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Hyperacusis, as I see it.
The post below I wrote on another forum and have posted it here as it might be of some help to anyone that has hyperacusis. It is just my personal opinion and not professional medical advice. Michael Leigh Hyperacusis, As I See It. Some members have asked for my opinion on hyperacusis as they
The post below I wrote on another forum and have posted it here as it might be of some help to anyone that has hyperacusis. It is just my personal opinion and not professional medical advice. Michael Leigh Hyperacusis, As I See It. Some members have asked for my opinion on hyperacusis as they
Hidden
in
British Tinnitus Association
7 years ago
Amantadine anti viral used in parkinsonĀ“s
I visited my neurologist yesterday and although I think I am doing great, she prescribed 100mg once a day of amantadine (hope that is the name in english). As anyone been prescribed this? does anyone know how it is supposed to help. I have researched but the contraindications seem to be what I do
I visited my neurologist yesterday and although I think I am doing great, she prescribed 100mg once a day of amantadine (hope that is the name in english). As anyone been prescribed this? does anyone know how it is supposed to help. I have researched but the contraindications seem to be what I do
isabelalfaiate
in
Ataxia UK
7 years ago
Head Rushes š¢
I see my endo on Friday and I know she's going to up my dose to 150mg of Levo. For the last couple of days I've been having like head rushes. Is this connected? I have a constant mega headache as well. I'm soooo tired. I'm sooo angry. I'm being mean and I can't help it. I literally can't be bothered
I see my endo on Friday and I know she's going to up my dose to 150mg of Levo. For the last couple of days I've been having like head rushes. Is this connected? I have a constant mega headache as well. I'm soooo tired. I'm sooo angry. I'm being mean and I can't help it. I literally can't be bothered
Zuzka1
in
Thyroid UK
8 years ago
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Questions and fears
It's Jake again . Soon you will all get to know me as the most nervous 22 year old in the world haha. Okay I should probably stop googling all these sites and studies and what not because it's doing me no good. My two biggest fears now are (heck I haven't even been diagnosed WITH PV and if I am it's
It's Jake again . Soon you will all get to know me as the most nervous 22 year old in the world haha. Okay I should probably stop googling all these sites and studies and what not because it's doing me no good. My two biggest fears now are (heck I haven't even been diagnosed WITH PV and if I am it's
JW1995
in
MPN Voice
8 years ago
Hydrotherapy
Hiya everyone! I went to see the physio today following my diagnosis. He didn't give me any exercises which I was surprised about but advised he would like to refer me to hydrotherapy. I can't swim normally as I have a cam leision on my hip bone but he feels it would really help. I had an MRI on my
Hiya everyone! I went to see the physio today following my diagnosis. He didn't give me any exercises which I was surprised about but advised he would like to refer me to hydrotherapy. I can't swim normally as I have a cam leision on my hip bone but he feels it would really help. I had an MRI on my
Jordana88
in
Fibromyalgia Action UK
8 years ago
Amino acids for E.D.
I have read that argenine, citrulline, and pine bark extract can help with ED does anyone know if this is true, and if so in what doses and over what time period.
I have read that argenine, citrulline, and pine bark extract can help with ED does anyone know if this is true, and if so in what doses and over what time period.
Petergallery
in
Erectile Dysfunction Support
8 years ago
Near fainting
I forgot to mention near fainting spells, 2, to my last post. Does anyone experience this. Also very scary. This is why an MRI was ordered. All normal. Cardiology workup is next. I feel like I just cannot fight this any more. Too many terrifying symptoms. Love and Hugs. Kinsalelady.
I forgot to mention near fainting spells, 2, to my last post. Does anyone experience this. Also very scary. This is why an MRI was ordered. All normal. Cardiology workup is next. I feel like I just cannot fight this any more. Too many terrifying symptoms. Love and Hugs. Kinsalelady.
