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steroid injection for back pain with pain team?
hello, I have had back pain for as long as I remember however 3 years ago was the first episode of severe spasm in my whole back making me collapse and couldn’t be moved for hours. I was put on gabapentin for 2.5 years which I have tapered off because I’m not sure the problem was nerve pain and the mri
hello, I have had back pain for as long as I remember however 3 years ago was the first episode of severe spasm in my whole back making me collapse and couldn’t be moved for hours. I was put on gabapentin for 2.5 years which I have tapered off because I’m not sure the problem was nerve pain and the mri
Louiseelaine
in
Stanmore Young Spine Group
7 months ago
Low BP in afib and covid
After all the years I have finally caught COVID. Had a headache for a couple of days which has gone now. Not much coughing, just feel a bit achy and weak.Unfortunately, it's sent me into an afib episode although my heart rate is staying below 100bpm in fact it's hovering around 70 to 80bpm. I was concerned
After all the years I have finally caught COVID. Had a headache for a couple of days which has gone now. Not much coughing, just feel a bit achy and weak.Unfortunately, it's sent me into an afib episode although my heart rate is staying below 100bpm in fact it's hovering around 70 to 80bpm. I was concerned
Karendeena
in
AF Association
6 months ago
Rash any advice?
I have noticed this rash over last 2 or 3 months. Its not itchy or raised. Any advice most welcome. Im taking 100mcg teva levo and 15mcg thybon henning. Vit d, magnesium glycinate. Any advice most welcome 🌸🌸🌸🌸🌸
I have noticed this rash over last 2 or 3 months. Its not itchy or raised. Any advice most welcome. Im taking 100mcg teva levo and 15mcg thybon henning. Vit d, magnesium glycinate. Any advice most welcome 🌸🌸🌸🌸🌸
Geegee777
in
Thyroid UK
8 months ago
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sjogens?
I have post PV Myelofibrosis. When I was dx with PV I took Pegasys from April 22 @ 45mg then 60mg then 90mg fortnightly. (On Jakavi since August 23) So took Pegasys for about 16 months After a couple of months on Pegasys I started to experience close vision problems which could not be corrected with
I have post PV Myelofibrosis. When I was dx with PV I took Pegasys from April 22 @ 45mg then 60mg then 90mg fortnightly. (On Jakavi since August 23) So took Pegasys for about 16 months After a couple of months on Pegasys I started to experience close vision problems which could not be corrected with
Yanico
in
MPN Voice
8 months ago
shingles vaccine
Hi folks This is a brilliant site has keep me steady since my husband’s diagnosis of SLL now CLL. My Husband had been W&W for 6 years, now on acalabrutinib for two years with no side affect and doing well. He has been offered the shingles vaccine but he hasn’t had chickenpox’s, is it safe to get the
Hi folks This is a brilliant site has keep me steady since my husband’s diagnosis of SLL now CLL. My Husband had been W&W for 6 years, now on acalabrutinib for two years with no side affect and doing well. He has been offered the shingles vaccine but he hasn’t had chickenpox’s, is it safe to get the
Charles4
in
CLL Support
8 months ago
questions
In the summer, I noticed sporadic noises in one ear. It only happened at night, when lying down to sleep. It was almost like a deep and faint squeak. It lasted 2 days and went away. Months later, after developing a sinus cold, it returned. I did not react immediately as I thought it would pass. After
In the summer, I noticed sporadic noises in one ear. It only happened at night, when lying down to sleep. It was almost like a deep and faint squeak. It lasted 2 days and went away. Months later, after developing a sinus cold, it returned. I did not react immediately as I thought it would pass. After
Healthymetoday
in
Tinnitus UK
6 months ago
lung nodule / proposed surgery / scared and confused
Hello, thank you for this site. My best to all on this site for health and happiness. I’m not even sure where I may be at on this journey but am certainly scared and confused . In March of 2022 I had a kidney stone and a lung nodule was detected on right lower lobe and suggested follow up in 3 -6 months
Hello, thank you for this site. My best to all on this site for health and happiness. I’m not even sure where I may be at on this journey but am certainly scared and confused . In March of 2022 I had a kidney stone and a lung nodule was detected on right lower lobe and suggested follow up in 3 -6 months
ghostyinmass
in
Lung Cancer Support
6 months ago
Nose sprays for colds etc
I feel as if a have a cold brewing. Some time ago there were posts of a spray used in nose. Flu Guard ? I am not sure. I think a Vick one too. Could anyone advise please. Wish to nip in the bud. Thank you.
