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Sylvia Plath and B12?
Has anyone else pondered on the links here? Although I can find all sorts of discussion about her early stresses, repeated losses and struggle with depression, even chemical imbalances, possible bipolar, not a jot can I find about the B12 deficiency which she would have had at least at one point, even
Has anyone else pondered on the links here? Although I can find all sorts of discussion about her early stresses, repeated losses and struggle with depression, even chemical imbalances, possible bipolar, not a jot can I find about the B12 deficiency which she would have had at least at one point, even
bookish
in
Pernicious Anaemia Society
4 months ago
Spine metastasis
My father in law is 78 year old male with PCA with what appears to be a single spine metastasis. Gleason 7 ( 4+3) We have an appointment coming up with the radiation oncologist . Is this something they would get a PSMA TEST for to confirm and also would he just receive ADT with radiation to primary site
My father in law is 78 year old male with PCA with what appears to be a single spine metastasis. Gleason 7 ( 4+3) We have an appointment coming up with the radiation oncologist . Is this something they would get a PSMA TEST for to confirm and also would he just receive ADT with radiation to primary site
Telegraph2022
in
Advanced Prostate Cancer
4 months ago
Buprenorphine and antidepressants
I have had RLS for 50 years and depression right along with it. Wellbutrin has worked well, but I still get periods of severe depression on it. Since discontinuing the Pramipexole 3 months ago, the depression has been very severe. Not sure if was stopping the Pramipexole or starting the Bup. has anyone
I have had RLS for 50 years and depression right along with it. Wellbutrin has worked well, but I still get periods of severe depression on it. Since discontinuing the Pramipexole 3 months ago, the depression has been very severe. Not sure if was stopping the Pramipexole or starting the Bup. has anyone
teakabeagle
in
Restless Legs Syndrome
4 months ago
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Post release advice
Hi. it’s day 4 after a valve replacement, web removal and wall reduction, all has gone great and if the wire removal, X ray etc go well today I can leave. the temptation is to stay for support but think that’s normal nerves! Anyone got advice for coping with that when first go home and general advice
Hi. it’s day 4 after a valve replacement, web removal and wall reduction, all has gone great and if the wire removal, X ray etc go well today I can leave. the temptation is to stay for support but think that’s normal nerves! Anyone got advice for coping with that when first go home and general advice
TriumphLover
in
British Heart Foundation
9 months ago
Exercise making it worse?
Hi everyone, I have a question about exercise and endo. So basically I've been pretty much bedbound all of last year with rare weeks of being able to function, but lately I've experience a good couple of months of feeling better and being able to live! (Don't get me wrong still in pain but manageable
Hi everyone, I have a question about exercise and endo. So basically I've been pretty much bedbound all of last year with rare weeks of being able to function, but lately I've experience a good couple of months of feeling better and being able to live! (Don't get me wrong still in pain but manageable
Lavenderpetal
in
Endometriosis UK
4 months ago
To those newly diagnosed! There is hope!
I was diagnosed with Parkinson’s in Dec 2018. My form of Parkinson’s has a huge psychological element that many of you can relate to. It’s obvious because of how quickly I progressed while I was getting diagnosed . My Dad who was my best friend and business partner died unexpectedly in 2013, which destroyed
I was diagnosed with Parkinson’s in Dec 2018. My form of Parkinson’s has a huge psychological element that many of you can relate to. It’s obvious because of how quickly I progressed while I was getting diagnosed . My Dad who was my best friend and business partner died unexpectedly in 2013, which destroyed
38yroldmale
in
Cure Parkinson's
7 months ago
CBD - my Mum's journey so far
Hello - I am so grateful to have found this group as I have felt alone given this disease is rare and even the health care professionals are not aware of it. I've detailed her journey which may help others trying to get a diagnosis. In 2019 my Mum's speech became slurred (only the family at this
Hello - I am so grateful to have found this group as I have felt alone given this disease is rare and even the health care professionals are not aware of it. I've detailed her journey which may help others trying to get a diagnosis. In 2019 my Mum's speech became slurred (only the family at this
Lalamccoy
in
PSP Association
7 months ago
Red Light Therapy
I have been using Wellreds Coronet for two years. I sleep extremely well since I started using it ( I had terrible sleep problems for years ). Worth every penny ! I use their preset program 2 x/day
I have been using Wellreds Coronet for two years. I sleep extremely well since I started using it ( I had terrible sleep problems for years ). Worth every penny ! I use their preset program 2 x/day
Defiance
in
Cure Parkinson's
7 months ago
Update and Feeling Kicked…..
