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More advice please prior to GP consultation
Hi experts. I upped my pred dose to 20 mg 2 weeks ago believing I had PMR flare after dropping to 15 for 2 weeks. But with your knowledge and experience you suggested Piriformis syndrome - am still struggling with the PS pains but am fortunately having some sports therapy massage and stretching and exercising
Hi experts. I upped my pred dose to 20 mg 2 weeks ago believing I had PMR flare after dropping to 15 for 2 weeks. But with your knowledge and experience you suggested Piriformis syndrome - am still struggling with the PS pains but am fortunately having some sports therapy massage and stretching and exercising
Pocketdog
in
PMRGCAuk
3 years ago
Nebivolol timing and low blood pressure
I take 2.5mg Nebivolol and 200mg Flecainide daily, taking the Nebivolol in the mornings. I have low normal BP but recently have had readings in the 80/50 range which make me feel pretty bad. I drink water and keep my salt level up but every day down it goes about 2 hours after I take the Nebivolol
I take 2.5mg Nebivolol and 200mg Flecainide daily, taking the Nebivolol in the mornings. I have low normal BP but recently have had readings in the 80/50 range which make me feel pretty bad. I drink water and keep my salt level up but every day down it goes about 2 hours after I take the Nebivolol
Finvola
in
AF Association
3 years ago
A&E
Hi all, hope yr all ok, spent Easter in Monday and most of Tuesday in a&e with shooting pain in my temples and sore eye socket, had loads of different tests, lots of pain killers,60mg of pred as a precaution and turns out I was diagnosed with photosenry not sure I spelt that right, which is lights,brightness
Hi all, hope yr all ok, spent Easter in Monday and most of Tuesday in a&e with shooting pain in my temples and sore eye socket, had loads of different tests, lots of pain killers,60mg of pred as a precaution and turns out I was diagnosed with photosenry not sure I spelt that right, which is lights,brightness
Hidden
in
PMRGCAuk
3 years ago
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Dry mouth
Hi all , please can you help me , I have APS (diagnosed 3 years ago ) now I have a very dry mouth , I am pretty sure it's going to be Sjorgrens as I am very achey and tired too , waiting for a referral! I do know that these rotten Immune diseases seem to multiply with time , 7 years I'm told and that
Hi all , please can you help me , I have APS (diagnosed 3 years ago ) now I have a very dry mouth , I am pretty sure it's going to be Sjorgrens as I am very achey and tired too , waiting for a referral! I do know that these rotten Immune diseases seem to multiply with time , 7 years I'm told and that
Sevenstar
in
The Australian Sjögren's Syndrome Association
3 years ago
Glossopharyngeal neuralgia
Hell everyone, just wondering if any of you have experienced Glossopharyngeal neuralgia? I get severe pain left side of tongue, jaw ,base of tongue and throat sometimes radiating to my ear. It usually appears without warning, and is often associated with swallowing. I have limited systemic scleroderma
Hell everyone, just wondering if any of you have experienced Glossopharyngeal neuralgia? I get severe pain left side of tongue, jaw ,base of tongue and throat sometimes radiating to my ear. It usually appears without warning, and is often associated with swallowing. I have limited systemic scleroderma
UCTD
in
Scleroderma & Raynaud's UK (SRUK)
3 years ago
Trigger Warning: Living with suicidal ideation
Hi everyone....first off please let me say that I have no plans to hurt myself however I do feel that I live with the idea of it most days. I have ocd, ptsd, anxiety and depression due to an event that occurred 4 years ago. I have a wonderful therapist who I am doing emdr with, I take meds, etc.....
Hi everyone....first off please let me say that I have no plans to hurt myself however I do feel that I live with the idea of it most days. I have ocd, ptsd, anxiety and depression due to an event that occurred 4 years ago. I have a wonderful therapist who I am doing emdr with, I take meds, etc.....
Hidden
in
Anxiety and Depression Support
3 years ago
Should Progesterone injections be done at a specific time in FET?
