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Amitriptyline / Ketamine
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Covid Vaccine, medical conditions and allergies
I was just wondering whether anyone has taken any of the vaccines? Although I work within a hospital setting where some of my colleagues have already received it, had been sent a text by my GP stating I should book and appointment and now furloughed, I really do not wish to take it due to my allergies
I was just wondering whether anyone has taken any of the vaccines? Although I work within a hospital setting where some of my colleagues have already received it, had been sent a text by my GP stating I should book and appointment and now furloughed, I really do not wish to take it due to my allergies
AngieB68
in
Functional Neurological Disorder - FND Hope
3 years ago
A Different Perspective
Having been seen privately by an eminent rheumatologist.......a leading authority in the field of PMR/GCA, since my diagnosis in May 2019, I decided to change to NHS care, as weirdly there is much more support available in between appointments when you're under the NHS than as a private patient! I had
Having been seen privately by an eminent rheumatologist.......a leading authority in the field of PMR/GCA, since my diagnosis in May 2019, I decided to change to NHS care, as weirdly there is much more support available in between appointments when you're under the NHS than as a private patient! I had
Kendrew
in
PMRGCAuk
3 years ago
I am on 4mg Pred, 30mg Amitriptyline and 600mg Gabapentin .. should my diet factor in more foods with low stress on the immune system ? TIA
I am on 4mg Pred, 30mg Amitriptyline and 600mg Gabapentin .. should my diet factor in more foods with low stress on the immune system ? TIA 🤗
I am on 4mg Pred, 30mg Amitriptyline and 600mg Gabapentin .. should my diet factor in more foods with low stress on the immune system ? TIA 🤗
Capprice
in
PMRGCAuk
3 years ago
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Advice please
Hi, I was diagnosed with fibromyalgia in June 2018, the rheumatologist told G.P to add medication and refer me to a pain management clinic, I’m still waiting. My pain just keeps getting worse to the point of ending up in tears it literally makes me feel sick and stops me in my tracks. I have basically
Hi, I was diagnosed with fibromyalgia in June 2018, the rheumatologist told G.P to add medication and refer me to a pain management clinic, I’m still waiting. My pain just keeps getting worse to the point of ending up in tears it literally makes me feel sick and stops me in my tracks. I have basically
Emk68
in
Fibromyalgia Action UK
3 years ago
Me/cfs
Hi all.... so I have just got off the phone to my neurologist.... I was diagnosed with fibromyalgia in 2012 and today I have been diagnosed with Me/cfs.... I feel relieved that I have answers to my symptoms. I had a nerve conduction test done and she said that came back normal... I have strange sensation
Hi all.... so I have just got off the phone to my neurologist.... I was diagnosed with fibromyalgia in 2012 and today I have been diagnosed with Me/cfs.... I feel relieved that I have answers to my symptoms. I had a nerve conduction test done and she said that came back normal... I have strange sensation
Dazakella2010
in
Fibromyalgia Action UK
3 years ago
Does either (or both) Steroids/Amitriptyline cause heart palpitations/anxiety attack?
Hi guys, I just spent the past 25mins feeling my heart beat faster and faster, i stopped doing work and turned on a 5mins meditation video and my heart beat normalized thankfully. Looking back i have noticed that when I am higher steroids I sometimes get random increased heart palpitations but i
Hi guys, I just spent the past 25mins feeling my heart beat faster and faster, i stopped doing work and turned on a 5mins meditation video and my heart beat normalized thankfully. Looking back i have noticed that when I am higher steroids I sometimes get random increased heart palpitations but i
Sandy1212
in
LUPUS UK
3 years ago
Peripheral neuralgia
I saw the neurologist yesterday and he told me that what I have is common (10% of people feel as if they are wearing socks, have burning toes, etc), but the name of the condition is longer than that town in Wales. It means that no-one knows what causes it. So now I have another condition that "nobody
I saw the neurologist yesterday and he told me that what I have is common (10% of people feel as if they are wearing socks, have burning toes, etc), but the name of the condition is longer than that town in Wales. It means that no-one knows what causes it. So now I have another condition that "nobody
MaggieSylvie
in
Leukaemia Support
4 years ago
Diltiazem and Amitriptyline
Hi folks I suffer from coronary artery spams. Does anyone take diltiazem and amitriptyline at the same time . My GP has prescribed amitriptyline (25mg) and I take 200mg of diltiazem daily. The reason for the amitriptyline is to help reduce my anxiety and to replace diazepam , which has been very helpful
Hi folks I suffer from coronary artery spams. Does anyone take diltiazem and amitriptyline at the same time . My GP has prescribed amitriptyline (25mg) and I take 200mg of diltiazem daily. The reason for the amitriptyline is to help reduce my anxiety and to replace diazepam , which has been very helpful
Battle2020
in
British Heart Foundation
4 years ago
Infusion.
