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More to add to my sh*tshow
Well as if the year hasn't been sh*t enough. I went into AF on Friday night and now on Digoxin and Eliquis blood thinners. This just tops my shitty year off.......I hope these 2 drugs don't make the RLS worse. The universe has really given me a kick in the teeth this year, with spinal surgery resulting
Well as if the year hasn't been sh*t enough. I went into AF on Friday night and now on Digoxin and Eliquis blood thinners. This just tops my shitty year off.......I hope these 2 drugs don't make the RLS worse. The universe has really given me a kick in the teeth this year, with spinal surgery resulting
Hidden
in
Restless Legs Syndrome
7 months ago
Spinal cord stimulation for treatment of neuropathy
I came across the following article: Spinal Cord Stimulation May Help Diabetic Neuropathy A link to the article: https://www.medscape.com/viewarticle/990791?ecd=soc_fb_230419_mscpedt_news_mdscp_stimulation&faf=1 I wondered whether there has been research on spinal cord stimulation for treatment of
I came across the following article: Spinal Cord Stimulation May Help Diabetic Neuropathy A link to the article: https://www.medscape.com/viewarticle/990791?ecd=soc_fb_230419_mscpedt_news_mdscp_stimulation&faf=1 I wondered whether there has been research on spinal cord stimulation for treatment of
WiscGuy
in
Pernicious Anaemia Society
1 year ago
tortuous world of pain
I have no words, I have been to see 2 pain specialists, 2 neurologists for ongoing nerve damage pain, back pain and restless leg pain and symptoms..e.g continual torturing tugging, electric prod like pain and jerking of whole limb. I discovered when I had my last spinal operation that the Buprenorphine
I have no words, I have been to see 2 pain specialists, 2 neurologists for ongoing nerve damage pain, back pain and restless leg pain and symptoms..e.g continual torturing tugging, electric prod like pain and jerking of whole limb. I discovered when I had my last spinal operation that the Buprenorphine
Hidden
in
Neuropathy Support
7 months ago
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Torturous world of RLS
I have no words, I have been to see 2 pain specialists, 2 neurologists for ongoing nerve damage pain, back pain and restless leg pain and symptoms..e.g continual torturing tugging, electric prod like pain and jerking of whole limb. I discovered when I had my last spinal operation that the Buprenorphine
I have no words, I have been to see 2 pain specialists, 2 neurologists for ongoing nerve damage pain, back pain and restless leg pain and symptoms..e.g continual torturing tugging, electric prod like pain and jerking of whole limb. I discovered when I had my last spinal operation that the Buprenorphine
Hidden
in
Restless Legs Syndrome
7 months ago
Bad cold sore should I wait to inject Methotrexate?
I was at the dentist last Thursday - not my usual one - and she was a bit rough! She split my lip in the corner and it's came out with large cold sores which are not healing! 😔 I'm considering not injecting today to give them a better chance to heal - what do you think? They're sore and I can't eat
I was at the dentist last Thursday - not my usual one - and she was a bit rough! She split my lip in the corner and it's came out with large cold sores which are not healing! 😔 I'm considering not injecting today to give them a better chance to heal - what do you think? They're sore and I can't eat
marie66
in
NRAS
17 days ago
Cold & sore throat PAF
hi, I’ve had a cold and cough for 7 days now and having been having AF episodes lasting from 30mins - 5hours almost daily. Normally I would get an episode once a month at worst. Can colds and coughs bring on more regular occurances of AF?
hi, I’ve had a cold and cough for 7 days now and having been having AF episodes lasting from 30mins - 5hours almost daily. Normally I would get an episode once a month at worst. Can colds and coughs bring on more regular occurances of AF?
tom0985
in
Atrial Fibrillation Support
1 month ago
colds and coughs
I am recently diagnosed with RA, I am on immune blockers. And I keep getting colds and coughs. is this due to my immune system being reduced. And is there anything I can do to treat this? Thank you.
