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Chostochondritus after cardioversion ?
Hi everyone, after a successful cardioversion I felt amazing. However, after six weeks I was told it has failed. I still felt alot better but recently it has been getting worse with some dizziness and more episodes. However, after being at A E 3 times since, the docs are sure that the chest pain on
Hi everyone, after a successful cardioversion I felt amazing. However, after six weeks I was told it has failed. I still felt alot better but recently it has been getting worse with some dizziness and more episodes. However, after being at A E 3 times since, the docs are sure that the chest pain on
Sailblue
in
AF Association
4 months ago
A tooth with a life of it's own!
Hi, all. I wrote in several months ago about a painful tooth. My dentist couldn't find anything wrong with it. He finally referred me to an endodontist, and he did a root canal. Found several issues. Would have been nice if that had been the end of it, but no! The pain would not go away, and I
Hi, all. I wrote in several months ago about a painful tooth. My dentist couldn't find anything wrong with it. He finally referred me to an endodontist, and he did a root canal. Found several issues. Would have been nice if that had been the end of it, but no! The pain would not go away, and I
orangemax
in
PMRGCAuk
7 months ago
This is perplexing - Coffee's effectiveness on Parkinson prevention
I drank a lot of coffee from my teens until diagnosis at age 48. Yet study after study appears to support the efficacy of coffee in Parkinsons prevention. https://neurosciencenews.com/caffeine-genetics-parkinsons-24920/
I drank a lot of coffee from my teens until diagnosis at age 48. Yet study after study appears to support the efficacy of coffee in Parkinsons prevention. https://neurosciencenews.com/caffeine-genetics-parkinsons-24920/
pdpatient
in
Cure Parkinson's
7 months ago
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seeking more info with yet more questions
Hello. As I begin to write this it's 5:45 in the morning here. Trying to get at least some type of sleep. Still having loads of anxiety but trying to calm myself down to at least write this. Glancing over once in a while to check oxymeter, heart rate ranging from 92 to 104, oxygen steady at 96-97.
Hello. As I begin to write this it's 5:45 in the morning here. Trying to get at least some type of sleep. Still having loads of anxiety but trying to calm myself down to at least write this. Glancing over once in a while to check oxymeter, heart rate ranging from 92 to 104, oxygen steady at 96-97.
gbn_
in
Atrial Fibrillation Support
4 months ago
Chemo Vs ADT
So this is possibly the dumbest question I have asked. But the knowledge on this forum is worth tapping into even for people like me who struggle with all the complexities of PC. So, - ADT suppresses PC but will not kill it. Chemo on the other hand finds the PC cells and kills them. So why do
So this is possibly the dumbest question I have asked. But the knowledge on this forum is worth tapping into even for people like me who struggle with all the complexities of PC. So, - ADT suppresses PC but will not kill it. Chemo on the other hand finds the PC cells and kills them. So why do
Mike58
in
Advanced Prostate Cancer
5 months ago
Hello
Introducing myself, as I'll be looking through posts in the coming weeks... I'm 61, recently diagnosed with AF, but reckon I've been suffering for about 2 years. Biosprolol, Apixaban and Digoxin. Due to do the 'zaps' in 8-12 weeks.
Introducing myself, as I'll be looking through posts in the coming weeks... I'm 61, recently diagnosed with AF, but reckon I've been suffering for about 2 years. Biosprolol, Apixaban and Digoxin. Due to do the 'zaps' in 8-12 weeks.
