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Gastroparesis or side effects?
Hi everyone, Could anyone give me a clue what's going on please? I suspect I have gastroparesis as my "digestive system" to put it politely has ceased to function. Been 4 times to A&E with fecal impaction causing vomiting, fainting and delirium. They clear the blockage and give me laxatives to take
Hi everyone, Could anyone give me a clue what's going on please? I suspect I have gastroparesis as my "digestive system" to put it politely has ceased to function. Been 4 times to A&E with fecal impaction causing vomiting, fainting and delirium. They clear the blockage and give me laxatives to take
notlob
in
Ehlers-Danlos Support UK
8 years ago
I'm new here, any help and advice welcomed
I am new here. I have been recently diagnosed with fibromyalgia after suffering for 18 months of terrible pain and not knowing why. My pain is chronic, I have limited mobility and feel burnt out from having to deal with this each day. I'm now on pregabalin and nortriptyline for the pain, depression
I am new here. I have been recently diagnosed with fibromyalgia after suffering for 18 months of terrible pain and not knowing why. My pain is chronic, I have limited mobility and feel burnt out from having to deal with this each day. I'm now on pregabalin and nortriptyline for the pain, depression
ValT28
in
Fibromyalgia Action UK
8 years ago
SLE, SJÖGREN and Periphery Neuropathy/ Poly -Neuropathy.
I have been on here for quite a while responding to your many posts, and all of a sudden I am blown away by a missed diagnosis. For years I am having lost sensations in fingers , toes, overall reduced feeling in my skin, inexplicable heat on my chest which was wiped away as being a menopausal symptom
I have been on here for quite a while responding to your many posts, and all of a sudden I am blown away by a missed diagnosis. For years I am having lost sensations in fingers , toes, overall reduced feeling in my skin, inexplicable heat on my chest which was wiped away as being a menopausal symptom
morlobach
in
LUPUS UK
8 years ago
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Jamsam
l've been suffer with lBS for about ten years . have lost a stone in weight since last year have tried most things. also diverticulitis. the wind is the most debilitating issues that builds through the day and then l have try to release it before l can get some sleep at night l'm taking nortriptyline
l've been suffer with lBS for about ten years . have lost a stone in weight since last year have tried most things. also diverticulitis. the wind is the most debilitating issues that builds through the day and then l have try to release it before l can get some sleep at night l'm taking nortriptyline
janwoods
in
IBS Network
8 years ago
Increasing my dose of Nortriptyline??
Hi guys, Just wondering if anyone has experience of Nortriptyline? Was on Gabapentin and Amytriptyline for a while but have come off it as it didn't really make much of a difference pain wise and they both made me feel really dreadful. I've been on Nortriptyline now for about 6 weeks, it's helping me
Hi guys, Just wondering if anyone has experience of Nortriptyline? Was on Gabapentin and Amytriptyline for a while but have come off it as it didn't really make much of a difference pain wise and they both made me feel really dreadful. I've been on Nortriptyline now for about 6 weeks, it's helping me
Toplady
in
Pain Concern
8 years ago
I'm new here
Hi I'm new to this site. After being in severe pain mainly from back passage and perineum and had mri/ct scans and a pelvic floor repair due to rectocele and cystocele I still have the pain every doctor I have seen says something different now I have been referred to dr Telford at wythenshawe hospital
Hi I'm new to this site. After being in severe pain mainly from back passage and perineum and had mri/ct scans and a pelvic floor repair due to rectocele and cystocele I still have the pain every doctor I have seen says something different now I have been referred to dr Telford at wythenshawe hospital
Kphee21
in
Pelvic Pain Support Network
8 years ago
Running out of patience with fibromyalgia
Hi, I'm 25 and live with fibromyalgia, hypo-thyroidism, auto-immune urticaria and angiodema. I work as an ops manager (which can be stressful), try to go to the gym 4/5 times per week and eat a healthy balanced diet. I don't feel sorry for myself (because why would I?!), I'm pragmatic and I get on with
Hi, I'm 25 and live with fibromyalgia, hypo-thyroidism, auto-immune urticaria and angiodema. I work as an ops manager (which can be stressful), try to go to the gym 4/5 times per week and eat a healthy balanced diet. I don't feel sorry for myself (because why would I?!), I'm pragmatic and I get on with
Amayc
in
Pain Concern
8 years ago
Sleep issues - anyone have experience with the sleep tracker apps?
