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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
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
7 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
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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
Flecainide & Constipation!
Hi, Ever since my Flecainide was increased to 150mg twice daily I have suffered with never-ending constipation causing very impacted and large hard to pass stools. Naturally I have tried all sorts of remedies (have always consumed prunes every day together with a high fibre oats/wheat-bran/toasted
Hi, Ever since my Flecainide was increased to 150mg twice daily I have suffered with never-ending constipation causing very impacted and large hard to pass stools. Naturally I have tried all sorts of remedies (have always consumed prunes every day together with a high fibre oats/wheat-bran/toasted
Fib36
in
AF Association
6 months ago
Effects of fenbendazole and vitamin E succinate on the growth and survival of prostate cancer cells
As I mentioned in a previous reply , here is an article on Fenben and VES.I added the VES (400mg} to my Fenben protocol few weeks age taken along with Tudca and Bovine Lactoferrin for my morning dosing. Mid afternoon it's Fenben/DMSO , Evening is Ivermectin / Tudca / Lactoferrin. Herbs etc in between
As I mentioned in a previous reply , here is an article on Fenben and VES.I added the VES (400mg} to my Fenben protocol few weeks age taken along with Tudca and Bovine Lactoferrin for my morning dosing. Mid afternoon it's Fenben/DMSO , Evening is Ivermectin / Tudca / Lactoferrin. Herbs etc in between
85745
in
Advanced Prostate Cancer
8 months ago
Its not getting better its beginning to drive me mad
Ive had this annoying noise in my ears for a few years now? Its really getting on my nerves now as it has got progressively louder, im 55 years old and cant explain how completly frustrated right now ? Knowing its getting louder as i get older .IT has an annoying habit of changing pitch from a high pitch
Ive had this annoying noise in my ears for a few years now? Its really getting on my nerves now as it has got progressively louder, im 55 years old and cant explain how completly frustrated right now ? Knowing its getting louder as i get older .IT has an annoying habit of changing pitch from a high pitch
Philbeard
in
Tinnitus UK
8 months ago
update
hi to those of you that follow me on here and those who don’t just wanted to do a quick update. So I saw Transplant consultant last month and he said I probably won’t live 5 years without a transplant. I went back yesterday as follow up as they are now seeing me monthly, and we’ll I was totally surprised
hi to those of you that follow me on here and those who don’t just wanted to do a quick update. So I saw Transplant consultant last month and he said I probably won’t live 5 years without a transplant. I went back yesterday as follow up as they are now seeing me monthly, and we’ll I was totally surprised
Harriet-sarah
in
British Liver Trust
8 months ago
Doctor wants me to start Hydrea
I am 44 years old. I was diagnosed with ET 3 years ago. My platelet count had been pretty steady at around 700, sometimes it would spike to mid 700s or up to as high as 800. My last visit was 846 and the Doctor began to panic a little bit. She wanted me to start Hydrea 500mg 3 times a week to get things
I am 44 years old. I was diagnosed with ET 3 years ago. My platelet count had been pretty steady at around 700, sometimes it would spike to mid 700s or up to as high as 800. My last visit was 846 and the Doctor began to panic a little bit. She wanted me to start Hydrea 500mg 3 times a week to get things
JT1622
in
MPN Voice
8 months ago
Endo supplements
Hi all, Just wondered if anyone take any supplements/vitamins or something that they find helps keep their periods regular. I was on the combined pill for 8 years and decided to come off it as I wanted my body back. When on the pill I was taking breaks to have my period, but now I've been off for
Hi all, Just wondered if anyone take any supplements/vitamins or something that they find helps keep their periods regular. I was on the combined pill for 8 years and decided to come off it as I wanted my body back. When on the pill I was taking breaks to have my period, but now I've been off for
Endo_hub
in
Endometriosis UK
8 months ago
Total knee replacement
19 days post op - been very tough especially when COVID thrown into the mix! My muscle tone wasn’t great pre-op but is now nonexistent. Is it possible to build muscle tone with PMR? Without PMR it’s possible to build good muscle tone with regular exercises but no matter how frequently I do my post op
19 days post op - been very tough especially when COVID thrown into the mix! My muscle tone wasn’t great pre-op but is now nonexistent. Is it possible to build muscle tone with PMR? Without PMR it’s possible to build good muscle tone with regular exercises but no matter how frequently I do my post op
Toffeeboyblue
in
PMRGCAuk
5 months ago
Foraminotomy
has anybody had a posterior endoscopic foraminotomy? In particular for bone spurs. I could be looking at this surgery once injections have been exhausted. Would be interested in hearing from people about how they found it, did it work, and crucially what was your post op experience like, pain levels,
has anybody had a posterior endoscopic foraminotomy? In particular for bone spurs. I could be looking at this surgery once injections have been exhausted. Would be interested in hearing from people about how they found it, did it work, and crucially what was your post op experience like, pain levels,
yorkshirelad1
in
Pain Concern
6 months ago
Labyrinthitis & tinnitus
Had mild tinnitus for a while which I could cope with, but since the onset of labyrinthitis back in March the tinnitus has got much worse, particularly recently..anyone had similar?..Currently in bed after another labyrinthitis 'episode'.
