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Spinal cord injuries
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Morphine user
Hi all, I'm new to this page so hope I am able to get some advice. I've been on morphine for about 5 years, now taking 120mg twice daily along with gabapentin and naproxen and others 🙄, I have had failed spinal surgery. I am not getting a break from pain even with everything I'm on and I'm wondering
Hi all, I'm new to this page so hope I am able to get some advice. I've been on morphine for about 5 years, now taking 120mg twice daily along with gabapentin and naproxen and others 🙄, I have had failed spinal surgery. I am not getting a break from pain even with everything I'm on and I'm wondering
Saz2603
in
Action on Pain
4 years ago
Results In !! 150mcgs to 175mcgs Levo
Good Morning All - Well just received the medicheck results from going from a TSH fo 10..and feeling really poorly dated 20 may 2020 to 14 July i waited 10 weeks : I increased my daily 150mcgs to 175mcgs bloods taken 07.30am fasting other than water. Ferritin 125 - (13-50) vitB12 active 150 - (37.5
Good Morning All - Well just received the medicheck results from going from a TSH fo 10..and feeling really poorly dated 20 may 2020 to 14 July i waited 10 weeks : I increased my daily 150mcgs to 175mcgs bloods taken 07.30am fasting other than water. Ferritin 125 - (13-50) vitB12 active 150 - (37.5
Christinah61
in
Thyroid UK
4 years ago
My neuropathy has decreased that It's barley noticeable at times. Stress and inactivity increases it though.
Why? I don't know. I might to start to believe a 100% recovery might be around the corner somewhere. Some changes I've made though, I've increased my injection slightly these past two months. I noticed major change in increasing my exercise regimen followed by ice baths, cold therapy and breathing
Why? I don't know. I might to start to believe a 100% recovery might be around the corner somewhere. Some changes I've made though, I've increased my injection slightly these past two months. I noticed major change in increasing my exercise regimen followed by ice baths, cold therapy and breathing
Geckowacko
in
Pernicious Anaemia Society
4 years ago
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Challenges
Just a thought I want to share. I know most can relate to most of what I’ve written... John 14:27 27 Peace I leave with you; my peace I give you. I do not give to you as the world gives. Do not let your hearts be troubled and do not be afraid. Three years ago, I was diagnosed with MS. Was it a shock
Just a thought I want to share. I know most can relate to most of what I’ve written... John 14:27 27 Peace I leave with you; my peace I give you. I do not give to you as the world gives. Do not let your hearts be troubled and do not be afraid. Three years ago, I was diagnosed with MS. Was it a shock
robster1
in
My MSAA Community
4 years ago
Two years later from near death. PA, low B12.
Two years later after near death experience due to PA. Neuropathy still alive, but changing very SLOWLY and still making progression. I found out a website that sells ampules 5MG (5000ug A.K.A. micro grams) methylcobalamin the good stuff. http://balans-arnhem.ccvshop.nl/Webwinkel-Product-143400297
Two years later after near death experience due to PA. Neuropathy still alive, but changing very SLOWLY and still making progression. I found out a website that sells ampules 5MG (5000ug A.K.A. micro grams) methylcobalamin the good stuff. http://balans-arnhem.ccvshop.nl/Webwinkel-Product-143400297
Geckowacko
in
Pernicious Anaemia Society
4 years ago
New shoes 😁👟👟
Ok so not been on here last week was so busy with my last assignment and finishing uni that i didnt have time for anything, but think my legs were probably grateful for the extra week off to be fair! Finally got my gait analysis done and told i have a really good gait so at least i know it not how i
Ok so not been on here last week was so busy with my last assignment and finishing uni that i didnt have time for anything, but think my legs were probably grateful for the extra week off to be fair! Finally got my gait analysis done and told i have a really good gait so at least i know it not how i
Shar71
Graduate
in
Couch to 5K
4 years ago
Continuous colds
Hi, I'm waiting to see a rheumatologist and have been reading up on lupus. I suffer with constant and what seems like continuous colds, could this have anything to do with lupus. Before bloods showed lupus markers I had visited the gp and they put me on some nasal spray. I used it religiously for about
Hi, I'm waiting to see a rheumatologist and have been reading up on lupus. I suffer with constant and what seems like continuous colds, could this have anything to do with lupus. Before bloods showed lupus markers I had visited the gp and they put me on some nasal spray. I used it religiously for about
Dartsnerd
in
LUPUS UK
4 years ago
Splitting nails & lupus
Morning all, this maybe a silly question but does anybody else suffer from splitting nails? Since being diagnosed with lupus, I have had increased amounts of ridges on them but now the nails are splitting down to the nail bed. Also, my thumb nails are separating, as in, the back of the nail appears to
Morning all, this maybe a silly question but does anybody else suffer from splitting nails? Since being diagnosed with lupus, I have had increased amounts of ridges on them but now the nails are splitting down to the nail bed. Also, my thumb nails are separating, as in, the back of the nail appears to
MoominMomma
in
LUPUS UK
4 years ago
Am I taking too much vitamins?
