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Stem cell and bone marrow transplants
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Bubbles or foam in urine.
Hi, I hope everyone is doing well. I had my kidney transplant about 5 months ago. My urine has always foam or bubbles (I'm not sure) in there. There is also no protein in my urine. My doctor's told me the only way there will be foam in my urine is when there is protein in it. They too find it unusually
Hi, I hope everyone is doing well. I had my kidney transplant about 5 months ago. My urine has always foam or bubbles (I'm not sure) in there. There is also no protein in my urine. My doctor's told me the only way there will be foam in my urine is when there is protein in it. They too find it unusually
K___B
in
Kidney Disease
3 years ago
TRAVELLING ABROAD, POST LIVER TRANSPLANT.
Hello there everyone. I was wondering if anyone has had any experience with health insurance while travelling to America and other places where insurance is extremely expensive and sometimes extortionately so. I received a list of recommended providers from the administrators on here but I seemed to
Hello there everyone. I was wondering if anyone has had any experience with health insurance while travelling to America and other places where insurance is extremely expensive and sometimes extortionately so. I received a list of recommended providers from the administrators on here but I seemed to
Hidden
in
British Liver Trust
3 years ago
After 2nd Vaccine Antibodies
As a kidney transplant In the USA, whose responsibility is it to test me to find out if my body has made antibodies after the second covid vaccine? Also, how long do I have to wait to be tested for antibodies?
As a kidney transplant In the USA, whose responsibility is it to test me to find out if my body has made antibodies after the second covid vaccine? Also, how long do I have to wait to be tested for antibodies?
Hidden
in
Kidney Transplant
3 years ago
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Spinal Fusion-break Identified while being on the Lung Transplant List.
Good evening all, I have been listed on the Lung Transplant List for over 2 1/2 years now. They noticed right at the start of my evaluation that I had the start of osteoporosis which they put down to years of taking prednisolone. Even though I had this they were still happy to list me. I have recently
Good evening all, I have been listed on the Lung Transplant List for over 2 1/2 years now. They noticed right at the start of my evaluation that I had the start of osteoporosis which they put down to years of taking prednisolone. Even though I had this they were still happy to list me. I have recently
Joseph260268
in
Lung Conditions Community Forum
3 years ago
coping with anxiety and depression due to a child needing a kidney transplant
Anyone have a child awaiting kidney transplant? How do you deal or cope with all the emotions, not to mention anxiety and depression? Our 12 year old needs a kidney and my husband is not a match. I am a blood type match however, I have scar tissue on my kidneys from many many infections and I am over
Anyone have a child awaiting kidney transplant? How do you deal or cope with all the emotions, not to mention anxiety and depression? Our 12 year old needs a kidney and my husband is not a match. I am a blood type match however, I have scar tissue on my kidneys from many many infections and I am over
Crissylately
in
Parents of Children with Kidney Disease
3 years ago
Thriving with Congestive Heart Failure and a Left Ventricular Assist Device as I await a Heart Transplant.
Hi all- I am a retired dental surgeon with Congestive Heart Failure. I currently have a Left Ventricular Assist Device and am hoping for a call for a heart transplant in the next few weeks. I will be glad to share my experiences over the past twenty years with any of you. I have had 2 aortic valve replacement
Hi all- I am a retired dental surgeon with Congestive Heart Failure. I currently have a Left Ventricular Assist Device and am hoping for a call for a heart transplant in the next few weeks. I will be glad to share my experiences over the past twenty years with any of you. I have had 2 aortic valve replacement
Hidden
in
British Heart Foundation
3 years ago
Ongoing liver assessment stress
Over the last few weeks my husband has been assessed on an outpatient basis to see whether he's suitable for a liver transplant. His last test was this week on Wednesday when he had to do a treadmill test to see how fit his heart is. Just by chance we were looking at his medical record on line and
Over the last few weeks my husband has been assessed on an outpatient basis to see whether he's suitable for a liver transplant. His last test was this week on Wednesday when he had to do a treadmill test to see how fit his heart is. Just by chance we were looking at his medical record on line and
Corrine1
in
British Liver Trust
3 years ago
METAVIVE experience and why I stopped. (a long post sorry!!) Please read and tell me what you think...
