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Parkinson’s and vagal nerve stimulation, promising human studies.
RESULTS: PD patients showed instable gait with insufficient range of motion during usual walking. [u]
Active taVNS improved gait characteristics including step length, stride velocity, stride length, and step length variability compared with sham taVNS after completion of the 7-day therapy.
[/u]
RESULTS: PD patients showed instable gait with insufficient range of motion during usual walking. [u]
Active taVNS improved gait characteristics including step length, stride velocity, stride length, and step length variability compared with sham taVNS after completion of the 7-day therapy.
[/u]
House2
in
Cure Parkinson's
4 months ago
Is Baclofen part of asthma treatment?
I was taken off Montelukast by my Asthma specialist after more than twenty years. Baclofen was given but I had to stop taking it after two weeks because my cough didn't get better. My GP asked me to stop. I couldn't get in touch with my specialist. Should I restart the Baclofen?
I was taken off Montelukast by my Asthma specialist after more than twenty years. Baclofen was given but I had to stop taking it after two weeks because my cough didn't get better. My GP asked me to stop. I couldn't get in touch with my specialist. Should I restart the Baclofen?
Ossing
in
Asthma Community Forum
4 months ago
Lyme disease
Reply to Steve n. Yes have Lyme . Diagnosed with ME so sadly no treatment. Very interested to hear about new treatment.
Reply to Steve n. Yes have Lyme . Diagnosed with ME so sadly no treatment. Very interested to hear about new treatment.
Shelley1234567
in
Pernicious Anaemia Society
4 months ago
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Vitamin and mineral deficiencies/Thyroid dysfunction.. Chicken or Egg?
Before I spend my hard earned money on going to a private ENDO because the NHS is failing me I wanted to ask what you all thought about the problem of iron deficiency and vitamin D deficiency and how this relates to underactive thyroid . I read a lot here about how these vitamins should be optimal for
Before I spend my hard earned money on going to a private ENDO because the NHS is failing me I wanted to ask what you all thought about the problem of iron deficiency and vitamin D deficiency and how this relates to underactive thyroid . I read a lot here about how these vitamins should be optimal for
doingitfordad
in
Thyroid UK
7 months ago
Pernicious anaemia, no stomach acid and pain
I have had pernicious anaemia for 18 years and injections every 10 weeks. I have suffered with reflux, heartburn and congestion for many years. Last year a 24hr manometry test revealed I had zero stomach acid. Doctors offer me no advice at all to help with my digestive issues. This includes when I have
I have had pernicious anaemia for 18 years and injections every 10 weeks. I have suffered with reflux, heartburn and congestion for many years. Last year a 24hr manometry test revealed I had zero stomach acid. Doctors offer me no advice at all to help with my digestive issues. This includes when I have
Suesue246
in
Pernicious Anaemia Society
7 months ago
Prostate cancer
My prostate condition started around eight years ago when I had urinary track infection which also led to prostatitis. Ever since then, my PSA jumped from 2 to 7.8 during the last 5 years. I had two biopsies… first one, four years ago, they detected no positive cancer cells in my prostate. However
My prostate condition started around eight years ago when I had urinary track infection which also led to prostatitis. Ever since then, my PSA jumped from 2 to 7.8 during the last 5 years. I had two biopsies… first one, four years ago, they detected no positive cancer cells in my prostate. However
Yuncoinc7148
in
Fight Prostate Cancer
4 months ago
Liver Biopsy report, can anyone interpret?
