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Shingles
Would be keen to hear from anyone with S.L.E. & Shingles. !st time I have had Shingles (S.L.E. 9yrs). A bit surprised at how painful it is & how low I feel. Left side under breast wraps around to spine. On Antivirals & Endep for pain (not making much of a difference) Dr said it may last 3 months. Yikes
Would be keen to hear from anyone with S.L.E. & Shingles. !st time I have had Shingles (S.L.E. 9yrs). A bit surprised at how painful it is & how low I feel. Left side under breast wraps around to spine. On Antivirals & Endep for pain (not making much of a difference) Dr said it may last 3 months. Yikes
Kazunlocked
in
LUPUS UK
6 years ago
Help
Need help..I'm coming off endep and side effects are awful they told me to take 1/2tablet 3 days then mine for 2 then to start my new one which is flouexetine.. any suggestions for coming off one to go on another and what experience has other people had..finding it really hard please help me
Need help..I'm coming off endep and side effects are awful they told me to take 1/2tablet 3 days then mine for 2 then to start my new one which is flouexetine.. any suggestions for coming off one to go on another and what experience has other people had..finding it really hard please help me
cazza1972
in
Anxiety Support
6 years ago
Male hypo's support and advice
I take high dose of
zenpep
enzymes with every meal to provide absorbtion. It's hard to wade through info and support on here as most hypo's are female and struggle with weight issues. I have no eyebrows.
I take high dose of
zenpep
enzymes with every meal to provide absorbtion. It's hard to wade through info and support on here as most hypo's are female and struggle with weight issues. I have no eyebrows.
Jeffreyt
in
Thyroid UK
6 years ago
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Hip pain
I have been recently been diagnosed with severe osteoarthritis in my right hip. The stabbing pain has moved down my right thigh and knee and below that as well. When I put weight on my right leg the sharp pain makes it difficult to stand and walk. I had a CT and full body bone scan because I feared that
I have been recently been diagnosed with severe osteoarthritis in my right hip. The stabbing pain has moved down my right thigh and knee and below that as well. When I put weight on my right leg the sharp pain makes it difficult to stand and walk. I had a CT and full body bone scan because I feared that
Brightman
in
Pain Concern
7 years ago
What do pain management units do?
My rheumy refereed me to the pain management unit at the hospital just over a year ago. I had completely forgotten until I got a letter saying I have to attend a group info session and then they will make an appt. Do they just do group therapy, CBT stuff as I am not interested in that? I also really
My rheumy refereed me to the pain management unit at the hospital just over a year ago. I had completely forgotten until I got a letter saying I have to attend a group info session and then they will make an appt. Do they just do group therapy, CBT stuff as I am not interested in that? I also really
Someonesmother
in
NRAS
7 years ago
Constant Muscle Pain, 10 years and counting, Undiagnosed
I've always had muscle pain but since 2006 when I was told I had mild scoliosis and went to see a Skeletal Massage Therapists....it has only gotten worse every year. Been me I'm already immune to pain killers so that's never been an option for me. Basically I am in pain 24/7 now...and all centered in
I've always had muscle pain but since 2006 when I was told I had mild scoliosis and went to see a Skeletal Massage Therapists....it has only gotten worse every year. Been me I'm already immune to pain killers so that's never been an option for me. Basically I am in pain 24/7 now...and all centered in
Hidden
in
Pain Concern
7 years ago
A seasoned veteran but also new
Hey everyone! I'm new to HealthUnlocked~ The name's Keira. Average mid twenties nerdy artsy aussie female with a love of learning and adventure...which has all had to stop with the growing number of health related issues that have grown. Bit of a veteran with dealing with health declines as I do have
Hey everyone! I'm new to HealthUnlocked~ The name's Keira. Average mid twenties nerdy artsy aussie female with a love of learning and adventure...which has all had to stop with the growing number of health related issues that have grown. Bit of a veteran with dealing with health declines as I do have
Hidden
in
IBS Network
7 years ago
Vasculitis
Hi I live in Townsville in Australia and have an auto immune condition Vasculitis. I have had Peripheral Vasculitis for two years and have a ride of symptoms and experiences. I went from working a full time hectic job to one day experiencing what they called " dropped foot" to having to stop working
Hi I live in Townsville in Australia and have an auto immune condition Vasculitis. I have had Peripheral Vasculitis for two years and have a ride of symptoms and experiences. I went from working a full time hectic job to one day experiencing what they called " dropped foot" to having to stop working
Vrainbird
in
Vasculitis UK
8 years ago
Madapor & endep
Hi My mum has PD and has been presribed 50mg of madapar 3 times a day with Endep for headaches / depression. She is constantly getting nausea and headaches and is in bed most of the day . Does any one take this medication and if this is normal.. Any alternatives from the above would be appreciated Thanks
Hi My mum has PD and has been presribed 50mg of madapar 3 times a day with Endep for headaches / depression. She is constantly getting nausea and headaches and is in bed most of the day . Does any one take this medication and if this is normal.. Any alternatives from the above would be appreciated Thanks
PSZ28
in
Cure Parkinson's
8 years ago
Migraines and medical marijuana
Hi there, has anyone tried medical marijuana for migraines? I read a scientific report online from the New Scientist claiming the data is not complete yet to produce concrete proof of its pain reduction capacity. I did however, read it is good for neuropathic pain. So are migraines technically neuropathic
Hi there, has anyone tried medical marijuana for migraines? I read a scientific report online from the New Scientist claiming the data is not complete yet to produce concrete proof of its pain reduction capacity. I did however, read it is good for neuropathic pain. So are migraines technically neuropathic
Claudeminh
in
National Migraine Centre
8 years ago
CRPS
Hello everyone. I am new to this, i have recently been diagnosed with CRPS of the right foot, pain mainly radiating to the big toe, ball of my foot and side of my foot. This happend after id been in an induced coma for one week and then hospital for an extra week bedbound. I straight away upon discharge
Hello everyone. I am new to this, i have recently been diagnosed with CRPS of the right foot, pain mainly radiating to the big toe, ball of my foot and side of my foot. This happend after id been in an induced coma for one week and then hospital for an extra week bedbound. I straight away upon discharge
Tanjaaa
in
Pain Concern
8 years ago
Confusion
Hi, I'm new to this site but was wondering if anyone is taken Thyroxine and Endep (amitriptyline) and if so if they've had any side effects like confusion and brain processing. I had radioactive iodine treatment for an overactive thyroid 25 years ago and since then have been on 100mg thyroxine daily.