Hi everyone. I've not been on here for a long time. I'm at my worst ever at the mo and just feel so down and low. The pains are constant, I cant sleep, sleepwalking is back again. I know this whole crappy situation isn't helping anyone right now and we just have to learn to live with it but why should
Hi everyone. I've not been on here for a long time. I'm at my worst ever at the mo and just feel so down and low. The pains are constant, I cant sleep, sleepwalking is back again. I know this whole crappy situation isn't helping anyone right now and we just have to learn to live with it but why should
QUEENIE74
in
Fibromyalgia Action UK
4 years ago
Neurology appointment
Hi guys, I have just had a video call with a neurologist from Walton center and for the first time, since diagnoses in 2015, I have had a full explanation of my symptoms. First he explained that the pain receptors in my system have been switched on by a past injury, mild head trauma and neck injury.
Hi guys, I have just had a video call with a neurologist from Walton center and for the first time, since diagnoses in 2015, I have had a full explanation of my symptoms. First he explained that the pain receptors in my system have been switched on by a past injury, mild head trauma and neck injury.
Jan1964
in
Fibromyalgia Action UK
4 years ago
Ms or not
Hi guys don’t even know if you remember me my mum had MS she passed away at 47 two years ago since then I was diagnosed with MS I took my ms Diagnosis to an MS specialist Dr Omar Malik in Charing cross hospital he told me that I didn’t have MS and my lesions were in the wrong area of the brain. He told
Hi guys don’t even know if you remember me my mum had MS she passed away at 47 two years ago since then I was diagnosed with MS I took my ms Diagnosis to an MS specialist Dr Omar Malik in Charing cross hospital he told me that I didn’t have MS and my lesions were in the wrong area of the brain. He told
Buckley123
in
My MSAA Community
4 years ago
GP reducing pain relief
Hi guys I’m at my wits end. I have stage 4 rectovaginal endo. I have had one surgery that confirmed this in 2016 and no further surgery. My last consultant follow up was a round 6 months ago. I am managing just about with analgesia and sheer powering through as I’m reluctant to have the surgery as much
Hi guys I’m at my wits end. I have stage 4 rectovaginal endo. I have had one surgery that confirmed this in 2016 and no further surgery. My last consultant follow up was a round 6 months ago. I am managing just about with analgesia and sheer powering through as I’m reluctant to have the surgery as much
Naffers
in
Endometriosis UK
4 years ago
Amitriptyline - Dosages etc.
What dosages are people on & what time/s of day are they taking it? Has anyone come off it with success ? Are you taking it for IBS C or D ? I take mine for the nerve pain I suffer with with IBS-C & just wondering how everybody else uses it. Thanks in advance
What dosages are people on & what time/s of day are they taking it? Has anyone come off it with success ? Are you taking it for IBS C or D ? I take mine for the nerve pain I suffer with with IBS-C & just wondering how everybody else uses it. Thanks in advance
bringiton54321
in
IBS Network
4 years ago
Fatigue affecting my wirk
Hi, I’ve just been recently diagnosed with fibromyalgia. I’m on amitriptyline at night although it’s not having any impact yet. Also I’m a teaching assistant at a primary Schl and I’m finding it really hard to stay awake in the afternoons. My eyes just want to close. Anyone else feel the same?