Hello all, got my cirrhosis dx in march from a biopsy, however I have the full report, is there anything else of note from it other than I have cirrhosis from fat in the liver? The biopsy followed a high fibroscan read of 30.7kPa. Thank you Specimen: Liver, very high fibroscan reading ?cirrhosis
Hello all, got my cirrhosis dx in march from a biopsy, however I have the full report, is there anything else of note from it other than I have cirrhosis from fat in the liver? The biopsy followed a high fibroscan read of 30.7kPa. Thank you Specimen: Liver, very high fibroscan reading ?cirrhosis
aranshaw
in
British Liver Trust
4 months ago
Liver issues
Hi everyone, i have history of alcohol abuse from past 6 years and i left alcohol from 1 year. I had done liver elastography and mean ARFI comes 1.07m/sec and afetr 3 days i had done fibbroscan whih shows median stiffnes 9 kpa.After that i left alcohol and complete absebteeism from 1 year. Few months
Hi everyone, i have history of alcohol abuse from past 6 years and i left alcohol from 1 year. I had done liver elastography and mean ARFI comes 1.07m/sec and afetr 3 days i had done fibbroscan whih shows median stiffnes 9 kpa.After that i left alcohol and complete absebteeism from 1 year. Few months
Jhon789
in
British Liver Trust
4 months ago
Still confused about PSA and Testosterone testing
I have been reading posts here for some time and there seems to be a split between those who only get PSA tests each time they go to their doctors and those that get both tests each time. I had a baseline testosterone test before Lupron and before radiation. I am now doing my 6 month follow up and
I have been reading posts here for some time and there seems to be a split between those who only get PSA tests each time they go to their doctors and those that get both tests each time. I had a baseline testosterone test before Lupron and before radiation. I am now doing my 6 month follow up and
Mgtd
in
Advanced Prostate Cancer
4 months ago
Anti-nuclear factor levels
Hi all, this is my first time posting here. I'm wondering whether anyone can help me make sense of blood results. Anti-nuclear Factor DNA states positive. Specifically Anti-RO60 which is 26.0.I have some typical symptoms of Lupus including butterfly rash on face and develop itchy rash on exposed skin
Hi all, this is my first time posting here. I'm wondering whether anyone can help me make sense of blood results. Anti-nuclear Factor DNA states positive. Specifically Anti-RO60 which is 26.0.I have some typical symptoms of Lupus including butterfly rash on face and develop itchy rash on exposed skin
Funkyweirdo
in
LUPUS UK
7 months ago
Need Prostate Cancer Support Group. Need group that has been around for awhile,informative & nice guys..Experienced with Hypogonadal and TRT
Need Prostate Cancer Support Group... Need group that has been around for awhile..meets at night...west coast preferred but anywhere, informative and nice guys..please reply with contact info...experienced with hypogonadal & TRT if possible..a plus..thanks
Need Prostate Cancer Support Group... Need group that has been around for awhile..meets at night...west coast preferred but anywhere, informative and nice guys..please reply with contact info...experienced with hypogonadal & TRT if possible..a plus..thanks
JWS13
in
Advanced Prostate Cancer
4 months ago
Sterlings Reply
Please forgive the lateness but here it is:Four years after prostectomy my psa began to rise. I had eight weeks of radiation to the prostate bed. Psa returned to nondetectable for eleven years. Two years ago my psa began to rise at an alarming rate it was doubling monthly if not more. I started eligard
Please forgive the lateness but here it is:Four years after prostectomy my psa began to rise. I had eight weeks of radiation to the prostate bed. Psa returned to nondetectable for eleven years. Two years ago my psa began to rise at an alarming rate it was doubling monthly if not more. I started eligard
Praying2BHealthy
in
Advanced Prostate Cancer
4 months ago
Recompensated Liver.