Kinsalelady
in
MPN Voice
8 years ago
For US Medicare patients
Good news: Did you know there will be an increase in benefit cap limits for outpatient therapy, physical therapy, speech-language pathology and occupational therapy for Medicare recipients in 2017? Once the caps are reached, thereās an exception process that allows for medically necessary therapy costs
Good news: Did you know there will be an increase in benefit cap limits for outpatient therapy, physical therapy, speech-language pathology and occupational therapy for Medicare recipients in 2017? Once the caps are reached, thereās an exception process that allows for medically necessary therapy costs
Christine47
in
PSP Association
8 years ago
Ginger
I found myself fancying a ginger beer last evening and so had one, only to then have a better evening. A quick Google reveals there is a correlation with RLS due to the anti-inflammatory properties, although for now I'm sceptical about whether one ginger beer could have had so immediate effect. What
I found myself fancying a ginger beer last evening and so had one, only to then have a better evening. A quick Google reveals there is a correlation with RLS due to the anti-inflammatory properties, although for now I'm sceptical about whether one ginger beer could have had so immediate effect. What
OldHollow
in
Restless Legs Syndrome
8 years ago
Are YOU getting old?
This was passed to me by a (ex?) friend and I thought it would draw a few wistful smiles as we have the younger folk around during this holiday season. AS i GET OLDER I REALIZE: 1. I talk to myself, because sometimes I need expert advice. 2. Sometimes I roll my eyes out loud. 3. I don't need anger
This was passed to me by a (ex?) friend and I thought it would draw a few wistful smiles as we have the younger folk around during this holiday season. AS i GET OLDER I REALIZE: 1. I talk to myself, because sometimes I need expert advice. 2. Sometimes I roll my eyes out loud. 3. I don't need anger
violetsnowdrop
in
PMRGCAuk
8 years ago
Occupational Health Review
Hi all I'm hoping that someone will be able to relate to my particular work situation and, perhaps, give me some advice. I've just been moved into a job not by choice, and am being told it requires me to travel between 4 and 8 hours in a day to various meetings. I have tried to explain that I will find
Hi all I'm hoping that someone will be able to relate to my particular work situation and, perhaps, give me some advice. I've just been moved into a job not by choice, and am being told it requires me to travel between 4 and 8 hours in a day to various meetings. I have tried to explain that I will find
Hidden
in
NRAS
8 years ago
Chest crushing cold though out my body so bad is if dont get into a hot shower . I can't breath .
Chest crushing cold though out my body so bad if dont get into a hot shower . I can't breath . I have pains all over my body all the time . i feel like Im going to die all the tume but i don't . this happens on a regular basis . i have never been diagnosed with fibro they cant find out whats wrong
Chest crushing cold though out my body so bad if dont get into a hot shower . I can't breath . I have pains all over my body all the time . i feel like Im going to die all the tume but i don't . this happens on a regular basis . i have never been diagnosed with fibro they cant find out whats wrong
Bommarito1
in
Fibromyalgia Action UK
8 years ago
Im new :-) pain when breathing deeply
0 Replies Hey everyone. im new. came here as ive lurked alot. and you all seem like a knowledgable bunch :-). So about two weeks ago I suddenly devolped apain in my top left rib. under my breast. if I lay lie on the sofa with my back against the arm rest it hurts when I breath in if I lean over to tie
0 Replies Hey everyone. im new. came here as ive lurked alot. and you all seem like a knowledgable bunch :-). So about two weeks ago I suddenly devolped apain in my top left rib. under my breast. if I lay lie on the sofa with my back against the arm rest it hurts when I breath in if I lean over to tie
Freshsmellingmustard
in
Lung Conditions Community Forum
8 years ago
B12 makes me anxious and jittery
Hey there. On Nov. 02 I got my first B12 shot. Then sublingual 1000mu every day. Didn't felt much the first days. Then become tired, which I liked. Yes it was a warm, chilling, comfortable feeling. Stayed in bed all day, which I can, because I often work at home. My physical symptoms improve constantly
Hey there. On Nov. 02 I got my first B12 shot. Then sublingual 1000mu every day. Didn't felt much the first days. Then become tired, which I liked. Yes it was a warm, chilling, comfortable feeling. Stayed in bed all day, which I can, because I often work at home. My physical symptoms improve constantly
Hidden
in
Pernicious Anaemia Society
8 years ago
Zzzzzzzzzzzzzzzz
A couple of posters have complained about difficulty sleeping. This is a breathing exercise that might help with sleep and/or anxiety. worth a try. https://www.youtube.com/watch?v=gz4G31LGyog sweet dreams :)
A couple of posters have complained about difficulty sleeping. This is a breathing exercise that might help with sleep and/or anxiety. worth a try. https://www.youtube.com/watch?v=gz4G31LGyog sweet dreams :)
wellness1
in
Thyroid UK
8 years ago
ASAP/ALAP counts - what constitutes numbers to be worried about ?