Hi, I'm new to this site but was wondering if anyone is taken Thyroxine and Endep (amitriptyline) and if so if they've had any side effects like confusion and brain processing. I had radioactive iodine treatment for an overactive thyroid 25 years ago and since then have been on 100mg thyroxine daily.
Jac66
in
Thyroid UK
8 years ago
I'm scared and don't know how I'll cope on a 5 day camp!
Hi everyone I recently joined here to share my story with people who understand what im going through. When I was 10 I was vomiting a lot and having horrible pains, so bad that I had a term off school. During this time I was going back and forth to hospital under going tests until nothing come back after
Hi everyone I recently joined here to share my story with people who understand what im going through. When I was 10 I was vomiting a lot and having horrible pains, so bad that I had a term off school. During this time I was going back and forth to hospital under going tests until nothing come back after
Flower58
in
Endometriosis UK
8 years ago
Rectal muscle spasm
Hi! I am suffering from what appears to be a rectal muscle spasm. I have extreme pain following a BM sometimes lasting up to 8 hours. Lying down is the only thing to take the edge off the pain. In desperation I had Botox injected in November. I seemed worse following the Botox procedure but was told
Hi! I am suffering from what appears to be a rectal muscle spasm. I have extreme pain following a BM sometimes lasting up to 8 hours. Lying down is the only thing to take the edge off the pain. In desperation I had Botox injected in November. I seemed worse following the Botox procedure but was told
Hidden
in
Pelvic Pain Support Network
9 years ago
Migraines from viral meningitis
Dear all, I had viral meningitis in October 2012 and its nearly 3 years after now! I have chronic migraines from the VM and have had for over 2 years. Off and on. Sometimes more on than off. I am trying botox injections from my neurologist every 3 months as well as daily propranolol and endep. Just wondering
Dear all, I had viral meningitis in October 2012 and its nearly 3 years after now! I have chronic migraines from the VM and have had for over 2 years. Off and on. Sometimes more on than off. I am trying botox injections from my neurologist every 3 months as well as daily propranolol and endep. Just wondering
Claudeminh
in
Meningitis Now
9 years ago
Weight loss and Fibromyalgia
Hello, I'm wondering if anyone knows of any good ways to lose weight with Fibromyalgia? I've gained 20kg in the past 2 years, and It's really making me feel more depressed :/ I also don't have much money to do certain things :/ Any ideas? p.s I am on Endep, Lexapro, Norimin and Atenalol, but recently
Hello, I'm wondering if anyone knows of any good ways to lose weight with Fibromyalgia? I've gained 20kg in the past 2 years, and It's really making me feel more depressed :/ I also don't have much money to do certain things :/ Any ideas? p.s I am on Endep, Lexapro, Norimin and Atenalol, but recently
KeiraT
in
Fibromyalgia Action UK
10 years ago
Living with CRPS Type 2
I'm male 42yr old panelbeater who cut my fingers at work accident 18 months ago. Deep cuts severing nerves. Had swelling initially with burning and stabbing pain. To cut a long story short I'm In AGONY all the time now. My fingers and wrist are contracted and deformed and I have 20/10 nerve pain every
I'm male 42yr old panelbeater who cut my fingers at work accident 18 months ago. Deep cuts severing nerves. Had swelling initially with burning and stabbing pain. To cut a long story short I'm In AGONY all the time now. My fingers and wrist are contracted and deformed and I have 20/10 nerve pain every
rrusty71
in
Action on Pain
10 years ago
Had a phone call from rhuemy yesterday conserning positive anti RNP
Have been told that need to have more tests done but she said looks as though i have a CTD of some kind she reassured me that because all other tests have come back negative is a good thing. At my first appointment she informed me osteo and more likely fibro so put me on endep and (celebrex to use
Have been told that need to have more tests done but she said looks as though i have a CTD of some kind she reassured me that because all other tests have come back negative is a good thing. At my first appointment she informed me osteo and more likely fibro so put me on endep and (celebrex to use
Hopey
in
LUPUS UK
10 years ago
I can go on Topamax or endep for treatment of my migraines which occur weekly, which will work more quickly at reducing the migraines?
westie49
in
National Migraine Centre
10 years ago
Soula’s PN Weather Update
Posted by soula in About, My pain on http://www.pudendalnerve.com.au/2013/09/21/soulas-pn-weather-update/ Soula's PN Weather ReportIt’s been a while since I posted a personal update but it’s probably accurate to say that PN’s weather patterns need to be documented seasonally. I mostly have turbulence
Posted by soula in About, My pain on http://www.pudendalnerve.com.au/2013/09/21/soulas-pn-weather-update/ Soula's PN Weather ReportIt’s been a while since I posted a personal update but it’s probably accurate to say that PN’s weather patterns need to be documented seasonally. I mostly have turbulence
Hidden
in
Pelvic Pain Support Network
11 years ago
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