I feel as if a have a cold brewing. Some time ago there were posts of a spray used in nose. Flu Guard ? I am not sure. I think a Vick one too. Could anyone advise please. Wish to nip in the bud. Thank you.
Dottie11
in
Lung Conditions Community Forum
6 months ago
Biologic with covid
Testing positive for covid and am am taking a biologic.Like my head the info is a bit wooly, but I think it maybe that I should suspend the biologic until covid test is negative. Presume this is correct as i think it should make sense. Is anyone in similar circumstances able to confirm or otherwise?
Testing positive for covid and am am taking a biologic.Like my head the info is a bit wooly, but I think it maybe that I should suspend the biologic until covid test is negative. Presume this is correct as i think it should make sense. Is anyone in similar circumstances able to confirm or otherwise?
Wantplaytennis
in
NRAS
6 months ago
Unexplained increase in mortality rates
I'd like to begin by saying I'm not a conspiracy theorist by any stretch of the imagination but having heard so many stories (mostly first hand and through personal experience) since the outbreak of Covid in Jan 2020 I am beginning to question what's going on. A recent publication in LANCET, no less
I'd like to begin by saying I'm not a conspiracy theorist by any stretch of the imagination but having heard so many stories (mostly first hand and through personal experience) since the outbreak of Covid in Jan 2020 I am beginning to question what's going on. A recent publication in LANCET, no less
SuperSanta
in
British Heart Foundation
6 months ago
covid 19 and Funcational Gait Disorder
Hi All I’ve had Funcational Gait disorder for 12 long years now, so cannot walk very far and rely on my mobility scooter and walking stick to get around. Last Sunday I came down with covid and it seems to have attacked my legs so I’m almost unable to stand let alone walk a few steps. Has anyone else
Hi All I’ve had Funcational Gait disorder for 12 long years now, so cannot walk very far and rely on my mobility scooter and walking stick to get around. Last Sunday I came down with covid and it seems to have attacked my legs so I’m almost unable to stand let alone walk a few steps. Has anyone else
lorettapalmer
in
Functional Neurological Disorder - FND Hope
7 months ago
Hepatic Peliosis (What is it?)
RE: Hepatic Peliosis (What is it?) Hi all, I have been diagnosed with Hepatic Peliosis of the liver. What is it? and is there any treatments please? Does anyone else have Hepatic Peliosis ? How are your dealing with this etc? Any information would be helpful. Thank you. Regards, Kevin Walker
RE: Hepatic Peliosis (What is it?) Hi all, I have been diagnosed with Hepatic Peliosis of the liver. What is it? and is there any treatments please? Does anyone else have Hepatic Peliosis ? How are your dealing with this etc? Any information would be helpful. Thank you. Regards, Kevin Walker
kevpwalker
in
British Liver Trust
5 months ago
Need advice on what to do next!