14 months after my SCT I am going through a period of chronic GvHD in my liver. After 2 months of corticoids I have been switched to Jakavi - progressively increased from 2x5mg to 2x15mg per day. The Doctor has explained to me they are following my ASAT and ALAT counts to monitor progress; these counts
14 months after my SCT I am going through a period of chronic GvHD in my liver. After 2 months of corticoids I have been switched to Jakavi - progressively increased from 2x5mg to 2x15mg per day. The Doctor has explained to me they are following my ASAT and ALAT counts to monitor progress; these counts
crapaud
in
MPN Voice
8 years ago
Emollients - Epimax instead of Diprobase
I asked my GP for some more Diprobase, but was refused as my NHS area's formulary no longer lists it. I remembered a nurse using Fifty:50 so asked for that, and it was allowed. The formulary now lists Epimax as the first choice alternative to Aproderm, Aqueous cream, Aquamax, Diprobase cream, E45 cream
I asked my GP for some more Diprobase, but was refused as my NHS area's formulary no longer lists it. I remembered a nurse using Fifty:50 so asked for that, and it was allowed. The formulary now lists Epimax as the first choice alternative to Aproderm, Aqueous cream, Aquamax, Diprobase cream, E45 cream
SmallBlueThing
in
LSN
8 years ago
Hydrotherapy pool
Hi , I've been referred for physio and hydrotherapy treatment by my surgeon after surgery on my knee , my question is , are there Steps to get in and out of the pool as I'm unsteady on my feet and don't like the sound of a hoist ! Hope someine can help me asap please.
Hi , I've been referred for physio and hydrotherapy treatment by my surgeon after surgery on my knee , my question is , are there Steps to get in and out of the pool as I'm unsteady on my feet and don't like the sound of a hoist ! Hope someine can help me asap please.
291155
in
Fibromyalgia Action UK
8 years ago
Bad Lower Back Pain
I started gettting noticeable back pain a year ago and it has been getting progressively worse over time. I have went to physical therapy for multiple injuries, this being one of them, but the pain has not subsided. I am 14, if that helps. I play very competitive hockey and am currently dealing with
I started gettting noticeable back pain a year ago and it has been getting progressively worse over time. I have went to physical therapy for multiple injuries, this being one of them, but the pain has not subsided. I am 14, if that helps. I play very competitive hockey and am currently dealing with
Zaxonite
in
Pain Concern
8 years ago
CHC
We are being reassessed for CHC really worried because from my understanding we could loose it? Because George is not going to die soon, I don't know how I will cope without it, I explained that this illness is unpredictable and compulsive behaviour really feel stressed out, just sitting here crying,
We are being reassessed for CHC really worried because from my understanding we could loose it? Because George is not going to die soon, I don't know how I will cope without it, I explained that this illness is unpredictable and compulsive behaviour really feel stressed out, just sitting here crying,
Yvonneandgeorge
in
PSP Association
8 years ago
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