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Shingles vaccine
Hi, has anyone had the shingles vaccine, I have had shingles 5 times over the years and have been advised to have the vaccine, bit worried about possible reaction?Thanx
Hi, has anyone had the shingles vaccine, I have had shingles 5 times over the years and have been advised to have the vaccine, bit worried about possible reaction?Thanx
Den73
in
PMRGCAuk
8 months ago
Rheumatoid Meningitis Recovery
Has anyone out there had rheumatoid meningitis? I was recently treated for it and am looking for others who have had this experience or just experience with recovering from aseptic meningitis in general. I was diagnosed with RF positive RA in 2012. My disease has been stable on Cimzia for 6+ years.
Has anyone out there had rheumatoid meningitis? I was recently treated for it and am looking for others who have had this experience or just experience with recovering from aseptic meningitis in general. I was diagnosed with RF positive RA in 2012. My disease has been stable on Cimzia for 6+ years.
ChiChiCo
in
Meningitis Now
1 year ago
Shingles vaccine
Has anyone on methotrexate and infliximab had the shingles vaccine ? Do you have to get it every year ?
Has anyone on methotrexate and infliximab had the shingles vaccine ? Do you have to get it every year ?
Grounsel
in
NRAS
8 months ago
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Advice please...
My fibro always gets worse in cold weather so bath soaks are my best friends at the moment, however, my boiler and heating stopped working few days ago, I called my housing association and they fixed the heaters, but for hot water I was told its not considered emergency as you can boil kettles of water
My fibro always gets worse in cold weather so bath soaks are my best friends at the moment, however, my boiler and heating stopped working few days ago, I called my housing association and they fixed the heaters, but for hot water I was told its not considered emergency as you can boil kettles of water
YMEPLEASE
in
Fibromyalgia Action UK
3 months ago
PBC and nails / gel polish / acrylic
hi everyone, just a quick question.. I wondered has anyone had any issues with having their nails done with gel polish. I had to switch from gel polish to acrylic as my nails kept having a reaction to the gel - and often developed a fungal infection. Once I switched to acrylic they were much better
hi everyone, just a quick question.. I wondered has anyone had any issues with having their nails done with gel polish. I had to switch from gel polish to acrylic as my nails kept having a reaction to the gel - and often developed a fungal infection. Once I switched to acrylic they were much better
Deemum
in
PBC Foundation
3 months ago
Question on tapering
Everytime I start reducing my pred I develop a Cold sore on my lip, does an yone else have this problem?
Everytime I start reducing my pred I develop a Cold sore on my lip, does an yone else have this problem?
Kiwisufferer2019
in
PMRGCAuk
5 months ago
lupus and shingles
Hey guys, I hope you’re all keeping safe and well. Just wondering if anyone has any tips or advice on how to manage having lupus and shingles! I got diagnosed on Wednesday and it’s safe to say I’m suffering a bit. Is there anything I should be looking out for? Avoiding? Thanks in advance!
Hey guys, I hope you’re all keeping safe and well. Just wondering if anyone has any tips or advice on how to manage having lupus and shingles! I got diagnosed on Wednesday and it’s safe to say I’m suffering a bit. Is there anything I should be looking out for? Avoiding? Thanks in advance!
Krishny18
in
LUPUS UK
1 year ago
More red spots on nails
Still don't know what these are. Anyone else get them?
Still don't know what these are. Anyone else get them?
Brychni
in
NRAS
6 months ago
Lyme Disease
Hello, I hope everyone is feeling as well as possible. Can I ask about links between Lyme Disease and RA? What is actually known? My daughter was talking about ticks the other day (we are both walkers) when I said I had had (in my late teens) a bullseye mark from a tick on my leg, she said ‘well that
Hello, I hope everyone is feeling as well as possible. Can I ask about links between Lyme Disease and RA? What is actually known? My daughter was talking about ticks the other day (we are both walkers) when I said I had had (in my late teens) a bullseye mark from a tick on my leg, she said ‘well that
Lyndy
in
NRAS
10 months ago
shingles vaccine
no you can't have the shingles as it is a live vaccine. You don't get offered the shingles vaccine until you are 70
no you can't have the shingles as it is a live vaccine. You don't get offered the shingles vaccine until you are 70
bunnycaramel
in
NRAS
10 months ago
Shingles Vaccine
I have RA and am currently taking hydroxychloroquin, methotrexate and amgevita. I’m trying to work out whether at age 61 with a compromised immune system, I will qualify for the new shingrix (shingles non-live) vaccine on the NHS? Does anyone know?
I have RA and am currently taking hydroxychloroquin, methotrexate and amgevita. I’m trying to work out whether at age 61 with a compromised immune system, I will qualify for the new shingrix (shingles non-live) vaccine on the NHS? Does anyone know?
