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Pain management
Any tips on how to manage pain without resorting to painkillers please. I have painkillers but rarely use them and want to keep it that way. I have a very sore left arm which is far less painful when I mould it to my body and keep it inactive. Thank goodness I am right handed. Doc is looking into it.
Any tips on how to manage pain without resorting to painkillers please. I have painkillers but rarely use them and want to keep it that way. I have a very sore left arm which is far less painful when I mould it to my body and keep it inactive. Thank goodness I am right handed. Doc is looking into it.
Amanba
in
Anxiety and Depression Support
1 year ago
Concern about getting more Covid-19 vaccines.
I was diagnosed under 2 years ago. I guess I’ve had it since 2007. Just wondering about getting more Covid-19 vaccines. I have believed it is a good idea to get them. But every time I have I get some very odd things I’ve never experienced before. Rash. Sore in my eye. Eye infection. I cut my arm and
I was diagnosed under 2 years ago. I guess I’ve had it since 2007. Just wondering about getting more Covid-19 vaccines. I have believed it is a good idea to get them. But every time I have I get some very odd things I’ve never experienced before. Rash. Sore in my eye. Eye infection. I cut my arm and
Y5cc8j
in
CLL Support
1 year ago
Scared to death
Had my laser iridotomy today.Anxious all day.Had it done wasn't too bad.However my pressure spiked at 39. Started shaking. Doctor was fab.Gave me medication loads of drops Got to take tablets for 3 days and immflammatory drops for 7 days. Going to go back tomorrow to get pressuees checked.tablets run
Had my laser iridotomy today.Anxious all day.Had it done wasn't too bad.However my pressure spiked at 39. Started shaking. Doctor was fab.Gave me medication loads of drops Got to take tablets for 3 days and immflammatory drops for 7 days. Going to go back tomorrow to get pressuees checked.tablets run
Paula1710
in
Glaucoma UK
1 year ago
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Glycine
is glycine powder safe for Rls ? To use at night before bed? It helps me as well as magnesium glycinate but I am not using for rls. Anyone know?
is glycine powder safe for Rls ? To use at night before bed? It helps me as well as magnesium glycinate but I am not using for rls. Anyone know?
RCHD
in
Restless Legs Syndrome
1 year ago
Broken clavicle pain? Broke my clavicle after a epileptic seizure in 2011, but cold weather means dull pain! Must be others same situation?
I use my laptop a lot, a dull pain just does not go away, whilst writing, I have HPT so pain killers out of question! I suppose some sort of cream would be best, even magnesium oil joint spray like I use for my osteoarthritis on my knees might help? doubtful! Is anybody same situation as refracturing
I use my laptop a lot, a dull pain just does not go away, whilst writing, I have HPT so pain killers out of question! I suppose some sort of cream would be best, even magnesium oil joint spray like I use for my osteoarthritis on my knees might help? doubtful! Is anybody same situation as refracturing
Adlon57
in
Bone Health and Osteoporosis UK
1 year ago
Mixed up with recent diagnosis
Hi everyone. It has been so good to read all the different posts about Glaucoma and Glaucoma suspect and interocular eye pressure. I was with private consultant here in Ireland just three days ago who did visual field test and put in the dye etc. to exam my optic nerve. She said optic nerve seemed normal
Hi everyone. It has been so good to read all the different posts about Glaucoma and Glaucoma suspect and interocular eye pressure. I was with private consultant here in Ireland just three days ago who did visual field test and put in the dye etc. to exam my optic nerve. She said optic nerve seemed normal
Emerneurosis
in
Glaucoma UK
1 year ago
Eye side effects on biologics for rheumatoid arthritis
Has anyone else has very dry and sore eyes on biologics? Did it get better over time or did you have to stop/ switch to an alternative? I had this with adalimumab (Amgevita) so switched to etanercept (Benepali) but the same thing is happening again. I’m so keen to get better but my eyes are very sore
Has anyone else has very dry and sore eyes on biologics? Did it get better over time or did you have to stop/ switch to an alternative? I had this with adalimumab (Amgevita) so switched to etanercept (Benepali) but the same thing is happening again. I’m so keen to get better but my eyes are very sore
Cocobean1
in
NRAS
1 year ago
symptoms flare-up
The last 3 weeks or so I have notice some dormant b12 symptoms (nerve
pain
in hands, feet, and right arm. Weird
eye
blurriness) flaring. Have any of you had b12 symptoms reappear (despite continued regular injections. Weekly in my case) because of a new onset iron or cofactor deficiency?
