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1st lap endo 2nd lap no endo help I'm confussed?
Haa anyone had same experience as me? I'm feeling lost upset confussed. A year ago I was diagnosed with endometriosis /adenomyosis and pcos I had lost my job to being in and out hospitals in extreme flare ups. To the point I now have morphine at home to reduce chance of me needing to stay in hospital
Haa anyone had same experience as me? I'm feeling lost upset confussed. A year ago I was diagnosed with endometriosis /adenomyosis and pcos I had lost my job to being in and out hospitals in extreme flare ups. To the point I now have morphine at home to reduce chance of me needing to stay in hospital
Confussedpenguin101
in
Endometriosis UK
21 days ago
1st lap endometriosis 2nd lap no endo help???
Haa anyone had same experience as me? I'm feeling lost upset confussed. A year ago I was diagnosed with endometriosis /adenomyosis and pcos I had lost my job to being in and out hospitals in extreme flare ups. To the point I now have morphine at home to reduce chance of me needing to stay in hospital
Haa anyone had same experience as me? I'm feeling lost upset confussed. A year ago I was diagnosed with endometriosis /adenomyosis and pcos I had lost my job to being in and out hospitals in extreme flare ups. To the point I now have morphine at home to reduce chance of me needing to stay in hospital
Confussedpenguin101
in
The Endometriosis Foundation
21 days ago
Active B12 test results
Hi all, Not been on here for a few weeks due to feeling exhausted. I've managed to complete the Active B12 test (thank you Richmond nursing in Llanelli) for fitting me in for the blood draw. I waited with baited breath for my test results to be put on my Medichecks account and I was so shocked when
Hi all, Not been on here for a few weeks due to feeling exhausted. I've managed to complete the Active B12 test (thank you Richmond nursing in Llanelli) for fitting me in for the blood draw. I waited with baited breath for my test results to be put on my Medichecks account and I was so shocked when
Allywales8663
in
Pernicious Anaemia Society
22 days ago
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Not PCa related, but interesting new delivery techniques:
"It is a responsive therapy strategy towards the various cell states. This intelligent nanomachine with controlled release of anti-cancer drug in specific cancer cell subtypes can reduce the side effect to normal cells and facilitate the targeted therapy, which is promising as a theranostics nanoplatform
"It is a responsive therapy strategy towards the various cell states. This intelligent nanomachine with controlled release of anti-cancer drug in specific cancer cell subtypes can reduce the side effect to normal cells and facilitate the targeted therapy, which is promising as a theranostics nanoplatform
Maxone73
in
Advanced Prostate Cancer
6 months ago
Morning update on so confused.....
morning all, thank you for your help. So have just got latest bloods in. this is the picture so far... begining of june started as week knees going up stairs, then more Hyper symptoms- Hot flushing, sweating, weeing alot, skin burning at night, loss of weight, right eye red and puffy. tremors
morning all, thank you for your help. So have just got latest bloods in. this is the picture so far... begining of june started as week knees going up stairs, then more Hyper symptoms- Hot flushing, sweating, weeing alot, skin burning at night, loss of weight, right eye red and puffy. tremors
KimyH
in
Thyroid UK
26 days ago
Blood results
Hello everyone, I have ARLD, I saw my Grastro Consultant on the 20th August, He told me my bloods were normal and my liver is functioning normally , he order a endoscopy and a ct scan to be done before I see him again in three months time , I found the appointment over whelming a lot to take in,
Hello everyone, I have ARLD, I saw my Grastro Consultant on the 20th August, He told me my bloods were normal and my liver is functioning normally , he order a endoscopy and a ct scan to be done before I see him again in three months time , I found the appointment over whelming a lot to take in,
Orangutan_lover
in
British Liver Trust
30 days ago
EMG and NCT tests query
after over 2 years of waiting to be referred, i finally have an appt with neurophysology for EMG and NCT tests but they have booked the appt at 8.30 in the morning. thing is that the symptoms of awful burning/frozen sensation which iniatially were only in my right foot (started about 6 years ago at
after over 2 years of waiting to be referred, i finally have an appt with neurophysology for EMG and NCT tests but they have booked the appt at 8.30 in the morning. thing is that the symptoms of awful burning/frozen sensation which iniatially were only in my right foot (started about 6 years ago at
Crochet_fan
in
Neuropathy Support
6 months ago
Group Therapy #3
Got a group meeting today and i'm nervous because I feel that people can pick up on my body language and read into it and notice, i'm nervous. Also afraid that I wont be able to stop observing the people around me and what they're doing and that will be noticed as well. I'd like some advice please.
