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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
5 months ago
Indapamide
I have been on 10mg Amlodipine and 10mg Ramipril for some years now. My blood pressure has slight increased to 135/96. Due to the raised DBP, my doctors wants me to add Indapamide. Is anybody taking Indapamide? are there any side affects? Would be interested in hearging from anyone who is
I have been on 10mg Amlodipine and 10mg Ramipril for some years now. My blood pressure has slight increased to 135/96. Due to the raised DBP, my doctors wants me to add Indapamide. Is anybody taking Indapamide? are there any side affects? Would be interested in hearging from anyone who is
AnimalNatureLover
in
High Blood Pressure Support
5 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
5 months ago
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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
5 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
5 months ago
covid and metratrexate for RA
morning all!! I tested positive for covid on the 24th of February and was told by the Rheumatologist nurses and the consultant to stop the metratrexate and just take painkillers which that is what I’ve been doing!I'm having a massive flur up as I haven’t had any RA meds for over a month as before the
morning all!! I tested positive for covid on the 24th of February and was told by the Rheumatologist nurses and the consultant to stop the metratrexate and just take painkillers which that is what I’ve been doing!I'm having a massive flur up as I haven’t had any RA meds for over a month as before the
Mybirthday1975
in
NRAS
5 months ago
Warfarin and Prednisone/Prednisolone ?
Hello everyone, Just wondering if anyone has taken Perdnisone or Prednisolone with Warfarin ? Experienced any drug interactions ? Many thanks, Rosegardens
Hello everyone, Just wondering if anyone has taken Perdnisone or Prednisolone with Warfarin ? Experienced any drug interactions ? Many thanks, Rosegardens
rosegardens
in
Atrial Fibrillation Support
5 months ago
Has anyone taken Perdnisone or Prednisolone with Warfarin ?
Hello everyone, Just wondering if anyone has taken Perdnisone or Prednisolone with Warfarin ? Experienced any drug interactions ? Many thanks, Rosegardens
Hello everyone, Just wondering if anyone has taken Perdnisone or Prednisolone with Warfarin ? Experienced any drug interactions ? Many thanks, Rosegardens
rosegardens
in
Hughes Syndrome APS Forum
5 months ago
Has anyone taken Perdnisone or Prednisolone with Warfarin ?
Hello everyone, Just wondering if anyone has taken Perdnisone or Prednisolone with Warfarin ? Experienced any drug interactions ? Many thanks, Rosegardens
Hello everyone, Just wondering if anyone has taken Perdnisone or Prednisolone with Warfarin ? Experienced any drug interactions ? Many thanks, Rosegardens
rosegardens
in
Anticoagulation Support
5 months ago
Has anyone succeeded using bluetooth microphone to amplify patients voice so it can be heard on bluetooth hearing aids?
Hi, My wife (78) was diagnosed with PSP about 30 months ago and is in slow decline. Her voice is getting weaker and I am finding it difficult to hear what she says, much of it is mumbled. My hearing aids are bluetooth enabled, so I wondered if anyone had managed to amplify a patient's voice using
Hi, My wife (78) was diagnosed with PSP about 30 months ago and is in slow decline. Her voice is getting weaker and I am finding it difficult to hear what she says, much of it is mumbled. My hearing aids are bluetooth enabled, so I wondered if anyone had managed to amplify a patient's voice using
Legobuilder
in
PSP Association
5 months ago
Has anyone tried Piracetam for Parkinson's disease.
Hi, was diagnosed with Parkinson's August 2023. Taking one Levocarb CR 200/50 MG for tremor. Also using Coronet 4 light helmet therapy twice daily and symbyx 904 PD care laser on gut alternate days ,along with vibratory gloves alternate days with great results. Heard that Piracetam might help,wondering
Hi, was diagnosed with Parkinson's August 2023. Taking one Levocarb CR 200/50 MG for tremor. Also using Coronet 4 light helmet therapy twice daily and symbyx 904 PD care laser on gut alternate days ,along with vibratory gloves alternate days with great results. Heard that Piracetam might help,wondering
Logon206500
in
Cure Parkinson's
5 months ago
Dutasteride increases PSA Doubling Time after PSA Recurrence
These two Kaplan-Meier plots compare Dutasteride (0.5 mg/day) to Placebo in a randomized, double-blind trial from 2012 of 187 men who have progressed to
PSA Failure.
In the upper plot, Dutasteride increases the
Doubling Time
from, for example, 9 months to 18 months (factor of 2X). In
These two Kaplan-Meier plots compare Dutasteride (0.5 mg/day) to Placebo in a randomized, double-blind trial from 2012 of 187 men who have progressed to
PSA Failure.
