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New 2024 AUA/ASTRO/SUO Guidelines for Salvage Therapy
https://www.auanet.org/guidelines-and-quality/guidelines/salvage-therapy-for-prostate-cancer Not surprising. I think they should recommend adjuvant ADT at a PSA≥0.35 instead of ≥0.7 because I think patients are hoping for curative SRT and not just equivalent survival. https://www.prostatecancer.news
https://www.auanet.org/guidelines-and-quality/guidelines/salvage-therapy-for-prostate-cancer Not surprising. I think they should recommend adjuvant ADT at a PSA≥0.35 instead of ≥0.7 because I think patients are hoping for curative SRT and not just equivalent survival. https://www.prostatecancer.news
Tall_Allen
in
Advanced Prostate Cancer
5 months ago
Parkinson's Nurse update
Hi all, thank you for all your previous posts, they were most helpful. Since then we have had a few medical professionals visit. The Parkinsons Nurse is coming to see my father-in-law tomorrow. Is there any questions we need to be asking? The OT and Physio visited yesterday and recommended a new commode
Hi all, thank you for all your previous posts, they were most helpful. Since then we have had a few medical professionals visit. The Parkinsons Nurse is coming to see my father-in-law tomorrow. Is there any questions we need to be asking? The OT and Physio visited yesterday and recommended a new commode
Loveispatient23
in
PSP Association
7 months ago
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
4 months ago
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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
4 months ago
recurrence after lobectomy
Hello, I am 53 and live in the UK and I stop smoking in my late 20’. I had a lobectomy of my right lower lobe in April 2022 to remove a minimally invasive adenocarcinoma staged pT1 N0, M0, PL0, R0 (found by complete accident on an abdomen CT scan.) I begged for adjuvant therapy after the operation
Hello, I am 53 and live in the UK and I stop smoking in my late 20’. I had a lobectomy of my right lower lobe in April 2022 to remove a minimally invasive adenocarcinoma staged pT1 N0, M0, PL0, R0 (found by complete accident on an abdomen CT scan.) I begged for adjuvant therapy after the operation
Bibicata
in
The Roy Castle Lung Cancer Foundation
8 months ago
Transformation of Richter's Transformation Treatment to combination targeted therapy - tislelizumab +zanubrutinib (ASH 2023)
Richter's Transformation treatments are typically fixed term R-CHOP*, or modifications of that chemoimmunity therapy. So it's encouraging to hear that [i]"In a phase 2 trial, anti-PD-1 inibitor tislelizumab + next gen BTK inhibitor zanubrutinib had an overall response rate of 58.3% in patients with Richter's
Richter's Transformation treatments are typically fixed term R-CHOP*, or modifications of that chemoimmunity therapy. So it's encouraging to hear that [i]"In a phase 2 trial, anti-PD-1 inibitor tislelizumab + next gen BTK inhibitor zanubrutinib had an overall response rate of 58.3% in patients with Richter's
AussieNeil
Partner
in
CLL Support
8 months ago
Pain everywhere.
I've been 10+ yrs searching for answers. I had some bladder problems in 2013. Doctors did surgery. I almost died. Apparently they told me my blood vessels looked funny. They didn't know if they "knicked " me or what but I lost 8 pints of blood very quickly. They barely got me transfusion in time. I chalked
I've been 10+ yrs searching for answers. I had some bladder problems in 2013. Doctors did surgery. I almost died. Apparently they told me my blood vessels looked funny. They didn't know if they "knicked " me or what but I lost 8 pints of blood very quickly. They barely got me transfusion in time. I chalked
CountryGirl9636
in
Partners for Behcet's
8 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
4 months ago
Blood results interpretation required
Hi there, I need help interpreting my results. My symptoms are brain fog, joint aches, lack of energy and anxiety. These have been with me all my life. They got better in 2022 when I started combination therapy. However, I do not think I have reached my optimum (whatever that is) because these symptoms
Hi there, I need help interpreting my results. My symptoms are brain fog, joint aches, lack of energy and anxiety. These have been with me all my life. They got better in 2022 when I started combination therapy. However, I do not think I have reached my optimum (whatever that is) because these symptoms
Carlax
in
Thyroid UK
5 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
4 months ago
How you can help make ibrutinib plus venetoclax fixed duration therapy a reality for Australians with previously untreated CLL
In Australia, no new medicine can be listed on the Pharmaceutical Benefits Scheme (PBS) unless it has first been recommended by the Pharmaceutical Benefits Advisory Committee (PBAC). In March 2024, PBAC will again consider a submission to recommend a 15-month combination therapy of ibrutinib plus venetoclax
In Australia, no new medicine can be listed on the Pharmaceutical Benefits Scheme (PBS) unless it has first been recommended by the Pharmaceutical Benefits Advisory Committee (PBAC). In March 2024, PBAC will again consider a submission to recommend a 15-month combination therapy of ibrutinib plus venetoclax
CLLerinOz
Administrator
in
CLL Support
8 months ago
Studies comparing Levo mono vs Levo/Lio combo T4/T3 treatment
Batty1shared an article here https://healthunlocked.com/thyroiduk/posts/150566060/why-don’t-doctors-know-deal-with-this-hypothyroid-issue That lead me to a rabbit hole on the American Thyroid Association website. Sharing a summary of what I found to be a very comprehensive presentation of studies
Batty1shared an article here https://healthunlocked.com/thyroiduk/posts/150566060/why-don’t-doctors-know-deal-with-this-hypothyroid-issue That lead me to a rabbit hole on the American Thyroid Association website. Sharing a summary of what I found to be a very comprehensive presentation of studies
FallingInReverse
in
Thyroid UK
5 months ago
PSA rising on Triplet Therapy after <18m
Hi all. Hope you are keeping your spirits high. This is a follow up to a post I made in 2022 about my father. I haven't posted since, which reflects the period of relative normalcy that followed the commencement of ADT (triplet therapy) at MSK. I want to pause to appreciate that since I know most of
Hi all. Hope you are keeping your spirits high. This is a follow up to a post I made in 2022 about my father. I haven't posted since, which reflects the period of relative normalcy that followed the commencement of ADT (triplet therapy) at MSK. I want to pause to appreciate that since I know most of
nyc_son
in
Advanced Prostate Cancer
5 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
5 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
5 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
5 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
5 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
5 months ago
Private Blood Test Results
Hello, Diagnosed with Hashimoto’s 2019, it was a long and sickly road to diagnosis and treatment. Levothyroxine only didn’t work for me and after a couple of not so great endo appointments I finally found a really good endocrinologist who agreed to add in liothyronine and commenced me on 20mcg
Hello, Diagnosed with Hashimoto’s 2019, it was a long and sickly road to diagnosis and treatment. Levothyroxine only didn’t work for me and after a couple of not so great endo appointments I finally found a really good endocrinologist who agreed to add in liothyronine and commenced me on 20mcg
Lassithi
in
Thyroid UK
5 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
5 months ago
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