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Amitriptyline / Ketamine
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Nothing But Pain
Has anyone out there had a tot removal, by tot I mean trans obturator tape/mesh removed and have been left with the anchors either side on sits bone. Despite having this tape removed back in sept 2013 and taking pregabalin and amitriptyline for the nerve damage that was caused after the prolapse repair
Has anyone out there had a tot removal, by tot I mean trans obturator tape/mesh removed and have been left with the anchors either side on sits bone. Despite having this tape removed back in sept 2013 and taking pregabalin and amitriptyline for the nerve damage that was caused after the prolapse repair
stenosis49
in
Pain Concern
7 years ago
Amitriptyline Withdrawals / Slowly giving up
Sat here at 0330 after trying and failing to sleep for 3 and a half hours. Amitriptyline withdrawals kicking my a**e! My GP said you'll either not get addicted or get addicted and judging from my personality, I knew id probably end up getting addicted. Guess I was right lol! Slowly giving up now, nothing
Sat here at 0330 after trying and failing to sleep for 3 and a half hours. Amitriptyline withdrawals kicking my a**e! My GP said you'll either not get addicted or get addicted and judging from my personality, I knew id probably end up getting addicted. Guess I was right lol! Slowly giving up now, nothing
TheInjuredBiker
in
Anxiety Support
7 years ago
Hip & back pain
Hi everyone, in so much pain with my hips & lower back, it's not sciatica as it's not going down my legs. Sitting down & getting up is horrendous, even trying to sit on the toilet is a struggle. Had chronic back pain for a long time & can only take amitriptyline & paracetamol as too many side effects
Hi everyone, in so much pain with my hips & lower back, it's not sciatica as it's not going down my legs. Sitting down & getting up is horrendous, even trying to sit on the toilet is a struggle. Had chronic back pain for a long time & can only take amitriptyline & paracetamol as too many side effects
Hidden
in
Myalgic Encephalomyelitis Community
7 years ago
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RLS driving me mad
I have suffered fir ten years now and find older I get the worse it gets 67 now my pain constant put me on 5 miles of Oxynorm but it's not working now,find that my arms are just as bad as the legs. I also take liquid ketamine for pain and this helps but don't like to take it every night as it upsets
I have suffered fir ten years now and find older I get the worse it gets 67 now my pain constant put me on 5 miles of Oxynorm but it's not working now,find that my arms are just as bad as the legs. I also take liquid ketamine for pain and this helps but don't like to take it every night as it upsets
Conifer
in
Restless Legs Syndrome
7 years ago
Betaine HCL with Pepsin and breastfeeding
Hi everyone, I've been having issues with digestion for years and after reading about it I think I might have low stomach acid. I have Hashimoto's and I have a lot of digestion/gut issues, so I think my gut isn't too well. I thought about getting a good Betaine HCL + Pepsin supplement, but I'm breastfeeding
Hi everyone, I've been having issues with digestion for years and after reading about it I think I might have low stomach acid. I have Hashimoto's and I have a lot of digestion/gut issues, so I think my gut isn't too well. I thought about getting a good Betaine HCL + Pepsin supplement, but I'm breastfeeding
AnaReis
in
Thyroid UK
7 years ago
Endo pain
Hi I've been diagnostic with endometriosis 18 month ago after suFeering with agonising pain since June 15 when I got sterilised. I've been on prostap whigh was faborn but you can only take for 6 months at a time. The pill doesn't agree with me (attempted suicide). Most recently had the mirena coil fitted
Hi I've been diagnostic with endometriosis 18 month ago after suFeering with agonising pain since June 15 when I got sterilised. I've been on prostap whigh was faborn but you can only take for 6 months at a time. The pill doesn't agree with me (attempted suicide). Most recently had the mirena coil fitted
Suzied2b
in
Endometriosis UK
7 years ago
Background migraine
Hi, I have been having a bad background migraine for few years now. I also have migraine attacks occasionally which can last from a few days to a few weeks. I have had scans and been to see neurologists. A couple of months ago, I came to the national migraine centre. Apart from some medication for migraine
Hi, I have been having a bad background migraine for few years now. I also have migraine attacks occasionally which can last from a few days to a few weeks. I have had scans and been to see neurologists. A couple of months ago, I came to the national migraine centre. Apart from some medication for migraine
Windflower24
in
National Migraine Centre
7 years ago
hallucinations ......side effect of medication?
