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Going from gabapentin to pregabalin..
Has anyone gone from gabapentin to pregabalin?? I’m currently taking 3,200 mg of gabapentin a day and the pain team have recommended I move to pregabalin as I’m still really struggling with pain.. So I’m just wandering if you’ve made the move and how you found it?
Has anyone gone from gabapentin to pregabalin?? I’m currently taking 3,200 mg of gabapentin a day and the pain team have recommended I move to pregabalin as I’m still really struggling with pain.. So I’m just wandering if you’ve made the move and how you found it?
Lynzhoppy1
in
Pain Concern
6 years ago
Diet and lifestyle
Hi Well after the failed attempt at an ablation where the surgeon decided last minute that the arrythmias were too many for treatment under sedation and I would need general I decided that maybe it wasn't for me after all. I have an appointment to see them again on the 2nd July and in the last 6 weeks
Hi Well after the failed attempt at an ablation where the surgeon decided last minute that the arrythmias were too many for treatment under sedation and I would need general I decided that maybe it wasn't for me after all. I have an appointment to see them again on the 2nd July and in the last 6 weeks
Hidden
in
AF Association
6 years ago
New member in NJ
Recently diagnosed at early stages and only drug i am on now is rasagiline which makes me feel a bit woozy. I am in the supplement business and have always been physically active so I hope to be able to offer some support for all.
Recently diagnosed at early stages and only drug i am on now is rasagiline which makes me feel a bit woozy. I am in the supplement business and have always been physically active so I hope to be able to offer some support for all.
Jandeb
in
Cure Parkinson's
6 years ago
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Appointment with Dr Costantini in Viterbo, Italy
Yesterday my husband had his appointment with Dr Costantini. We decided to hire a driver from our hotel in Rome. My husband was not keen on taking the train and we figured it was money well spent. Dr Costantini is very passionate about treating Parkinsons and also confident about the success of treating
Yesterday my husband had his appointment with Dr Costantini. We decided to hire a driver from our hotel in Rome. My husband was not keen on taking the train and we figured it was money well spent. Dr Costantini is very passionate about treating Parkinsons and also confident about the success of treating
nellie58
in
Cure Parkinson's
6 years ago
Foot pain - pelvic pain connection
Hi all. In addition to pelvic pain I have developed severe foot pain which has forced me to resign my job. 3 physical therapists say with confidence that the foot pain is coming from the pelvic region even though nerve conduction and EMG tests are negative. But nobody seems to be able to reduce the
Hi all. In addition to pelvic pain I have developed severe foot pain which has forced me to resign my job. 3 physical therapists say with confidence that the foot pain is coming from the pelvic region even though nerve conduction and EMG tests are negative. But nobody seems to be able to reduce the
Pelviccrusader
in
Pelvic Pain Support Network
6 years ago
New here
I have been dealing with Peripheral neuropathy for at least 10 yrs,was on Cymbalta and Lyrica which seemed to work.Recently have stopped taking as many prescriptions as I can for side effect reasons and now the pain has started to come back.Really don’t want to start up on meds again if possible and
I have been dealing with Peripheral neuropathy for at least 10 yrs,was on Cymbalta and Lyrica which seemed to work.Recently have stopped taking as many prescriptions as I can for side effect reasons and now the pain has started to come back.Really don’t want to start up on meds again if possible and
Terry1313
in
Neuropathy Support
6 years ago
MMP Mucous Membrane Pemphigoid...anyone else?
I woke up Tuesday with bumps in my mouth. Went to the periodontist this morning and she gave me this diagnosis. I have to go back in 10 days and she will do a biopsy for confirmation. I also have retinal vasculitis. Does anyone have any experience with this? Thanks
I woke up Tuesday with bumps in my mouth. Went to the periodontist this morning and she gave me this diagnosis. I have to go back in 10 days and she will do a biopsy for confirmation. I also have retinal vasculitis. Does anyone have any experience with this? Thanks
arcr
in
Vasculitis UK
6 years ago
Brain fog
Hi All I’ve heard this term used regularly by bloggers and it is used on official sites but do it is a bit of a ‘catch all’ term! I am not sure if my ‘brain fog’ is the same as other people’s. My ‘brain fog’ occurs sometimes just after my 12 week b12 injection and then somewhere between weeks 6 - 8.