Hey guys, sorry, yet again, for going quiet for a while. I always read the daily digest and try to keep up with all the posts. I wonder if anyone has any experience with the sleep tracker apps? I recently started using one and realised just how poor my sleep actually is. My deep sleep never amounts to
Hey guys, sorry, yet again, for going quiet for a while. I always read the daily digest and try to keep up with all the posts. I wonder if anyone has any experience with the sleep tracker apps? I recently started using one and realised just how poor my sleep actually is. My deep sleep never amounts to
ladytelita
in
Fibromyalgia Action UK
8 years ago
Continuing saga
Hi! I wrote on here a few months back asking advice on finding someone to look outside the box after being treated for 5 years for sero neg RA and was no further on. Got a lot of interesting feedback from people on here, thank you, so thought I'd update you and ask your opinion on a couple of other things
Hi! I wrote on here a few months back asking advice on finding someone to look outside the box after being treated for 5 years for sero neg RA and was no further on. Got a lot of interesting feedback from people on here, thank you, so thought I'd update you and ask your opinion on a couple of other things
Lynnels
in
NRAS
8 years ago
Fibromyalgia and costochondritis
Hi Everyone, I started getting terrible burning pains between my shoulder blades about 5/6 years ago and felt I could not lift my arms and felt tired, other symptoms appeared,but I just thought that I had pulled a muscle and it would go, unfortunately it only went for short periods and i just put up
Hi Everyone, I started getting terrible burning pains between my shoulder blades about 5/6 years ago and felt I could not lift my arms and felt tired, other symptoms appeared,but I just thought that I had pulled a muscle and it would go, unfortunately it only went for short periods and i just put up
Hidden
in
My Fibro Community
8 years ago
LSVT Big!
I'm 64, diagnosed with PD 18 months ago but have had symptoms of no left arm swing, rigidity of torso, leaning forwards when walking, and bradykinesia for some years before that, no tremor. I was initially started on Madopar with no positive response, just bad reactions and I felt so sick I couldn't
I'm 64, diagnosed with PD 18 months ago but have had symptoms of no left arm swing, rigidity of torso, leaning forwards when walking, and bradykinesia for some years before that, no tremor. I was initially started on Madopar with no positive response, just bad reactions and I felt so sick I couldn't
grower
in
Cure Parkinson's
9 years ago
Is there a link between fibromalgia and underactive thyroid ??
Hi, first time on here. Most of my adult life I have suffered from pain related illnesses ever since I had glandular fever at age 19. I am not the type of person to run to the doctor everytime I feel pain but when it goes on and on for months/ years with no let up you want some answers as to what is
Hi, first time on here. Most of my adult life I have suffered from pain related illnesses ever since I had glandular fever at age 19. I am not the type of person to run to the doctor everytime I feel pain but when it goes on and on for months/ years with no let up you want some answers as to what is
Angeren14
in
Fibromyalgia Action UK
9 years ago
Constant pins and needles
Hi, I am 24 years old, I have been living with pins and needles constantly for the last 7 months in my hands, feet and tounge, I also have a constant ringing noise in my ear. Blood tests, nerve conduction study, osteopath visit twice, CT brain and spine scan, neurologist examination, eye test all came
Hi, I am 24 years old, I have been living with pins and needles constantly for the last 7 months in my hands, feet and tounge, I also have a constant ringing noise in my ear. Blood tests, nerve conduction study, osteopath visit twice, CT brain and spine scan, neurologist examination, eye test all came
Hannahfox2015
in
NRAS
9 years ago
Nortriptyline
not sure if this is due to taking the above but of late i have developed a tremor in my hands the right is the worst to the extent that i need to hold cups with both hands so i dont spill my drinks when putting to my mouth. Also sometimes my husband says i have said something and i am certain i said
not sure if this is due to taking the above but of late i have developed a tremor in my hands the right is the worst to the extent that i need to hold cups with both hands so i dont spill my drinks when putting to my mouth. Also sometimes my husband says i have said something and i am certain i said
prim50
in
Pain Concern
9 years ago
injections not worked
well three week since my nerve block injections and i am still getting the leg,foot and now lower back pain. For the first week i really thought it had worked then increased my activities and bingo back it came. Drove with breaks for 80 miles only to suffer that night and following day with serve pain
well three week since my nerve block injections and i am still getting the leg,foot and now lower back pain. For the first week i really thought it had worked then increased my activities and bingo back it came. Drove with breaks for 80 miles only to suffer that night and following day with serve pain
prim50
in
Pain Concern
9 years ago
GON?
