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Normal Pressure Glaucoma
I have suspected Normal Pressure Glaucoma and have been prescribed single use Monopost eye drops. I have been putting them in for about three weeks and since then I have been having mild headaches. The pressure in my left eye is 9 and in my right eye 10. Because I am a type 1 Diabetic I have an eye
I have suspected Normal Pressure Glaucoma and have been prescribed single use Monopost eye drops. I have been putting them in for about three weeks and since then I have been having mild headaches. The pressure in my left eye is 9 and in my right eye 10. Because I am a type 1 Diabetic I have an eye
AnnieJo41
in
Glaucoma UK
8 months ago
Theme Parks & Continuing Life
hi all, creeping up to 1 year since my TBI. I stayed in hosp for 4 days before being discharged but despite this my TBI was classed as ‘severe’. I am lucky in the sense of I seem to have recovered really well. I don’t have any symptoms anymore apart from the odd BPPV spell which I fix with the epley.
hi all, creeping up to 1 year since my TBI. I stayed in hosp for 4 days before being discharged but despite this my TBI was classed as ‘severe’. I am lucky in the sense of I seem to have recovered really well. I don’t have any symptoms anymore apart from the odd BPPV spell which I fix with the epley.
sunnygiraffe
in
Headway
8 months ago
Getting bombarded with ads for RA treatment Honey bee venom cream?.
Amazing too good to be true claims for this but there seems to be a few bits of research on it being anti inflammatory. Anyone tried it ? Still taking the meds....
Amazing too good to be true claims for this but there seems to be a few bits of research on it being anti inflammatory. Anyone tried it ? Still taking the meds....
welsh12
in
NRAS
4 months ago
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Dry skin
Does anyone feel that Hydroxyurea causes your skin to dry out and wrinkle faster?
Does anyone feel that Hydroxyurea causes your skin to dry out and wrinkle faster?
Winchie
in
MPN Voice
8 months ago
MGUS and PMR/GCA
If true, this is a little unsettling... MGUS can be a precursor to Multiple Myeloma. Quote from article: "A study of United States veterans suggested that subjects with autoimmune conditions where autoantibodies are detectable are at increased risk of developing MGUS [46]. Furthermore, a recent
If true, this is a little unsettling... MGUS can be a precursor to Multiple Myeloma. Quote from article: "A study of United States veterans suggested that subjects with autoimmune conditions where autoantibodies are detectable are at increased risk of developing MGUS [46]. Furthermore, a recent
kp60
in
PMRGCAuk
4 months ago
bladder stones
When my urologist did my biopsy he also removed bladder stones by breaking them in pieces and retrieving them thru my supra pubic catheter portal. Unfortunately all of them could not be be retrieved and they moved down my urethra to the point where the enlarged prostate pinched off urine flow. They
When my urologist did my biopsy he also removed bladder stones by breaking them in pieces and retrieving them thru my supra pubic catheter portal. Unfortunately all of them could not be be retrieved and they moved down my urethra to the point where the enlarged prostate pinched off urine flow. They
agnut
in
Fight Prostate Cancer
8 months ago
Enterosgel
Hi I’ve been suffering from haemorrhoids for a few months. It’s been getting better very gradually by eating a very high fibre diet to keep my stool very soft. But this has had the side effect of causing urgency several times a day. It’s making it very difficult to leave the house. I’ve had ibs for
Hi I’ve been suffering from haemorrhoids for a few months. It’s been getting better very gradually by eating a very high fibre diet to keep my stool very soft. But this has had the side effect of causing urgency several times a day. It’s making it very difficult to leave the house. I’ve had ibs for
MurphysSoulMate
in
IBS Network
4 months ago
Altered sensation after Dilator exercises
Hi all,I would really appreciate some support and guidance as I have a hypertonic pelvic floor muscle (for about 8-9 years). I have tried many approaches over the years but recently return to focus on physiotherapy and dilator stretches - on an intensive approach this time- completing a passive stretch
Hi all,I would really appreciate some support and guidance as I have a hypertonic pelvic floor muscle (for about 8-9 years). I have tried many approaches over the years but recently return to focus on physiotherapy and dilator stretches - on an intensive approach this time- completing a passive stretch
HopefulOphelia
in
Pelvic Pain Support Network
8 months ago
bladder/urinary tract endo
Hi all, has anyone got confirmed bladder endometriosis? I'm interested to hear about symptoms and whether you saw your gynaecologist or/and a urologist. Thanks!
Hi all, has anyone got confirmed bladder endometriosis? I'm interested to hear about symptoms and whether you saw your gynaecologist or/and a urologist. Thanks!
PopcornPJ
in
Endometriosis UK
4 months ago
Dry eyes
Hi helpful warriors I am on 35 mg of pred for next 2 weeks, then tapering to 30. Does pred cause dry eyes? ( did have cataract removal surgery in June of 2023.) Since diagnosis of GCA in late July 2023 I have had very dry eyes. I am on Thealoz Duo drops (3% Trehalose, 0.15 Sodium Hyaluronate).
Hi helpful warriors I am on 35 mg of pred for next 2 weeks, then tapering to 30. Does pred cause dry eyes? ( did have cataract removal surgery in June of 2023.) Since diagnosis of GCA in late July 2023 I have had very dry eyes. I am on Thealoz Duo drops (3% Trehalose, 0.15 Sodium Hyaluronate).