Thank you to everyone who helped me with my last post on this board regarding DNR. I’m relieved to say that my father was released and is possibly back on track to regain some of the weight lost at hospital. Still waiting to hear if it’s lymphoma. As for me I am feeling kinda kicked down this week.
Thank you to everyone who helped me with my last post on this board regarding DNR. I’m relieved to say that my father was released and is possibly back on track to regain some of the weight lost at hospital. Still waiting to hear if it’s lymphoma. As for me I am feeling kinda kicked down this week.
RoseFlowerDew
in
Pernicious Anaemia Society
1 year ago
RANDOMIZED CONTROLLED TRIAL EVALUATING THE CARDIO-METABOLIC EFFECTS OF LEVOTHYROXINE AND LIOTHYRONINE
An interesting preprint paper re liothyronine. (Apologies for SHOUTING - using capitals - but I usually try to copy exactly.) [i]Thyroid. 2023 Sep 19.[/i] [i]doi: 10.1089/thy.2023.0135. Online ahead of print.[/i] [i]
PRELIMINARY RESULTS OF A DOUBLE-BLIND RANDOMIZED CONTROLLED TRIAL EVALUATING THE
An interesting preprint paper re liothyronine. (Apologies for SHOUTING - using capitals - but I usually try to copy exactly.) [i]Thyroid. 2023 Sep 19.[/i] [i]doi: 10.1089/thy.2023.0135. Online ahead of print.[/i] [i]
PRELIMINARY RESULTS OF A DOUBLE-BLIND RANDOMIZED CONTROLLED TRIAL EVALUATING THE
helvella
Thyroid UK
in
Thyroid UK
7 months ago
Why is this so hard, someone to talk to
Hi everyone. I had treatment resistant depression for my entire adult life, I've been on pretty much every med, hospitalized, ECT tms and ketamine. Nothings helped. I've gone the DBT and cbt route. I've been suicidal. Can anyone out there relate? I'm married with a 13 year old which makes it harder.
Hi everyone. I had treatment resistant depression for my entire adult life, I've been on pretty much every med, hospitalized, ECT tms and ketamine. Nothings helped. I've gone the DBT and cbt route. I've been suicidal. Can anyone out there relate? I'm married with a 13 year old which makes it harder.
Coffeeshop
in
Anxiety and Depression Support
4 months ago
Seasonal Affective Disorder and photosensitive retinal ganglion cells
I think I suffer from Seasonal Affective Disorder (SAD) and it has got much worse since I lost most. of trhe vision in my left eye and some peripheral vision in both eyes in 2021. I've seen some interesting reports into the recently discovered third set of photoreceptive cells in teh retina "photosensitive
I think I suffer from Seasonal Affective Disorder (SAD) and it has got much worse since I lost most. of trhe vision in my left eye and some peripheral vision in both eyes in 2021. I've seen some interesting reports into the recently discovered third set of photoreceptive cells in teh retina "photosensitive
Tarsius
in
Anxiety and Depression Support
7 months ago
Msa 7 months on
The symptoms still kicking on 7 months in. Still out of wheelchair (I'd say just)I've bought a mobility scooter. The council have been really helpful and speech therapy have been excellent. Old friends have been good to catch up with for an hour or so but I don't know if it's common but insomnia and
The symptoms still kicking on 7 months in. Still out of wheelchair (I'd say just)I've bought a mobility scooter. The council have been really helpful and speech therapy have been excellent. Old friends have been good to catch up with for an hour or so but I don't know if it's common but insomnia and
thedjsupreme
in
Multiple System Atrophy Trust
7 months ago
What the Dr says...
