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Tongue / Graves disease
Can the thyroid affect the tongue? I was borderline again last time and have a blood test end of Feb due to be discharged if ok but I think as I keep being borderline they're not sure what to do with me. As to whether my body is naturally on borderline as I don't really get many of the symptoms Mild
Can the thyroid affect the tongue? I was borderline again last time and have a blood test end of Feb due to be discharged if ok but I think as I keep being borderline they're not sure what to do with me. As to whether my body is naturally on borderline as I don't really get many of the symptoms Mild
kittyelen
in
Thyroid UK
8 months ago
lidocaine infusion?
Good afternoon everyone. I have Occipital/Trigeminal Neuralgia and have had a variety of treatments for the past 7 years. Most recently a nerve block which went wrong and left me in worse pain. My last option is a lidocaine infusion which I am waiting for. I take Pregablin/codeine/migraine meds etc
Good afternoon everyone. I have Occipital/Trigeminal Neuralgia and have had a variety of treatments for the past 7 years. Most recently a nerve block which went wrong and left me in worse pain. My last option is a lidocaine infusion which I am waiting for. I take Pregablin/codeine/migraine meds etc
armao
in
Pain Concern
1 year ago
All About myself Indeed
My name is John Stefan and I am from London. I do Live in Peterborough and I have been Living in Peterborough for a very Long time since 2008. Before that I moved from Place to Place but have been settled Here in Peterborough since the above named year Indeed. Also I am a Christian and I have been studying
My name is John Stefan and I am from London. I do Live in Peterborough and I have been Living in Peterborough for a very Long time since 2008. Before that I moved from Place to Place but have been settled Here in Peterborough since the above named year Indeed. Also I am a Christian and I have been studying
Hidden
in
Mencap
8 months ago
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Support after Diagnosis and advice
I've had my diagnosis now of chronic pain and fibromyalgia last week over a very lengthy appointment, still in loads of pain and even morning stiffness and aches, no mention of using a walking aid if I really need it. we discussed pain relief which after the nurse decided to stay on paracetamol until
I've had my diagnosis now of chronic pain and fibromyalgia last week over a very lengthy appointment, still in loads of pain and even morning stiffness and aches, no mention of using a walking aid if I really need it. we discussed pain relief which after the nurse decided to stay on paracetamol until
Kat32A
in
Fibromyalgia Action UK
8 months ago
Viral Meningitis
Dear all,I am from Germany but I did not find any useful forums where I can read about similar syptoms and post meningitis peoblems! I had meningitis and was brought in hospital on 16.3 with a painful headache and fever.luckily the next day a doctor said he wants to do a „puncture“ to be sure it is not
Dear all,I am from Germany but I did not find any useful forums where I can read about similar syptoms and post meningitis peoblems! I had meningitis and was brought in hospital on 16.3 with a painful headache and fever.luckily the next day a doctor said he wants to do a „puncture“ to be sure it is not
Walkingintheforest
in
Meningitis Now
1 year ago
Aciclovir as prevention for shingles
I wish to express my deepest thanks to all fellow members who have responded to my recent enquiry. There has been consensus in all replies confirming that prescribing Aciclovir is standard practice.
I wish to express my deepest thanks to all fellow members who have responded to my recent enquiry. There has been consensus in all replies confirming that prescribing Aciclovir is standard practice.