Hi all, my son increased his dosage of amitriptyline to 50 mg last night ( has to increase by 10 mg every 5/7 days as part of his management plan) . He was experiencing hallucinations. Has anyone else experienced this? I have told him he should carry on with his meds and see how he goes, obviously if
Hi all, my son increased his dosage of amitriptyline to 50 mg last night ( has to increase by 10 mg every 5/7 days as part of his management plan) . He was experiencing hallucinations. Has anyone else experienced this? I have told him he should carry on with his meds and see how he goes, obviously if
joben45
in
Headway
7 years ago
Botox Injections.
Hi, I have suffered from RLS on and off for years, but it became so severe a couple of years ago I went to my GP for some medication. He first prescribed Amitriptyline, but this didn't work, so I now take 0.0176mg nightly of Praminexole which does work 95% of the time, but the side effects are tough
Hi, I have suffered from RLS on and off for years, but it became so severe a couple of years ago I went to my GP for some medication. He first prescribed Amitriptyline, but this didn't work, so I now take 0.0176mg nightly of Praminexole which does work 95% of the time, but the side effects are tough
Barnaby97
in
Restless Legs Syndrome
7 years ago
Heat and RLS
Hi, I have just joined the community, I didn't know you existed. Do people find that their RLS is worse in the summer when it's hot. I stretch my calf muscles out in the evening and I take Amitriptyline at night to help most of the time it helps. I would love some advice on how to stop the heat getting
Hi, I have just joined the community, I didn't know you existed. Do people find that their RLS is worse in the summer when it's hot. I stretch my calf muscles out in the evening and I take Amitriptyline at night to help most of the time it helps. I would love some advice on how to stop the heat getting
cyclinglady
in
Restless Legs Syndrome
7 years ago
Churg Strauss Struggles
Hi everyone, I know I have dropped off this site for about a year now but after finally being diagnosed with Churg Strauss last October through a private referral to a rheumatologist in London my life has been a roller coaster! My asthma consultant at The Brompton consistently refused to believe I
Hi everyone, I know I have dropped off this site for about a year now but after finally being diagnosed with Churg Strauss last October through a private referral to a rheumatologist in London my life has been a roller coaster! My asthma consultant at The Brompton consistently refused to believe I
meganoscar123
in
Lung Conditions Community Forum
7 years ago
Amitriptyline, Day 2
Hi, I'm in my early 40's and have sufferedswith ibs-d since my teens. There are certain foods that seem to exacerbate my symptoms, but for me the overriding issue is stress; working with my GP and following my Hospital appts I have tried several methods to manage my stress, but nothing I do can over
Hi, I'm in my early 40's and have sufferedswith ibs-d since my teens. There are certain foods that seem to exacerbate my symptoms, but for me the overriding issue is stress; working with my GP and following my Hospital appts I have tried several methods to manage my stress, but nothing I do can over
ArnoldAx
in
IBS Network
7 years ago
Alcahol and amitryptline
Well first of all I know I can't spell I have always had a little drinking problem since stopping smoking weed I am now on a mix of propananol citoalopran and amitriptyline I have been having major mood swings weight gain I try to be good food wise and always end up stuffing my face some days I am really
Well first of all I know I can't spell I have always had a little drinking problem since stopping smoking weed I am now on a mix of propananol citoalopran and amitriptyline I have been having major mood swings weight gain I try to be good food wise and always end up stuffing my face some days I am really
Cosseryt
in
Fibromyalgia Action UK
7 years ago
Systemic enzymes on empty stomach
Hi there folks, had PA for decades and b12 injections etc, but recently developing carpal tunnel syndrome (which can be exacerbated by low b12). I'd like to add systemic enzymes to my supps as they can assist with CTS. Blood tests always show high levels of B12. Sometimes wonder if I still have pernicious