The last 3 weeks or so I have notice some dormant b12 symptoms (nerve
pain
in hands, feet, and right arm. Weird
eye
blurriness) flaring. Have any of you had b12 symptoms reappear (despite continued regular injections. Weekly in my case) because of a new onset iron or cofactor deficiency?
MuppDog
in
Pernicious Anaemia Society
4 months ago
3 days after circimsision, shit be wildin.
So I'm 3 days in and I think for the most part everything is going ok. I was given pain killers but decided after the 1st day to stop taking them cause I felt like they weren't worth the side effects. A couple concerns I have is that I'm really horny for no reason, it's like if I get the slightest thought
So I'm 3 days in and I think for the most part everything is going ok. I was given pain killers but decided after the 1st day to stop taking them cause I felt like they weren't worth the side effects. A couple concerns I have is that I'm really horny for no reason, it's like if I get the slightest thought
CDG65
in
Men's Health Forum (Penis Health)
1 year ago
Free at last!
Well almost, transport should be here in 10 minutes. Can't wait to get home. Not one person in the whole hospital knows or wants to know about MSA with the exception of my consultant. The ward sister has flatly refused to let him know that I'm in on the basis that I just need nursing care and as
Well almost, transport should be here in 10 minutes. Can't wait to get home. Not one person in the whole hospital knows or wants to know about MSA with the exception of my consultant. The ward sister has flatly refused to let him know that I'm in on the basis that I just need nursing care and as
Polesden11
in
Multiple System Atrophy Trust
1 year ago
APs and Fatigue
Hi I have had APS since 2016, living in Norway and have “fatigue”. This is by far the most demanding problem with my APS. I read on the APS support UK page the following recommendation: “Take 200-400g hydroxychloroquine daily. This drug has long been used to treat fatigue and joint pain in autoimmune
Hi I have had APS since 2016, living in Norway and have “fatigue”. This is by far the most demanding problem with my APS. I read on the APS support UK page the following recommendation: “Take 200-400g hydroxychloroquine daily. This drug has long been used to treat fatigue and joint pain in autoimmune
Jonr
in
Hughes Syndrome APS Forum
1 year ago
Not diagnosed yet, suffering for many years
Hi everyone, My name is Kimberly, I live in Northwestern United States. I have been struggling with symptoms for years and had no idea this could be MS. I’ve had a hard time going up stairs as well as walking on flat ground for several months, maybe a year. My legs feel as though they weigh a hundred
Hi everyone, My name is Kimberly, I live in Northwestern United States. I have been struggling with symptoms for years and had no idea this could be MS. I’ve had a hard time going up stairs as well as walking on flat ground for several months, maybe a year. My legs feel as though they weigh a hundred
GrmaK
in
My MSAA Community
1 year ago
Itchy eyes
I know that glaucoma makes our eyes sensitive, and I do use lubricating eye drops SO many times during the day, but I still find that my eyes - especially inner eye, and around the base of the lids - gets really itchy. And of course we can't scratch our eyes. So does anybody else find this, and if so
I know that glaucoma makes our eyes sensitive, and I do use lubricating eye drops SO many times during the day, but I still find that my eyes - especially inner eye, and around the base of the lids - gets really itchy. And of course we can't scratch our eyes. So does anybody else find this, and if so
PBX142
in
Glaucoma UK
1 year ago
Hi fellow sufferers.
