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Bronscospopy results
Hi There, I had a bronscospopy on Tuesday. I haven't heard anything back yet does that mean it's Not lung cancer. Thorax scan in January showed some abnormalities. Consultant wasn't sure if old infection or fungal disease ect or even TB. Many Thanks Emma
Hi There, I had a bronscospopy on Tuesday. I haven't heard anything back yet does that mean it's Not lung cancer. Thorax scan in January showed some abnormalities. Consultant wasn't sure if old infection or fungal disease ect or even TB. Many Thanks Emma
EmmaB66
in
The Roy Castle Lung Cancer Foundation
1 month ago
Next NoSilverBullet Zoom webinar on 13th of November: Interview of Dr Wayne Markman, CEO of Symbyx, on "Light therapy for Parkinson's".
I am delighted to announce that our next NoSilverBullet Zoom webinar will be taking place at 8.00pm London time on Monday the 13th of November. I will have the pleasure of interviewing Dr Wayne Markman, CEO of Symbyx, on "Light therapy for Parkinson's" Please use the Eventbrite link below to register
I am delighted to announce that our next NoSilverBullet Zoom webinar will be taking place at 8.00pm London time on Monday the 13th of November. I will have the pleasure of interviewing Dr Wayne Markman, CEO of Symbyx, on "Light therapy for Parkinson's" Please use the Eventbrite link below to register
Michel0220
in
Cure Parkinson's
6 months ago
Surgeon in Liverpool as requested thyroid bloods and thyroid antibodies 🤗
Hi everyone ❤️ Just posting this, as some members who have been following my struggle with thyroid medication these past 4 years, I decided to discontinue the T4 teva, the silly endo put me back on after taking me off the t3 which was not working due to gastric issues, forgetting also that teva t4 did
Hi everyone ❤️ Just posting this, as some members who have been following my struggle with thyroid medication these past 4 years, I decided to discontinue the T4 teva, the silly endo put me back on after taking me off the t3 which was not working due to gastric issues, forgetting also that teva t4 did
birkie
in
Thyroid UK
1 month ago
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Efficacy and safety of new‑generation BTKis (primarily acalabrutinib and zanubrutinib) in CLL/SLL: a systematic review and meta‑analysis
The meta-analysis of 20 studies on CLL/SLL patients treated with new-generation BTKis was based on papers selected from [i]"A comprehensive search on PubMed, Embase, Cochrane Library, and ClinicalTrials.gov. up to January 31, 2023".[/i] The full study title is
Efficacy and safety of new‑generation
The meta-analysis of 20 studies on CLL/SLL patients treated with new-generation BTKis was based on papers selected from [i]"A comprehensive search on PubMed, Embase, Cochrane Library, and ClinicalTrials.gov. up to January 31, 2023".[/i] The full study title is
Efficacy and safety of new‑generation
AussieNeil
Administrator
in
CLL Support
6 months ago
over 40 conception
I’m 41 going through my first cycle. I wanted to try and improve my chances of success due to my age. So have been taking coenzyme q10, regularly, as well as low dose melatonin, and omega 3 oils, folic acid and multivitamins. Also undergoing acupuncture and light therapy to improve egg quality. I’ve
I’m 41 going through my first cycle. I wanted to try and improve my chances of success due to my age. So have been taking coenzyme q10, regularly, as well as low dose melatonin, and omega 3 oils, folic acid and multivitamins. Also undergoing acupuncture and light therapy to improve egg quality. I’ve
Coffeeone
in
Fertility Network UK
6 months ago
Finding the Right Treatment
I have been really depressed for the last two years. I have been diagnosed with treatment resistant depression. I have tried 10 different medications, I do weekly therapy, see a psychiatric NP and I have finally resorted to ECT until my insurance company stopped paying for anesthesia. I can't afford
I have been really depressed for the last two years. I have been diagnosed with treatment resistant depression. I have tried 10 different medications, I do weekly therapy, see a psychiatric NP and I have finally resorted to ECT until my insurance company stopped paying for anesthesia. I can't afford
sunshinefan
in
Anxiety and Depression Support
2 months ago
New to this group
Hi all. I am new to this group. I am not new to mental illness having been diagnosed since 2006, but in the last two year, my depression has gotten much worse and landed me in the hospital 5 times. It also has me having a new diagnosis of treatment resistant depression. I have tried many medications,
Hi all. I am new to this group. I am not new to mental illness having been diagnosed since 2006, but in the last two year, my depression has gotten much worse and landed me in the hospital 5 times. It also has me having a new diagnosis of treatment resistant depression. I have tried many medications,
sunshinefan
in
Anxiety and Depression Support
2 months ago
New Consultant-Different Plan
Long story short- long battle to get diagnosis although received in 2019 and Hashimoto’s confirmed. After several attempts to stabilise on mono therapy I was lucky enough after several years of strife and illness to be allocated an endo who listened to me, took cortisol levels (low) addisons test (
Long story short- long battle to get diagnosis although received in 2019 and Hashimoto’s confirmed. After several attempts to stabilise on mono therapy I was lucky enough after several years of strife and illness to be allocated an endo who listened to me, took cortisol levels (low) addisons test (
Lassithi
in
Thyroid UK
3 months ago
support groups/meetings
good morning , hope all are as well as can be, I’m wondering if anyone knows of any support groups coffee mornings ect for people with fibro and other chronic health conditions in the south east wales area of uk ,thanks for reading 🙏