Hi there folks, had PA for decades and b12 injections etc, but recently developing carpal tunnel syndrome (which can be exacerbated by low b12). I'd like to add systemic enzymes to my supps as they can assist with CTS. Blood tests always show high levels of B12. Sometimes wonder if I still have pernicious
Katejc33
in
Pernicious Anaemia Society
7 years ago
Feeling lost and confused 😪
Having battled with fibro for over 10 years , I feel I've been lucky with not using lots of medication. I used amitriptyline 50mg at night , a weekly massage , paracetamol and codeine . I've had a major flare up and been prescribed Gabapentine , it's giving me horrendous side effects and I've only been
Having battled with fibro for over 10 years , I feel I've been lucky with not using lots of medication. I used amitriptyline 50mg at night , a weekly massage , paracetamol and codeine . I've had a major flare up and been prescribed Gabapentine , it's giving me horrendous side effects and I've only been
Kathy41
in
Fibromyalgia Action UK
7 years ago
SAH & BLEED INTO SPINE
Hello campers! I saw a neurosurgeon last week who knew about my case for first time last week and she explained everything about 'my' SAH and a bleed into the spine. The presence of the blood aggravated/inflamed the spine, resulting in pain, sensations that keep you up at night...a bit like restless
Hello campers! I saw a neurosurgeon last week who knew about my case for first time last week and she explained everything about 'my' SAH and a bleed into the spine. The presence of the blood aggravated/inflamed the spine, resulting in pain, sensations that keep you up at night...a bit like restless
magdolna
in
Headway
7 years ago
Chronic pain clinic appointment
OK ladies I need your help. My long awaited appointment has come through for the pelvic pain clinic in Oxford. I need to ask questions. I am currently taking 150 mg of Pregablin and 75 mg of Amitriptyline. They don't seem to be helping with the pain. Just makes my head feel like it's stuffed full
OK ladies I need your help. My long awaited appointment has come through for the pelvic pain clinic in Oxford. I need to ask questions. I am currently taking 150 mg of Pregablin and 75 mg of Amitriptyline. They don't seem to be helping with the pain. Just makes my head feel like it's stuffed full
Wendymcconnell
in
Pelvic Pain Support Network
7 years ago
struggling bigtime newbie (update and advice)
Hello again everyone. I recently posted for the first time. Just to recap, I have been diagnosed Hypo 15 months ago after many months feeling ill. Been increasing slowly to 100 levo to get to a tsh of 1 or under. Felt quite bad when I went from 50 to 75 but it seemed to settle a bit but I was still
Hello again everyone. I recently posted for the first time. Just to recap, I have been diagnosed Hypo 15 months ago after many months feeling ill. Been increasing slowly to 100 levo to get to a tsh of 1 or under. Felt quite bad when I went from 50 to 75 but it seemed to settle a bit but I was still
mythreecats
in
Thyroid UK
7 years ago
Getting a Diagnosis
Hi, I am new to this forum. I have not received a diagnosis of Fibro, my Dr seems to be reluctant to commit to this. I have been tested for Lupus, polymyalgia and Multiple Sclerosis - all negative. I had a traumatic event some 6 years ago (actually there were several one after another), I think these
Hi, I am new to this forum. I have not received a diagnosis of Fibro, my Dr seems to be reluctant to commit to this. I have been tested for Lupus, polymyalgia and Multiple Sclerosis - all negative. I had a traumatic event some 6 years ago (actually there were several one after another), I think these
vivdk
in
Fibromyalgia Action UK
7 years ago
22 months post vm 35 female
So glad I found this forum. I got sick August of 2015. Little did I know what exactly would play out. I started with mono and continued to deteriorate which led to diagnosis of vm and 9 day hospitalization. I'm in the medical profession and am in awe of lack of information regarding recovery from vm.
So glad I found this forum. I got sick August of 2015. Little did I know what exactly would play out. I started with mono and continued to deteriorate which led to diagnosis of vm and 9 day hospitalization. I'm in the medical profession and am in awe of lack of information regarding recovery from vm.
Bcamron
in
Meningitis Now
7 years ago
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