Hi Ladies, Just a quick one, im having PIO injections for this transfer and have done it before bed so far. Last unsuccessful cycle I did them during day. Does this affect anything? My clinic haven't advised a specific time. Im a carer and its hard to do the shot at the same time daily if im busy with
Hi Ladies, Just a quick one, im having PIO injections for this transfer and have done it before bed so far. Last unsuccessful cycle I did them during day. Does this affect anything? My clinic haven't advised a specific time. Im a carer and its hard to do the shot at the same time daily if im busy with
Hidden
in
Fertility Network UK
3 years ago
CLL and Numb Chin Syndrome
Hi everyone. I am 40 year old male in the UK and was diagnosed with CLL in Feb 2019. I have been on w&w for the entire time. I have had no real symptoms with the exception of swolen glands and fatigue. Also my Spleen is swollen. Over the last few days I'e noticed that the righ side of chin feels numb
Hi everyone. I am 40 year old male in the UK and was diagnosed with CLL in Feb 2019. I have been on w&w for the entire time. I have had no real symptoms with the exception of swolen glands and fatigue. Also my Spleen is swollen. Over the last few days I'e noticed that the righ side of chin feels numb
Devans81
in
CLL Support
3 years ago
I feel like things just keep getting added to my plate
These past few weeks I’ve felt like I’ve been just stretched to the limit. I feel like stressful thing after stressful thing just keeps happening. Two weeks ago I had my last dentist appointment after months of repeated visits. I hadn’t been to a dentist in a year and that had consequences. But finally
These past few weeks I’ve felt like I’ve been just stretched to the limit. I feel like stressful thing after stressful thing just keeps happening. Two weeks ago I had my last dentist appointment after months of repeated visits. I hadn’t been to a dentist in a year and that had consequences. But finally
DemureRose
in
Anxiety Support
3 years ago
EMF MCS light sensitivity questions
Hey! I am wondering if anyone on here has EMF sensitivity and MCS and how you manage it and/ or any products that you have found that help symptoms (my main symptom is a bright red, hot, swelling face and then swelling all over the body). It is mainly when I use my phone or watch the tv for a long time
Hey! I am wondering if anyone on here has EMF sensitivity and MCS and how you manage it and/ or any products that you have found that help symptoms (my main symptom is a bright red, hot, swelling face and then swelling all over the body). It is mainly when I use my phone or watch the tv for a long time
Girlwithallergy
in
LUPUS UK
3 years ago
update on soreness after injections
I asked members here about washing out with saline after injections recently as I had started getting keratitis ( severe inflammation / inability to tolerate light/ pain) after last two lots of injections ( I have had 38 now) in both eyes. Studies were vague about whether washing iodine out after injection
I asked members here about washing out with saline after injections recently as I had started getting keratitis ( severe inflammation / inability to tolerate light/ pain) after last two lots of injections ( I have had 38 now) in both eyes. Studies were vague about whether washing iodine out after injection
rosyG
in
Macular Society
3 years ago
I walked!
