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starting Romosozumab soon
I am new to this forum and have just been reading the wealth of information about osteoporosis.. Thank god for what a wonderful group I can learn from. T12 fracture in Feb then 4 more lumbar fractures in March 30th 2024. My GP whom is just the best ever contacted an endocrinologist and he suggested
I am new to this forum and have just been reading the wealth of information about osteoporosis.. Thank god for what a wonderful group I can learn from. T12 fracture in Feb then 4 more lumbar fractures in March 30th 2024. My GP whom is just the best ever contacted an endocrinologist and he suggested
234me
in
Bone Health and Osteoporosis UK
3 months ago
Misoprostol medical miscarriage. Constant cramping.
I had Misoprostol medical induced miscarriage on Monday 8th. I had 4 hours of heavy bleeding and extreme cramps on the Monday. Then Tuesday, weds and Thurs I felt physically fine. Then Friday morning in the middle of the night I woke up with extreme cramps again. Not as bad as Monday. But bad enough
I had Misoprostol medical induced miscarriage on Monday 8th. I had 4 hours of heavy bleeding and extreme cramps on the Monday. Then Tuesday, weds and Thurs I felt physically fine. Then Friday morning in the middle of the night I woke up with extreme cramps again. Not as bad as Monday. But bad enough
Trex123
in
Fertility Network UK
3 months ago
Demodex Blepharitis treatments?
Hello, all. Glaucoma diagnosed late 2019. Initially drops tolerated ok think Latanoprost plus other.After a while developed bad red eyes, itching. Tried various drops since including preservative free, had both cataracts done. Tablets Azetazoloimide? Worked well, not able stay on them! Stopped taking
Hello, all. Glaucoma diagnosed late 2019. Initially drops tolerated ok think Latanoprost plus other.After a while developed bad red eyes, itching. Tried various drops since including preservative free, had both cataracts done. Tablets Azetazoloimide? Worked well, not able stay on them! Stopped taking
TVTech
in
Glaucoma UK
6 months ago
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What is classed as a flare?
Hi, I was diagnosed in November, had a steroid injection and started on MTX, once the steroid started wearing off the pain and swelling in my knees returned straight away but not in my hands, they have been great. Had a load of fluid sucked out of my knee and another steroid injection about 6 weeks ago
Hi, I was diagnosed in November, had a steroid injection and started on MTX, once the steroid started wearing off the pain and swelling in my knees returned straight away but not in my hands, they have been great. Had a load of fluid sucked out of my knee and another steroid injection about 6 weeks ago
Cat-E
in
NRAS
3 months ago
New results…
Hi everyone, just a bit of background info: These are my NHS test results from Nov 2023: t4 13.8 (7-17) tsh 0.10 (0.20 - 4.50) although the TSH came back slightly under range at that time, thankfully the GP said “no action” so I have carried on with 75mcg (have been having my usual brands - no
Hi everyone, just a bit of background info: These are my NHS test results from Nov 2023: t4 13.8 (7-17) tsh 0.10 (0.20 - 4.50) although the TSH came back slightly under range at that time, thankfully the GP said “no action” so I have carried on with 75mcg (have been having my usual brands - no
JoJoloveschocolate
in
Thyroid UK
3 months ago
Side effects?
Good Afternoon, I just wanted to ask if anyone else who has been on Dienogest or is on Dienogest has had bleeding in between their menstrual cycles as well? I know it’s in the patient information leaflet but I was slightly startled when I saw significant bleeding yesterday that was accompanied by agonising
Good Afternoon, I just wanted to ask if anyone else who has been on Dienogest or is on Dienogest has had bleeding in between their menstrual cycles as well? I know it’s in the patient information leaflet but I was slightly startled when I saw significant bleeding yesterday that was accompanied by agonising
Vee2508
in
Endometriosis UK
3 months ago
PV and AMD?
