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Red eye and GCA
I have had a red eye for 3 days. No pain just uncomfortable and not affectiing sight. I have had GCA diagnosed since March (second time around) and now on 6 mg for the last month and staying on that for next month. Went to pharmacy who told me to ring 111 and see dr. After 1 hour on phone waiting for
I have had a red eye for 3 days. No pain just uncomfortable and not affectiing sight. I have had GCA diagnosed since March (second time around) and now on 6 mg for the last month and staying on that for next month. Went to pharmacy who told me to ring 111 and see dr. After 1 hour on phone waiting for
MaryHelen2
in
PMRGCAuk
2 years ago
Covid anyone?
For Christmas I received a positive Covid result. I am fully vaccinated and boosted. I had an inflamed spine from a long car ride. So i was on solumedrol 1000 mg once a month and PT(My DMT Copaxone). This was working for me. On December 20th another intravenous solumedrol. I became fatigued and had
For Christmas I received a positive Covid result. I am fully vaccinated and boosted. I had an inflamed spine from a long car ride. So i was on solumedrol 1000 mg once a month and PT(My DMT Copaxone). This was working for me. On December 20th another intravenous solumedrol. I became fatigued and had
TonyiaR7
in
My MSAA Community
2 years ago
Improvement seen after giving Vitamin B2 (Riboflavin)
Wanted to share this information with the board. I have been giving my mother Vitamin B2 (Riboflavin) for almost 2 months now and there is definitely improvement in her energy levels, balance and walking. She is getting 50mg dose once in hours, 3 times a day (for a total of 150mg/day). Giving it
Wanted to share this information with the board. I have been giving my mother Vitamin B2 (Riboflavin) for almost 2 months now and there is definitely improvement in her energy levels, balance and walking. She is getting 50mg dose once in hours, 3 times a day (for a total of 150mg/day). Giving it
John_morris71
in
Cure Parkinson's
2 years ago
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IBS-C & Sibo
I’ve got IBS-C and have recently been diagnosed with Sibo , I’ve had a 2 week course of antibiotics, Rifaximin, but they’ve done nothing , in fact I feel worse now , my stomach is in turmoil, so I’m assuming I still have it , but I haven’t been re tested yet , so I can’t be sure . I gather from my consultant
I’ve got IBS-C and have recently been diagnosed with Sibo , I’ve had a 2 week course of antibiotics, Rifaximin, but they’ve done nothing , in fact I feel worse now , my stomach is in turmoil, so I’m assuming I still have it , but I haven’t been re tested yet , so I can’t be sure . I gather from my consultant
Gardenlover2020
in
IBS Network
2 years ago
Down to 6mg but feeling it! Shall I persevere?
I went to Cape Verde on holiday at the start of December and was worried I may have a flare. I was on 7.5mg pred and I was great. Since then I’ve gone down to 6mg which I’ve now been on for about 8 days and am feeling weak. I have some pain in my upper arms but not unbearable like when diagnosed and
I went to Cape Verde on holiday at the start of December and was worried I may have a flare. I was on 7.5mg pred and I was great. Since then I’ve gone down to 6mg which I’ve now been on for about 8 days and am feeling weak. I have some pain in my upper arms but not unbearable like when diagnosed and
MiloCollie
in
PMRGCAuk
2 years ago
Treatment options
Hello all, I have some questions regarding treatment, just wondered if anyone can help. 1. Has anyone (in the UK) managed to get medication other than SSRI plus antipsychotic? Either NHS or private? If so, how? 2. Has anyone tried multiple SSRIs with little to no success, then tried another that does
Hello all, I have some questions regarding treatment, just wondered if anyone can help. 1. Has anyone (in the UK) managed to get medication other than SSRI plus antipsychotic? Either NHS or private? If so, how? 2. Has anyone tried multiple SSRIs with little to no success, then tried another that does
noname_squirrel
in
My OCD Community
2 years ago
Second ablation
I am also struggling with having a second ablation. While propafenone is stopping the AFIB, it is causing causing fatigue and weakness which is affecting my qol. I can not take anticoagulants so I have had Watchman device, pacemaker, and a first ablation. It was very successful for several years.