good morning , hope all are as well as can be, I’m wondering if anyone knows of any support groups coffee mornings ect for people with fibro and other chronic health conditions in the south east wales area of uk ,thanks for reading 🙏
Nevercansleep
in
Fibromyalgia Action UK
2 months ago
DENOSUNAB
I have stage 4 incurable lung cancerI have been on this drug for 20 months in respect of my bone cancer. My scans to date have all been stable and continue to show that the cancer has shrunk or disappeared to date. However, as my targeted therapy treatment (Brigatinib) is working, I am enquiring whether
I have stage 4 incurable lung cancerI have been on this drug for 20 months in respect of my bone cancer. My scans to date have all been stable and continue to show that the cancer has shrunk or disappeared to date. However, as my targeted therapy treatment (Brigatinib) is working, I am enquiring whether
Gymbuddie
in
The Roy Castle Lung Cancer Foundation
6 months ago
Depression
I am really struggling with depression. I am antidepressant resistent. I have tried everything. Tried ECT and magnetic therapy. Had 32 trans magnetic stimulation txs Mon-Fri in Oct and Nov. I know I will hang in there. I hang in there and then I go into a deep depression when it gets harder and harder
I am really struggling with depression. I am antidepressant resistent. I have tried everything. Tried ECT and magnetic therapy. Had 32 trans magnetic stimulation txs Mon-Fri in Oct and Nov. I know I will hang in there. I hang in there and then I go into a deep depression when it gets harder and harder
mauv
in
Anxiety and Depression Support
2 months ago
My Story
Hello all! I've never really shared my story.. If you can relate, have suggestions or anything feel free to comment or message me. Thanks in advance. My first panic attack and anxiety started when I was 10. I developed a fear of elevators. It made going to places, like doctors, hotels, ect. very difficult
Hello all! I've never really shared my story.. If you can relate, have suggestions or anything feel free to comment or message me. Thanks in advance. My first panic attack and anxiety started when I was 10. I developed a fear of elevators. It made going to places, like doctors, hotels, ect. very difficult
DogLover91
in
Anxiety and Depression Support
2 months ago
confused
i drink quite a bit. went in for my blood work about 2 months ago, liver stuff was high. DR sent me to get a sonogram. they came back and said i had a fatty liver and should cut back on my drinking. i went in this week to DR because my lower legs were swollen. no clots but when the nurse called me she
i drink quite a bit. went in for my blood work about 2 months ago, liver stuff was high. DR sent me to get a sonogram. they came back and said i had a fatty liver and should cut back on my drinking. i went in this week to DR because my lower legs were swollen. no clots but when the nurse called me she
hopingnottoolate
in
British Liver Trust
2 months ago
Diverticulitis &Severe Pain.
Hi all,Hope you’re all as good as you can be. I have Diverticulitis,now this is the 4th time in about the last 6mths. Now it’s quite new to me so I’m finding it difficult to understand about diet Ect. All I get from my GP is low fibre during a flare up,high fibre when I’m not. Well I have pain
Hi all,Hope you’re all as good as you can be. I have Diverticulitis,now this is the 4th time in about the last 6mths. Now it’s quite new to me so I’m finding it difficult to understand about diet Ect. All I get from my GP is low fibre during a flare up,high fibre when I’m not. Well I have pain
Breathless1943
in
Bowel Disease Support
2 months ago
Still depressed after ECT
I recently had ECT done (14treatments) I was feeling like it had changed my life and I was able to live again. But now I am back to feeling low moods, no motivation, and all the other symptoms associated with depression and anxiety. I was in a treatement facility and recently came back home, so maybe
I recently had ECT done (14treatments) I was feeling like it had changed my life and I was able to live again. But now I am back to feeling low moods, no motivation, and all the other symptoms associated with depression and anxiety. I was in a treatement facility and recently came back home, so maybe
Jersey24
in
Anxiety and Depression Support
2 months ago
Memory issues ??
Hi đź‘‹ I havnt posted in a while ,however I have had long standing JCA/RA among the rest that goes with it like MCTD . So after years of intense treatment from the age of 11 . I now find myself at the age of 60 with memory issues. To start it was around a year ago ,my gp thought I'd had a stroke as I
Hi đź‘‹ I havnt posted in a while ,however I have had long standing JCA/RA among the rest that goes with it like MCTD . So after years of intense treatment from the age of 11 . I now find myself at the age of 60 with memory issues. To start it was around a year ago ,my gp thought I'd had a stroke as I
Weemillie
in
NRAS
2 months ago
positive thinking
chris turner here 65 yr old male married over 40 yrs to cindy who has done so much as have her family to help me battle with liver disease/fibromyalgia/pht/enlarged spleen/liver diabetet type 2.other bits and bobs to deal with .ex butcher of 40 yrs ex biker 40yrs too ,no longer able to ride anymore and
chris turner here 65 yr old male married over 40 yrs to cindy who has done so much as have her family to help me battle with liver disease/fibromyalgia/pht/enlarged spleen/liver diabetet type 2.other bits and bobs to deal with .ex butcher of 40 yrs ex biker 40yrs too ,no longer able to ride anymore and
chrisuk
in
British Liver Trust
2 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
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