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Pessary Moved
Very new to this having been diagnosed with vaginal and bladder prolapse last year. Following Bladder cancer I have suffered for years with UTI’s and have been ‘uncomfortable’ down below for several decades with recurring thrush and other infections and as allways asked , I have not been sexually active
Very new to this having been diagnosed with vaginal and bladder prolapse last year. Following Bladder cancer I have suffered for years with UTI’s and have been ‘uncomfortable’ down below for several decades with recurring thrush and other infections and as allways asked , I have not been sexually active
Nonameme
in
Pelvic Pain Support Network
5 months ago
Double vision episode
Just had one. First since November 2021. Then I was on high dose pred for GCA, coming down. Continued to taper quite successfully, eventually to zero in November 2022. But PMR followed, so went onto 15mg pred, tapering again quite successfully. Down to 5 mg since 6th February. Clearly no blood test
Just had one. First since November 2021. Then I was on high dose pred for GCA, coming down. Continued to taper quite successfully, eventually to zero in November 2022. But PMR followed, so went onto 15mg pred, tapering again quite successfully. Down to 5 mg since 6th February. Clearly no blood test
Lutra2
in
PMRGCAuk
5 months ago
A shunt or not?
has anyone had the experience of having a shunt put in their eye for glaucoma at the same time as a cataract operation? I’ve had one very successful cataract operation and I’m about to have the second. The consultant wants to put in a shunt as the pressure in that eye is 22, Have never had any
has anyone had the experience of having a shunt put in their eye for glaucoma at the same time as a cataract operation? I’ve had one very successful cataract operation and I’m about to have the second. The consultant wants to put in a shunt as the pressure in that eye is 22, Have never had any
Orlando23
in
Glaucoma UK
5 months ago
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Fibro and Sjogrens
Hi all, I've been diagnosed with fibro for 8 years, but for last few months I've felt so much worse, with new symptoms of really painful dry red eyes, extremely dry mouth, dry skin with rashes and dry cough, and increased pain and fatigue. My gp says it's sjogrens, an autoimmune disease, and referred
Hi all, I've been diagnosed with fibro for 8 years, but for last few months I've felt so much worse, with new symptoms of really painful dry red eyes, extremely dry mouth, dry skin with rashes and dry cough, and increased pain and fatigue. My gp says it's sjogrens, an autoimmune disease, and referred
Janpan7
in
Fibromyalgia Action UK
5 months ago
1.5 mgs now blood tests all over the place
So I am into my third year with pmr. I have been at 1.5 mg prednisone for 2 weeks and had my quarterly bloodwork done. Ana is now positive. It was negative last quarter. I am positive for Sjogrens but I don't have any symptoms. Is this because of my lower dosage? I am a little stiff and slow , but
So I am into my third year with pmr. I have been at 1.5 mg prednisone for 2 weeks and had my quarterly bloodwork done. Ana is now positive. It was negative last quarter. I am positive for Sjogrens but I don't have any symptoms. Is this because of my lower dosage? I am a little stiff and slow , but
paleolady
in
PMRGCAuk
5 months ago
cranberry powder?
Has anyone used cranberry powder rather than tablets for uti prevention? I’ve had the all clear for mum to take it but she will struggle with the big tabs so looking for a powder equivalent. I may also go down the D mannose route but as that can cause diarrhoea am holding off…….diarrhoea led to a nasty
Has anyone used cranberry powder rather than tablets for uti prevention? I’ve had the all clear for mum to take it but she will struggle with the big tabs so looking for a powder equivalent. I may also go down the D mannose route but as that can cause diarrhoea am holding off…….diarrhoea led to a nasty
RT18
in
PMRGCAuk
5 months ago
Vision in the recovery weeks ( and long term) after a trabeculectomy.
