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This looks interesting :) I know people with PTSD who have benefited from EMDR ...
... so hope it will be beneficial to p/w FND too :) https://doi.org/10.1136/bmjopen-2023-073727
... so hope it will be beneficial to p/w FND too :) https://doi.org/10.1136/bmjopen-2023-073727
210272
in
Functional Neurological Disorder - FND Hope
11 months ago
Kindly suggest me what it is!!
Hi everyone, i have a question which is more like a concern. This is my recent OCT scan on 06/03/2023, as I'm diagnosed macular edema. And taken avastin injection in my eye. The central thickness was 219 (green part) and it remain same 219 after the inj, but the other swelling was reduced. Now my concern
Hi everyone, i have a question which is more like a concern. This is my recent OCT scan on 06/03/2023, as I'm diagnosed macular edema. And taken avastin injection in my eye. The central thickness was 219 (green part) and it remain same 219 after the inj, but the other swelling was reduced. Now my concern
iAdnanShah
in
Macular Society
1 year ago
Ongoing Headaches/anxiety
Hey all, I have had Hippocampal Sclerosis since the age of 8 months and am now 41. I had surgery in 2017 to eradicate my seizures which were occurring on average 3 times a week. Since the operation, I have only had one due to being trialed off medication. Apart from escaping the ongoing seizures,
Hey all, I have had Hippocampal Sclerosis since the age of 8 months and am now 41. I had surgery in 2017 to eradicate my seizures which were occurring on average 3 times a week. Since the operation, I have only had one due to being trialed off medication. Apart from escaping the ongoing seizures,
sguthrie
in
Epilepsy Action
1 year ago
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I've OHS in 10 days - tips and must haves?
Hello everyone, So, after the very unexpected heart attack (clot passing through the hole in my heart) 3 weeks ago, all of a sudden I have the date for my OHS to close the ASD (and maybe repair the stretched valves too). It's planned for 14 April. 10 days' time. I feel woefully unprepared. I need to
Hello everyone, So, after the very unexpected heart attack (clot passing through the hole in my heart) 3 weeks ago, all of a sudden I have the date for my OHS to close the ASD (and maybe repair the stretched valves too). It's planned for 14 April. 10 days' time. I feel woefully unprepared. I need to
LadyZ13
in
British Heart Foundation
1 year ago
Painkillers and Buserelin
Hi ladies Maybe a silly question - am day 6 into Buserelin injections and have had a splitting headache for the last 2 days Can I take any painkillers? Am worried I'll effect how the drugs will work if I take extra meds. Thanks a lot xx
Hi ladies Maybe a silly question - am day 6 into Buserelin injections and have had a splitting headache for the last 2 days Can I take any painkillers? Am worried I'll effect how the drugs will work if I take extra meds. Thanks a lot xx
Katieloulou1983
in
Fertility Network UK
1 year ago
filled with sadness and frustration
Taking a medication called roaccutane 20years ago has ruined my life. It has damaged my brain and i’ve been living with these awful side effects all through my 20s and 30s. I’m utterly fed up with chronic head pains, scorched sensations, cognitive problems, brain numbness/deadness, ringing in my head
Taking a medication called roaccutane 20years ago has ruined my life. It has damaged my brain and i’ve been living with these awful side effects all through my 20s and 30s. I’m utterly fed up with chronic head pains, scorched sensations, cognitive problems, brain numbness/deadness, ringing in my head
Dann2
in
Headway
1 year ago
I’m scared of treatment
Venetoclax and Obinutuzumab My Haematologist has suggested that I may need to start treatment with these drugs and Calquence. I’ve been on Watch & Wait since diagnosed in 2014 when WBC count was just above normal range. Now it’s about six times higher than normal range and my red cell count has gone
Venetoclax and Obinutuzumab My Haematologist has suggested that I may need to start treatment with these drugs and Calquence. I’ve been on Watch & Wait since diagnosed in 2014 when WBC count was just above normal range. Now it’s about six times higher than normal range and my red cell count has gone
tigerbeauty
in
CLL Support
1 year ago
so confused with different doctors and their differing advice
My
eye
pain
is back. My weird tongue thing is back and I’m the heaviest I’ve ever been in my life. He did prescribe iron and I’ve had an infusion once a week for 4 weeks. And also he prescribed vitamin D. I just don’t know where to go or what to do next.
