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ToeNail fungus treatment and Methotrexate
I’ve recently been recommended Curanail by my footcare practitioner for a toe nail fungus condition. I wondered if any one has used this while taking weekly methotrexate, and sometimes Naproxen.My blood test results are all fine and RA is well controlled atm. Looking at the instructions it can take
I’ve recently been recommended Curanail by my footcare practitioner for a toe nail fungus condition. I wondered if any one has used this while taking weekly methotrexate, and sometimes Naproxen.My blood test results are all fine and RA is well controlled atm. Looking at the instructions it can take
L-ttie
in
NRAS
2 months ago
Night Terrors
Good morning everyone, I last posted about my night terrors , so I visited my doctor who changed the 30mg lansoprazole I was taking to 20 Esomeprazole but unfortunately still getting the disturbing night terrors feel so upset this morning the nightmare was so bad last night I was too scared to go
Good morning everyone, I last posted about my night terrors , so I visited my doctor who changed the 30mg lansoprazole I was taking to 20 Esomeprazole but unfortunately still getting the disturbing night terrors feel so upset this morning the nightmare was so bad last night I was too scared to go
lmpieroni
in
Scleroderma & Raynaud's UK (SRUK)
2 months ago
Sepsis - a timely reminder
[i]“The paramedics were reluctant to take me in,” he said. “They thought I should go and see my GP. I could have gone back to sleep. And I would have died I suppose. After a bit of remonstration they agreed [to take me]. No doubt at all Kati saved my life. If we had got there two hours later I would
[i]“The paramedics were reluctant to take me in,” he said. “They thought I should go and see my GP. I could have gone back to sleep. And I would have died I suppose. After a bit of remonstration they agreed [to take me]. No doubt at all Kati saved my life. If we had got there two hours later I would
bennevisplace
in
CLL Support
2 months ago
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Thyroid Dysfunction and PD
So I thought I'd cross-search some of my health challenges and whadyaknow: https://academic.oup.com/cei/article/208/3/372/6578682. Shut your mush and take your Ldopa, though I'm non-responsive. Doc, I'm photophobic, can't open my eyes in the morning ALO, blepharospasm...Read it's predictive years before
So I thought I'd cross-search some of my health challenges and whadyaknow: https://academic.oup.com/cei/article/208/3/372/6578682. Shut your mush and take your Ldopa, though I'm non-responsive. Doc, I'm photophobic, can't open my eyes in the morning ALO, blepharospasm...Read it's predictive years before
Dabaa
in
Cure Parkinson's
2 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
1 year ago
Keeping Pegasys injections cool and monitoring temp
Hi, I have recently been diagnosed with Erdheim-Chester Disease after being treated for many years for an MPN, (ET) I have started on Pegasys Interferon and will be travelling by plane soon (yay) and am looking for advice to keep the injections cool. Does anyone use a fridge (or similar) thermometer
Hi, I have recently been diagnosed with Erdheim-Chester Disease after being treated for many years for an MPN, (ET) I have started on Pegasys Interferon and will be travelling by plane soon (yay) and am looking for advice to keep the injections cool. Does anyone use a fridge (or similar) thermometer
LeoTravels
in
MPN Voice
2 months ago
Kesimpta
Hello, Hope everyone is ok and enjoying some sunshine. Over in the UK we aren't blessed with too much, but at the moment it is very fine :-) Anyhow, I moved over from Tecfidera to Ksimpta around 4 months ago after a particularly nasty relapse last year, and wondered if anyone else has done the same
Hello, Hope everyone is ok and enjoying some sunshine. Over in the UK we aren't blessed with too much, but at the moment it is very fine :-) Anyhow, I moved over from Tecfidera to Ksimpta around 4 months ago after a particularly nasty relapse last year, and wondered if anyone else has done the same
Jasperdoo
in
My MSAA Community
2 months ago
Tremor Assessment
Has anyone had a tremor assessment prior to deep brain stimulation?
Has anyone had a tremor assessment prior to deep brain stimulation?
Ostap
in
Ataxia UK
4 months ago
itch left upper back
a while back someone posted the name of a condition relating to autoimmune illnesses where you have itching on your upper back, left hand side, no rash. It sometimes accompanies autoimmune illnesses. I use Sarna lotion which is what I seem to recall the poster using as well. Anyone remember the name
a while back someone posted the name of a condition relating to autoimmune illnesses where you have itching on your upper back, left hand side, no rash. It sometimes accompanies autoimmune illnesses. I use Sarna lotion which is what I seem to recall the poster using as well. Anyone remember the name
Twopies
in
PMRGCAuk
2 months ago
DBS: Medtronic question re. voice
Hi everyone. As many of you know I had DBS last August. Didn’t reverse my symptoms 5 years as was touted by my neuro but patched me up to fight another couple of rounds. When I was switched on, after a day or so I noticed that it was much harder to speak: volume and articulacy were much harder to produce
Hi everyone. As many of you know I had DBS last August. Didn’t reverse my symptoms 5 years as was touted by my neuro but patched me up to fight another couple of rounds. When I was switched on, after a day or so I noticed that it was much harder to speak: volume and articulacy were much harder to produce
jeeves19
in
Cure Parkinson's
4 months ago
Antibiotics for UTI symptoms
I suspect I have endometriosis after years of painful periods, painful sex and occasional bloating. My symptoms were menstruation specific. The last 2 years I have been almost been symptom free (for some unknown reason) but since Feb I have been having the classic tugging pain from my upper abdomen down
I suspect I have endometriosis after years of painful periods, painful sex and occasional bloating. My symptoms were menstruation specific. The last 2 years I have been almost been symptom free (for some unknown reason) but since Feb I have been having the classic tugging pain from my upper abdomen down
Mint_all_day
in
Endometriosis UK
2 months ago
Shingles
Hi all, My friend has Shingles. With PMR is it advisable to stay away until after breakout. Reading conflicting advice. Much appreciated yet again!! Thank you.