I have had narrow angle glaucoma for over 10 years and despite years of drops and a laser iridotomy in both eyes my glaucoma is slowly progressing. My sight loss in my left eye is not too bad at all ( patchy small areas) but I do feel my central vision is not as good in my left eye ( no cataract or other
I have had narrow angle glaucoma for over 10 years and despite years of drops and a laser iridotomy in both eyes my glaucoma is slowly progressing. My sight loss in my left eye is not too bad at all ( patchy small areas) but I do feel my central vision is not as good in my left eye ( no cataract or other
Cyclingalong
in
Glaucoma UK
5 months ago
ACR (Microalbumin/Creatinine Ratio)
My Urine’s ACR result is 8.4 mg/mmol. HbA1C is 8.5. I am very worried. Kindly advise or provide insights.
My Urine’s ACR result is 8.4 mg/mmol. HbA1C is 8.5. I am very worried. Kindly advise or provide insights.
Limeandlemon
in
Diabetes India
5 months ago
First MS Neuro Appointment!
Neuro confirmed in person that I have MS. I have RRMS. To get me out of the current flare, I started steroid infusions today, and will do 3 days of it. I am hopeful that it will really help. I'm looking forward to seeing what my 'new normal' is (more like impatiently waiting for this flare to be over
Neuro confirmed in person that I have MS. I have RRMS. To get me out of the current flare, I started steroid infusions today, and will do 3 days of it. I am hopeful that it will really help. I'm looking forward to seeing what my 'new normal' is (more like impatiently waiting for this flare to be over
MSFlea
in
My MSAA Community
5 months ago
Any practical tools to prevent computer vision syndrome?
Any practical tools to prevent computer vision syndrome (lower back and neck pain, eye dryness and strain)?
Any practical tools to prevent computer vision syndrome (lower back and neck pain, eye dryness and strain)?
bliinkai
in
Pain Concern
5 months ago
Dry-Needling and Low Level Laser Therapy By Physios: Does this really work and can it worsen tinnitus?
I triggered tinnitus and hyperacusis over 7 years ago now. Luckily it always went eventually but as of about 4 months ago it seems as if it is here to stay and a lot worse. An otologist told me that areas I said gave me pain could be consistent with TMJ issues and that he worked with a physio who could
I triggered tinnitus and hyperacusis over 7 years ago now. Luckily it always went eventually but as of about 4 months ago it seems as if it is here to stay and a lot worse. An otologist told me that areas I said gave me pain could be consistent with TMJ issues and that he worked with a physio who could
PuddingChipsAndGravy
in
Tinnitus UK
1 year ago
suspected epidural tumour
Hi all! Hope you are all doing well. My dad just got his scans back, and to go along with his rising PSA (over 260 now), the said they suspect he has an epidural tumour. Our MO typically glazes past his scan results as she doesn’t seem them significant, I want to make sure I am right to be worried here
Hi all! Hope you are all doing well. My dad just got his scans back, and to go along with his rising PSA (over 260 now), the said they suspect he has an epidural tumour. Our MO typically glazes past his scan results as she doesn’t seem them significant, I want to make sure I am right to be worried here
StayingSTRNG
in
Advanced Prostate Cancer
5 months ago
MRI/MRE
we’ll, I was stressing for nothing. The MRI was nothing. They use the 3T which is a little larger, not much, than the traditional MRI and did nit have the loud banging and clanging. It had a little noise but my country music drowned most of it out. Now the MRE is a little different story. Because I’
we’ll, I was stressing for nothing. The MRI was nothing. They use the 3T which is a little larger, not much, than the traditional MRI and did nit have the loud banging and clanging. It had a little noise but my country music drowned most of it out. Now the MRE is a little different story. Because I’
gwillistexas
in
PBC Foundation
1 year ago
From high hopes to not a lot of hope in one gruelling morning.