My
eye
pain
is back. My weird tongue thing is back and I’m the heaviest I’ve ever been in my life. He did prescribe iron and I’ve had an infusion once a week for 4 weeks. And also he prescribed vitamin D. I just don’t know where to go or what to do next.
Sppr
in
Thyroid UK
1 year ago
Peginterferon side effects!
Hi all, I have ET Jak2+ since 2021 and have been injecting 45mg Peginterferon weekly for 6 months and doing relatively ok until just recently. I now am experiencing severe aching arms and legs radiating down from my neck to my knees. It is so bad that I have to take pain killers daily. My blood pressure
Hi all, I have ET Jak2+ since 2021 and have been injecting 45mg Peginterferon weekly for 6 months and doing relatively ok until just recently. I now am experiencing severe aching arms and legs radiating down from my neck to my knees. It is so bad that I have to take pain killers daily. My blood pressure
Fairbank
in
MPN Voice
1 year ago
Fatty pad atrophy (ball of foot)
Hello, I am hoping there might be someone here who has experience of coping with fatty pad atrophy. I have recently been told by a podiatrist that this is the cause of the pain in the balls of my feet. I feel like I'm walking on my bones and have nerve pain due to the reduction in the fatty pad.
Hello, I am hoping there might be someone here who has experience of coping with fatty pad atrophy. I have recently been told by a podiatrist that this is the cause of the pain in the balls of my feet. I feel like I'm walking on my bones and have nerve pain due to the reduction in the fatty pad.
Dorunrun61
Graduate
in
Couch to 5K
1 year ago
Unusual bruise on eyelid
I woke up this morning to find I have a large bruise on my eyelid and my
eye
is a bit foggy no
pain
and no headache. I'm just curious to know if anyone here ever experienced anything similar. I will ring doctor and make appointment to have it checked.
I woke up this morning to find I have a large bruise on my eyelid and my
eye
is a bit foggy no
pain
and no headache. I'm just curious to know if anyone here ever experienced anything similar. I will ring doctor and make appointment to have it checked.
Chriss66
in
PMRGCAuk
10 months ago
cataract op for glaucoma
hi. Has anyone had a cataract operation to reduce eye pressure and did it work? I have not been able to use any eye drops for over a year as developed allergy to all. Laser only reduced pressure slightly. Was told optic nerve had deteriorated slightly over 5 years. As I am 75 I thought it would be ok
hi. Has anyone had a cataract operation to reduce eye pressure and did it work? I have not been able to use any eye drops for over a year as developed allergy to all. Laser only reduced pressure slightly. Was told optic nerve had deteriorated slightly over 5 years. As I am 75 I thought it would be ok
Islandhome
in
Glaucoma UK
1 year ago
Hashimotos double vision
Hello everyone. Just wondering if anyone else here has experienced double vision with Hashimoto's ? I have been feeling tired, heavy, low mood, brain fog, memory problems etc. I went to my optician for a routine check up 3 weeks ago and the letters on the chart were swimming around in a way I'd never
Hello everyone. Just wondering if anyone else here has experienced double vision with Hashimoto's ? I have been feeling tired, heavy, low mood, brain fog, memory problems etc. I went to my optician for a routine check up 3 weeks ago and the letters on the chart were swimming around in a way I'd never
Girtonian
in
Thyroid UK
1 year ago
PMR without steroids?