I am also struggling with having a second ablation. While propafenone is stopping the AFIB, it is causing causing fatigue and weakness which is affecting my qol. I can not take anticoagulants so I have had Watchman device, pacemaker, and a first ablation. It was very successful for several years.
N400033
in
AF Association
2 years ago
Thyroid and Breast implant illness
Hi all-Just went through this "explant" surgery two weeks ago. The surgeons assistant told me many many patients had huge improvements with hypothyroidism. Some said Hashimotos went away, and was proven on their labs. My endo has patients where she's seen this also. Anyone experience this ? Weird but
Hi all-Just went through this "explant" surgery two weeks ago. The surgeons assistant told me many many patients had huge improvements with hypothyroidism. Some said Hashimotos went away, and was proven on their labs. My endo has patients where she's seen this also. Anyone experience this ? Weird but
abartme
in
Thyroid UK
2 years ago
Does Glaucoma always spread to other eye?
I had suspected Glaucoma in c.2014 but after 2 years of regular hospital visits I was 'discharged' as they could not diagnose and the condition seemed stable. I have myopia (borderline for driving), congenital stationary night blindness (tested & diagnosed at Moorfields), plus something called congenital
I had suspected Glaucoma in c.2014 but after 2 years of regular hospital visits I was 'discharged' as they could not diagnose and the condition seemed stable. I have myopia (borderline for driving), congenital stationary night blindness (tested & diagnosed at Moorfields), plus something called congenital
t55ddy
in
Glaucoma UK
2 years ago
Will this interfere with my underactive thyroid?
Hi I wish to start taking a collagen supplement but it contains celadrin and bromelain. Does anybody know if these Ingredients could have any negative impact on my underactive thyroid? Any help much appreciated as quite often some supplements have things in them which can do more harm or undo the good
Hi I wish to start taking a collagen supplement but it contains celadrin and bromelain. Does anybody know if these Ingredients could have any negative impact on my underactive thyroid? Any help much appreciated as quite often some supplements have things in them which can do more harm or undo the good
TrishG67
in
Thyroid UK
2 years ago
Anyone had RAI or thyroidectomy for recurrent chronic thyroiditis?
Hello all and happy holidays. I don’t expect a reply as everyone will be busy but having had a 2 recent thyroid ultrasounds, the consultant radiologist said I had chronic thyroiditis which probably has been going on for quite a long time (don’t I know it- 2 months off work and still waiting for my body
Hello all and happy holidays. I don’t expect a reply as everyone will be busy but having had a 2 recent thyroid ultrasounds, the consultant radiologist said I had chronic thyroiditis which probably has been going on for quite a long time (don’t I know it- 2 months off work and still waiting for my body
Hidden
in
Thyroid UK
2 years ago
New lens in my glasses when they come. xx
Afternoon everyone and how are we all. I am here in my pjs now and resting, I have been and got my eyes tested now it has been four weeks since my cataract surgery. I am having a new lens in my right eye and they have ordered me a new lens for my regular glasses. Then it was a coffee and home as i
Afternoon everyone and how are we all. I am here in my pjs now and resting, I have been and got my eyes tested now it has been four weeks since my cataract surgery. I am having a new lens in my right eye and they have ordered me a new lens for my regular glasses. Then it was a coffee and home as i
sylvi
in
NRAS
3 years ago
JAK2 and TET2
Does anyone else here have this double mutation? After nearly three years of Pegasys my JAK2 has dropped from over 80% to c. 14% but my TET2 has only dropped from 55% to 40%. Got results of my recent BMB and no change in fibrosis, still ‘an increase in thin reticulin, especially in areas of focal clustering
Does anyone else here have this double mutation? After nearly three years of Pegasys my JAK2 has dropped from over 80% to c. 14% but my TET2 has only dropped from 55% to 40%. Got results of my recent BMB and no change in fibrosis, still ‘an increase in thin reticulin, especially in areas of focal clustering
Paul123456
in
MPN Voice
3 years ago
Abatacept swap from pens to syringes.