Hi all, My friend has Shingles. With PMR is it advisable to stay away until after breakout. Reading conflicting advice. Much appreciated yet again!! Thank you.
Fredddie
in
PMRGCAuk
1 year ago
Shingles and Ruxolitinib
I note that on the Blood Cancer web site is states that [i]Aciclovir is an anti-viral medication that prevents shingles, which can be a side effect of Ruxolitinib.[/i] [i]If you’re on Ruxolitinib, you have to be careful about your skin,[/i] I was told to be aware and careful of my skin when taking
I note that on the Blood Cancer web site is states that [i]Aciclovir is an anti-viral medication that prevents shingles, which can be a side effect of Ruxolitinib.[/i] [i]If you’re on Ruxolitinib, you have to be careful about your skin,[/i] I was told to be aware and careful of my skin when taking
nanmc
in
MPN Voice
2 months ago
update after Drs app.
saw the Dr who did listen to chest etc. and looked in throat for thrush symptons. He gave me a sputum jar for if it happens again in the next few days ,he wants mr to see the Asthma Nurse ( not much hope there) if it happens again he will send me to see a consult. He also asked who had prescribed the
saw the Dr who did listen to chest etc. and looked in throat for thrush symptons. He gave me a sputum jar for if it happens again in the next few days ,he wants mr to see the Asthma Nurse ( not much hope there) if it happens again he will send me to see a consult. He also asked who had prescribed the
MrsP70
in
Lung Conditions Community Forum
2 months ago
Cold immersion therapy for PC?
Has anyone had experience with using cold immersion, either ice baths or cold showers, to support recovery and treatment side effects?
Has anyone had experience with using cold immersion, either ice baths or cold showers, to support recovery and treatment side effects?
7OaksTom
in
Advanced Prostate Cancer
2 months ago
Insomnia
Hello, I was diagnosed PD when i was 37, now I'm 46 years old. 5 months ago i was DBS. After surgery, things did not go bad, but not as good I have expected. On March 7th i was reajusted the neurostimulator by my neourologist. On March 15th i started HDT Protocol, 50 mg sublingual on alternative days
Hello, I was diagnosed PD when i was 37, now I'm 46 years old. 5 months ago i was DBS. After surgery, things did not go bad, but not as good I have expected. On March 7th i was reajusted the neurostimulator by my neourologist. On March 15th i started HDT Protocol, 50 mg sublingual on alternative days
carlosgarcia2048
in
Cure Parkinson's
4 months ago
update
am now on 15mg norspan patch, this is keeping the leg at a bearable level. I still have to fight the tugging and pulling 24/7 but it is not so severe that I want to end it all when the patch is on. They seem to have given up now and not trying anything else. I have arranged nerve conduction studies
am now on 15mg norspan patch, this is keeping the leg at a bearable level. I still have to fight the tugging and pulling 24/7 but it is not so severe that I want to end it all when the patch is on. They seem to have given up now and not trying anything else. I have arranged nerve conduction studies
Hidden
in
Neuropathy Support
9 months ago
update
I am now on 15mg norspan patch, this is keeping the leg at a bearable level. I still have to fight the tugging and pulling 24/7 but it is not so severe that I want to end it all when the patch is on. They seem to have given up now and not trying anything else. I have arranged nerve conduction studies
I am now on 15mg norspan patch, this is keeping the leg at a bearable level. I still have to fight the tugging and pulling 24/7 but it is not so severe that I want to end it all when the patch is on. They seem to have given up now and not trying anything else. I have arranged nerve conduction studies
Hidden
in
Restless Legs Syndrome
9 months ago
As if MS wasn't enough, I have osteoporosis
HelloAs if MS wasn't enough, I now have osteoporosis. Which could be why I fell and broke my shoulder in December. My primary doctor has put me on boniva. So again I am afraid to take it. Side effects just don't sound l ike fun . I am only 53. I am taking vitamin D and eating 2 tums daily for
HelloAs if MS wasn't enough, I now have osteoporosis. Which could be why I fell and broke my shoulder in December. My primary doctor has put me on boniva. So again I am afraid to take it. Side effects just don't sound l ike fun . I am only 53. I am taking vitamin D and eating 2 tums daily for
jkdavid99
in
My MSAA Community
3 months ago
Itch Relief?
While vacationing last winter, I developed an unbearable itch on my feet. They felt like they were on fire and I was itching so hard I was afraid I’d tear the skin off. I grabbed some aloe vera (for sunburn) and rubbed it on my feet. Instant relief. Certainly easier than jumping in the shower! Hope
While vacationing last winter, I developed an unbearable itch on my feet. They felt like they were on fire and I was itching so hard I was afraid I’d tear the skin off. I grabbed some aloe vera (for sunburn) and rubbed it on my feet. Instant relief. Certainly easier than jumping in the shower! Hope
ILik3Pizza
in
PBC Foundation
3 months ago
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