Hubby (55) was just diagnosed with PMR that we suspect he's had for about two years. He'd like to try and work through it without taking prednisone since every post we read is about people trying to get off of it. Do you think it's possible to manage the pain with other means and methods long enough
Hubby (55) was just diagnosed with PMR that we suspect he's had for about two years. He'd like to try and work through it without taking prednisone since every post we read is about people trying to get off of it. Do you think it's possible to manage the pain with other means and methods long enough
Hidden
in
PMRGCAuk
1 year ago
Off topic maybe.
Having a conversation about holidays with hubby this morning. With everything that's been going on with me it's been a no no since October. The sulfasalazine, 3rd med Ive tried, is killing my sleep. Im stopping it for a few days to see if sleep returns. I'm a walking zombie! Hubby, Garry, says he doesn't
Having a conversation about holidays with hubby this morning. With everything that's been going on with me it's been a no no since October. The sulfasalazine, 3rd med Ive tried, is killing my sleep. Im stopping it for a few days to see if sleep returns. I'm a walking zombie! Hubby, Garry, says he doesn't
Haz58
in
NRAS
1 year ago
Pegasys - to start or not
It has been now 3 years with ET diagnosis. Lot of reading about MPN’s behind me, especially through this network of wonderful people. I am now seriously considering starting Pegasys and reserved today an appointment with my specialist to discuss how we would go about it. In my country this line of
It has been now 3 years with ET diagnosis. Lot of reading about MPN’s behind me, especially through this network of wonderful people. I am now seriously considering starting Pegasys and reserved today an appointment with my specialist to discuss how we would go about it. In my country this line of
Bigcheat
in
MPN Voice
1 year ago
Alternating meds
I wonder if anyone else has experience with a RLS therapy method of alternating .375 mg Pramipexole and Methadone 20-30 mg every 10 days? I also use marijuana which helps maybe 40% for about an hour. My case is very severe with many previous pharmacologic failures including Alpha 2 Ligands, Buprenorphine
I wonder if anyone else has experience with a RLS therapy method of alternating .375 mg Pramipexole and Methadone 20-30 mg every 10 days? I also use marijuana which helps maybe 40% for about an hour. My case is very severe with many previous pharmacologic failures including Alpha 2 Ligands, Buprenorphine
WelbyB
in
Restless Legs Syndrome
1 year ago
lap yesterday!
5 years and yesterday finally got the answers for my pain. Endometriosis found. My surgeon also mentioned adhesions? And my appendix was fused to scar tissue. Just wondering if anyone else has had this? What a mix of emotions I’m feeling today. It wasn’t just a bad period, can painkillers keep the pain
5 years and yesterday finally got the answers for my pain. Endometriosis found. My surgeon also mentioned adhesions? And my appendix was fused to scar tissue. Just wondering if anyone else has had this? What a mix of emotions I’m feeling today. It wasn’t just a bad period, can painkillers keep the pain
JAJ27
in
Endometriosis UK
1 year ago
Painkillers and afib
What painkillers are best suited to us afiiibbers? I recently took paracetamol and it turned my heartbeat irregular and fast ...although I think it may of been the caffeine in them I have bad toothache and taking antibiotics but so far have gone without painkillers for fear of having a af attack Any
What painkillers are best suited to us afiiibbers? I recently took paracetamol and it turned my heartbeat irregular and fast ...although I think it may of been the caffeine in them I have bad toothache and taking antibiotics but so far have gone without painkillers for fear of having a af attack Any
Sunnyann
in
AF Association
1 year ago
Mild Sjogrens? Is that a thing?
Neither are dry to the point of
pain
but my husband has noticed I've developed an
eye
'tic'. I'm sort of rolling my eyes and opening my eyes wide; I've realised it because my eyes are dry and feel sticky.
Neither are dry to the point of
pain
but my husband has noticed I've developed an
eye
'tic'. I'm sort of rolling my eyes and opening my eyes wide; I've realised it because my eyes are dry and feel sticky.
Hidden
in
Thyroid UK
1 year ago
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