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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
5 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
5 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
5 months ago
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PSA 4.7 (over 2 years it double and then doubled again) This is the Pathology report A: Prostate gland, left lateral posterior, biopsy: Benign prostatic tissue with mild chronic inflammation, no tumor present. B: Prostate gland, left lateral mid, biopsy: Benign prostatic tissue with mild chronic
PSA 4.7 (over 2 years it double and then doubled again) This is the Pathology report A: Prostate gland, left lateral posterior, biopsy: Benign prostatic tissue with mild chronic inflammation, no tumor present. B: Prostate gland, left lateral mid, biopsy: Benign prostatic tissue with mild chronic
Vortex12
in
Prostate Cancer Network
6 months ago
tramadol
I was on tramadol for at least 10 years----100 mg. then my doc took me off because a neurologist put me on Clonazepam for REM/SBD (rapid eye movement sleep behavior disorder.) But I was also getting cervical and lumbar rhizotomies...and still do every 12-14 months or so. I am now working with the VA
I was on tramadol for at least 10 years----100 mg. then my doc took me off because a neurologist put me on Clonazepam for REM/SBD (rapid eye movement sleep behavior disorder.) But I was also getting cervical and lumbar rhizotomies...and still do every 12-14 months or so. I am now working with the VA
Shadowperson
in
Pain Concern
11 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
5 months ago
Low B6... taking a complex with pyridoxine which obviously doesn't suit
Back to the search for the best B complex (Thorne being elusive at the moment and didn't do particularly well at keeping my B12 up)... one which contains pyridoxal 5' phosphate Does anyone rate Igennus Super B Complex? All suggestions welcome 🤗
Back to the search for the best B complex (Thorne being elusive at the moment and didn't do particularly well at keeping my B12 up)... one which contains pyridoxal 5' phosphate Does anyone rate Igennus Super B Complex? All suggestions welcome 🤗
TiggerMe
in
Thyroid UK
11 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
5 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
6 months ago
Can anyone help
Hi group. Ive been treated for underachieve thyroid for many years, mostly with Levothyroxine (current treatment) and for a brief period years ago Liothyronine (until it was stopped). My background is a healthcare professional and I understand the physiology side of the thyroid gland and associated
Hi group. Ive been treated for underachieve thyroid for many years, mostly with Levothyroxine (current treatment) and for a brief period years ago Liothyronine (until it was stopped). My background is a healthcare professional and I understand the physiology side of the thyroid gland and associated
SOT1512
in
Thyroid UK
8 months ago
Shingrix vaccine for immunosuppressed people aged 50+
I thought I would just post this from the gov.uk website because I have just a bit of struggle convincing our surgery that I was eligible, so maybe other people haven't been invited either. The full list is on chrome-extension://efaidnbmnnnibpcajpcglclefindmkaj/https://assets.publishing.service.gov.uk
I thought I would just post this from the gov.uk website because I have just a bit of struggle convincing our surgery that I was eligible, so maybe other people haven't been invited either. The full list is on chrome-extension://efaidnbmnnnibpcajpcglclefindmkaj/https://assets.publishing.service.gov.uk
Sharitone
in
PMRGCAuk
8 months ago
PEG Feeding
Hi....my step mum has PSP, she is bed bound and has carers come into her home 3 times a day to help my dad who is her full time carer. She is still able to eat and swallow although this is becoming a lot more difficult and time consuming and can no longer feed herself. The speech therapist spoke to my
Hi....my step mum has PSP, she is bed bound and has carers come into her home 3 times a day to help my dad who is her full time carer. She is still able to eat and swallow although this is becoming a lot more difficult and time consuming and can no longer feed herself. The speech therapist spoke to my
KingKenny73
in
PSP Association
8 months ago
LDH high
Looking back, my specialist tested my LDH at diagnosis and it was in fact elevated. He told me that it’s very common for MPN’s to cause elevated LDH levels and said with treatment we can correct them.. is that true? I was worried for a second about any organ or tissue damage, but he reassured and said