I am new here but have suffered from wet AMD since January 2021 and have had several injections of Eylea in both eyes since. I am currently stable and on an 8 week re-check each time. I also suffer from diplopia (double vision) and this eye problem conflicts with the AMD disease making it difficult
I am new here but have suffered from wet AMD since January 2021 and have had several injections of Eylea in both eyes since. I am currently stable and on an 8 week re-check each time. I also suffer from diplopia (double vision) and this eye problem conflicts with the AMD disease making it difficult
Mando007
in
Macular Society
1 year ago
Advice Needed
For years I’ve been suffering from pain in my bones, sleeplessness, depression and sometimes inability to do general things. I’ve seen my GP who has given me a variety of painkillers. I’ve had an appointment with a Consultant Rheumatologist which has been cancelled by the hospital several times, and
For years I’ve been suffering from pain in my bones, sleeplessness, depression and sometimes inability to do general things. I’ve seen my GP who has given me a variety of painkillers. I’ve had an appointment with a Consultant Rheumatologist which has been cancelled by the hospital several times, and
WelshWitchy
in
Fibromyalgia Action UK
1 year ago
Ocular hypertension
I have ocular hypertension and narrow angles. I have had a successful iridotomy but my pressures remain between 20-30 . Never higher and never lower. My glaucoma consultant whom I saw this week is happy. My eyes are stable. Good visual fields. No optic nerve damage. I use Tiopex and Latanopost drops
I have ocular hypertension and narrow angles. I have had a successful iridotomy but my pressures remain between 20-30 . Never higher and never lower. My glaucoma consultant whom I saw this week is happy. My eyes are stable. Good visual fields. No optic nerve damage. I use Tiopex and Latanopost drops
EthelPledge94
in
Macular Society
1 year ago
mtx and adalimumab/ Idacio
Hi please could anyone let me know if they have changed from mtx tablets to Idacio ? I was told that you still have to take mtx tablets but at a lower dose with Idacio ? I was told biologics can work within a couple of weeks ?? I don't know if I want to go down the biologics route yet, I am a bit
Hi please could anyone let me know if they have changed from mtx tablets to Idacio ? I was told that you still have to take mtx tablets but at a lower dose with Idacio ? I was told biologics can work within a couple of weeks ?? I don't know if I want to go down the biologics route yet, I am a bit
lindyloo2018
in
NRAS
1 year ago
putting down the burden
I have been practising albeit a bit as hoc putting things weighing me down into an imaginary bag and putting the heavy burden of that bag down. Knowing it’s still mine and I can retreive it should I want to at any time. I know this sounds simplistic but I simply couldn’t live with carrying it all around
I have been practising albeit a bit as hoc putting things weighing me down into an imaginary bag and putting the heavy burden of that bag down. Knowing it’s still mine and I can retreive it should I want to at any time. I know this sounds simplistic but I simply couldn’t live with carrying it all around
Lindyloo53
Volunteer
in
Heal My PTSD
1 year ago
Need to learn about my kidney disease diagnosis
Chronic Kidney Disease. I've just been diagnosed with Stage 3a. I know nothing and am starting from scratch. I would really like to see how others are dealing with this disease and get tips on diet, exercise and OTC medications which may be harming me, such as Tylenol and other painkillers and diet supplements
Chronic Kidney Disease. I've just been diagnosed with Stage 3a. I know nothing and am starting from scratch. I would really like to see how others are dealing with this disease and get tips on diet, exercise and OTC medications which may be harming me, such as Tylenol and other painkillers and diet supplements
Ladyprudence
in
Kidney Disease
1 year ago
Zolmitripan
Hello, I have just been told by my pharmacy that they can no longer get zolmitripan. They are the only pain killers that work for me. Has anyone else had problems getting it? Thanks
Hello, I have just been told by my pharmacy that they can no longer get zolmitripan. They are the only pain killers that work for me. Has anyone else had problems getting it? Thanks
Shenow
in
Migraine Support
1 year ago
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