Hi All I’ve heard this term used regularly by bloggers and it is used on official sites but do it is a bit of a ‘catch all’ term! I am not sure if my ‘brain fog’ is the same as other people’s. My ‘brain fog’ occurs sometimes just after my 12 week b12 injection and then somewhere between weeks 6 - 8.
Alfabeta
in
Pernicious Anaemia Society
6 years ago
Undiagnosed nerve pain
Hello. I am 44 years old, male from Sweden. Since October 2015 I've had really distressing nerve pain, most severe in my feet, but also in my face and lower back. I've had 4 neurological investigations (with EMG, nerve conduction studies and thermal thresholds), seen 7 neurologists and 30+ other doctors
Hello. I am 44 years old, male from Sweden. Since October 2015 I've had really distressing nerve pain, most severe in my feet, but also in my face and lower back. I've had 4 neurological investigations (with EMG, nerve conduction studies and thermal thresholds), seen 7 neurologists and 30+ other doctors
JakeBlake
in
Neuropathy Support
6 years ago
Hanna
Hi,new here, i have PA, and i get 2 times a week B12 injections, for over two years now, still i am not much better, numbness in feet, tingling in hands and feet, nerve pain up my legs, i am taking methyl. b 12 but it seems like that does not help. thank you
Hi,new here, i have PA, and i get 2 times a week B12 injections, for over two years now, still i am not much better, numbness in feet, tingling in hands and feet, nerve pain up my legs, i am taking methyl. b 12 but it seems like that does not help. thank you
Muttilina
in
Pernicious Anaemia Society
6 years ago
A new kind of pain
Don't know if my fibro is getting worse or I have developed some kind of neuropathy I've been getting sharp shooting pains in my legs and arms mostly legs instead of my usual burning pain I was borderline diabetic about a year ago and was meant to go a diabetes awareness thingy magig brain fog can't
Don't know if my fibro is getting worse or I have developed some kind of neuropathy I've been getting sharp shooting pains in my legs and arms mostly legs instead of my usual burning pain I was borderline diabetic about a year ago and was meant to go a diabetes awareness thingy magig brain fog can't
Hidden
in
Fibromyalgia Action UK
6 years ago
Numbness not getting better
Hello, About 5 months ago, I came to my primary with some tingles / numbness that kept popping up in my hands and feet. My primary checked my blood levels which was super low. She decided to give me B12 supplments (1000mcg) and I have been taken them since. At the same time, I decided to do a follow
Hello, About 5 months ago, I came to my primary with some tingles / numbness that kept popping up in my hands and feet. My primary checked my blood levels which was super low. She decided to give me B12 supplments (1000mcg) and I have been taken them since. At the same time, I decided to do a follow
onesneakymofo
in
Pernicious Anaemia Society
6 years ago
Hashimoto's neuropathy, Goitre, normal thyroid results- trying ALA, and magnesium spray for neuropathic symptoms
Hi all, Just wanted to ask if any of you suffering from neuropathies have tried magnesium oil spray, and Alpha Lipoic Acid supplements to help treat your condition? After much trawling around on the internet, I've come across many articles and patient reviews on both of the above, with the overall consensus
Hi all, Just wanted to ask if any of you suffering from neuropathies have tried magnesium oil spray, and Alpha Lipoic Acid supplements to help treat your condition? After much trawling around on the internet, I've come across many articles and patient reviews on both of the above, with the overall consensus
DaisyBelle85
in
Thyroid UK
6 years ago
Leg jerks
Has anybody experienced leg jerks or torso jerks while being on lyrica? I have constant almost unstoppable jerks which make me mad!It feels like an electrode is hitting me!These jerks give me pain at my lower left leg.I could also describe them as tics.