I posted a few times about Metavive here first: https://healthunlocked.com/thyroiduk/posts/145085653/metavive-experience and there later: https://healthunlocked.com/thyroiduk/posts/145251376/metavive-experience-feedback My decision to try Metavive (porcine l and ll) was to try to find a product I could
I posted a few times about Metavive here first: https://healthunlocked.com/thyroiduk/posts/145085653/metavive-experience and there later: https://healthunlocked.com/thyroiduk/posts/145251376/metavive-experience-feedback My decision to try Metavive (porcine l and ll) was to try to find a product I could
Starsw
in
Thyroid UK
3 years ago
Update to ? Tocilizumab
I recently wrote for advice prior to starting on Tocilizumab as I was little nervous about side effects. I have now had 3 injections and my CRP is back to normal so have started to taper my prednisone down again. However I have been having sharp pains in my head, Rt temporal area, but also above and
I recently wrote for advice prior to starting on Tocilizumab as I was little nervous about side effects. I have now had 3 injections and my CRP is back to normal so have started to taper my prednisone down again. However I have been having sharp pains in my head, Rt temporal area, but also above and
Hiland
in
PMRGCAuk
3 years ago
Kidney failure stage 4 and am worried?
My mother had a kidney failure she's on stage 4, her GFR was 17% on December 2020, now its increased to 25% (UP & DOWN) she was prepared for kidney transplant (I am the donor) , but now the doctor postponed transplant until it goes down (below 20%), does she really need to do the transplant now or she
My mother had a kidney failure she's on stage 4, her GFR was 17% on December 2020, now its increased to 25% (UP & DOWN) she was prepared for kidney transplant (I am the donor) , but now the doctor postponed transplant until it goes down (below 20%), does she really need to do the transplant now or she
MAK88
in
Kidney Disease
3 years ago
British Society for Immunology statement on COVID-19 vaccines for patients who are immunocompromised or immunosuppressed
For people currently undergoing whole organ or
stem
cell
transplant
and who may be severely immunocompromised, you should talk to your medical treatment team about the most suitable time to get your COVID-19 vaccination.
For people currently undergoing whole organ or
stem
cell
transplant
and who may be severely immunocompromised, you should talk to your medical treatment team about the most suitable time to get your COVID-19 vaccination.
crashdoll
in
NRAS
3 years ago
COVID vaccines and the immune system
This is for information only. There are many people out there who may have a weakened or lowered immune system due to several reasons including a liver transplant and who might be struggling with concerns over whether a covid vaccine is safe to have or not. There is a presentation being given on the
This is for information only. There are many people out there who may have a weakened or lowered immune system due to several reasons including a liver transplant and who might be struggling with concerns over whether a covid vaccine is safe to have or not. There is a presentation being given on the
Richard-Allen
in
British Liver Trust
3 years ago
Lupus life insurance is it possible!