Got a group meeting today and i'm nervous because I feel that people can pick up on my body language and read into it and notice, i'm nervous. Also afraid that I wont be able to stop observing the people around me and what they're doing and that will be noticed as well. I'd like some advice please.
EricJones
in
Anxiety and Depression Support
6 months ago
Any successful treatment with red light therapy for peripheral neuropathy?
Hello, I am wondering whether or not it’s worth pursuing some sort of photobiomodulation (red light) therapy as a way of addressing idiopathic peripheral neuropathy which, in my case, means numb feet with burning soles at night. Has anybody had any success with these types of intervention, either through
Hello, I am wondering whether or not it’s worth pursuing some sort of photobiomodulation (red light) therapy as a way of addressing idiopathic peripheral neuropathy which, in my case, means numb feet with burning soles at night. Has anybody had any success with these types of intervention, either through
1jay
in
Neuropathy Support
6 months ago
Treatment resistant psychosis
Hi everyone I was wondering if anyone here has had treatment resistant psychosis and has had to take clozapine or have ect treatment? I'm still struggling with a couple of delusions and was hoping to hear some success stories from others.
Hi everyone I was wondering if anyone here has had treatment resistant psychosis and has had to take clozapine or have ect treatment? I'm still struggling with a couple of delusions and was hoping to hear some success stories from others.
Zebrawhite
in
Action on Postpartum Psychosis
1 month ago
Still fighting for a diagnosis B12, PA
Due to my ongoing failing health I've had to do my own research as to the pathway of blood test results, symptoms and the progression/knock on effects of having doctors who refuse to help. I have had to be extremely proactive in my own diagnosis, following the path of autoimmune conditions (co-morbid
Due to my ongoing failing health I've had to do my own research as to the pathway of blood test results, symptoms and the progression/knock on effects of having doctors who refuse to help. I have had to be extremely proactive in my own diagnosis, following the path of autoimmune conditions (co-morbid
Allywales8663
in
Pernicious Anaemia Society
1 month ago
t3 Monotherapy
Hello everyone, I have been a reader of the forum for a while now and it is nice to know so many other people are struggling with un-resolved thyroid problems. This forum was the first place where I thought wow, these guys get it. I have hypermobile ehlers danlos syndrome, I was diagnosed with MS
Hello everyone, I have been a reader of the forum for a while now and it is nice to know so many other people are struggling with un-resolved thyroid problems. This forum was the first place where I thought wow, these guys get it. I have hypermobile ehlers danlos syndrome, I was diagnosed with MS
Jimjamio
in
Thyroid UK
6 months ago
help with results please
I’d be grateful if anyone could help with results please. I’m on combined therapy 50mg T4 and 35mg T3 TFT 0.02 (0.35-4.94) FT3 4.5 (2.4-6.00) FT4 8.1 (9.00-19.00) B12 433 (187-883) Vit D 126.1 >50 Thank you :)
I’d be grateful if anyone could help with results please. I’m on combined therapy 50mg T4 and 35mg T3 TFT 0.02 (0.35-4.94) FT3 4.5 (2.4-6.00) FT4 8.1 (9.00-19.00) B12 433 (187-883) Vit D 126.1 >50 Thank you :)
Bollieforme
in
Thyroid UK
6 months ago
Seyfried press-pulse metabolic strategy for aggressive advanced prostate cancer
I'm writing on behalf of my brother who was diagnosed one year ago with stage four prostate cancer metastasized to the bones. His oncologist initially started him on anti-androgens and radiation with some positive initial results. In the past couple of months his numbers are going in the wrong direction
I'm writing on behalf of my brother who was diagnosed one year ago with stage four prostate cancer metastasized to the bones. His oncologist initially started him on anti-androgens and radiation with some positive initial results. In the past couple of months his numbers are going in the wrong direction