Has anybody experienced leg jerks or torso jerks while being on lyrica? I have constant almost unstoppable jerks which make me mad!It feels like an electrode is hitting me!These jerks give me pain at my lower left leg.I could also describe them as tics.
Katerina22
in
Restless Legs Syndrome
6 years ago
Has anyone tried Pentazocine for pain
Has anyone been prescribed Pentazocine for pain? My doc has taken me off co-codomol as he believes this is giving me the bad headaches I have experienced for the past week although I am not convinced. Just wondered if this med is any good? Many thanks
Has anyone been prescribed Pentazocine for pain? My doc has taken me off co-codomol as he believes this is giving me the bad headaches I have experienced for the past week although I am not convinced. Just wondered if this med is any good? Many thanks
June56
in
Fibromyalgia Action UK
6 years ago
Acupuncture has really helped
I have rls and peripheral neuropathy, which means awful sleep and waking constantly with restless legs and hands swollen and tingly. 2 days ago I had acupuncture with a knowledgeable Chinese lady. I’ve had two great nights sleep and my fingers felt normal in the morning. She put needles in my neck, back
I have rls and peripheral neuropathy, which means awful sleep and waking constantly with restless legs and hands swollen and tingly. 2 days ago I had acupuncture with a knowledgeable Chinese lady. I’ve had two great nights sleep and my fingers felt normal in the morning. She put needles in my neck, back
callistodevi
in
Restless Legs Syndrome
6 years ago
Anyone suffering with neuropathy ?
I need help from anyone who is also suffering with neuropathy, mine hands, legs, feet. Any suggestions most welcomed. Been to 4 different neurologists practices, no help? Had this problem before treatment.
I need help from anyone who is also suffering with neuropathy, mine hands, legs, feet. Any suggestions most welcomed. Been to 4 different neurologists practices, no help? Had this problem before treatment.
Njsailorgirl
in
CLL Support
6 years ago
Advice B vitamins
Hi everyone, I have just finished my 6 loading doses of B12 injections. I gather I should have taken Folic Acid once started with them but I didn't realise at the time. I have in the cupboard some Vitamin B tablets and I wonder of you could advise whether they are suitable to take. Each tablet contains
Hi everyone, I have just finished my 6 loading doses of B12 injections. I gather I should have taken Folic Acid once started with them but I didn't realise at the time. I have in the cupboard some Vitamin B tablets and I wonder of you could advise whether they are suitable to take. Each tablet contains
Tanzanite55
in
Pernicious Anaemia Society
6 years ago
Telangiectasia
Good morning all. I have servers telangietasia on my face and hands, over the past few weeks i have developed many on y tongue and inner mouth, I did have a couple spring up about a year ago and there's been no trouble but now, the pain of them when I eat or drink is horrendous, I'm losing a !ot of
Good morning all. I have servers telangietasia on my face and hands, over the past few weeks i have developed many on y tongue and inner mouth, I did have a couple spring up about a year ago and there's been no trouble but now, the pain of them when I eat or drink is horrendous, I'm losing a !ot of
Joanne_Evans030365
in
Scleroderma & Raynaud's UK (SRUK)
6 years ago
Neuropathy --- my story!!
I've been reading a lot of posts on the topic of Neuropathy and I find the one common thread seems to be... WE ARE NOT ALONE!!! We are all suffering, in some form or to some degree with this incurable disease. We are never going to get rid of it; we can only try to manage it by whatever means works best
I've been reading a lot of posts on the topic of Neuropathy and I find the one common thread seems to be... WE ARE NOT ALONE!!! We are all suffering, in some form or to some degree with this incurable disease. We are never going to get rid of it; we can only try to manage it by whatever means works best
Ameka
in
Foggy's "Invisible Illness" Support
6 years ago
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