Hi everyone, it’s been a very long time since I’ve posted anything on this forum. Hope you’re all as well as you can possibly be, if not I hope you feel better soon. I have a question for you all and although it’s through the possible worst pandemic this country has been through, I would like to ask
Hi everyone, it’s been a very long time since I’ve posted anything on this forum. Hope you’re all as well as you can possibly be, if not I hope you feel better soon. I have a question for you all and although it’s through the possible worst pandemic this country has been through, I would like to ask
Wolf_1
in
LUPUS UK
3 years ago
Journey update: LVV/GCA, tocilizumab and exercise
I have been diagnosed with LVV/GCA beginning of February (though MRI/MRA and PET/CT were not fully conclusive). With the help of Tocilizumab I now arrived at 12.5 mg prednisolone per day. I know that this is a very fast taper but it worked well until now and from now on the steps will become much smaller
I have been diagnosed with LVV/GCA beginning of February (though MRI/MRA and PET/CT were not fully conclusive). With the help of Tocilizumab I now arrived at 12.5 mg prednisolone per day. I know that this is a very fast taper but it worked well until now and from now on the steps will become much smaller
DeepThought2
in
PMRGCAuk
3 years ago
Covid vaccine & PMR
Having had my vaccine today, I asked the nurse if my antibodies would produce equally as well as someone who didn’t have autoimmune issues. She said probably not but the only way to find out that would be to have an antibody test after the 2nd vaccine. I have thyroid issues, hashimotos, and PMR, has
Having had my vaccine today, I asked the nurse if my antibodies would produce equally as well as someone who didn’t have autoimmune issues. She said probably not but the only way to find out that would be to have an antibody test after the 2nd vaccine. I have thyroid issues, hashimotos, and PMR, has
Daisy1624
in
PMRGCAuk
3 years ago
Peripheral Neuropathy in feet
Hi everyone. I have painful , numb feet due to PN for about a year. Did not improve during dialysis and now that I recently had a kidney transplant I am hoping there may be some change? Treating it with pregabalin for the pain. Has anybody else had the same and found any improvement?
Hi everyone. I have painful , numb feet due to PN for about a year. Did not improve during dialysis and now that I recently had a kidney transplant I am hoping there may be some change? Treating it with pregabalin for the pain. Has anybody else had the same and found any improvement?
Weimarador
in
Kidney Transplant Patient Support
3 years ago
Hospital Service Experience for Bilirary Atresia, Leed, Uk
Our daughter will have another operation to attempt to try and clear her Jaundice next week. She had a Kasia on Dec' 14th (born 14/10/20). They will give her a DISDA scan tomorrow (17/02/20) and hopefully try and establish the location of the problem that is still preventing her Jaundice from clearing
Our daughter will have another operation to attempt to try and clear her Jaundice next week. She had a Kasia on Dec' 14th (born 14/10/20). They will give her a DISDA scan tomorrow (17/02/20) and hopefully try and establish the location of the problem that is still preventing her Jaundice from clearing
Dominic1975
in
Children's Liver Disease Foundation
3 years ago
VO2max vs cardio fitness
I'm new to this site. I'm a 74 year old man living in York, UK. My Fitbit gives me a score of 42 which is supposed to be excellent for my age. Not long ago I had a proper VO2 max test where I rode an exercise bike with a mask on and they measured my respiratory gases. I was given a score of 13. This
I'm new to this site. I'm a 74 year old man living in York, UK. My Fitbit gives me a score of 42 which is supposed to be excellent for my age. Not long ago I had a proper VO2 max test where I rode an exercise bike with a mask on and they measured my respiratory gases. I was given a score of 13. This
Andyv1
in
Bridge to 10K
3 years ago
Help for after Meningitis
Hello friends! I wish all of you a healthy 2021! My name is Fredy, I was born in Peru, but for problems in my country I moved to the USA, now I live in New York. In 2012 I got meningitis, 2 weeks in comma, when I woke up from coma, my brain was gone, after that took me like 4 years to understand something
Hello friends! I wish all of you a healthy 2021! My name is Fredy, I was born in Peru, but for problems in my country I moved to the USA, now I live in New York. In 2012 I got meningitis, 2 weeks in comma, when I woke up from coma, my brain was gone, after that took me like 4 years to understand something
menin
in
Meningitis Now
3 years ago
Transurethral Urinary Bladder Resection #2...coming up!
Well, mates...I made it for three years with the bladder neoplasia in check, and undergoing BCG vaccine every few months. Remember I could now go on the lung transplant list having been cancer free for three years. Well Thursday’s cystoscopy put an end to that (although my oncologist argues this type
Well, mates...I made it for three years with the bladder neoplasia in check, and undergoing BCG vaccine every few months. Remember I could now go on the lung transplant list having been cancer free for three years. Well Thursday’s cystoscopy put an end to that (although my oncologist argues this type
Sharp5Flat13
in
Lung Conditions Community Forum
3 years ago
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