Thank you to everybody on this site – I have found it very helpful. I was diagnosed with GCA in September. I have to say my GP and Bath Hospital were excellent though it was a shock. My sight tested OK in the Eye Clinic. I started on 60 prednisolone reducing, and I am coping quite well, but I am paranoid
Thank you to everybody on this site – I have found it very helpful. I was diagnosed with GCA in September. I have to say my GP and Bath Hospital were excellent though it was a shock. My sight tested OK in the Eye Clinic. I started on 60 prednisolone reducing, and I am coping quite well, but I am paranoid
Gladys911
in
PMRGCAuk
5 months ago
Anyone opted for private Cataract surgery?
Hi, I have seronegative RA and am on Benepali. Have just had a routine eye test and been told I need cataract surgery. I thought I needed new glasses but it turns out it's cataracts! Anyway my optician has referred me on the NHS via my GP but I'm wondering about going private as I have no idea how long
Hi, I have seronegative RA and am on Benepali. Have just had a routine eye test and been told I need cataract surgery. I thought I needed new glasses but it turns out it's cataracts! Anyway my optician has referred me on the NHS via my GP but I'm wondering about going private as I have no idea how long
Chann
in
NRAS
5 months ago
Sjogrens - eye pain/migraine
I'm getting severe headaches that are around my eyes. I wake up with my head & eyes killing me. Is this just dry eyes? My light sensitivity is off the charts. Has anyone else expierenced this? Is this a Sjogren symptom?
I'm getting severe headaches that are around my eyes. I wake up with my head & eyes killing me. Is this just dry eyes? My light sensitivity is off the charts. Has anyone else expierenced this? Is this a Sjogren symptom?
Texgirl
in
NRAS
5 months ago
My Cancer and other health issues update.
After months of pretty bad news over my bladder cancer which is high grade and had spread to the inner linings of my bladder. I was told I could not have BCG anymore and that was gloomy news. I have an appointment tomorrow for a new three bladder cancer BCG Treatment. I was surprised I was having
After months of pretty bad news over my bladder cancer which is high grade and had spread to the inner linings of my bladder. I was told I could not have BCG anymore and that was gloomy news. I have an appointment tomorrow for a new three bladder cancer BCG Treatment. I was surprised I was having
Ern007
in
Lung Conditions Community Forum
5 months ago
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