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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
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
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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
Pain patches gor RLS relief??
I'm still very satisfied with my Therapulse which really works for me..but is not a cure. Wondering if anyone has tried these pain patches that are advertised on FB eg Kailo?? They seem expensive and are just pain relieving patches that stick to your body, legs etc..but do they help?I may look on Amazon
I'm still very satisfied with my Therapulse which really works for me..but is not a cure. Wondering if anyone has tried these pain patches that are advertised on FB eg Kailo?? They seem expensive and are just pain relieving patches that stick to your body, legs etc..but do they help?I may look on Amazon
Allyp69
in
Restless Legs Syndrome
2 years 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
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
Severe Nerve Pain
Hello everyone. I’m new here does anyone have or had this issue. I’m suffering from so much Nerve pain I developed Tremors in my left hand then my right now my entire body shakes my head jerks I get bad headaches from pain and nausea. I’m active I work warehouse which is extremely physical which flares
Hello everyone. I’m new here does anyone have or had this issue. I’m suffering from so much Nerve pain I developed Tremors in my left hand then my right now my entire body shakes my head jerks I get bad headaches from pain and nausea. I’m active I work warehouse which is extremely physical which flares
MsDiva54
in
Pain Concern
2 years ago
Pegusus Interferon
Hello hello MPN friends l have not been on the site for awhile as l began new meds interferon ten weeks ago and at the time needed to sit quitley with what this means for me. Three weeks in l struggled with intense migraine and spent most of my time on pain killers with my duvet over my head. The
Hello hello MPN friends l have not been on the site for awhile as l began new meds interferon ten weeks ago and at the time needed to sit quitley with what this means for me. Three weeks in l struggled with intense migraine and spent most of my time on pain killers with my duvet over my head. The
Hidden
in
MPN Voice
2 years ago
Amlopidine
Hi all...a few weeks ago there was a thread on here about a possible connection between high eye pressure/eye conditions and Amlopidine blood pressure tablets I have since attended two appointments at Kings College Hospital ....glaucoma clinic (I'm a glaucoma suspect) and medical retina clinic (
Hi all...a few weeks ago there was a thread on here about a possible connection between high eye pressure/eye conditions and Amlopidine blood pressure tablets I have since attended two appointments at Kings College Hospital ....glaucoma clinic (I'm a glaucoma suspect) and medical retina clinic (
EthelPledge94
in
Glaucoma UK
1 year ago
EMDR !
Hey guys ! I had my second session today for EMDR therapy for some trauma healing and I feel like it’s not working at all . Should I have more patience with this ? Thanks
Hey guys ! I had my second session today for EMDR therapy for some trauma healing and I feel like it’s not working at all . Should I have more patience with this ? Thanks
Sushi2345
in
My OCD Community
1 year ago
Just diagnosed
HiI've just been diagnosed with Primary Angle closure.Opthamologist says no glaucoma.Im on pilocarpine drops.Eye pressure both eyes 25.Apparantley my eyes are small.Have dry eyes too Bit scared to be honest having anxiety I'm having laser peripheral iridotomy I was shaking today getting the tests nearly
HiI've just been diagnosed with Primary Angle closure.Opthamologist says no glaucoma.Im on pilocarpine drops.Eye pressure both eyes 25.Apparantley my eyes are small.Have dry eyes too Bit scared to be honest having anxiety I'm having laser peripheral iridotomy I was shaking today getting the tests nearly
Paula1710
in
Glaucoma UK
1 year ago
Just struggling to comprehend things and if I’m ok.. 21 man
So like I struggled with acid reflux a couple week back thinking it was a heart issue they gave me ECG and bloods and everything fine. So every settled down, but like last week I got this arm pain that went away. But on the 23rd I got like upper belly tightness and felt heavy. Then the 24th, I got like
So like I struggled with acid reflux a couple week back thinking it was a heart issue they gave me ECG and bloods and everything fine. So every settled down, but like last week I got this arm pain that went away. But on the 23rd I got like upper belly tightness and felt heavy. Then the 24th, I got like
Dshadzz07
in
British Heart Foundation
2 years ago
PMR? and lack of energy
Hi my husband has been very ill with PMR or some related rheumatoid ailment. Put on various doses of prednisone starting 15 reduced to nil then increased to 40 mg after hospital consultation. He is very weak no energy taking all thes tablets plus slow release painkiller and getting nowhere. It would
Hi my husband has been very ill with PMR or some related rheumatoid ailment. Put on various doses of prednisone starting 15 reduced to nil then increased to 40 mg after hospital consultation. He is very weak no energy taking all thes tablets plus slow release painkiller and getting nowhere. It would
Radley3941
in
PMRGCAuk
2 years ago
Happy hungry Christmas
I hope everyone has a lovely day. Unfortunately we had a power cut last night at 1am and another today at 12.45 just when most people had put their turkeys in. It came back 5 minutes ago. They obviously just reset a fuse during the night which didn't fix it. So no heating, lights, phones, TV or even
I hope everyone has a lovely day. Unfortunately we had a power cut last night at 1am and another today at 12.45 just when most people had put their turkeys in. It came back 5 minutes ago. They obviously just reset a fuse during the night which didn't fix it. So no heating, lights, phones, TV or even
Qualipop
in
British Heart Foundation
2 years ago
Seeing an MPN Specialist tomorrow!
I have an appointment at Stanford with an MPN Specialist tomorrow. Going on 5 years with ET+CALR and currently taking aspirin and 2 pills of Hydrea daily AND 90mcg of Pegasys once a week. We are in a transitional period right now and I will eventually just be taking Pegasys and aspirin. Took my 4th dose
I have an appointment at Stanford with an MPN Specialist tomorrow. Going on 5 years with ET+CALR and currently taking aspirin and 2 pills of Hydrea daily AND 90mcg of Pegasys once a week. We are in a transitional period right now and I will eventually just be taking Pegasys and aspirin. Took my 4th dose
Zeppelin11
in
MPN Voice
1 year ago
omeprazole use with ani inflammatory medication. Magnesium oil spray.
hi, sorry to hear about your struggles. I’ve been on omeprazole for many years to treat acid reflux. If you’re on any anti inflammatory drugs, these can cause stomach acid and that’s probably why you have been given them. For pain I use magnesium oil spray from Holland and Barrett I find it helps a
hi, sorry to hear about your struggles. I’ve been on omeprazole for many years to treat acid reflux. If you’re on any anti inflammatory drugs, these can cause stomach acid and that’s probably why you have been given them. For pain I use magnesium oil spray from Holland and Barrett I find it helps a
Primrose59
in
Fibromyalgia Action UK
2 years ago
EMDR therapy for depression?
https://my.clevelandclinic.org/health/treatments/22641-emdr-therapy Anyone experienced EMDR therapy? Would you give it a try? Thoughts?
https://my.clevelandclinic.org/health/treatments/22641-emdr-therapy Anyone experienced EMDR therapy? Would you give it a try? Thoughts?
Renizzle2023
in
Anxiety and Depression Support
1 year ago
Newly diagnosed
I still feel unsure as the information I have been given is quite sketchy. My initial fibroscan in July 2022 seemed to be quite disconcerting as had a liver stiffness of 41.9Kpa with CAP 400, which apparently is the most they could record, so was a little concerned. But nothing was really discussed
I still feel unsure as the information I have been given is quite sketchy. My initial fibroscan in July 2022 seemed to be quite disconcerting as had a liver stiffness of 41.9Kpa with CAP 400, which apparently is the most they could record, so was a little concerned. But nothing was really discussed
FAB1962
in
British Liver Trust
2 years ago
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