MausenMumma
in
AF Association
4 months ago
degarelix v/s eligard "lupron"
my baseline psa was1316 with a elevated alkaline phosphatase of 270 12/2021 , on 01/13/2021 my psa had risen to 1665 to avoid a further psa spike I was given a loading dose of 240 mg of degarelix followed by 80 mg every 28 days for 18months then for 3 mouths this last summer a three month dose of
my baseline psa was1316 with a elevated alkaline phosphatase of 270 12/2021 , on 01/13/2021 my psa had risen to 1665 to avoid a further psa spike I was given a loading dose of 240 mg of degarelix followed by 80 mg every 28 days for 18months then for 3 mouths this last summer a three month dose of
yardsailor
in
Advanced Prostate Cancer
8 months ago
update
hi to those of you that follow me on here and those who don’t just wanted to do a quick update. So I saw Transplant consultant last month and he said I probably won’t live 5 years without a transplant. I went back yesterday as follow up as they are now seeing me monthly, and we’ll I was totally surprised
hi to those of you that follow me on here and those who don’t just wanted to do a quick update. So I saw Transplant consultant last month and he said I probably won’t live 5 years without a transplant. I went back yesterday as follow up as they are now seeing me monthly, and we’ll I was totally surprised
Harriet-sarah
in
British Liver Trust
8 months ago
Update on PSA
Aug 4 - diagnosed PCa, gleason 9 Aug 5 - started casodex Aug 17 - started lupron 3 mth Had my first blood work done yesterday (Oct 5) and PSA is now at 0.56. Was over 9 in June. So, I kind of feel good in knowing that as expected the meds are working and lowering PSA. Meaning I can move forward
Aug 4 - diagnosed PCa, gleason 9 Aug 5 - started casodex Aug 17 - started lupron 3 mth Had my first blood work done yesterday (Oct 5) and PSA is now at 0.56. Was over 9 in June. So, I kind of feel good in knowing that as expected the meds are working and lowering PSA. Meaning I can move forward
Yzinger
in
Advanced Prostate Cancer
8 months ago
Woot💙PSA dropped after being the same for two consecutive months
Hey y'all,#stageIVpca Back story : PSA at 552.2 on 10/13/14 - 15 Taxoteres in 2015, 6 more in 2020, 18 Cabazitaxels in '21/'22. 28 IMRTs Spring 2023 as PSA was rising 50% every month earlier 2023, hitting 34 😳 Still on track for 552.2 miles on 10/13/23 to mark the 9th year with #stageivpca when PSA
Hey y'all,#stageIVpca Back story : PSA at 552.2 on 10/13/14 - 15 Taxoteres in 2015, 6 more in 2020, 18 Cabazitaxels in '21/'22. 28 IMRTs Spring 2023 as PSA was rising 50% every month earlier 2023, hitting 34 😳 Still on track for 552.2 miles on 10/13/23 to mark the 9th year with #stageivpca when PSA
dockam
in
Advanced Prostate Cancer
8 months ago
cirrhosis and rheumatoid arthritis
My partner originally decompensated now compensated has suffered from bad aches and pains since diagnosis with ALD - always told it was a side effect of cirrhosis but as he started to become decompensated they started to entertain the idea it might be something else. Cut to almost 2 years later and
My partner originally decompensated now compensated has suffered from bad aches and pains since diagnosis with ALD - always told it was a side effect of cirrhosis but as he started to become decompensated they started to entertain the idea it might be something else. Cut to almost 2 years later and
Rshc
in
British Liver Trust
6 months ago
Parkinson's patient experiences improvements following stem cell infusions
research being done at Hope Biosciences in Sugarland, TX https://www.frontiersin.org/articles/10.3389/fneur.2023.1257080/full Conclusions Overall, HB-adMSC therapy was efficacious in improving the patient's experience with a progressively degenerative neurological disease such as PD. Administration
research being done at Hope Biosciences in Sugarland, TX https://www.frontiersin.org/articles/10.3389/fneur.2023.1257080/full Conclusions Overall, HB-adMSC therapy was efficacious in improving the patient's experience with a progressively degenerative neurological disease such as PD. Administration
Boscoejean
in
Cure Parkinson's
8 months ago
Scientists identify 11 new genes linked to aggressive prostate cancer
"It's the largest study published so far to compare the inherited genetic influences which separate aggressive and non-aggressive prostate cancers." https://www.icr.ac.uk/news-archive%2Fscientists-identify-11-new-genes-linked-to-aggressive-prostate-cancer?utm_medium=email&utm_source=rasa_io&utm_campaign
"It's the largest study published so far to compare the inherited genetic influences which separate aggressive and non-aggressive prostate cancers." https://www.icr.ac.uk/news-archive%2Fscientists-identify-11-new-genes-linked-to-aggressive-prostate-cancer?utm_medium=email&utm_source=rasa_io&utm_campaign
V10fanatic
in
Advanced Prostate Cancer
8 months ago
Medication and Memory
I was diagnosed with AFib in July and my daily medication is 12-5 Bisoprolol, as well as Digoxin, Rivaroxaban and Perindopril. I’ve always had a brilliant memory but have recently become concerned that I cannot retain information for very long at all. I also seem to get spurts of random, fleeting and
I was diagnosed with AFib in July and my daily medication is 12-5 Bisoprolol, as well as Digoxin, Rivaroxaban and Perindopril. I’ve always had a brilliant memory but have recently become concerned that I cannot retain information for very long at all. I also seem to get spurts of random, fleeting and
Jonhel
in
AF Association
4 months ago
The Holidays can be hard!
