Search
Search
About
Log in
Join
Experiences with
Eye pain
Posts
Communities
16,503 public posts
Filter results
No more spaghetti or jelly legs!
I recently posted a question just prior to my neurology visit about my gate being off and got some really good answers however after visiting my neurologist I was put on a medication called ampyra. You have to get it from a specialty pharmacy and my copay is 47$ a month but it is ms specific. It takes
I recently posted a question just prior to my neurology visit about my gate being off and got some really good answers however after visiting my neurologist I was put on a medication called ampyra. You have to get it from a specialty pharmacy and my copay is 47$ a month but it is ms specific. It takes
Mark1499
in
My MSAA Community
8 months ago
cateract surgery
Hello: I’m a little worried about having cateract surgery as I like most have tremor or dyskinesia. The doctor asked could I be still. Funny. Anyone experience this? Any thoughts? Thanks.
Hello: I’m a little worried about having cateract surgery as I like most have tremor or dyskinesia. The doctor asked could I be still. Funny. Anyone experience this? Any thoughts? Thanks.
Ep0522
in
Cure Parkinson's
8 months ago
I didn’t know if I’d be able to come back…..
Hello It’s been months since I posted to all the lovely supportive people here. I’m very sorry but I couldn’t face it as I had an injury, which a physio said meant that I might not be able to run again. I was devastated. But the amazing news is after nearly 4 months of not running I started very slowly
Hello It’s been months since I posted to all the lovely supportive people here. I’m very sorry but I couldn’t face it as I had an injury, which a physio said meant that I might not be able to run again. I was devastated. But the amazing news is after nearly 4 months of not running I started very slowly
LindySearle
Graduate10
in
Bridge to 10K
7 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Back and hips - is this a Flare??
Hi wonderful people, When I first had PMR and at each previous flare, the pain has been across my shoulders and down the backs of my legs. I am currently feeling it badly in my lower back and pelvic girdle and am not sure if it is a flare or summat else. I am somewhat stressed and know that this
Hi wonderful people, When I first had PMR and at each previous flare, the pain has been across my shoulders and down the backs of my legs. I am currently feeling it badly in my lower back and pelvic girdle and am not sure if it is a flare or summat else. I am somewhat stressed and know that this
MDT1
in
PMRGCAuk
7 months ago
Edinburgh Endo Clinic
Hello! Just wondering if anyone has been on a loooong waiting list to be seen by an Endo specialist for the first time since diagnosis? Currently, it's an 80-week waiting time in Edinburgh. I know there is an option to go privately but I am just totally shocked that someone has to suffer from pain etc
Hello! Just wondering if anyone has been on a loooong waiting list to be seen by an Endo specialist for the first time since diagnosis? Currently, it's an 80-week waiting time in Edinburgh. I know there is an option to go privately but I am just totally shocked that someone has to suffer from pain etc
Axolotl23
in
Endometriosis UK
7 months ago
Anticoagulant users
G'day, Just after some input from NOAC and Warfarin users. I use Warfarin and have done so for nearly 14 years. No sweat ! Never had bleed problems but have had an assortment of bruising problems in that time usually from DIY mishaps. All sorts of pretty colours of blues, greens, yellows and purples
G'day, Just after some input from NOAC and Warfarin users. I use Warfarin and have done so for nearly 14 years. No sweat ! Never had bleed problems but have had an assortment of bruising problems in that time usually from DIY mishaps. All sorts of pretty colours of blues, greens, yellows and purples
BenHall1
in
Atrial Fibrillation Support
7 months ago
Who has had cataract surgery with a bleb?
So as is the way with this condition, you cruise for a while then your eyes decide they do not wish to play ball! So basically I’ve been noticing a decrease in clarity with my right eye. The Glaucoma clinic doesn’t think I’m an urgent case so I’m waiting till November where I will see a nurse 😒.
So as is the way with this condition, you cruise for a while then your eyes decide they do not wish to play ball! So basically I’ve been noticing a decrease in clarity with my right eye. The Glaucoma clinic doesn’t think I’m an urgent case so I’m waiting till November where I will see a nurse 😒.