I have no Idea what the weird numbers mean after it apart from ug. I included these incase it makes sense to someone else. I'm low in Vitamin D and iron , I always have been since a kid. I've only just noticed what each of the packet says , more concerned with taking both the multivitamin and the
I have no Idea what the weird numbers mean after it apart from ug. I included these incase it makes sense to someone else. I'm low in Vitamin D and iron , I always have been since a kid. I've only just noticed what each of the packet says , more concerned with taking both the multivitamin and the
Hidden
in
Fibromyalgia Action UK
4 years ago
Sores in nose - chemotherapy
Apart from a runny nose with chemotherapy (Carboplatin/Pemetrexed) I'm also getting sores that are very similar to cold sores - tried betnovate cream, but not much good, then tried Zovirax which is better, but doesn't clear them and still forms scabs that bleed. It can be very sore and painful. Any
Apart from a runny nose with chemotherapy (Carboplatin/Pemetrexed) I'm also getting sores that are very similar to cold sores - tried betnovate cream, but not much good, then tried Zovirax which is better, but doesn't clear them and still forms scabs that bleed. It can be very sore and painful. Any
MacColl
in
Lung Conditions Community Forum
4 years ago
HAS ANYONE WITH PD HAD SPINAL CORD STIMULATOR IMPLANTED FOR POSTURE CORRECTION,PAIN MODULATION AND MOTOR FUNCTION?
Hi,friends,this procedure might be relatively new. I have read that it is similarly to DBS,but it targets the spinal cord instead of the brain.I was wondering,if anyone had this procedure done,please share your experience. How effective is it?Is it safer ,compared to DBS? Thanks in advance.
Hi,friends,this procedure might be relatively new. I have read that it is similarly to DBS,but it targets the spinal cord instead of the brain.I was wondering,if anyone had this procedure done,please share your experience. How effective is it?Is it safer ,compared to DBS? Thanks in advance.
OREOLU
in
Cure Parkinson's
4 years ago
Triple Inhaled Therapy at Two Glucocorticoid Doses in Moderate-to-Very-Severe COPD.
Triple fixed-dose regimens of an inhaled glucocorticoid, a long-acting muscarinic antagonist (LAMA), and a long-acting β2-agonist (LABA) for chronic obstructive pulmonary disease (COPD) have been studied at single dose levels of inhaled glucocorticoid, but studies at two dose levels are lacking. Triple
Triple fixed-dose regimens of an inhaled glucocorticoid, a long-acting muscarinic antagonist (LAMA), and a long-acting β2-agonist (LABA) for chronic obstructive pulmonary disease (COPD) have been studied at single dose levels of inhaled glucocorticoid, but studies at two dose levels are lacking. Triple
2greys
in
Lung Conditions Community Forum
4 years ago
Swelling feet ,ankles
Hi all ,has anyone found while using Trimbow ,or the likes ect ,have side effects of swollen feet and ankles
Hi all ,has anyone found while using Trimbow ,or the likes ect ,have side effects of swollen feet and ankles
Alice70
in
Lung Conditions Community Forum
4 years ago
Respiratory Deficits and Trans phobia.
