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Sibelium and mental health
Hello, ive been taking sibelium 5mg for about 4 months, it has been going ok sk far, the only symptoms i experienced were drowsiness and increased appetite, but recently i got a really bad stomach flu and had to take antibiotics, although my pharmacist and drs told me there is no interactions, i felt
Hello, ive been taking sibelium 5mg for about 4 months, it has been going ok sk far, the only symptoms i experienced were drowsiness and increased appetite, but recently i got a really bad stomach flu and had to take antibiotics, although my pharmacist and drs told me there is no interactions, i felt
Kevin160
in
National Migraine Centre
2 years ago
Gentamicin
I have Bronchiectasis and have had it a long time .I have a New Consultant and she has put me on inhaled Gentamicin one month on ,one month off ,which I have just started..My main concern is hearing loss which they say c an happen. .I wear hearing aids already which is a recent experience.My Consultant
I have Bronchiectasis and have had it a long time .I have a New Consultant and she has put me on inhaled Gentamicin one month on ,one month off ,which I have just started..My main concern is hearing loss which they say c an happen. .I wear hearing aids already which is a recent experience.My Consultant
cat50
in
Lung Conditions Community Forum
2 years ago
Physiotherapy and hydrotherapy questions
hi I have been diagnosed with fibromyalgia since March time it has taken 15 months to get this diagnosed with a rheumatologist. Anyway, I wanted to put this question out there and ask if anyone has had physio for this and do you have to get referred by a doctor and does anyone know if you can get hydrotherapy
hi I have been diagnosed with fibromyalgia since March time it has taken 15 months to get this diagnosed with a rheumatologist. Anyway, I wanted to put this question out there and ask if anyone has had physio for this and do you have to get referred by a doctor and does anyone know if you can get hydrotherapy
fibrogirl41
in
Fibromyalgia Action UK
2 years ago
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Husband progressing quickly
Hi! My husband is 68 years old. He was officially diagnosed with PSP IN 2020 , but has been showing symptoms since 2015. He is barely walking now. He falls very frequently. He is on a rollater or he could not get around at all. Everything is so hard for him to do. He has not driven in 3 or 4 years. He
Hi! My husband is 68 years old. He was officially diagnosed with PSP IN 2020 , but has been showing symptoms since 2015. He is barely walking now. He falls very frequently. He is on a rollater or he could not get around at all. Everything is so hard for him to do. He has not driven in 3 or 4 years. He
Hidden
in
PSP Association
2 years ago
Stomach flu
Oh my goodness the pains on my stomach are awful I used sick day rules for two days but couldn’t sleep I’m assuming high pred dose. Iv taken Imodium but it’s persistent. I’m doing BRAT diet but not gonna eat today. Back to 10.5mg pred I do have hip pain! Any advice pleeeeeeaaaseeee
Oh my goodness the pains on my stomach are awful I used sick day rules for two days but couldn’t sleep I’m assuming high pred dose. Iv taken Imodium but it’s persistent. I’m doing BRAT diet but not gonna eat today. Back to 10.5mg pred I do have hip pain! Any advice pleeeeeeaaaseeee
Uglow
in
PMRGCAuk
2 years ago
The PSP-CBD Ice Cream Challenge 2022 Day 8
Oak Island -The Smith's Cove Excavation Seems appropriate for the finale of season 9 today. Acorns (fans of the show) will get this. BTW, the lettering is made from milk chocolate... I used a mold. The first letter 'T' represents the lead cross found on the shoreline. I made the cofferdam with graham
Oak Island -The Smith's Cove Excavation Seems appropriate for the finale of season 9 today. Acorns (fans of the show) will get this. BTW, the lettering is made from milk chocolate... I used a mold. The first letter 'T' represents the lead cross found on the shoreline. I made the cofferdam with graham
daddyt
in
PSP Association
2 years ago
A bit of drama on Besremi
(there's a sort of survey question near the end) I've been on it for 3 months now. From starting dose of 50mcg for HU transition my dose last week was ~110. -That evening I had high sensitivity to light, looking at the overhead kitchen light was nearly like looking at the sun. Even the white sink
(there's a sort of survey question near the end) I've been on it for 3 months now. From starting dose of 50mcg for HU transition my dose last week was ~110. -That evening I had high sensitivity to light, looking at the overhead kitchen light was nearly like looking at the sun. Even the white sink
EPguy
in
MPN Voice
2 years ago
L5 S1 fusion, laminectomy and bilateral foraminotomy
I am coming up on 3 months post op. I go to therapy 2 x a week and can walk moderately for 15-30 minutes a day but every time I think I am making progress as far as being pain free I have a bad spell needing meds, ice and heat again. I am 60 and may just be slow to heal?