Vich81
in
Glaucoma UK
9 months ago
Laparoscopy found nothing - symptoms all point to endometriosis
I don’t suppose anyone has been in the same situation as me and can help? I have suffered from a range of issues from 15 with periods; bleeding and pain with intercourse, severe leg pain, always bleeding/spotting outside of periods, bad period pains, UTI like symptoms and odd bowel movements around
I don’t suppose anyone has been in the same situation as me and can help? I have suffered from a range of issues from 15 with periods; bleeding and pain with intercourse, severe leg pain, always bleeding/spotting outside of periods, bad period pains, UTI like symptoms and odd bowel movements around
puddl0503
in
Endometriosis UK
7 months ago
Endo on the bladder
Anyone else have the bladder and bowel endo? Willing to try anything, for any kind of relief. I have endo on and going into my bladder and now also effecting my bowel. It's triggered normally about day 3 of my period and last for a good 3 weeks. The first few days I just have to be near a toilet, when
Anyone else have the bladder and bowel endo? Willing to try anything, for any kind of relief. I have endo on and going into my bladder and now also effecting my bowel. It's triggered normally about day 3 of my period and last for a good 3 weeks. The first few days I just have to be near a toilet, when
Country-Girl100
in
Endometriosis UK
7 months ago
arthritis
having cervicogenic headaches from arthritis in neck. Any painkillers better than paracetamol that we can safely take? Thanks again.
having cervicogenic headaches from arthritis in neck. Any painkillers better than paracetamol that we can safely take? Thanks again.
Lindaj754
in
AF Association
7 months ago
How to deal with side effect of hot flashes and feeling hot all the time from pain meds?
How do you deal with the side effect of hot flashes and feeling hot all the time that is being caused from your pain medicine or antidepressants used for pain? I take Tramadol at the highest dosage everyday for my severe nerve pain from CRPS because it's the only thing that works for me. However it makes
How do you deal with the side effect of hot flashes and feeling hot all the time that is being caused from your pain medicine or antidepressants used for pain? I take Tramadol at the highest dosage everyday for my severe nerve pain from CRPS because it's the only thing that works for me. However it makes
Hidden
in
Neuro Support
7 months ago
How to deal with side effects of feeling hot from pain meds and antidepressants for pain?
How do you deal with the side effect of feeling hot all the time and having hot flashes that are caused from your pain medicine or your antidepressant used for pain? I take Tramadol at the highest dosage for my severe nerve pain from CRPS because it's the only thing that works for me however I find that
How do you deal with the side effect of feeling hot all the time and having hot flashes that are caused from your pain medicine or your antidepressant used for pain? I take Tramadol at the highest dosage for my severe nerve pain from CRPS because it's the only thing that works for me however I find that
Hidden
in
Neuropathy Support
7 months ago
Eugenol
I just happened to come across some information relating to cirrhosis. It is called eugenol and it comes from cloves. The NIH as recently as 2021 has done studies and as far as I can tell it is helping the liver to heal. I am not a scientist so the big scientific words are beyond me so I am not sure
I just happened to come across some information relating to cirrhosis. It is called eugenol and it comes from cloves. The NIH as recently as 2021 has done studies and as far as I can tell it is helping the liver to heal. I am not a scientist so the big scientific words are beyond me so I am not sure
leanne5000
in
British Liver Trust
10 months ago
RSV and Flare
hi everyone, I seem to be in the wars a bit at the moment and need some advice: - diagnosed PMR and RA April 23 - dosage of 30mg pred and 20 mg methotrexate - gradually reduced pred to 10.5 as per Rhumetologist instructions - had a flare in calf muscles, increased pred to 12.5 - travelled to NYC
hi everyone, I seem to be in the wars a bit at the moment and need some advice: - diagnosed PMR and RA April 23 - dosage of 30mg pred and 20 mg methotrexate - gradually reduced pred to 10.5 as per Rhumetologist instructions - had a flare in calf muscles, increased pred to 12.5 - travelled to NYC
MegfromOz
in
PMRGCAuk
7 months ago
compressed vertebrae, i asked dr about stronger pain medication and they said no -- i wonder why?