Had mild tinnitus for a while which I could cope with, but since the onset of labyrinthitis back in March the tinnitus has got much worse, particularly recently..anyone had similar?..Currently in bed after another labyrinthitis 'episode'.
Cityfan1
in
Tinnitus UK
8 months ago
Easy squeeze eye drops
Happy and healthy new year to you lovely people. I have recently had a hand op and my other hand is giving up the ghost. I have Sjögren’s syndrome as well as ra and have to put eye drops in regularly. I was wondering if any of you use eye drops that are easy to squeeze or if any of you use a bottle applicator
Happy and healthy new year to you lovely people. I have recently had a hand op and my other hand is giving up the ghost. I have Sjögren’s syndrome as well as ra and have to put eye drops in regularly. I was wondering if any of you use eye drops that are easy to squeeze or if any of you use a bottle applicator
debjw
in
NRAS
5 months ago
Lyrica can it just mask inflammation
Hi. I'm still waiting for the rhumatologist and for the moment my gp want my to try lyrica to remove the pain. Does it work for inflammatory pain? If i stop feeling the pain but the inflammation is still there can i rupture something by moving to much again? I have achille inflammation, pain in my rib
Hi. I'm still waiting for the rhumatologist and for the moment my gp want my to try lyrica to remove the pain. Does it work for inflammatory pain? If i stop feeling the pain but the inflammation is still there can i rupture something by moving to much again? I have achille inflammation, pain in my rib
Shadow35
in
NRAS
8 months ago
Buprenorphine
Does anyone have any idea on how much Buprenorphine I should take for RLS. . I Also, Ihave severe pain and have to go through surgery which involves putting a rod through 10 levels on my spine . Will Buprenorphine be sufficient or can another med be added?
Does anyone have any idea on how much Buprenorphine I should take for RLS. . I Also, Ihave severe pain and have to go through surgery which involves putting a rod through 10 levels on my spine . Will Buprenorphine be sufficient or can another med be added?
Josana13
in
Restless Legs Syndrome
1 year ago
Interstitial Cystitis with negative biopsy?
Hi everyone, I had a cystoscopy done during a surgery for endometriosis under general and the report says 'petichiae seen on double fill' and a question of Interstitial Cystitis. They took a biopsy and that shows 'a few scattered mast cells' but reports 'negative for significant inflammation'. One Urogynae
Hi everyone, I had a cystoscopy done during a surgery for endometriosis under general and the report says 'petichiae seen on double fill' and a question of Interstitial Cystitis. They took a biopsy and that shows 'a few scattered mast cells' but reports 'negative for significant inflammation'. One Urogynae
G3miniStar
in
Bladder Health UK
8 months ago
Muscle movements upwards
I'm.not sure I have FND. Muscles move involuntarily up.my back neck and head. Trying to balance. I've got tinnitus. Alll fter using olive oil in right ear in 2020 to soften wax. Not stopped ever. Issues with balance but never dizzy. More like there is a boat inside me! My brain can often be calculating
I'm.not sure I have FND. Muscles move involuntarily up.my back neck and head. Trying to balance. I've got tinnitus. Alll fter using olive oil in right ear in 2020 to soften wax. Not stopped ever. Issues with balance but never dizzy. More like there is a boat inside me! My brain can often be calculating
Chandalierglass
in
Functional Neurological Disorder - FND Hope
8 months ago
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