HI folks.First of all Merry Christmas to you all. I was diagnosed with Decompensated Cirrhosis in 2021 and after having all my scheduled MRI Liver/ spleen scans my results have all came back no features of concern.. AFT blood monitoring results normal range. The only symptom I had was jaundice in my
HI folks.First of all Merry Christmas to you all. I was diagnosed with Decompensated Cirrhosis in 2021 and after having all my scheduled MRI Liver/ spleen scans my results have all came back no features of concern.. AFT blood monitoring results normal range. The only symptom I had was jaundice in my
Nip1
in
British Liver Trust
4 months ago
He and liver disease
I am so scared about damage to my liver , I’m worried I have Hepatic encephalopathy. I stupidly took to many over the counter tablets over a course of a month ( paracetamol) , I ended up in ANE but blood work come back ok and wasn’t ever treated however I’m worried I left it to long to go to the hospital
I am so scared about damage to my liver , I’m worried I have Hepatic encephalopathy. I stupidly took to many over the counter tablets over a course of a month ( paracetamol) , I ended up in ANE but blood work come back ok and wasn’t ever treated however I’m worried I left it to long to go to the hospital
Chickenlady34
in
British Liver Trust
4 months ago
Importance of ADT
Are there any good outcomes without using ADT ( hormone therapy)? I delayed it for a couple of years with bad results. My history -- [u]
2021
[/u]: Age 78. PSA was 7.79, Gleason 4+3=7. Small lesion in prostate, with perineural invasion. Had 20 IMRT for prostate. No ADT. [u]
2022
[/u]: PSA
Are there any good outcomes without using ADT ( hormone therapy)? I delayed it for a couple of years with bad results. My history -- [u]
2021
[/u]: Age 78. PSA was 7.79, Gleason 4+3=7. Small lesion in prostate, with perineural invasion. Had 20 IMRT for prostate. No ADT. [u]
2022
[/u]: PSA
vintage42
in
Advanced Prostate Cancer
4 months ago
INR control
Hi don't know if this is of any interest to anyone ,but my INR has always been impossible to stabilize My heamatologist suggested taking a small dose of vitamin K and increasing the warfarin dose I didn't do this as don't want to be taking any more supplements, So I decided to massively increase my intake
Hi don't know if this is of any interest to anyone ,but my INR has always been impossible to stabilize My heamatologist suggested taking a small dose of vitamin K and increasing the warfarin dose I didn't do this as don't want to be taking any more supplements, So I decided to massively increase my intake
mully
in
Hughes Syndrome APS Forum
3 months ago
Anyone has this issue
I was given my B12 injection today and told I need to book a review with a GP as my B12 level is good and that I could now take oral B12 instead. My experience before on oral B12 is it didn’t work for me. Every bit of research I have read states Pernicious Anaemia doesn’t go away and you need B12 injections
I was given my B12 injection today and told I need to book a review with a GP as my B12 level is good and that I could now take oral B12 instead. My experience before on oral B12 is it didn’t work for me. Every bit of research I have read states Pernicious Anaemia doesn’t go away and you need B12 injections
1998cd
in
Pernicious Anaemia Society
7 months ago
Restless Leg - Interesting Article
Article says iron is not getting across the BBB. Wonder if helps with PD.
They are trying to sell, but Interesting . I already take some of the things mentioned. Says I need Lactobacillus plantarum 299. My probiotic has Lactobacillus plantarum but does not state 299. The article has links, but
Article says iron is not getting across the BBB. Wonder if helps with PD.
They are trying to sell, but Interesting . I already take some of the things mentioned. Says I need Lactobacillus plantarum 299. My probiotic has Lactobacillus plantarum but does not state 299. The article has links, but
Gcf51
in
Cure Parkinson's
4 months ago
Devon and Cornwall Lupus Group Information day - Saturday 14th October - Everyone welcome!
Come join the Devon and Cornwall Lupus Group for our next Information day, next Saturday. It will be a great opportunity to learn, network and support LUPUS UK and those affected by the disease. If you would like more information or to RSVP, please contact DCLG.secretary@gmail.com.
Come join the Devon and Cornwall Lupus Group for our next Information day, next Saturday. It will be a great opportunity to learn, network and support LUPUS UK and those affected by the disease. If you would like more information or to RSVP, please contact DCLG.secretary@gmail.com.
michaellasmith
Administrator
in
LUPUS UK
7 months ago
SteveN
I am posting this here because the site won’t let me do anything else! I wanted to know if there are any Lyme disease sufferers on here, or any with ADHD/Autism? I am a Lyme disease sufferer and have spent about the last 5 years trying to test a theory about finding/engineering a treatment or cure.
I am posting this here because the site won’t let me do anything else! I wanted to know if there are any Lyme disease sufferers on here, or any with ADHD/Autism? I am a Lyme disease sufferer and have spent about the last 5 years trying to test a theory about finding/engineering a treatment or cure.
Weavernat
in
Pernicious Anaemia Society
4 months ago
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