Hi everyone :) I've been on and off medication for the last 2 years, tried Migraleve, Pizotifen, PropranololTopiramate, Amitriptyline, Nortriptyline and thats not all of them :/ I'm still in school and since my exams are next week, I've stopped taking the medication because of the nasty side effects.
Hi everyone :) I've been on and off medication for the last 2 years, tried Migraleve, Pizotifen, PropranololTopiramate, Amitriptyline, Nortriptyline and thats not all of them :/ I'm still in school and since my exams are next week, I've stopped taking the medication because of the nasty side effects.
arjuna
in
National Migraine Centre
9 years ago
Help...Extended ibs Flare
Hi I have had ibs for 22 years and like many it comes and goes usually a few days here and there may be a week but I'm now going into my 4th week and it's never been this bad it's so painful the bloating the diarrhoea mixed in with more solid mucus covered stools and the most terrible wind the smell
Hi I have had ibs for 22 years and like many it comes and goes usually a few days here and there may be a week but I'm now going into my 4th week and it's never been this bad it's so painful the bloating the diarrhoea mixed in with more solid mucus covered stools and the most terrible wind the smell
Tonichick
in
IBS Network
9 years ago
nortriptyline and increase in hot flushes
Since putting up my dose of nortriptyline to 40mg a night i seem to be having more hot flushes then my normal menopausal dose also i have become more irritable and suffer with anxiety too. dont know if it is connected or not maybe its just all to do with my menopause .
Since putting up my dose of nortriptyline to 40mg a night i seem to be having more hot flushes then my normal menopausal dose also i have become more irritable and suffer with anxiety too. dont know if it is connected or not maybe its just all to do with my menopause .
prim50
in
Pain Concern
9 years ago
Pain patch advice
Silly question, but how do I ask a GP for pain patch? My regular GP is off on extended leave due to ill health so I have to see someone else. Keep putting off making an appointment as I really don't know how to ask. I've been very stressed and unwell of late. I was in hospital with pneumonia a short
Silly question, but how do I ask a GP for pain patch? My regular GP is off on extended leave due to ill health so I have to see someone else. Keep putting off making an appointment as I really don't know how to ask. I've been very stressed and unwell of late. I was in hospital with pneumonia a short
ladytelita
in
Fibromyalgia Action UK
9 years ago
Central sensitivity syndrome
I have FMS / Myfacial pain with trigeminal neuralgia features octial neuralgia migraines IBS Rosacea and central sensitivity syndrome . I was wondering if anyone else has been dx with central sensitivity syndrome . I have been having trouble with meds . I take gabapentin . My nuero has tried me on amytriplyine
I have FMS / Myfacial pain with trigeminal neuralgia features octial neuralgia migraines IBS Rosacea and central sensitivity syndrome . I was wondering if anyone else has been dx with central sensitivity syndrome . I have been having trouble with meds . I take gabapentin . My nuero has tried me on amytriplyine
kgarrett1
in
Fibromyalgia Action UK
9 years ago
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