In the upper plot, Dutasteride increases the
Doubling Time
from, for example, 9 months to 18 months (factor of 2X). In
janebob99
in
Advanced Prostate Cancer
5 months ago
Starting fresh - probiotics
Hello people. I recently became disillusioned with the supplements I was taking. It came about because I restarted berberine after a three month break. My normal brand, renew by science, have doubled their strength, and within a day or two I was finding I was ridiculously tired, like I'd run a marathon
Hello people. I recently became disillusioned with the supplements I was taking. It came about because I restarted berberine after a three month break. My normal brand, renew by science, have doubled their strength, and within a day or two I was finding I was ridiculously tired, like I'd run a marathon
Karmaone
in
Cure Parkinson's
5 months ago
Dragging a millstone up a mountain. RLS blind spot, patient’s apparently don’t know best.
Hello friends, it’s a while since my last post but was waiting until I had some good news to share with you all but as the title of the post indicates the opposite. I have a wonderful Consultant Dr Jose Thomas who specialises in sleep disorders and RLS, the downside is he is based in Wales uk and I
Hello friends, it’s a while since my last post but was waiting until I had some good news to share with you all but as the title of the post indicates the opposite. I have a wonderful Consultant Dr Jose Thomas who specialises in sleep disorders and RLS, the downside is he is based in Wales uk and I
HipHop1972
in
Restless Legs Syndrome
5 months ago
distortion on Amsler grid
Hi, I’m 44 years old and developed eye pain a couple of weeks ago, it was pretty intense and mostly in the outer corner of my left eye though a little in my right eye too. I thought I had an eye infection so booked an eye test with an OCT scan, my eye test was fine, OCT scan was fine too and my prescription
Hi, I’m 44 years old and developed eye pain a couple of weeks ago, it was pretty intense and mostly in the outer corner of my left eye though a little in my right eye too. I thought I had an eye infection so booked an eye test with an OCT scan, my eye test was fine, OCT scan was fine too and my prescription
Phoenix_24
in
Macular Society
5 months ago
Cushings and thyroid
So I've been having multiple tests for hormones and a dexamethasone 1mcg suppression test Wass done as my cortisol remained higher than 50 (the cut or is 50mnol and mine wasac 85. I was wondering if anyone has had cushing tests on here and if this lack of suppression can be caused by anything else. I
So I've been having multiple tests for hormones and a dexamethasone 1mcg suppression test Wass done as my cortisol remained higher than 50 (the cut or is 50mnol and mine wasac 85. I was wondering if anyone has had cushing tests on here and if this lack of suppression can be caused by anything else. I
jparsss
in
Thyroid UK
5 months ago
multaq
hi guys So the dr has taken me off propafenone after being on for a few years and doing well with episodes being around 9 months apart. Started me on multaq and now episodes every 3 weeks, actually in af now for second day. My INR is 2.3 so can I wait until 7 days before going for the dreaded cardioversion
hi guys So the dr has taken me off propafenone after being on for a few years and doing well with episodes being around 9 months apart. Started me on multaq and now episodes every 3 weeks, actually in af now for second day. My INR is 2.3 so can I wait until 7 days before going for the dreaded cardioversion
Henry716
in
Atrial Fibrillation Support
5 months ago
Pradaxa. Benefits and problems
Been on Pradaxa since 2016. Seems to do the job, but having started on 150mg found that bleeding from the anus was very unpleasant. The doctor reduced the dose to 110mg and that solved the problem. Taking the tablet gave me a lot of wind, but drinking plenty of water solved that. Pradaxa terrifies dentists
Been on Pradaxa since 2016. Seems to do the job, but having started on 150mg found that bleeding from the anus was very unpleasant. The doctor reduced the dose to 110mg and that solved the problem. Taking the tablet gave me a lot of wind, but drinking plenty of water solved that. Pradaxa terrifies dentists
Rsb417
in
Atrial Fibrillation Support
5 months ago
eylea injections
Hi everyone. I have the eyelea injections in both eyes, it is often painful for 3-4 days after and i always have bloodshot eyes. My question is, when should i return to work after these injections? I work in an acute mental health unit where there is risk of aggression and violence ?
Hi everyone. I have the eyelea injections in both eyes, it is often painful for 3-4 days after and i always have bloodshot eyes. My question is, when should i return to work after these injections? I work in an acute mental health unit where there is risk of aggression and violence ?
90rach
in
Macular Society
5 months ago
Anybody had Haematuria in urine and or bladder symptoms?
So I'm new here, awaiting the official report but TVs ultrasound done last week and I was told at the time he thinks I have endometriosis.Reason for scan was recent UTI like symptoms without any positive cultures, history of v heavy painful periods, acute lower back and abdo pain etc.. I am constantly
So I'm new here, awaiting the official report but TVs ultrasound done last week and I was told at the time he thinks I have endometriosis.Reason for scan was recent UTI like symptoms without any positive cultures, history of v heavy painful periods, acute lower back and abdo pain etc.. I am constantly
XLozX
in
Endometriosis UK
5 months ago
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