I've had PV since 2015 and have been on Jakafi for 18 months. I've recently been diagnosed with age-related macular degeneration and have been treated with intravitreous avastin. I've seen some papers suggesting that AMD is more common for people with MPNs. Has anyone else had this experience? Steve
I've had PV since 2015 and have been on Jakafi for 18 months. I've recently been diagnosed with age-related macular degeneration and have been treated with intravitreous avastin. I've seen some papers suggesting that AMD is more common for people with MPNs. Has anyone else had this experience? Steve
sbs_patient
in
MPN Voice
6 months ago
PIC - Punctate Inner Choroidopathy
Hi. I have just received a diagnosis for the above condition. I understand it’s extremely rare and would like to hear about other people’s experiences. I’m literally just on the journey and have had the first of 3 ‘rescue’ injections to prevent further sight loss. Would be good to connect with others
Hi. I have just received a diagnosis for the above condition. I understand it’s extremely rare and would like to hear about other people’s experiences. I’m literally just on the journey and have had the first of 3 ‘rescue’ injections to prevent further sight loss. Would be good to connect with others
Rome2023
in
Macular Society
6 months ago
small eyey
I don’t look like my eyes are normal size but the consultant says they are small, not deep and short ??? Says cataract op would be difficult when the time comes . Says further laser surgery not possible. has anyone else been told this ? I worries me for the future
I don’t look like my eyes are normal size but the consultant says they are small, not deep and short ??? Says cataract op would be difficult when the time comes . Says further laser surgery not possible. has anyone else been told this ? I worries me for the future
Sufitzy
in
Glaucoma UK
6 months ago
GP visit!
So I went to see my GP yesterday and discussed my symptoms, and asked about B12 injections. Got the same old story - test within range, symptoms aren’t bad enough, try oral B12 for three months, despite my explaining that I have low stomach acid and problems with malabsorption, which she again dismissed
So I went to see my GP yesterday and discussed my symptoms, and asked about B12 injections. Got the same old story - test within range, symptoms aren’t bad enough, try oral B12 for three months, despite my explaining that I have low stomach acid and problems with malabsorption, which she again dismissed
Chickens44
in
Pernicious Anaemia Society
3 months ago
Could BAT be our last chance?
My husband (on Lupron, castration resistant and tried every treatment) checked into the hospital 10 days ago for intense bone pain that requires heavy morphine. He has weakened bone marrow with low platelets and low red blood cells. He's getting palliative radiation for pain in a few places. Can't walk
My husband (on Lupron, castration resistant and tried every treatment) checked into the hospital 10 days ago for intense bone pain that requires heavy morphine. He has weakened bone marrow with low platelets and low red blood cells. He's getting palliative radiation for pain in a few places. Can't walk
Chris_Ali
in
Advanced Prostate Cancer
3 months ago
Leg pain.
My balance isn't very good. But the pain in my left leg is really bad. Keeps me awake at night, and hinders me during the day. Leg hurts all around at hip level, my knee seems to be swollen and the leg swells by the night. have had bone scan but still waiting for results. ( 4. To 5 months.now. ) Taking
My balance isn't very good. But the pain in my left leg is really bad. Keeps me awake at night, and hinders me during the day. Leg hurts all around at hip level, my knee seems to be swollen and the leg swells by the night. have had bone scan but still waiting for results. ( 4. To 5 months.now. ) Taking
mag123ben
in
MPN Voice
3 months ago
Moving the right way
Ralph was good this morning, not out of bed because he'd already had some work done, they changed the tracheotomy tube for a smaller one. Drs did their rounds and are going to tell SALT to not do the other tube through the nose and shock as they think in a few days it may not be necessary. His secretions
Ralph was good this morning, not out of bed because he'd already had some work done, they changed the tracheotomy tube for a smaller one. Drs did their rounds and are going to tell SALT to not do the other tube through the nose and shock as they think in a few days it may not be necessary. His secretions
Hidden
in
British Heart Foundation
3 months ago
Gabapentin and pain meds which one to go for?