Sometimes we dont think about the people that are alone during the holiday season. How difficult it can be with no one to reach out to. I know, l have been there. I knew l was loved, and so are you! MSAA is offering Talkspace, a private online therapy service. 🙂 Limited Space ! Dont do it alone
Sometimes we dont think about the people that are alone during the holiday season. How difficult it can be with no one to reach out to. I know, l have been there. I knew l was loved, and so are you! MSAA is offering Talkspace, a private online therapy service. 🙂 Limited Space ! Dont do it alone
Jesmcd2
CommunityAmbassador
in
My MSAA Community
5 months ago
Feeling Sad and scared.
Mick has been diagnosed with pancreatic cancer which the Medics think has spread too the Liver.I will give more details when I feel that I can cope. Regards Jenni uk
Mick has been diagnosed with pancreatic cancer which the Medics think has spread too the Liver.I will give more details when I feel that I can cope. Regards Jenni uk
very
in
CLL Support
5 months ago
Slow-SPEED ‘Slowing Parinson’s early through exercise dosage’
The Slow-SPEED project is the world's first large-scale research into potentially disease-retardant treatment in the prodromal phase of Parkinson's. But the results will undoubtedly also be important after diagnosis and PD at a more advanced stage. This 4-year study investigates in people at a higher
The Slow-SPEED project is the world's first large-scale research into potentially disease-retardant treatment in the prodromal phase of Parkinson's. But the results will undoubtedly also be important after diagnosis and PD at a more advanced stage. This 4-year study investigates in people at a higher
Esperanto
in
Cure Parkinson's
8 months ago
Ablation question
Hi I’ had my 3rd CV last Thursday . It was reverted after 1st go, and everything was great first time in over 3 years in sinus ryrhmn, I was elated and loved checking my Kardia seeing HR in sinus rythmn! However today I’ve gone back to AF mode , whilst I’m pleased it lasted almost 6 days last two previous
Hi I’ had my 3rd CV last Thursday . It was reverted after 1st go, and everything was great first time in over 3 years in sinus ryrhmn, I was elated and loved checking my Kardia seeing HR in sinus rythmn! However today I’ve gone back to AF mode , whilst I’m pleased it lasted almost 6 days last two previous
Janelr
in
AF Association
4 months ago
Auditory hallucinations
Hello, My mum was diagnosed in Feb 21 with Parkinson’s. She has recently been experiencing distressing crashing sounds (usually when she wakes, but not always). I appreciate this is probably Parkinson’s related, and would like to hear from anyone else suffering a similar experience. She has been on
Hello, My mum was diagnosed in Feb 21 with Parkinson’s. She has recently been experiencing distressing crashing sounds (usually when she wakes, but not always). I appreciate this is probably Parkinson’s related, and would like to hear from anyone else suffering a similar experience. She has been on
NJCOL
in
Cure Parkinson's
8 months ago
Nees help
i’m a 43-year-old guy who’s been diagnosed with Parkinson’s for five years. The meds for Parkinson sort of help. I’ve tried lots and lots of things, but the thing that made me feel the very best was B12. I think I have pernicious, anemia and Parkinson’s. I also have a very low B2 levels. If I don’t
i’m a 43-year-old guy who’s been diagnosed with Parkinson’s for five years. The meds for Parkinson sort of help. I’ve tried lots and lots of things, but the thing that made me feel the very best was B12. I think I have pernicious, anemia and Parkinson’s. I also have a very low B2 levels. If I don’t
38yroldmale
in
Pernicious Anaemia Society
5 months ago
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