Has anyone been told their abatacept pen will be changed to an injection syringe? The rheumatology nurse rang today to inform me that due to a world shortage of abatacept pens the providers, forgotten the new name but they were Health care at Home, will be moving people into normal prefilled syringes
Has anyone been told their abatacept pen will be changed to an injection syringe? The rheumatology nurse rang today to inform me that due to a world shortage of abatacept pens the providers, forgotten the new name but they were Health care at Home, will be moving people into normal prefilled syringes
rounder
in
NRAS
3 years ago
Eye infection every 3-4 Weeks - PA link?
I am now having my 4th eye (both eyes) infection in 5 months. I have been using Chloramphenical 0.5% eye drops for 5 days (4 times a day) it gets rid of it but it recurs approx every 3-4 weeks. Contacted the Drs today who arranged for both eyes to be swapped this afternoon. Could this be linked to PA
I am now having my 4th eye (both eyes) infection in 5 months. I have been using Chloramphenical 0.5% eye drops for 5 days (4 times a day) it gets rid of it but it recurs approx every 3-4 weeks. Contacted the Drs today who arranged for both eyes to be swapped this afternoon. Could this be linked to PA
LJH50
in
Pernicious Anaemia Society
3 years ago
What are your opinions on the case of George Lopez from 2020?
Could the PD community benefit from such cases? I liked the fact that they used a new type of syringe. "“You can’t teleport cells into a brain,” Schweitzer said. You need a needle that delivers the cells to a precise spot and does so without squeezing them. Yet in some previous cell therapies, “more
Could the PD community benefit from such cases? I liked the fact that they used a new type of syringe. "“You can’t teleport cells into a brain,” Schweitzer said. You need a needle that delivers the cells to a precise spot and does so without squeezing them. Yet in some previous cell therapies, “more
Hidden
in
Cure Parkinson's
3 years ago
4th Transfer BFN 💔
Absolutely broken today after our 4th transfer result. It's also 4 months to the day from our surgery for our MMC in August (transfer #3) 😔 That bright white FRER stick is quite terrifying. I think the next step is to take a look at immunes. I assume I don't need an ERA as we did achieve implantation
Absolutely broken today after our 4th transfer result. It's also 4 months to the day from our surgery for our MMC in August (transfer #3) 😔 That bright white FRER stick is quite terrifying. I think the next step is to take a look at immunes. I assume I don't need an ERA as we did achieve implantation
Hoop123
in
Fertility Network UK
3 years ago
I’m back
Hi everyone, Sorry I’ve not been around for some time, I’ve been feeling very poorly just lately. I’ve now got a condition called uveitis, I’ve been feeling very ill, unable to eat much and generally unwell. Yesterday due to severe eye pain I went to emergency eye hospital and it turns out I’ve got uveitis
Hi everyone, Sorry I’ve not been around for some time, I’ve been feeling very poorly just lately. I’ve now got a condition called uveitis, I’ve been feeling very ill, unable to eat much and generally unwell. Yesterday due to severe eye pain I went to emergency eye hospital and it turns out I’ve got uveitis
2013mayo
in
PMRGCAuk
3 years ago
Sore eyes and light sensitivity
Hi there, So quick (ish) back story. I have Hashimotos, diagnosed late 2019. Treated with levo slowly increasing to 150mcg daily by March 2021 with various ups and downs in fatigue, dizziness and foot pain in between. Around this time i started experience photosensitivity and sore eyes (my eyes have
Hi there, So quick (ish) back story. I have Hashimotos, diagnosed late 2019. Treated with levo slowly increasing to 150mcg daily by March 2021 with various ups and downs in fatigue, dizziness and foot pain in between. Around this time i started experience photosensitivity and sore eyes (my eyes have
pandacat2
in
Thyroid UK
3 years ago
Pegasys and insomnia
I’m now on a maintenance dose of pegasys. Started pegasys in 2016. In the Early years within 30mins of injecting I felt very tired and experienced a good deep sleep on my injection nights. Over the last year - not every time - maybe 50% of the injections I have difficulty sleeping. I feel relaxed but
I’m now on a maintenance dose of pegasys. Started pegasys in 2016. In the Early years within 30mins of injecting I felt very tired and experienced a good deep sleep on my injection nights. Over the last year - not every time - maybe 50% of the injections I have difficulty sleeping. I feel relaxed but
EleanorPV
in
MPN Voice
3 years ago
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