Hi, I’ve just been recently diagnosed with fibromyalgia. I’m on amitriptyline at night although it’s not having any impact yet. Also I’m a teaching assistant at a primary Schl and I’m finding it really hard to stay awake in the afternoons. My eyes just want to close. Anyone else feel the same?
Blun01
in
Fibromyalgia Action UK
4 years ago
Tinnitus and Amitriptyline 10mg.
Hello. My Gp proscribed Amitriptyline 10mg. I took the first dose in the evening & the following day I woke up without tinnitus. However it gradually appeared during the day & it was even louder than before so I stopped the medication as I do not want to risk making it worse. My question is for those
Hello. My Gp proscribed Amitriptyline 10mg. I took the first dose in the evening & the following day I woke up without tinnitus. However it gradually appeared during the day & it was even louder than before so I stopped the medication as I do not want to risk making it worse. My question is for those
DiegoDiegales
in
British Tinnitus Association
4 years ago
Having joint pain and swelling and prescribed Amitriptyline
Morning all! I hope you are all okay during lockdown. I have had joint pain for almost the entirety of the time I was diagnosed. My joints are usually quite puffy. The drs gave me an ultrasound and found no or hardly any inflammation so they don’t think the lupus is attacking my joint so more immunosuppression
Morning all! I hope you are all okay during lockdown. I have had joint pain for almost the entirety of the time I was diagnosed. My joints are usually quite puffy. The drs gave me an ultrasound and found no or hardly any inflammation so they don’t think the lupus is attacking my joint so more immunosuppression
Sandy1212
in
LUPUS UK
4 years ago
Help and advice please!
I have had PMR for 6 and a half years, with GCA after two years. Nearly 3 years ago I managed to reduce Pred. to 3.5mgs with a small amount of returning pain. I then had a rheumatologist appointment and was told that according to blood test results, PMR was gone and the pain and fatigue I was experiencing
I have had PMR for 6 and a half years, with GCA after two years. Nearly 3 years ago I managed to reduce Pred. to 3.5mgs with a small amount of returning pain. I then had a rheumatologist appointment and was told that according to blood test results, PMR was gone and the pain and fatigue I was experiencing
k-mac
in
PMRGCAuk
4 years ago
Itching and burning skin all over
Hi there . I've been suffering from burning and itching skin all over for nearly 2 years. Been tested for everything. They gave now decided its fibromyalgia. Have had ketamine infusions and nerve blocks. Stopped taking any medication I was on when it started about 4 months ago to see was it due to
Hi there . I've been suffering from burning and itching skin all over for nearly 2 years. Been tested for everything. They gave now decided its fibromyalgia. Have had ketamine infusions and nerve blocks. Stopped taking any medication I was on when it started about 4 months ago to see was it due to
Rebelpear1991
in
Pernicious Anaemia Society
4 years ago
Side effects of Amitriptyline
I have tried taking 10mg of Amitriptyline I am OK for about 10 days then I stop sleeping and it effects my brain. As a matter of interest has anybody else had this problem.
I have tried taking 10mg of Amitriptyline I am OK for about 10 days then I stop sleeping and it effects my brain. As a matter of interest has anybody else had this problem.
AML80
in
Pain Concern
4 years ago
IBS/Bleeding update
I am back with an update. I arranged to speak to my GP but due to a error in the system the appointment was not actually booked. I had called up to check that the pictures I'd taken for my GP to reference had been added to my file, which they had, but kind of hit a wall for a moment. I explained what
I am back with an update. I arranged to speak to my GP but due to a error in the system the appointment was not actually booked. I had called up to check that the pictures I'd taken for my GP to reference had been added to my file, which they had, but kind of hit a wall for a moment. I explained what
Yasai
in
IBS Network
4 years ago
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