Research has shown that transgender individuals with chest binding have abnormal lung function. Co-incidentally, Daniel Radcliffe has become embroiled with the creator of Harry Potter, GK Rowling, in an exchange of on-line differences of opinion about the acceptable definition of what a transgender person
Research has shown that transgender individuals with chest binding have abnormal lung function. Co-incidentally, Daniel Radcliffe has become embroiled with the creator of Harry Potter, GK Rowling, in an exchange of on-line differences of opinion about the acceptable definition of what a transgender person
Cateran
in
Lung Conditions Community Forum
4 years ago
What are the black thick mucus parts coming out of my nose?
Hello pals, I am an asthamtic 27 yro girl for 9 years now, been controlling my symptoms very well. I started to smoke for 4 years now. It's been a month now that my sinuses get dry and blocked at night that i cannot breathe but through my mouth. So I went to the pharmacy and they prescribed a nose
Hello pals, I am an asthamtic 27 yro girl for 9 years now, been controlling my symptoms very well. I started to smoke for 4 years now. It's been a month now that my sinuses get dry and blocked at night that i cannot breathe but through my mouth. So I went to the pharmacy and they prescribed a nose
KhaCB
in
Lung Conditions Community Forum
4 years ago
Staggering Levo, HRT, vit, cod liver oil capsules.
Hi I'm here to ask how should I stagger my medicines. I have hypothyroidism, I'm on levothyroxine, which I take first thing and have started HRT 6 mnths ago plus anti histamines, basically I take them all together in the morning. And I used to take cod lever oil capsules after dinner, now I'm adding
Hi I'm here to ask how should I stagger my medicines. I have hypothyroidism, I'm on levothyroxine, which I take first thing and have started HRT 6 mnths ago plus anti histamines, basically I take them all together in the morning. And I used to take cod lever oil capsules after dinner, now I'm adding
G2-1_g
in
Thyroid UK
4 years ago
Gp stopped my b12 injection and Iv had pernicious anemia 11 years , is this allowed apparently due to new research says my gp
I was refused my b12 injection for PA 18 month ago by my gp apparently new research came to light ,antibodies was negative so I do not require lifelong injections no more :- is this even possible ? I was told when diagnosed 11 year ago it’s lifelong as my body dont absorb it do t matter what oral
I was refused my b12 injection for PA 18 month ago by my gp apparently new research came to light ,antibodies was negative so I do not require lifelong injections no more :- is this even possible ? I was told when diagnosed 11 year ago it’s lifelong as my body dont absorb it do t matter what oral
Ashp24
in
Pernicious Anaemia Society
4 years ago
Anybody tried 'the Breather' device?
Hi all, anybody tried the 'Breather' (https://www.pnmedical.com/product/the-breather/)? I bought it like 11 days ago and have been trying to use it at least 2-3 times a day since. I'm actually struggling to use it the specified amount of times, but am finding it easier to blow into after using setting
Hi all, anybody tried the 'Breather' (https://www.pnmedical.com/product/the-breather/)? I bought it like 11 days ago and have been trying to use it at least 2-3 times a day since. I'm actually struggling to use it the specified amount of times, but am finding it easier to blow into after using setting
DaveT81
in
Lung Conditions Community Forum
4 years ago
Lupus/APS and cod liver oil
Hi, I'm 49, and have lupus with antiphospholipid syndrome. I'm currently on lifelong warfarin, statins, vit D, hydroxychloroquine and methotrexate injections. The inflammatory arthritis is very painful, would cod liver oil be safe to take with anticoagulants? I think the oil would help with the inflammation
Hi, I'm 49, and have lupus with antiphospholipid syndrome. I'm currently on lifelong warfarin, statins, vit D, hydroxychloroquine and methotrexate injections. The inflammatory arthritis is very painful, would cod liver oil be safe to take with anticoagulants? I think the oil would help with the inflammation
Gerardina
in
LUPUS UK
4 years ago
Neuropathy pain and hoping for a spinal cord simulator
Hi there good evening to everyone, can anyone advise me on how and where I can find a hospital in the UK which would hopefully give me a trial for a spinal cord stimulator on the nhs, in so much pain for over a year now, has totally affected my life in every way possible, I was so independent, now I
Hi there good evening to everyone, can anyone advise me on how and where I can find a hospital in the UK which would hopefully give me a trial for a spinal cord stimulator on the nhs, in so much pain for over a year now, has totally affected my life in every way possible, I was so independent, now I
midashomes64
in
Pain Concern
5 years ago
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