Mum's got probably vertebral pain, is on an otc pain tablet, plus a step up from that, the prescription version. a dr friend of mine said she should be on something stronger like oxycodone. i asked specialist if Mum could have a stronger pain medication, and was told no. why's that? maybe cause elderly
Mum's got probably vertebral pain, is on an otc pain tablet, plus a step up from that, the prescription version. a dr friend of mine said she should be on something stronger like oxycodone. i asked specialist if Mum could have a stronger pain medication, and was told no. why's that? maybe cause elderly
MayGodBlessYou
in
Bone Health and Osteoporosis UK
7 months ago
Being taking off Pegasys. :( Looking for alternatives
Hi all, I have ET & PV with Jak2. I am 40. I have been on aspirin for over 10 years, but had to start Pegasys 3 months ago. I haven't tolerated it well. Severe shortness of breath etc. My hematologist reduced my dose to 30 per week, but I am suffering with hypertension (150 to 69/96 on average) and
Hi all, I have ET & PV with Jak2. I am 40. I have been on aspirin for over 10 years, but had to start Pegasys 3 months ago. I haven't tolerated it well. Severe shortness of breath etc. My hematologist reduced my dose to 30 per week, but I am suffering with hypertension (150 to 69/96 on average) and
JustKeepSw1mming
in
MPN Voice
9 months ago
Adenomyosis/Endometriosis Pain Management
Hi All, Just looking for a bit of advice. I was diagnosed with Adenomyosis and Fibroids at 38. Its only been a year and a half but Im struggling hugely. I am very depressed and cant motivate myself day to day. I have constant pain in my lower abdomen, tailbone and Left bum. My pain has progressed
Hi All, Just looking for a bit of advice. I was diagnosed with Adenomyosis and Fibroids at 38. Its only been a year and a half but Im struggling hugely. I am very depressed and cant motivate myself day to day. I have constant pain in my lower abdomen, tailbone and Left bum. My pain has progressed
ABFr23
in
Endometriosis UK
7 months ago
a little drama
I have just reduced to 5mg. And like many others my energy is crashing. So a bit of a roller coaster and trying to plan things so that I don’t have too much excitement all at once! Wednesday my husband was diagnosed with detached retina, yesterday was an hour and a half trip to eye hospital for his
I have just reduced to 5mg. And like many others my energy is crashing. So a bit of a roller coaster and trying to plan things so that I don’t have too much excitement all at once! Wednesday my husband was diagnosed with detached retina, yesterday was an hour and a half trip to eye hospital for his
Alazarin
in
PMRGCAuk
9 months ago
Pain in one Eye.
For some months I've had a spot
pain
in one
eye
. When I rub my eye I can feel like a bruise would if pressed lightly. I have drops for dry eyes but using those does not make any difference. I have had a lens replacement in both eyes but there is not vision change.
For some months I've had a spot
pain
in one
eye
. When I rub my eye I can feel like a bruise would if pressed lightly. I have drops for dry eyes but using those does not make any difference. I have had a lens replacement in both eyes but there is not vision change.
omits
in
Men's Health Forum
3 months ago
Airing Pain 140: Out now!
[i]
Airing Pain
[/i] edition 140: Childhood Pain - Adverse Experiences and Parental Relationships is now available to listen to here: https://painconcern.org.uk/airing-pain-140-childhood-experiences/ Full transcript is available online and to download, as well as a captioned video on YouTube.
[i]
Airing Pain
[/i] edition 140: Childhood Pain - Adverse Experiences and Parental Relationships is now available to listen to here: https://painconcern.org.uk/airing-pain-140-childhood-experiences/ Full transcript is available online and to download, as well as a captioned video on YouTube.
PainConcernHelpline
Pain Concern
in
Pain Concern
7 months ago
1
...
31
32
33
...
100
Next page
10
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Endometriosis UK
2479 results
NRAS
1175 results
Fibromyalgia Action UK
1161 results
View top 10 communities
Sort by
Most Relevant
Newest