Recently diagnosed with Hashimotos following endocrinologist appt, which was actually to investigate causes for my hair loss (lost 60% of hair after covid vaccination, then Covid itself in early 2022). Also been suffering other symptoms for around 2 years - weight gain, tired all the time, joint pains
Recently diagnosed with Hashimotos following endocrinologist appt, which was actually to investigate causes for my hair loss (lost 60% of hair after covid vaccination, then Covid itself in early 2022). Also been suffering other symptoms for around 2 years - weight gain, tired all the time, joint pains
ErnieBear
in
Thyroid UK
7 months ago
Methotrexate and sinus/nasal issues
I've been on MTX for a year now and over the months I keep saying I feel like I'm coming down with a cold but it doesn't happen. I get a blockage in the back of my nasal passage and that causes post nasal drip and a sore throat. I was taking sulphasalazine but have stopped that as I felt so tired on
I've been on MTX for a year now and over the months I keep saying I feel like I'm coming down with a cold but it doesn't happen. I get a blockage in the back of my nasal passage and that causes post nasal drip and a sore throat. I was taking sulphasalazine but have stopped that as I felt so tired on
Gottarelax
in
NRAS
8 months ago
post quadruple bypass
I first started having problems in my legs in 2010.I was sent to vascular specialist who stated there was nothing wrong and from that I was sent for heart tests and again I was told there was nothing wrong.The pain was increasing in my right calf and was then in my left calf.I explained I was scared
I first started having problems in my legs in 2010.I was sent to vascular specialist who stated there was nothing wrong and from that I was sent for heart tests and again I was told there was nothing wrong.The pain was increasing in my right calf and was then in my left calf.I explained I was scared
wardywill
in
British Heart Foundation
7 months ago
Covid
Two members of my family have Covid.. My mum is suffering from ET. She bever got vaccinated cos she got scared at that time due to many cases of thrombosis and sudden deaths we had in my country.. Anyone else who hasn't got the vaccine and went through Covid. We were maked and kept distance and all but
Two members of my family have Covid.. My mum is suffering from ET. She bever got vaccinated cos she got scared at that time due to many cases of thrombosis and sudden deaths we had in my country.. Anyone else who hasn't got the vaccine and went through Covid. We were maked and kept distance and all but
PHGR
in
MPN Voice
7 months ago
Hair issues
hi I forgot to ask my rheum nurse about my hair. I’m on methotrexate and seems to be ok with no abnormal hair loss but since taking it I haven’t had my hair highlighted . Anybody advice with this ? I have left message on advice line but wondering others people’s experience. Thanks
hi I forgot to ask my rheum nurse about my hair. I’m on methotrexate and seems to be ok with no abnormal hair loss but since taking it I haven’t had my hair highlighted . Anybody advice with this ? I have left message on advice line but wondering others people’s experience. Thanks
Teddyboy17
in
NRAS
8 months ago
one year olds vaccines
Our grandson aged one is having jabs. I looked up and these are scheduled for one year olds. MMR is a weakened vaccine. Does anyone know if it’s safe to be around him as a immunosuppressed or where to find out in green book please ? Hib/MenC Pneumococcal conjugate vaccine (PCV13) Meningococcal
Our grandson aged one is having jabs. I looked up and these are scheduled for one year olds. MMR is a weakened vaccine. Does anyone know if it’s safe to be around him as a immunosuppressed or where to find out in green book please ? Hib/MenC Pneumococcal conjugate vaccine (PCV13) Meningococcal
Mozart150
in
NRAS
8 months ago
stomach acid
I don't understand this stomach acid 'thing'. I take a proton pump inhibitor for high stomach acid but people insist that as you get older you're stomach acid reduce. I'm 79. Also that doctors erroneously mistake low stomach acid for high!! What is going on? Any thoughts
I don't understand this stomach acid 'thing'. I take a proton pump inhibitor for high stomach acid but people insist that as you get older you're stomach acid reduce. I'm 79. Also that doctors erroneously mistake low stomach acid for high!! What is going on? Any thoughts
fiftyone
in
Thyroid UK
8 months ago
Free Covid Rapid Lateral Flow Test
Does anyone know how to obtain Covid Rapid Lateral Flow Tests free-of-charge in the U.K.? The Gov U.K. site says they are not available direct but are available via your local Pharmacy. None of my local pharmacy stores issue these tests free-of-charge under the NHS but are happy to charge £13 each, even
Does anyone know how to obtain Covid Rapid Lateral Flow Tests free-of-charge in the U.K.? The Gov U.K. site says they are not available direct but are available via your local Pharmacy. None of my local pharmacy stores issue these tests free-of-charge under the NHS but are happy to charge £13 each, even
Richardmint
in
CLL Support
7 months ago
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