RamsesII
in
CLL Support
7 months ago
Sciatica
Hi all. I have been suffering with back pain for several years. In regards to medication, you name it, I've tried it. I've have two lots of steroid injections which had no effect whatsoever and then finally in 2022 I had radio frequency ablation which was brilliant. I had instant relief from this. I
Hi all. I have been suffering with back pain for several years. In regards to medication, you name it, I've tried it. I've have two lots of steroid injections which had no effect whatsoever and then finally in 2022 I had radio frequency ablation which was brilliant. I had instant relief from this. I
Stormtrooper4
in
Pain Concern
8 months ago
I had b12 injections stopped during covid I’m now getting them again
I was diagnosed with pernicious anemia many years ago I was put on b12 injections,some years later I started experiencing numbness in my left leg burning sensation in my hands was sent to see a neurologist who did MRI scans and told there was degeneration in the nerves in my spine which was due to my
I was diagnosed with pernicious anemia many years ago I was put on b12 injections,some years later I started experiencing numbness in my left leg burning sensation in my hands was sent to see a neurologist who did MRI scans and told there was degeneration in the nerves in my spine which was due to my
bigE20
in
Pernicious Anaemia Society
8 months ago
non live shingles vaccine
I will be having my shingles vaccine soon (70 in May) - should I ask for non live vaccine - Shingrax? I take 6 mg of prednisolone a day - GP says live vaccine ok if on less than 7.5 mg but check with nurse - should I go private if GP won’t let offer non live vaccine?
I will be having my shingles vaccine soon (70 in May) - should I ask for non live vaccine - Shingrax? I take 6 mg of prednisolone a day - GP says live vaccine ok if on less than 7.5 mg but check with nurse - should I go private if GP won’t let offer non live vaccine?
Daffodilia
in
PMRGCAuk
2 years ago
what next?
Hello, I was diagnosed with exercise induced asthma in Jan 2022 and since then have tried various inhalers. I’m currently on Luforbec using the MART regime, so twice a day as standard and then when needed before exercise. I’ve also been taking Montelukast for the last six months. However my asthma still
Hello, I was diagnosed with exercise induced asthma in Jan 2022 and since then have tried various inhalers. I’m currently on Luforbec using the MART regime, so twice a day as standard and then when needed before exercise. I’ve also been taking Montelukast for the last six months. However my asthma still
Rosewren
in
Asthma Community Forum
8 months ago
Early signs of PA
I've been giving some thought to how long I've had PA. I was diagnosed about 2 years ago. BUT, when i look back at old photos of myself, my skin colour changed to be quite yellowy (my mum says my dad and his mum both had the yellowy skin tone). This yellowy colour has faded out and I'm much more "white
I've been giving some thought to how long I've had PA. I was diagnosed about 2 years ago. BUT, when i look back at old photos of myself, my skin colour changed to be quite yellowy (my mum says my dad and his mum both had the yellowy skin tone). This yellowy colour has faded out and I'm much more "white
Sailinglady
in
Pernicious Anaemia Society
8 months ago
Should I wait to start my Low Dose Naltrexone (LDN) for the first time if I’ve had a Covid or annual Flu vaccine?
Should I wait to start my Low Dose Naltrexone (LDN) for the first time if I’ve had a Covid or annual Flu vaccine? Answered by Pharmacist Stephen Dickson, LDN Specialist https://youtu.be/KjUKG5O28WA?si=GdB1rjXWdmr5zZ0b
Should I wait to start my Low Dose Naltrexone (LDN) for the first time if I’ve had a Covid or annual Flu vaccine? Answered by Pharmacist Stephen Dickson, LDN Specialist https://youtu.be/KjUKG5O28WA?si=GdB1rjXWdmr5zZ0b
Shewulf
Administrator
in
LDN Research Trust
8 months ago
MS heart disease etc sleeping solid
On an MS flare after month of covid.... i realized how strong i was previous to covid to now flat on floor. It seems true deep sleep is so important. Restoring the muscles....downloading the brain from stresses , Has anyone created thier space for sleep and how? Basically i live in my bed/room so im
On an MS flare after month of covid.... i realized how strong i was previous to covid to now flat on floor. It seems true deep sleep is so important. Restoring the muscles....downloading the brain from stresses , Has anyone created thier space for sleep and how? Basically i live in my bed/room so im
jackiesj
in
Anxiety and Depression Support
8 months ago
Immunocompromised?