Groda
in
PMRGCAuk
8 months ago
Swollen Stomach IBS_C
Hi everyone. Ive had gut problems for years. Diarrhoea mostly. My stomach has been swollen for a few months now with difficulty having a normal BM. Its usually sludge like...sorry about the description. A colonoscopy 2 years ago showed dilated colon and the gastro Dr said I have IBS _C . He said
Hi everyone. Ive had gut problems for years. Diarrhoea mostly. My stomach has been swollen for a few months now with difficulty having a normal BM. Its usually sludge like...sorry about the description. A colonoscopy 2 years ago showed dilated colon and the gastro Dr said I have IBS _C . He said
granny34
in
IBS Network
5 months ago
Vertigo
Iv been taking betahistine for 6weeks,for vertigo,been ok till last tues,now i keep getting up with vertigo,its not going away,the tablets are suppose to stop it, before i only had it every so often ,i take the tablets you put on your gum to melt for attacks they help but give me me bit of a headache
Iv been taking betahistine for 6weeks,for vertigo,been ok till last tues,now i keep getting up with vertigo,its not going away,the tablets are suppose to stop it, before i only had it every so often ,i take the tablets you put on your gum to melt for attacks they help but give me me bit of a headache
Puggles2
in
AF Association
8 months ago
That was a busy week!
last week I did run Kent 5k I was meant to have done the 10k but due to my ongoing injury problem did the 5k instead! Since the dark nights have descended I have been struggling with my fear of falling and causing more damage to my shoulder! I broke my shoulder in January and it has been classified
last week I did run Kent 5k I was meant to have done the 10k but due to my ongoing injury problem did the 5k instead! Since the dark nights have descended I have been struggling with my fear of falling and causing more damage to my shoulder! I broke my shoulder in January and it has been classified
BGood
in
Couch to 5K
8 months ago
IBS meds not working....
Hello, I have been struggling with an IBS flare for 3 months, I'm taking Alverine and Peppermint capsules. My GP has checked for celiac disease which thankfully was normal, had my poo checked twice, bloods are fine except for inflammation markers slightly raised, checked my thyroid but it's fine as
Hello, I have been struggling with an IBS flare for 3 months, I'm taking Alverine and Peppermint capsules. My GP has checked for celiac disease which thankfully was normal, had my poo checked twice, bloods are fine except for inflammation markers slightly raised, checked my thyroid but it's fine as
Kooks
in
IBS Network
5 months ago
Tinnitus worse since Ear infection/ Burst Eardrum
Hi everyoneEarlier this week I got a bad ear infection and urgent care think I may have burst my eardrum too, I have a Cookie Bite Hearing Loss which has been causing me to have tinnitus since I was about 14 so for about 6 years now but I've found that my tinnitus is worse since I got the infection especially
Hi everyoneEarlier this week I got a bad ear infection and urgent care think I may have burst my eardrum too, I have a Cookie Bite Hearing Loss which has been causing me to have tinnitus since I was about 14 so for about 6 years now but I've found that my tinnitus is worse since I got the infection especially
Lilmix03
in
Tinnitus UK
8 months ago
imurel
hi I was started on imurel in November alongside 10mgs prednisol. with a view to getting me off steroids. The pains in my head have mostly gone and I am starting to feel better now. I did start on 60 mgs prednisol when first diagnosed with PMR 15 months ago reduced to 10 mgs but then diagnosed with
hi I was started on imurel in November alongside 10mgs prednisol. with a view to getting me off steroids. The pains in my head have mostly gone and I am starting to feel better now. I did start on 60 mgs prednisol when first diagnosed with PMR 15 months ago reduced to 10 mgs but then diagnosed with
NormaB
in
PMRGCAuk
4 months ago
Pulsatile tinnitus
Hi there. Does anyone else have pulsatile T. Mostly it comes and goes, always one-sided as the T is that side. I can make it go away by turning my head to the opposite side. But when i turn it back the T comes back. Shrugging my shoulders helps as well as stretching my neck. Have spoken to the doctor
Hi there. Does anyone else have pulsatile T. Mostly it comes and goes, always one-sided as the T is that side. I can make it go away by turning my head to the opposite side. But when i turn it back the T comes back. Shrugging my shoulders helps as well as stretching my neck. Have spoken to the doctor
penelope2
in
Tinnitus UK
6 months ago
No more spaghetti or jelly legs!
I recently posted a question just prior to my neurology visit about my gate being off and got some really good answers however after visiting my neurologist I was put on a medication called ampyra. You have to get it from a specialty pharmacy and my copay is 47$ a month but it is ms specific. It takes
I recently posted a question just prior to my neurology visit about my gate being off and got some really good answers however after visiting my neurologist I was put on a medication called ampyra. You have to get it from a specialty pharmacy and my copay is 47$ a month but it is ms specific. It takes
Mark1499
in
My MSAA Community
8 months ago
Anaesthetic ablation.
I’m in Oz. Had a successful (so far) catheter ablation last year. Twilight anaesthesia. Not GA. No problem and no after affects.
I’m in Oz. Had a successful (so far) catheter ablation last year. Twilight anaesthesia. Not GA. No problem and no after affects.
Blissygirl
in
AF Association
8 months ago
cateract surgery
Hello: I’m a little worried about having cateract surgery as I like most have tremor or dyskinesia. The doctor asked could I be still. Funny. Anyone experience this? Any thoughts? Thanks.
Hello: I’m a little worried about having cateract surgery as I like most have tremor or dyskinesia. The doctor asked could I be still. Funny. Anyone experience this? Any thoughts? Thanks.
Ep0522
in
Cure Parkinson's
8 months ago
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