4mybrother
in
Advanced Prostate Cancer
2 months ago
Omg just received the prescription for peppermint capsules 🙈
Hi AGAIN everyone ❤️ This saga is beyond belief🤷♀️ just reading the leaflet accompanying the peppermint oil capsules. First there's a lot of 💩 fillers in it , as well as containing 0.2 ml of actual peppermint oil, it also contains the following. Gelatin, glycerol, purified water, titanium divide
Hi AGAIN everyone ❤️ This saga is beyond belief🤷♀️ just reading the leaflet accompanying the peppermint oil capsules. First there's a lot of 💩 fillers in it , as well as containing 0.2 ml of actual peppermint oil, it also contains the following. Gelatin, glycerol, purified water, titanium divide
birkie
in
Thyroid UK
2 months ago
Update on visit to gp🙈
Hi everyone ❤️ Update on visit to gp yesterday, firstly I will say she was one of the most down to earth gps I've ever seen👍 she had all my information to hand, she'd obviously done her homework which is rare with some , if not all gps today. I took my roseway information and tablets [ NDT] with me
Hi everyone ❤️ Update on visit to gp yesterday, firstly I will say she was one of the most down to earth gps I've ever seen👍 she had all my information to hand, she'd obviously done her homework which is rare with some , if not all gps today. I took my roseway information and tablets [ NDT] with me
birkie
in
Thyroid UK
2 months ago
Covid again - watch this space!- Update
Hi all, remember my post above from last week well I said I would update Monday after the test. You guessed it…. I fell really ill. I went out for a walk Monday morning and wasn’t feeling that bad but Monday afternoon it started taking hold of me, just feeling really poorly (what do I mean by poorly?
Hi all, remember my post above from last week well I said I would update Monday after the test. You guessed it…. I fell really ill. I went out for a walk Monday morning and wasn’t feeling that bad but Monday afternoon it started taking hold of me, just feeling really poorly (what do I mean by poorly?
Investigator1
in
Vasculitis UK
2 months ago
Group Therapy #2
So i went to my second group therapy. It went well, know seemed to be paying much attention to my body language (like I'm afraid of) no one seemed to see me see them carrying on and being themselves. (hyper focusing on them). But the one thing I cant stop from happening is hearing background sounds such
So i went to my second group therapy. It went well, know seemed to be paying much attention to my body language (like I'm afraid of) no one seemed to see me see them carrying on and being themselves. (hyper focusing on them). But the one thing I cant stop from happening is hearing background sounds such
EricJones
in
Anxiety and Depression Support
7 months ago
Psa and sacrolotic joint
I was diagnosed with psa 6 months ago .due to scalp psoriasis and swollen toes fingers knee pain ect .does any one else suffer from sacrolitis with there's and there spine neck my hips are so painful should I ask my rheumatology doctor other questions .does this happen with psa .he said my mri showed
I was diagnosed with psa 6 months ago .due to scalp psoriasis and swollen toes fingers knee pain ect .does any one else suffer from sacrolitis with there's and there spine neck my hips are so painful should I ask my rheumatology doctor other questions .does this happen with psa .he said my mri showed
Vic1977
in
Beyond Psoriasis
2 months ago
Update on me
Before I go to visit Ralph this morning, thought I'd write a bit about me. I rang this morning to see how his first night was, he'd vomited a little which she said was due to the stress of the move, but then he was fine and slept well. Last night was the first decent sleep I've had since his operation
Before I go to visit Ralph this morning, thought I'd write a bit about me. I rang this morning to see how his first night was, he'd vomited a little which she said was due to the stress of the move, but then he was fine and slept well. Last night was the first decent sleep I've had since his operation
Hidden
in
British Heart Foundation
7 months ago
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