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Urgent Synarel - help!
Hi everyone I have just had my final scan today, before ER on Monday. I take my trigger shot tomorrow- and im sure the Dr said to me to take my last Synarel/nafarelin nasal spray as usual (I have been taking it twice each nostril, 9am and 9pm) However, the paper instructions she has written down state
Hi everyone I have just had my final scan today, before ER on Monday. I take my trigger shot tomorrow- and im sure the Dr said to me to take my last Synarel/nafarelin nasal spray as usual (I have been taking it twice each nostril, 9am and 9pm) However, the paper instructions she has written down state
MollyHar
in
Fertility Network UK
4 months ago
Unsure how to proceed after flare continues
I wrote awhile back about having a return of PMR symptoms after successfully (over a year and a half) tapering to 5mg and staying on that dose for two months. The weather had gotten a lot colder here in Seattle and I attributed the flare partly to that. I increased my dose to 10mg for a week and had
I wrote awhile back about having a return of PMR symptoms after successfully (over a year and a half) tapering to 5mg and staying on that dose for two months. The weather had gotten a lot colder here in Seattle and I attributed the flare partly to that. I increased my dose to 10mg for a week and had
Donna5658
in
PMRGCAuk
4 months ago
update on my health issues
Hi everyone, I can no longer work and had to give my job up due to my many disabilities that I have. I receive Personal Independence Payment and Employment and Support Allowance. Today I received a phone call to tell me that I can no longer get Employment and Support Allowance. I received nil points
Hi everyone, I can no longer work and had to give my job up due to my many disabilities that I have. I receive Personal Independence Payment and Employment and Support Allowance. Today I received a phone call to tell me that I can no longer get Employment and Support Allowance. I received nil points
Imagine1
in
Pain Concern
8 months ago
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help with results please
I’d be grateful if anyone could help with results please. I’m on combined therapy 50mg T4 and 35mg T3 TFT 0.02 (0.35-4.94) FT3 4.5 (2.4-6.00) FT4 8.1 (9.00-19.00) B12 433 (187-883) Vit D 126.1 >50 Thank you :)
I’d be grateful if anyone could help with results please. I’m on combined therapy 50mg T4 and 35mg T3 TFT 0.02 (0.35-4.94) FT3 4.5 (2.4-6.00) FT4 8.1 (9.00-19.00) B12 433 (187-883) Vit D 126.1 >50 Thank you :)
Bollieforme
in
Thyroid UK
4 months ago
Surgery follow-up appointment
Hi all I had my surgery on the 30th of March, where they found four bits of endo. I did have stomach pains in my first month, but then I had an infection. From the second month after my surgery, I had stomach pains again, although it was at a lower intensity and frequency. Over the last couple of
Hi all I had my surgery on the 30th of March, where they found four bits of endo. I did have stomach pains in my first month, but then I had an infection. From the second month after my surgery, I had stomach pains again, although it was at a lower intensity and frequency. Over the last couple of
Bookobssessed
in
Endometriosis UK
8 months ago
Diabetic and Eye Damage
I have been insulin dependant diabetic for 40 years, which has been the cause of my eye conditions. I was one of the first patients my consultant gave eye injection, I've had three steroid implants, lots of Lazer and eye injections. Last year I had a sever bleed at the back of the eye resulting in
I have been insulin dependant diabetic for 40 years, which has been the cause of my eye conditions. I was one of the first patients my consultant gave eye injection, I've had three steroid implants, lots of Lazer and eye injections. Last year I had a sever bleed at the back of the eye resulting in
123charl
in
Macular Society
4 months ago
Headaches!
Hi everyone.....I'm started my PMR journey middle of January so have only been on Prednisolone for 6 weeks... I started on 20mg and now on 10mg I did up dosage for 2 weeks so was taking 12mg because I felt poorly... But my question is I've had a headache almost constantly for weeks....is it the press
Hi everyone.....I'm started my PMR journey middle of January so have only been on Prednisolone for 6 weeks... I started on 20mg and now on 10mg I did up dosage for 2 weeks so was taking 12mg because I felt poorly... But my question is I've had a headache almost constantly for weeks....is it the press
Tescohednesford
in
PMRGCAuk
4 months ago
Endo Diagnosis
Hi, I am unsure where to start off trying to get a diagnosis of endometriosis. I've been struggling for about 4 years now and have found out my gran and my mum both have endometriosis with them experiencing the same symptoms. All my symptoms line up with others that have endometriosis as well. My first
Hi, I am unsure where to start off trying to get a diagnosis of endometriosis. I've been struggling for about 4 years now and have found out my gran and my mum both have endometriosis with them experiencing the same symptoms. All my symptoms line up with others that have endometriosis as well. My first
LivePink
in
Endometriosis UK
8 months ago
Tapering with a high ESR Reading?