I am coming up on 3 months post op. I go to therapy 2 x a week and can walk moderately for 15-30 minutes a day but every time I think I am making progress as far as being pain free I have a bad spell needing meds, ice and heat again. I am 60 and may just be slow to heal?
Jeaniem130
in
Pain Concern
2 years ago
Do I need to be checked out
Hi I had an AF episode a week ago and then went into fast Sinus with a heart beat of 140. 6 days later I went into Kings for a routine endoscopy for my 3 yearly verecies check for my liver cirrhosis. My heart was still tackicardic. First they could not get the camera down my throat due to severe swallowing
Hi I had an AF episode a week ago and then went into fast Sinus with a heart beat of 140. 6 days later I went into Kings for a routine endoscopy for my 3 yearly verecies check for my liver cirrhosis. My heart was still tackicardic. First they could not get the camera down my throat due to severe swallowing
MalcolmCClark
in
Atrial Fibrillation Support
2 years ago
Help Ulster University research access to rehab services
If you have PSP or CBD and are living in Northern Ireland could you help researchers at Ulster University learn more about access to rehabilitation services (including physio, occupational therapy, speech therapists, psychologists)? This research will involve joining a 90-minutes virtual Focus Group
If you have PSP or CBD and are living in Northern Ireland could you help researchers at Ulster University learn more about access to rehabilitation services (including physio, occupational therapy, speech therapists, psychologists)? This research will involve joining a 90-minutes virtual Focus Group
HelenPSPA
in
PSP Association
2 years ago
An Unusual False-Positive Uptake of Radioiodine Caused by Breast Implants
Posting this simply to let everyone know! If the issue applies, make sure you discuss properly with anyone who wants to give you radioactive iodine. I suspect it will be at the obscure end of the scale. [i]Clin Nucl Med. 2022 Mar 30. doi: 10.1097/RLU.0000000000004165. Online ahead of print.
An
Posting this simply to let everyone know! If the issue applies, make sure you discuss properly with anyone who wants to give you radioactive iodine. I suspect it will be at the obscure end of the scale. [i]Clin Nucl Med. 2022 Mar 30. doi: 10.1097/RLU.0000000000004165. Online ahead of print.
An
helvella
Thyroid UK
in
Thyroid UK
2 years ago
Learning to live with Covid
Since all the rules were dropped in favour of learning to live with covid, I’ve been expecting to see comments on here, perhaps I missed them. As someone who was born with PCD, survived war living in industrial Birmingham, going to bed in cold damp air raid shelter, did my bit by collecting shrapnel
Since all the rules were dropped in favour of learning to live with covid, I’ve been expecting to see comments on here, perhaps I missed them. As someone who was born with PCD, survived war living in industrial Birmingham, going to bed in cold damp air raid shelter, did my bit by collecting shrapnel
Morrison10
in
Lung Conditions Community Forum
2 years ago
MUSIC THERAPY FOR ALIEN HAND
My husband who suffers from CBD is increasingly plagued by his hand clenching and clawing, especially at night. We have tried different objects, such as a rubber ball and rolled up towels but they don't ease the problem. I'm wondering about soothing music with headphones as a brain distraction.
My husband who suffers from CBD is increasingly plagued by his hand clenching and clawing, especially at night. We have tried different objects, such as a rubber ball and rolled up towels but they don't ease the problem. I'm wondering about soothing music with headphones as a brain distraction.