Hi everyone. What a day. Particularly what a morning. This is my third post. I was commenced on Mycophenolate by the Royal Hallamshire Consultant in early January. I attended for my second consultation this morning. Appointment was 10.20am. Arrived 9.30am. Car park full. Had to park half mile away and
Hi everyone. What a day. Particularly what a morning. This is my third post. I was commenced on Mycophenolate by the Royal Hallamshire Consultant in early January. I attended for my second consultation this morning. Appointment was 10.20am. Arrived 9.30am. Car park full. Had to park half mile away and
DaveLister
in
Lung Conditions Community Forum
5 months ago
Experiences with fast protein digestion
I am getting tired of not having any protein during the day or just fasting all day and I would like to be able to get "cheat days" once in a while. In this quest, I am convinced that there might be ways to digest food and in particular, protein faster 🧀🍕 Has anyone tried anything that you have found
I am getting tired of not having any protein during the day or just fasting all day and I would like to be able to get "cheat days" once in a while. In this quest, I am convinced that there might be ways to digest food and in particular, protein faster 🧀🍕 Has anyone tried anything that you have found
pdpatient
in
Cure Parkinson's
5 months ago
autoimmune hearing problems
I’ve posted this on SRUK forum too. Sorry this goes on a bit. Along with my UCTD with systemic sclerosis gut problems I’ve developed, I’ve had hearing problems for years. I’ve never really thought it could be another autoimmune problem but recently I couldn’t hear my own voice. I wear hearing aids and
I’ve posted this on SRUK forum too. Sorry this goes on a bit. Along with my UCTD with systemic sclerosis gut problems I’ve developed, I’ve had hearing problems for years. I’ve never really thought it could be another autoimmune problem but recently I couldn’t hear my own voice. I wear hearing aids and
Halfwayuphill
in
LUPUS UK
1 year ago
autoimmune ear problems?
Sorry this goes on a bit. Along with my UCTD with systemic sclerosis gut problems I’ve developed, I’ve had hearing problems for years. I’ve never really thought it could be another autoimmune problem but recently I couldn’t hear my own voice. I wear hearing aids and have just got new ones and thought
Sorry this goes on a bit. Along with my UCTD with systemic sclerosis gut problems I’ve developed, I’ve had hearing problems for years. I’ve never really thought it could be another autoimmune problem but recently I couldn’t hear my own voice. I wear hearing aids and have just got new ones and thought
Halfwayuphill
in
Scleroderma & Raynaud's UK (SRUK)
1 year ago
Possible lung metastasis
hi everyone I am 10 years just gone since the start of my journey, usual operation and chemo in 2014. then recurrence in the bowel in 2018 with resection and further chemo. I now have a single lung lesion noticed in March last year. Its now grown from 6mm in October to 9mm now. I have been told that
hi everyone I am 10 years just gone since the start of my journey, usual operation and chemo in 2014. then recurrence in the bowel in 2018 with resection and further chemo. I now have a single lung lesion noticed in March last year. Its now grown from 6mm in October to 9mm now. I have been told that
Bettyxxx
in
My Ovacome
5 months ago
Functional practitoner
In my search for answers, other than taking pills only for any manifestations of illness which occur (I have Sjogrens disease also), I am speaking with a functional practitioner tonight as they claim to find out causes of and then treat so it should be interesting. Doctors just give you more and more
In my search for answers, other than taking pills only for any manifestations of illness which occur (I have Sjogrens disease also), I am speaking with a functional practitioner tonight as they claim to find out causes of and then treat so it should be interesting. Doctors just give you more and more
Poshy
in
IBS Network
5 months ago
Please, help. Eustaquian tube obstruction instead of tinnitus?
I was almost surely diagnosed with tinnitus after seeing a couple of doctors but I'm experiencing things that make me positive I instead just have my Eustaquian tube closed either by wax or mucus from a large series of un-properly cured colds. 1. I've been having this mucus sensation in the back of
I was almost surely diagnosed with tinnitus after seeing a couple of doctors but I'm experiencing things that make me positive I instead just have my Eustaquian tube closed either by wax or mucus from a large series of un-properly cured colds. 1. I've been having this mucus sensation in the back of
Mirror665
in
Tinnitus UK
1 year ago
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