CagneysMum
in
NRAS
10 months ago
whenever i raise euthyrox100mg i get hbp headache nausea
is two weeks now i raised euthyrox from 75 yo 100mg and i dont think i can tolerate twice i tried and got hbp that even pills dont take it down
is two weeks now i raised euthyrox from 75 yo 100mg and i dont think i can tolerate twice i tried and got hbp that even pills dont take it down
morcan54
in
Thyroid UK
13 days ago
Shingles Vaccine
Shingles Vaccine From September 2023 you will be eligible for vaccine from age 65. Advertised on TV yesterday Rose
Shingles Vaccine From September 2023 you will be eligible for vaccine from age 65. Advertised on TV yesterday Rose
Rose54
in
PMRGCAuk
10 months ago
Separation/Divorce
Hi all, My husband and I are separating due to me having a brain cancer surgery injury. Can you recommend solicitors that are/have been really helpful with this sort of thing? Thanks in advance
Hi all, My husband and I are separating due to me having a brain cancer surgery injury. Can you recommend solicitors that are/have been really helpful with this sort of thing? Thanks in advance
NewGoldie
in
Headway
2 months ago
Treatment has hit a wall. I can not sit without pain.
I have not been able to sit without horrid pain since August. I did too much — and I have not recovered. On top of that, the nerve blocks I have been getting to try to help this pain for years, like pudendal nerve block, trigger point injections into my pelvic floor, si joint injections, and caudal injections
I have not been able to sit without horrid pain since August. I did too much — and I have not recovered. On top of that, the nerve blocks I have been getting to try to help this pain for years, like pudendal nerve block, trigger point injections into my pelvic floor, si joint injections, and caudal injections
kellerfly
in
Pelvic Pain Support Network
13 days ago
Nerve damage
Since my carpal tunnel, cubitunnel and median nerve surgery 2 years ago, I have experienced horrible, constant seeking nerve pain in my left arm. My hand is deformed and I have no use of my arm and hand. After 2 hand surgeons, 2 PT's and a neurologist, all of whom said there was nothing they could do
Since my carpal tunnel, cubitunnel and median nerve surgery 2 years ago, I have experienced horrible, constant seeking nerve pain in my left arm. My hand is deformed and I have no use of my arm and hand. After 2 hand surgeons, 2 PT's and a neurologist, all of whom said there was nothing they could do
mariootsi
in
Neuropathy Support
13 days ago
Pain management pudendal neuralgia
I had a fall from height 11 months ago. Struggling to get anywhere with medical professionals, there is no urgency & I have been made to feel neurotic at times. I’m finding the ones I have seen don’t really know about PN. My osteopath suspected PN in October & GP referred me to MSK spinal specialist
I had a fall from height 11 months ago. Struggling to get anywhere with medical professionals, there is no urgency & I have been made to feel neurotic at times. I’m finding the ones I have seen don’t really know about PN. My osteopath suspected PN in October & GP referred me to MSK spinal specialist
Chocolategrigio
in
Pelvic Pain Support Network
1 month ago
Pudendal nerve block
Has anyone had a pudendal nerve block? My endo specialist wants to give it ago to see if it offers me any relief from the chronic pelvic pain? I'm scared
Has anyone had a pudendal nerve block? My endo specialist wants to give it ago to see if it offers me any relief from the chronic pelvic pain? I'm scared
En89
in
Endometriosis UK
1 month ago
Need Relief
I have been experiencing pancreatic pain for 6 mos now. Have been to the ED 5 times in that time period. I thought I knew what pain was with my lower back issues - but I was unfortunately mistaken. During these acute pancreatic episodes - the best way to describe the pain is to say that I was out of
I have been experiencing pancreatic pain for 6 mos now. Have been to the ED 5 times in that time period. I thought I knew what pain was with my lower back issues - but I was unfortunately mistaken. During these acute pancreatic episodes - the best way to describe the pain is to say that I was out of
TVspike
in
Chronic Pancreatitis Support
1 month ago
An update
Several months ago, I wrote on here ‘A while back, I was seen by a lady at the pain clinic, who said that I have ‘Scoliosis convex to the right with minor anterior vertebral body height loss at T12, L3 and L4. Disc space narrowing at the lumbosacral level with hypertrophy of the lower lumbar facet joints
Several months ago, I wrote on here ‘A while back, I was seen by a lady at the pain clinic, who said that I have ‘Scoliosis convex to the right with minor anterior vertebral body height loss at T12, L3 and L4. Disc space narrowing at the lumbosacral level with hypertrophy of the lower lumbar facet joints
DollyDutchGirl
in
Pain Concern
1 month ago
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