Perrywrinkle
in
PSP Association
2 years ago
Anyone tried Iqoro?
I’m running out of ideas to solve my coughing caused by acid reflux. I’ve tried PPi’s over the years. Recently tried famitodine. Nothing seems to work. Gaviscon Advance helps a little. I am careful with what I eat and drink. My coughing starts after I have eaten or drunk something. Lasts about 15
I’m running out of ideas to solve my coughing caused by acid reflux. I’ve tried PPi’s over the years. Recently tried famitodine. Nothing seems to work. Gaviscon Advance helps a little. I am careful with what I eat and drink. My coughing starts after I have eaten or drunk something. Lasts about 15
Heatherfeb
in
Oesophageal & Gastric Cancer
2 years ago
Ototoxic drugs
I was scrolling through some old posts looking for something about habituation. But what caught my eye was a post about ototoxic drugs - those medications which may have an adverse effect on T, specifically. Either currently or in the past I’ve been prescribed several of those mentioned and none of these
I was scrolling through some old posts looking for something about habituation. But what caught my eye was a post about ototoxic drugs - those medications which may have an adverse effect on T, specifically. Either currently or in the past I’ve been prescribed several of those mentioned and none of these
Happyrosie
in
Tinnitus UK
2 years ago
Et + Cutaneous Mastocytosis
Blessed Day to everyone! Does anyone here having ET and cutaneous Mastocytosis or systemic Mastocytosis? Can I know what symptoms currently you facing ? Did you have headaches almost everyday 😞.
Blessed Day to everyone! Does anyone here having ET and cutaneous Mastocytosis or systemic Mastocytosis? Can I know what symptoms currently you facing ? Did you have headaches almost everyday 😞.
Ryna-Ally
in
MPN Voice
2 years ago
IBS Help
I am new here and hoping for some help. Have had stomach issues for a number of years but in the last 3 years it has got a lot worse. Pain under ribs mainly left side, pain in chest and sometimes moves to upper back. Lots of burping especially after eating or drinking and some acid. Loose stools in
I am new here and hoping for some help. Have had stomach issues for a number of years but in the last 3 years it has got a lot worse. Pain under ribs mainly left side, pain in chest and sometimes moves to upper back. Lots of burping especially after eating or drinking and some acid. Loose stools in
Old-Owl
in
IBS Network
2 years ago
Hyperacusis, tinnitus & headache
Hi, not been on here for a while but I suffer from Hyperacusis & tinnitus daily. Not sure if the tinnitus is worse or the Hyperacusis which does make it worse. I now have bad heads every day, these are from the top of my head down over my forehead and eyes. Does anyone else have this or is it a separate
Hi, not been on here for a while but I suffer from Hyperacusis & tinnitus daily. Not sure if the tinnitus is worse or the Hyperacusis which does make it worse. I now have bad heads every day, these are from the top of my head down over my forehead and eyes. Does anyone else have this or is it a separate
CalleLaurel
in
British Tinnitus Association
2 years ago
Rare diseases
Does any body on this site, have a very rare lung disease called pulmonary langerhans cell histiocytosis?
Does any body on this site, have a very rare lung disease called pulmonary langerhans cell histiocytosis?
Sandrapez
in
Lung Conditions Community Forum
2 years ago
A traffic jam in a city in my head day and night.
I go to bed at 9pm and put on a speaker head band with sleep music or crickets. This helps me fall asleep most of the time within minutes rather than without. My T wakes me/keeps me awake every night after 4-5 hours sleep without fail. I'm awake for 1-2 hours, and I often get up and read (write this
I go to bed at 9pm and put on a speaker head band with sleep music or crickets. This helps me fall asleep most of the time within minutes rather than without. My T wakes me/keeps me awake every night after 4-5 hours sleep without fail. I'm awake for 1-2 hours, and I often get up and read (write this
daverussell
in
Tinnitus UK
2 years ago
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