I'm taking gabapentin 900 all day for periodic limb movement disorder however I have a very painful arthritic shoulder and torn rotator cuff. The Dr has tried me on codeine but it made me very ill. Does anyone know what pain medication can be taken with gabapentin (I've tried paracetamol, co-codamol,
I'm taking gabapentin 900 all day for periodic limb movement disorder however I have a very painful arthritic shoulder and torn rotator cuff. The Dr has tried me on codeine but it made me very ill. Does anyone know what pain medication can be taken with gabapentin (I've tried paracetamol, co-codamol,
Speedbuggy
in
Restless Legs Syndrome
3 months ago
Pegasys for MF transitioning from hydroxycarbamide
My darling wife, had her appointment today, and her blood is well below par her Hgb is 82 hematocrit 0.27, platelets 213 which is good, white cells 45. The hematologist was talking about introducing pegasys interferon injections, after her 3 bags of red cells and a ferinject. She is worried about losing
My darling wife, had her appointment today, and her blood is well below par her Hgb is 82 hematocrit 0.27, platelets 213 which is good, white cells 45. The hematologist was talking about introducing pegasys interferon injections, after her 3 bags of red cells and a ferinject. She is worried about losing
jointpain
in
MPN Voice
6 months ago
Hashi symptoms still or tired/dry eyes?
Hey everyone, Still on my journey to "optimal" health and lab's whilst having Hashimoto's. Diagnosed 18 month ago. I have a strange one for you, or, not so strange, right now I'm not sure. So, currently on 162.5mcg of Levo and 10 mcg of Lio. I would say symptom wise I am feeling the best I have in
Hey everyone, Still on my journey to "optimal" health and lab's whilst having Hashimoto's. Diagnosed 18 month ago. I have a strange one for you, or, not so strange, right now I'm not sure. So, currently on 162.5mcg of Levo and 10 mcg of Lio. I would say symptom wise I am feeling the best I have in
dexterholland91
in
Thyroid UK
6 months ago
Anti thyroglobulin Antibody High
I'd a mole removed from my right shoulder blade last November that was initially feared to be cancerous, but thankfully wasn't so. Since then I have an annoying pain in my right upper abdomen. Have had an endoscopy( am awaiting report but consultant didn't seem overly concerned) had a cystoscopy which
I'd a mole removed from my right shoulder blade last November that was initially feared to be cancerous, but thankfully wasn't so. Since then I have an annoying pain in my right upper abdomen. Have had an endoscopy( am awaiting report but consultant didn't seem overly concerned) had a cystoscopy which
TOTTY1
in
Thyroid UK
3 months ago
ablation
Hello, my husband suffers with AF and after 3 failed cardioversions last year, he had an ablation yesterday though the chest. He was in theatre for a few hours and he is still in absolute agony in his chest, shoulders and back and can not move. Hes in hospital and they’re giving him painkillers, but
Hello, my husband suffers with AF and after 3 failed cardioversions last year, he had an ablation yesterday though the chest. He was in theatre for a few hours and he is still in absolute agony in his chest, shoulders and back and can not move. Hes in hospital and they’re giving him painkillers, but
Bexmm
in
British Heart Foundation
3 months ago
Not sure what to do....
Advice, personal experiences, and comments most welcome.... Apologies for the long post, but it covers my story so far to provide context. So.... probably the same story as many of you here: I have probably had endo for a very very long time, frequent visits to doctors re bleeding and pain etc. to be
Advice, personal experiences, and comments most welcome.... Apologies for the long post, but it covers my story so far to provide context. So.... probably the same story as many of you here: I have probably had endo for a very very long time, frequent visits to doctors re bleeding and pain etc. to be
fed_up_of_endo
in
Endometriosis UK
3 months ago
Diagnosed with new non-invasive procedure: Relieved but I feel emotional
I have now been formally diagnosed- I scored 0.90008 out of 1 on my test which means I have a very high After many Gp visits, countless prescriptions of high painkillers, doctors saying it is period pain (no 💩) and my referral pushed for key hole …. I finally have an answer and closer to some physical
I have now been formally diagnosed- I scored 0.90008 out of 1 on my test which means I have a very high After many Gp visits, countless prescriptions of high painkillers, doctors saying it is period pain (no 💩) and my referral pushed for key hole …. I finally have an answer and closer to some physical
Butterfly0509
in
Endometriosis UK
3 months ago
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