Hi everyone I have looked at some pinned articles and still wanted to put this question out there. As a person who is Stage 0, is in W&W who has healthy RBC, Platelets and Immunoglobulin numbers… am I still considered immunocompromised? My WBC number is currently around 34. I work in large crowds
Hi everyone I have looked at some pinned articles and still wanted to put this question out there. As a person who is Stage 0, is in W&W who has healthy RBC, Platelets and Immunoglobulin numbers… am I still considered immunocompromised? My WBC number is currently around 34. I work in large crowds
Audioblender
in
CLL Support
9 months ago
Covid Strikes Again!
I had my second bout of covid just last week. However this time I was mentally ready. My immune systems in tip top shape with the now very healthy diet I eat, full of vitamins and minerals that my body needs. It was mild, with me having a mild temperature for a day and a runny nose for a week. One
I had my second bout of covid just last week. However this time I was mentally ready. My immune systems in tip top shape with the now very healthy diet I eat, full of vitamins and minerals that my body needs. It was mild, with me having a mild temperature for a day and a runny nose for a week. One
natswright
in
Lung Conditions Community Forum
8 months ago
Home at last!
After 2 months (!) in hospital I finally got home on Friday. My hands were very stiff one day, the next I couldn't move them at all. That was very scary. They decided I had a virus, which took a week to get over, then I caught another - I had high temperature and a very phlegmy chest. They also put
After 2 months (!) in hospital I finally got home on Friday. My hands were very stiff one day, the next I couldn't move them at all. That was very scary. They decided I had a virus, which took a week to get over, then I caught another - I had high temperature and a very phlegmy chest. They also put
Kit10
in
My MSAA Community
8 months ago
asthma cough
I’d love it if anyone has any tips for calming an asthma cough without resorting to steroid tablets. It’s only just over a month since my last lot and I’d really like to try and avoid them if possible. It’s driving me and everyone else mad!
I’d love it if anyone has any tips for calming an asthma cough without resorting to steroid tablets. It’s only just over a month since my last lot and I’d really like to try and avoid them if possible. It’s driving me and everyone else mad!
Gymbearo
in
Asthma Community Forum
4 months ago
Covid and Uk free tests
Hi I have Covid again after being negative from the first bout 3 weeks again! Haven’t been anywhere so don’t know how its reared its head again, waiting on Respiratory Team to contact me again. In the UK we can get free tests with CLL, anyone got the free ones from the Chemist and what do we need to
Hi I have Covid again after being negative from the first bout 3 weeks again! Haven’t been anywhere so don’t know how its reared its head again, waiting on Respiratory Team to contact me again. In the UK we can get free tests with CLL, anyone got the free ones from the Chemist and what do we need to
uide3095
in
CLL Support
8 months ago
raised euthyrox and i get cough morning night to the point of choking and is strips of pink blood
every morning i get rib throat and cough with strips of pink blood . also wher thyroid is located is sore to swalow and night time i cough same thing all day after the morning i dont cough i just sore when i swallow i dont have cold it feel as if my thyroid swolen up and is making me
every morning i get rib throat and cough with strips of pink blood . also wher thyroid is located is sore to swalow and night time i cough same thing all day after the morning i dont cough i just sore when i swallow i dont have cold it feel as if my thyroid swolen up and is making me
morcan54
in
Thyroid UK
4 months ago
COVID survivors may be at a greater risk of developing Parkinson’s–like symptoms, researchers warn. What to know to protect your health
COVID survivors may be at a greater risk of developing Parkinson’s disease–like symptoms, researchers warn. What you need to know to protect your health
https://finance.yahoo.com/news/covid-survivors-may-greater-risk-170451040.html "The virus was able to infect cells from all the aforementioned
COVID survivors may be at a greater risk of developing Parkinson’s disease–like symptoms, researchers warn. What you need to know to protect your health
https://finance.yahoo.com/news/covid-survivors-may-greater-risk-170451040.html "The virus was able to infect cells from all the aforementioned
Bolt_Upright
in
Cure Parkinson's
8 months ago
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