I am recently diagnosed with RA, I am on immune blockers. And I keep getting colds and coughs. is this due to my immune system being reduced. And is there anything I can do to treat this? Thank you.
Toiletseat
in
NRAS
1 month ago
Tips for knee pain at 68
Hi everyone, I'm Lyndon. I Woke up Saturday morning with a horrible surprise - knee pain. It's centered on the front left side of my right knee, a dull ache that's been keeping me up at night and making it tough to move around. At 68, I've had my fair share of aches and pains, but this is new territory
Hi everyone, I'm Lyndon. I Woke up Saturday morning with a horrible surprise - knee pain. It's centered on the front left side of my right knee, a dull ache that's been keeping me up at night and making it tough to move around. At 68, I've had my fair share of aches and pains, but this is new territory
LyndonH
in
Pain Concern
1 month ago
new surgery just doesn’t understand.
I have
spinal
cord
injuries
, a below knee amputation and osteoporosis and kyphosis. This new surgery freaked out about the amount of MST I was on so I halved it.
I have
spinal
cord
injuries
, a below knee amputation and osteoporosis and kyphosis. This new surgery freaked out about the amount of MST I was on so I halved it.
MSTKing
in
Pain Concern
1 year ago
Mechanical mitral valve enquiries
Sorry for the long post but please share for me. I'm looking to speak to anyone that has had a Mitral metal heart valve replacement and required another operation specifically spinal surgery. Part of my new surgery requires me to have heperin injections instead of warfarin. I know some people have their
Sorry for the long post but please share for me. I'm looking to speak to anyone that has had a Mitral metal heart valve replacement and required another operation specifically spinal surgery. Part of my new surgery requires me to have heperin injections instead of warfarin. I know some people have their
Lynnsyd2
in
British Heart Foundation
8 months ago
9 years PMR and counting!
Hello all, firstly, I cannot express my gratitude for this site well enough. It has educated me, waylaid my apprehensions and relieved my moments of aloneness - thank you all. My background is ICU nursing and then psychologist in private practice specialising in aged competency issues, head injuries
Hello all, firstly, I cannot express my gratitude for this site well enough. It has educated me, waylaid my apprehensions and relieved my moments of aloneness - thank you all. My background is ICU nursing and then psychologist in private practice specialising in aged competency issues, head injuries
AussieKid
in
PMRGCAuk
8 months ago
Cold sores
Hi looking for ABIT advice, my partner was diagnosed with CLL in 2016 he finished O&V treatment 2022 and all has been well with now 6 monthly review with his consultant. he's recently started to suffer from recurring coldsores and some joint pain that don't seem to be healing, he has no other previous
Hi looking for ABIT advice, my partner was diagnosed with CLL in 2016 he finished O&V treatment 2022 and all has been well with now 6 monthly review with his consultant. he's recently started to suffer from recurring coldsores and some joint pain that don't seem to be healing, he has no other previous
Hd07
in
CLL Support
3 months ago
skin issue
I have had CLL for about four years. I am currently on active surveillance and treatment naive. I had a spinal fusion on July 17 for L4-5 due to Spondylolisthesis. I feel like I’m recovering as well as I can expect from the surgery. My hemoglobin dropped to 10 post surgery so I have been very tired but
I have had CLL for about four years. I am currently on active surveillance and treatment naive. I had a spinal fusion on July 17 for L4-5 due to Spondylolisthesis. I feel like I’m recovering as well as I can expect from the surgery. My hemoglobin dropped to 10 post surgery so I have been very tired but
BlueJk
in
CLL Support
8 months ago
Spinal Cord Stimulator
I am waiting to begin a trial for the Spinal Cord Stimulator. The doctor will put an external wire going up my spinal cord and have a battery pack on my back for a few days. The Stimulator is supposed to stop the lumbar pain from reaching the brain. If it works, the doctor will install an internal stimulator