Looking back, my specialist tested my LDH at diagnosis and it was in fact elevated. He told me that it’s very common for MPN’s to cause elevated LDH levels and said with treatment we can correct them.. is that true? I was worried for a second about any organ or tissue damage, but he reassured and said
JAKboy
in
MPN Voice
11 months ago
update on prolotherapy
I have had my first prolotherapy injections, they don't hurt much at all.......I must admit the next day I thought oh no I have done the wrong thing....my legs were so bad I wanted to jump off the bridge. Today they have settled down a bit. I suppose this has happened because the prolotherapy causes
I have had my first prolotherapy injections, they don't hurt much at all.......I must admit the next day I thought oh no I have done the wrong thing....my legs were so bad I wanted to jump off the bridge. Today they have settled down a bit. I suppose this has happened because the prolotherapy causes
Hidden
in
Neuropathy Support
8 months ago
update on prolotherapy and llltherapy
I have had my first prolotherapy injections, they don't hurt much at all.......I must admit the next day I thought oh no I have done the wrong thing....my legs were so bad I wanted to jump off the bridge. Today they have settled down a bit. I suppose this has happened because the prolotherapy causes
I have had my first prolotherapy injections, they don't hurt much at all.......I must admit the next day I thought oh no I have done the wrong thing....my legs were so bad I wanted to jump off the bridge. Today they have settled down a bit. I suppose this has happened because the prolotherapy causes
Hidden
in
Restless Legs Syndrome
8 months ago
Group therapy for arthritic pain including PMR
Does anyone know of any face-to-face groups within the Portsmouth area? Or, does anyone know who to contact to find out? Any advice would be gratefully received. Thank you
Does anyone know of any face-to-face groups within the Portsmouth area? Or, does anyone know who to contact to find out? Any advice would be gratefully received. Thank you
Markandevie
in
PMRGCAuk
8 months ago
European Society for Medical Oncology Congress - ESMO 2023 - Two Significant Lutetium Trials -mCRPC
Those following information coming from the ESMO Congress over the last few weeks will be aware of the many presentations focussed on the use of Lutetium. [i]
PSMAfore Study Unveils Game-Changing Results for Prostate Cancer Treatment
[/i] One such highlight was the results from the PSMAfore
Those following information coming from the ESMO Congress over the last few weeks will be aware of the many presentations focussed on the use of Lutetium. [i]
PSMAfore Study Unveils Game-Changing Results for Prostate Cancer Treatment
[/i] One such highlight was the results from the PSMAfore
marnieg46
in
Fight Prostate Cancer
8 months ago
How prostate cancer transforms into aggressive NEPC following treatment with anti-androgen therapy.
This could be a game changer as it could stop PCa from progressing. Science is going to save us. The development of effective anti-androgen therapies for prostate cancer is a major scientific advance. However, some men who receive these targeted treatments are more likely to develop a deadly treatment-resistant
This could be a game changer as it could stop PCa from progressing. Science is going to save us. The development of effective anti-androgen therapies for prostate cancer is a major scientific advance. However, some men who receive these targeted treatments are more likely to develop a deadly treatment-resistant
Scout4answers
in
Advanced Prostate Cancer
8 months ago
red light therapy
been using red light therapy for 3 years - has there been double bind trials and if so what were results? Thanks
been using red light therapy for 3 years - has there been double bind trials and if so what were results? Thanks
Coling
in
Cure Parkinson's
8 months ago
Discrimination at work, not sure if I need a representative or advocate to help if it goes to tribunal
I asked the manager and member of HR if they had read my
Occupational
Therapy
letter and they said no. It felt like a complete waste of time being referred to occupational health if they weren't going to follow up the outcome.
I asked the manager and member of HR if they had read my
Occupational
Therapy
letter and they said no. It felt like a complete waste of time being referred to occupational health if they weren't going to follow up the outcome.
Shanni91
in
Autism Support
1 year ago
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