My GP rang me yesterday because my ESR reading was 48 in a range of 1-30. He suggested I should increase the Pred. Because my cataract operation was cancelled for a fourth time yesterday, I dropped to 7 mg yesterday after being told, from 31 days on 7.5mg. I have read that ESR could denote
My GP rang me yesterday because my ESR reading was 48 in a range of 1-30. He suggested I should increase the Pred. Because my cataract operation was cancelled for a fourth time yesterday, I dropped to 7 mg yesterday after being told, from 31 days on 7.5mg. I have read that ESR could denote
Motida
in
PMRGCAuk
4 months ago
frustrated and anxious re appt
just feel this Is a safe space to have a rant was diagnosed beginning of October with NTG ( quite a lot of damage already , nerve damage, some peripheral vision loss ) Started on medication and was due to have a follow up appt after. 2 months ( so should have been December) However the hospital
just feel this Is a safe space to have a rant was diagnosed beginning of October with NTG ( quite a lot of damage already , nerve damage, some peripheral vision loss ) Started on medication and was due to have a follow up appt after. 2 months ( so should have been December) However the hospital
Crafty-gran
in
Glaucoma UK
4 months ago
Sore dry eyes
Good morning folks. I’ve been switched from Latanoprost to Monopost drops for both eyes. Bilateral NTG. I was getting a lot of headaches, eye pain and swelling around my right eye and a duty A&E ophthalmologist suggested I could be reacting to the preservatives in the Latanoprost drops. I’ve been on
Good morning folks. I’ve been switched from Latanoprost to Monopost drops for both eyes. Bilateral NTG. I was getting a lot of headaches, eye pain and swelling around my right eye and a duty A&E ophthalmologist suggested I could be reacting to the preservatives in the Latanoprost drops. I’ve been on
Maisie79
in
Glaucoma UK
4 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
11 months ago
Extremely high eye pressure while sleeping.
Hi, I have been diagnosed with glaucoma for about 12 years now and I also have uveitis since I was 2 years old. The last 4/5 years the main focus has been managing glaucoma as my uveitis is in remission. Recently I managed to get self monitoring eye pressure machine from Icare so I can keep track of
Hi, I have been diagnosed with glaucoma for about 12 years now and I also have uveitis since I was 2 years old. The last 4/5 years the main focus has been managing glaucoma as my uveitis is in remission. Recently I managed to get self monitoring eye pressure machine from Icare so I can keep track of
Biggs87
in
Glaucoma UK
4 months ago
sciatica and PD?
2 months ago after 2 10 hour train journeys I developed severe sciatic nerve pains down my right let and hip. these are making it very difficult/impossible to do my PD excercises. The GP only prescribes pain killers which don't really help. Web research seems to only suggest excercise stretching baby
2 months ago after 2 10 hour train journeys I developed severe sciatic nerve pains down my right let and hip. these are making it very difficult/impossible to do my PD excercises. The GP only prescribes pain killers which don't really help. Web research seems to only suggest excercise stretching baby
Nickcc
in
Cure Parkinson's
8 months ago
Eye issues related to hypothyroidism
Hi all, I was diagnosed with hypothyroidism in January of this year and started on 50mg levothyroxine. I’m having bloods every six weeks and working on my iron, vitamin D levels, folate and selenium. I’ll add my test results at the end for info. Overall I am feeling much better but I developed eye
Hi all, I was diagnosed with hypothyroidism in January of this year and started on 50mg levothyroxine. I’m having bloods every six weeks and working on my iron, vitamin D levels, folate and selenium. I’ll add my test results at the end for info. Overall I am feeling much better but I developed eye
Phoenix_24
in
Thyroid UK
4 months ago
Newsystem23
Not posted for a while, hope everyone is managing their lupus symptoms as best they can. I did think that using 50spf sun screen and taking hydroxychloroquine would keep my skin lupus at bay. However, I'm beginning to realise it is not just the sun and artificial light that my skin is sensitive to.
Not posted for a while, hope everyone is managing their lupus symptoms as best they can. I did think that using 50spf sun screen and taking hydroxychloroquine would keep my skin lupus at bay. However, I'm beginning to realise it is not just the sun and artificial light that my skin is sensitive to.
Newsystem23
in
LUPUS UK
4 months ago
Webinar:Do magnifying intraocular lenses work for people with macular disease?
Magnifying lenses, which are implanted are available to help those with macular disease see better. But, no trials have been done to prove how useful they are or who they are most suitable for. Dr Julie Silvestri from Royal Hospitals, Belfast, will be joining us for our first webinar of the month to
Magnifying lenses, which are implanted are available to help those with macular disease see better. But, no trials have been done to prove how useful they are or who they are most suitable for. Dr Julie Silvestri from Royal Hospitals, Belfast, will be joining us for our first webinar of the month to
Carol_MacularSociety
Partner
in
Macular Society
4 months ago
Glaucoma and macula degeneration
I've had glaucoma for nearly 30 yrs (I am 75) now diagnosed with macula degeneration in left eye . Anyone have the same ..what are the prospects ? Thank you..
I've had glaucoma for nearly 30 yrs (I am 75) now diagnosed with macula degeneration in left eye . Anyone have the same ..what are the prospects ? Thank you..
jesolo12
in
Glaucoma UK
4 months ago
Painful legs (burning sensation behind both knees)
Hi all Well, I’m hoping someone can provide a view on what is happening to me now! For the last couple of months I have had severe pain in the legs which has now started to become a burn behind my knees. It doesn’t improve or worsen on exercise and is particularly painful laying in bed. I used to
Hi all Well, I’m hoping someone can provide a view on what is happening to me now! For the last couple of months I have had severe pain in the legs which has now started to become a burn behind my knees. It doesn’t improve or worsen on exercise and is particularly painful laying in bed. I used to
Oldmasons
in
British Heart Foundation
8 months ago
Pegasys side effects
I was switched from 500 Hydroxyurea/day to 90mg Pegasys every two weeks. The pain in hips and thighs is substantial - headache also, but not as bothersome as the muscle pain. Has anyone else experience this on Pegasys. Also, has anyone tried CoQ10 for muscle pain and has it work? Thanks
I was switched from 500 Hydroxyurea/day to 90mg Pegasys every two weeks. The pain in hips and thighs is substantial - headache also, but not as bothersome as the muscle pain. Has anyone else experience this on Pegasys. Also, has anyone tried CoQ10 for muscle pain and has it work? Thanks
Dusty777
in
MPN Voice
4 months ago
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