Hi all , I hope everyone is doing ok. Just a question regarding what my GP said. I have Fybro, arthritis in my spine , had a hip replacement at 46, need a crutch or walking stick on good days , have plantar fascitis, PTSD and other forms of physical restrictions. Recent diagnosis of severe restrictive
Hi all , I hope everyone is doing ok. Just a question regarding what my GP said. I have Fybro, arthritis in my spine , had a hip replacement at 46, need a crutch or walking stick on good days , have plantar fascitis, PTSD and other forms of physical restrictions. Recent diagnosis of severe restrictive
Mrdiagnosis
in
Fibromyalgia Action UK
9 months ago
Self Anthem - Music therapy
So, I was remembering when I had a major breakdown when my life was falling apart everywhere I turned - after I realized that the life/relationship that I had invested so much of everything into was a big fat lie ... And I started to pick myself up and I heard this song and kept playing it over and over
So, I was remembering when I had a major breakdown when my life was falling apart everywhere I turned - after I realized that the life/relationship that I had invested so much of everything into was a big fat lie ... And I started to pick myself up and I heard this song and kept playing it over and over
HopeforMiami
in
Anxiety and Depression Support
7 months ago
update
Well the acupunture doesn't seem to be helping at this stage, have stopped it and trying reflexology and Low level laser therapy. The GP put me on 20mg Norspan patch from 15....it didn't seem to change the effect on my legs at the higher dose but it made me quite nauseated and sweaty and tired on higher
Well the acupunture doesn't seem to be helping at this stage, have stopped it and trying reflexology and Low level laser therapy. The GP put me on 20mg Norspan patch from 15....it didn't seem to change the effect on my legs at the higher dose but it made me quite nauseated and sweaty and tired on higher
Hidden
in
Neuropathy Support
7 months ago
update
Well the acupunture doesn't seem to be helping at this stage, have stopped it and trying reflexology and Low level laser therapy. The GP put me on 20mg Norspan patch from 15....it didn't seem to change the effect on my legs at the higher dose but it made me quite nauseated and sweaty and tired on higher
Well the acupunture doesn't seem to be helping at this stage, have stopped it and trying reflexology and Low level laser therapy. The GP put me on 20mg Norspan patch from 15....it didn't seem to change the effect on my legs at the higher dose but it made me quite nauseated and sweaty and tired on higher
Hidden
in
Restless Legs Syndrome
7 months ago
Ibs or celiac
hiya so for a few years off and on I’ve always had bloating , pains in adomin ect. But now constantly everytime I wee I always need a poo but I’m always straining . Couple of weeks ago I had bright pink blood in my sick. And for a couple of weeks I had mucus and blood in my stool. Doctors want to do
hiya so for a few years off and on I’ve always had bloating , pains in adomin ect. But now constantly everytime I wee I always need a poo but I’m always straining . Couple of weeks ago I had bright pink blood in my sick. And for a couple of weeks I had mucus and blood in my stool. Doctors want to do
Girlpower98
in
IBS Network
4 months ago
Struggling with impact on older children
When I was in hospital after PP last summer, I had amazing counselling on offer for me, for my partner, for my bonding with my baby. But, nothing for how my PP episode had impacted my older child. my son, who is now six, started to become very anxious about being left alone. This started when I was
When I was in hospital after PP last summer, I had amazing counselling on offer for me, for my partner, for my bonding with my baby. But, nothing for how my PP episode had impacted my older child. my son, who is now six, started to become very anxious about being left alone. This started when I was
MotherOfBears
in
Action on Postpartum Psychosis
7 months ago
Just an update .
I was due to have my hip replacement on 17th August, got to the hospital saw all the relevant people. A Dr came to put an arrow on my leg and asked me how long had i had the scratch on my hip ? I told him i wan not aware i had one ! He took a photo of it, i am not joking when i say it was not even an
I was due to have my hip replacement on 17th August, got to the hospital saw all the relevant people. A Dr came to put an arrow on my leg and asked me how long had i had the scratch on my hip ? I told him i wan not aware i had one ! He took a photo of it, i am not joking when i say it was not even an
Viv54
in
PMRGCAuk
9 months ago
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