I am waiting to begin a trial for the Spinal Cord Stimulator. The doctor will put an external wire going up my spinal cord and have a battery pack on my back for a few days. The Stimulator is supposed to stop the lumbar pain from reaching the brain. If it works, the doctor will install an internal stimulator
Kjun54321
in
Pain Concern
1 year ago
Grover’s disease
I have had CLL for about five years. I am currently on active surveillance and treatment naive. I had a spinal fusion on July 17 for L4-5 due to Spondylolisthesis. I feel like I’m recovering as well as I can expect from the surgery. My hemoglobin dropped to 10 post surgery so I have been very tired but
I have had CLL for about five years. I am currently on active surveillance and treatment naive. I had a spinal fusion on July 17 for L4-5 due to Spondylolisthesis. I feel like I’m recovering as well as I can expect from the surgery. My hemoglobin dropped to 10 post surgery so I have been very tired but
BlueJk
in
CLL America Support
8 months ago
still here
Hi All I like to try and update my journey so you can see that there are some longer term survivors. I am still on 0 PSA with advanced cancer. My journey is on my bio. I was diagnosed at 47 and now I’m 54 with no progression. My primary treatment was Zytiga and it is still working. I take a concoction
Hi All I like to try and update my journey so you can see that there are some longer term survivors. I am still on 0 PSA with advanced cancer. My journey is on my bio. I was diagnosed at 47 and now I’m 54 with no progression. My primary treatment was Zytiga and it is still working. I take a concoction
Apollo123
in
Advanced Prostate Cancer
4 months ago
Cold is good for you
Radio 4 currently has a series by Dr Michael Mosley, Cold Therapy. The third episode deals with exercising in the cold. One of his conclusions is that people who run reasonable distances for fun (as opposed to marathons, ultra runners, professionals) have their best performance at around 10-11C. Well
Radio 4 currently has a series by Dr Michael Mosley, Cold Therapy. The third episode deals with exercising in the cold. One of his conclusions is that people who run reasonable distances for fun (as opposed to marathons, ultra runners, professionals) have their best performance at around 10-11C. Well
Yesletsgo
Graduate10
in
Bridge to 10K
4 months ago
PIP Application form (Typing replies)
A little about me.I have been diagnosed with :- Lupus Rheumatoid Arthritis Fibromyalgia Underactive thyroid Hyperparathyrodism Carpal tunnel syndrome Osteoarthritis Depression Lower back spinal fusion Constant huge fatigue and brain fog I am planning on applying for PIP for the first time and
A little about me.I have been diagnosed with :- Lupus Rheumatoid Arthritis Fibromyalgia Underactive thyroid Hyperparathyrodism Carpal tunnel syndrome Osteoarthritis Depression Lower back spinal fusion Constant huge fatigue and brain fog I am planning on applying for PIP for the first time and
SLEepyhead123
in
NRAS
9 months ago
Lori, NURSE
I worked in a homeless program where I worked 70-70 hours a week. I was in a BSN program full time. I caught meningitis from the homeless program. I went from a thriving healthy nurse who got the scholarship for school by being an exemplary Nurse. At first I thought it was a bad flu with light sensitivity
I worked in a homeless program where I worked 70-70 hours a week. I was in a BSN program full time. I caught meningitis from the homeless program. I went from a thriving healthy nurse who got the scholarship for school by being an exemplary Nurse. At first I thought it was a bad flu with light sensitivity
FeelingDesperate
in
Meningitis Now
10 months ago
Colds/flu/viruses and Thyroxine
Just wondering is there any link to having Hashimotos and not having any colds/flu/viruses. The reason I ask is that I never got sick, with the usual colds etc for many years. I just started thyroxine a few months ago. Now I have a really horrible virus, coughing, temperature, flu like symptoms. This
Just wondering is there any link to having Hashimotos and not having any colds/flu/viruses. The reason I ask is that I never got sick, with the usual colds etc for many years. I just started thyroxine a few months ago. Now I have a really horrible virus, coughing, temperature, flu like symptoms. This
Sunflower535
in
Thyroid UK
7 months ago
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