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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
2 months ago
Aphasia
My husband is one month out of his tumor being 100% removed. His aphasia seems to be worse then it was 2 weeks out from surgery. He just started speech therapy this week. Is the decline normal?
My husband is one month out of his tumor being 100% removed. His aphasia seems to be worse then it was 2 weeks out from surgery. He just started speech therapy this week. Is the decline normal?
Nylo
in
Glioblastoma Support
7 months ago
Replace or reorganize neurons
Can someone explain :Does the parkinson's glove therapy assume we don't have a loss of Dopa. Neurons but they just need to be reorganized. Via vibration Where gene therapy assume we have a loss of Neurons that need to be replaced ? Which is it, replace or reorganize?
Can someone explain :Does the parkinson's glove therapy assume we don't have a loss of Dopa. Neurons but they just need to be reorganized. Via vibration Where gene therapy assume we have a loss of Neurons that need to be replaced ? Which is it, replace or reorganize?
bigl62
in
Cure Parkinson's
7 months ago
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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
Targeted Gene Therapy for Symptom Relief in Parkinson’s Disease
Very early, still a looooong way out, and results were only in animal models, but something to keep an eye on. https://www.brainpost.co/weekly-brainpost/2023/11/7/targeted-gene-therapy-for-symptom-relief-in-parkinsons-disease
Very early, still a looooong way out, and results were only in animal models, but something to keep an eye on. https://www.brainpost.co/weekly-brainpost/2023/11/7/targeted-gene-therapy-for-symptom-relief-in-parkinsons-disease
Neurosmith
in
Cure Parkinson's
7 months ago
still here
Hi All I like to try and update my journey so you can see that there are some longer term survivors. I am still on 0 PSA with advanced cancer. My journey is on my bio. I was diagnosed at 47 and now I’m 54 with no progression. My primary treatment was Zytiga and it is still working. I take a concoction
Hi All I like to try and update my journey so you can see that there are some longer term survivors. I am still on 0 PSA with advanced cancer. My journey is on my bio. I was diagnosed at 47 and now I’m 54 with no progression. My primary treatment was Zytiga and it is still working. I take a concoction
Apollo123
in
Advanced Prostate Cancer
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
3 months ago
Occupational therapy intervention for FND
Would anyone like to share their experiences of occupation therapy intervention for FND, especially in relation to the mitigation of shaking, vocalisations, and hypersensitivity to noise. How helpful did you find it?
Would anyone like to share their experiences of occupation therapy intervention for FND, especially in relation to the mitigation of shaking, vocalisations, and hypersensitivity to noise. How helpful did you find it?
Shimmyaway
in
Functional Neurological Disorder - FND Hope
7 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
3 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
3 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
3 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
3 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
3 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
3 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
3 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
3 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
4 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
7 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
7 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
3 months ago
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