I was determined to get on March 20th and walk. I made it about one block with my husbands help and it felt so good. Kinda late posting cause he had cataract surgery the following week and so many appointments and his daughter came from 500 miles away to drive us to hospital, and now I put in 3 drops
I was determined to get on March 20th and walk. I made it about one block with my husbands help and it felt so good. Kinda late posting cause he had cataract surgery the following week and so many appointments and his daughter came from 500 miles away to drive us to hospital, and now I put in 3 drops
agapepilgrim
in
My MSAA Community
3 years ago
Odd headache and feeling Strange to and detached
Hi all I've had anxiety for a little while and as I've got older I'm learning to understand the symptoms and deal with it a bit better but sometimes it can be very irritating I don't know if have anyone has ever experienced really weird headaches before or head pressures with feeling detached or numb
Hi all I've had anxiety for a little while and as I've got older I'm learning to understand the symptoms and deal with it a bit better but sometimes it can be very irritating I don't know if have anyone has ever experienced really weird headaches before or head pressures with feeling detached or numb
Thequeenbee30
in
Anxiety Support
3 years ago
Chronic closed narrow angle glucoma
I have been diagnosed with this a month ago. I have had a lot of laser treatments, tablets and eyedrops to bring the pressures down and keep them down. My left eye vision is all fogey now and can only see outlines of things, bit no details. Can anyone who has this tell me how they are finding it
I have been diagnosed with this a month ago. I have had a lot of laser treatments, tablets and eyedrops to bring the pressures down and keep them down. My left eye vision is all fogey now and can only see outlines of things, bit no details. Can anyone who has this tell me how they are finding it
Lynfreedom
in
Glaucoma UK
3 years ago
I want to hear from anybody who has had an Ahmed valve fitted
I have had Uveitis for over 5 years . In June 2020 I had an Ozurdex implant which worked very well. In December2020 I had a second Ozurdex implant and the pressure in my eye rose to a very high level and damaged the optic nerve. I now have Glaucoma and my vision is severely limited. My consultant spoke
I have had Uveitis for over 5 years . In June 2020 I had an Ozurdex implant which worked very well. In December2020 I had a second Ozurdex implant and the pressure in my eye rose to a very high level and damaged the optic nerve. I now have Glaucoma and my vision is severely limited. My consultant spoke
P0inteN0ire
in
Glaucoma UK
3 years ago
Retinal tear on left eye
Hi... I recently had two retinal tears to my eye and had emergency surgery. I was just wondering if anyone else had a similar experience and what was the outcome long term? Feeling a bit low and isolated 🥴
Hi... I recently had two retinal tears to my eye and had emergency surgery. I was just wondering if anyone else had a similar experience and what was the outcome long term? Feeling a bit low and isolated 🥴
Baggiebird67
in
IBS Network
3 years ago
Started on depixol 40mg depot inj fortnightly and now have severe RLS
Hi everyone I'm new here, hope everyone is doing OK. I have just been started on Depixol depot inj 40mg fortnightly. Previously I was on clopixol and previous to that was on depixol bylut don't remember the dose. While I was on clopixol I didn't have and RLS symptoms but the first time and now again
Hi everyone I'm new here, hope everyone is doing OK. I have just been started on Depixol depot inj 40mg fortnightly. Previously I was on clopixol and previous to that was on depixol bylut don't remember the dose. While I was on clopixol I didn't have and RLS symptoms but the first time and now again
Magpie2016
in
Restless Legs Syndrome
3 years ago
Not sure if I have IBS but need help.
Anyone on here know anything about eye problems and IBS. I suffer with episcleritis in my right eye which seems to come on when I eat gluten. When I eat gluten I get symptoms of IBS. I've been reading online some medics think eye problems are linked to IBS (amongst autoimmune disorders in general)
Anyone on here know anything about eye problems and IBS. I suffer with episcleritis in my right eye which seems to come on when I eat gluten. When I eat gluten I get symptoms of IBS. I've been reading online some medics think eye problems are linked to IBS (amongst autoimmune disorders in general)
Hidden
in
IBS Network
3 years ago
Registered blind
From looking at some posts, a, lot of you, quite rightly, are concerned you'll lose your vision. As you know I was born with glaucoma, but putting drops in every single day since at least 1983, my glaucoma, was stable enough to live a full life, driving etc. Over the years, from time to time, I've
From looking at some posts, a, lot of you, quite rightly, are concerned you'll lose your vision. As you know I was born with glaucoma, but putting drops in every single day since at least 1983, my glaucoma, was stable enough to live a full life, driving etc. Over the years, from time to time, I've
Jennymary
in
Glaucoma UK
3 years ago
Horizant Advice Please
I had my first dose last night and had a horrendous night, twitching and little sleep. How many days should I take it, before I give it up completely? I wouldn't say it was an allergic reaction, but just not the one I was hoping to get. The doctor told me to stop the Gabepentin cold turkey, which I did
I had my first dose last night and had a horrendous night, twitching and little sleep. How many days should I take it, before I give it up completely? I wouldn't say it was an allergic reaction, but just not the one I was hoping to get. The doctor told me to stop the Gabepentin cold turkey, which I did
Rwall
in
Restless Legs Syndrome
3 years ago
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