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coming off rotigotine patches
Hello, First post… Could someone please share their experience coming off rotigotine patches, and what helped you throughout this experience? Been on rotigotine for 4 or so years, and more recently started experiencing augmentation. Was on 2mg, in August GP suggested increasing to 3mg but that hardly
Hello, First post… Could someone please share their experience coming off rotigotine patches, and what helped you throughout this experience? Been on rotigotine for 4 or so years, and more recently started experiencing augmentation. Was on 2mg, in August GP suggested increasing to 3mg but that hardly
Artifcial
in
Restless Legs Syndrome
7 months ago
Where Are My People?
I was diagnosed with major depressive disorder over 5 years ago. It started with speech therapy but didn’t seem to help. I’ve been medicated since then but it doesn’t feel like it’s doing its job anymore. The last couple years have been a rollercoaster with changing meds multiple times, worsening depression
I was diagnosed with major depressive disorder over 5 years ago. It started with speech therapy but didn’t seem to help. I’ve been medicated since then but it doesn’t feel like it’s doing its job anymore. The last couple years have been a rollercoaster with changing meds multiple times, worsening depression
RottieFlood37
in
Major Depressive Disorder (MDD) Support
7 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
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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
COMBINATION THERAPY IS NOW UNDER REVIEW
This review indicates how and why combination therapy may be used in treatment. Interesting in itself, but another example of cherry-picking evidence ( we aren't mentioned in spite of starting this concept in 2012. Good cliquish admission where the "nonprofessionals"are best kept well out of the limelight
This review indicates how and why combination therapy may be used in treatment. Interesting in itself, but another example of cherry-picking evidence ( we aren't mentioned in spite of starting this concept in 2012. Good cliquish admission where the "nonprofessionals"are best kept well out of the limelight
diogenes
in
Thyroid UK
7 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
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
4 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
4 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
4 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
4 months ago
some great news….
My son will be turning 4 this January and that in and of itself is great news. Nothing is scarier than having just given birth and not knowing what the future of your precious new child will hold, like simply living. my son was born with PUV and severe reflux bilaterally. Of course there was renal
My son will be turning 4 this January and that in and of itself is great news. Nothing is scarier than having just given birth and not knowing what the future of your precious new child will hold, like simply living. my son was born with PUV and severe reflux bilaterally. Of course there was renal
MotherofBarbearians
in
Parents of Children with Kidney Disease
7 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
4 months ago
What are the most promising drugs/treatments on the horizon for PD symptom relief,slowing progression?
I see Buntanetap,Celeste light therapy and Cue1 as potentials. anyone have any thoughts? i dont know how much longer I can hang on.
I see Buntanetap,Celeste light therapy and Cue1 as potentials. anyone have any thoughts? i dont know how much longer I can hang on.
Jmellano
in
Cure Parkinson's
7 months ago
Newly diagnosed metastatic PC treatment options
Hi, I'm 68 years old. Here are the key points in my story so far: In July 2023 a blood test showed a PSA value of 45. On September 26 2023, prostate MRI showed a dominant tumor in the prostate with extension into the right seminal vesicle. Also the fat plane between the rectum and prostate is lost
Hi, I'm 68 years old. Here are the key points in my story so far: In July 2023 a blood test showed a PSA value of 45. On September 26 2023, prostate MRI showed a dominant tumor in the prostate with extension into the right seminal vesicle. Also the fat plane between the rectum and prostate is lost
ShorePine
in
Advanced Prostate Cancer
7 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
4 months ago
Memory issues ??
Hi 👋 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 👋 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
4 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
4 months ago
Robert
Robert was diagnosed with Parkinson’s in 2018 PSP in 2021 progression was slow at first. Last year Robert was walking with a cane and dragging his feet. In September he began to fall daily sometimes more. He got weaker every day and finally allowed me to call a rescue. What followed was a whirlwind
Robert was diagnosed with Parkinson’s in 2018 PSP in 2021 progression was slow at first. Last year Robert was walking with a cane and dragging his feet. In September he began to fall daily sometimes more. He got weaker every day and finally allowed me to call a rescue. What followed was a whirlwind
Wrski
in
PSP Association
7 months ago
Light Therapy Celeste
Photopharmics is getting ready to recruit for phase 3. For those interested: https://photopharmics.com/innovative-research-inclusive-trials-and-new-funding-drives-hope-for-people-with-parkinsons-disease/
Photopharmics is getting ready to recruit for phase 3. For those interested: https://photopharmics.com/innovative-research-inclusive-trials-and-new-funding-drives-hope-for-people-with-parkinsons-disease/
Pegcity
in
Cure Parkinson's
8 months ago
Diagnosed at 61
I had a my first tonic clonic seizure June 23. I'd been having focal seizures for 10 years but didn't know what they were, so never saw the doctor. I've had CT scan, MRI and all normal. Had an ECT and that showed abnormal electrical activity in my brain which shocked me. I started Lamotrigine in July
I had a my first tonic clonic seizure June 23. I'd been having focal seizures for 10 years but didn't know what they were, so never saw the doctor. I've had CT scan, MRI and all normal. Had an ECT and that showed abnormal electrical activity in my brain which shocked me. I started Lamotrigine in July
TheCoulerPurple
in
Epilepsy Action
4 months ago
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