Is my diagnose contratict itself ?
The mission of r/epilepsy is to provide a community forum for people who are affected by epilepsy. We exist to share ideas about the direction of epilepsy research, available treatment options for all seizure disorders, SUDEP, and to overcome the challenges and stigma created by epilepsy through lively discussion in a safe supportive environment.
Premonitory urge
Welcome to r/tourettes! This is a place for people with Tourette's/Tic Disorders and their allies to learn, chat, talk/complain about tics, and release some stress!
I‘m finaly tic free
Welcome to r/tourettes! This is a place for people with Tourette's/Tic Disorders and their allies to learn, chat, talk/complain about tics, and release some stress!
The door bell terrifies me, what can I do ?
Welcome! This is a community meant for a discussion of schizophrenia spectrum disorders, and related issues. Active participation is encouraged.
I'm so scared of the hospital.
Welcome! This is a community meant for a discussion of schizophrenia spectrum disorders, and related issues. Active participation is encouraged.
Post diagnose depression
The mission of r/epilepsy is to provide a community forum for people who are affected by epilepsy. We exist to share ideas about the direction of epilepsy research, available treatment options for all seizure disorders, SUDEP, and to overcome the challenges and stigma created by epilepsy through lively discussion in a safe supportive environment.
Am I loosing it again ?
Schizoaffective disorder is a chronic condition that affects approximately .3% of the American population. We often experience psychosis and mood instability. Symptoms can happen independently or overlap. To fight the isolation, fear, and confusion around this condition, we created a place for schizoaffective individuals, caregivers for schizoaffective individuals, and those curious about schizoaffective disorder. This is a place without judgement where one can vent, discuss symptoms, look for
Can medication stop the urge to tic ?
Welcome to r/tourettes! This is a place for people with Tourette's/Tic Disorders and their allies to learn, chat, talk/complain about tics, and release some stress!
My last aura was wild.
The mission of r/epilepsy is to provide a community forum for people who are affected by epilepsy. We exist to share ideas about the direction of epilepsy research, available treatment options for all seizure disorders, SUDEP, and to overcome the challenges and stigma created by epilepsy through lively discussion in a safe supportive environment.
Isn‘t the neurologist suppost to do test‘s ?
Welcome to r/tourettes! This is a place for people with Tourette's/Tic Disorders and their allies to learn, chat, talk/complain about tics, and release some stress!
Functional tic‘s vs Tourette‘s
Welcome to r/tourettes! This is a place for people with Tourette's/Tic Disorders and their allies to learn, chat, talk/complain about tics, and release some stress!
Is surgery worth it ?
The mission of r/epilepsy is to provide a community forum for people who are affected by epilepsy. We exist to share ideas about the direction of epilepsy research, available treatment options for all seizure disorders, SUDEP, and to overcome the challenges and stigma created by epilepsy through lively discussion in a safe supportive environment.
Autism and Comorbidity's. What are yours ? I go first.
Autism news, information and support. Please feel free to submit articles to enhance the knowledge, acceptance, understanding and research of Autism and ASD.
Gliosis spots (scar tissue) in brain matter. Any one else with it ?
The mission of r/epilepsy is to provide a community forum for people who are affected by epilepsy. We exist to share ideas about the direction of epilepsy research, available treatment options for all seizure disorders, SUDEP, and to overcome the challenges and stigma created by epilepsy through lively discussion in a safe supportive environment.
How to cope with anosognosia.
Welcome! This is a community meant for a discussion of schizophrenia spectrum disorders, and related issues. Active participation is encouraged.
Anyone who has/had positive voices ?
Welcome! This is a community meant for a discussion of schizophrenia spectrum disorders, and related issues. Active participation is encouraged.
Both relatives of mine with epilepsy don't live anymore, should I be worried ?
The mission of r/epilepsy is to provide a community forum for people who are affected by epilepsy. We exist to share ideas about the direction of epilepsy research, available treatment options for all seizure disorders, SUDEP, and to overcome the challenges and stigma created by epilepsy through lively discussion in a safe supportive environment.
I went nonverbal do to medical reasons and it feels right
Autism news, information and support. Please feel free to submit articles to enhance the knowledge, acceptance, understanding and research of Autism and ASD.
People think I‘m deaf
This is a subreddit for people with difficulties speaking, whether its partial or total loss of their voice. Anyone is welcome to post here, please be respectful of all members. Questions are encouraged
I got my self a sunflower lanyard ^_^
Autism news, information and support. Please feel free to submit articles to enhance the knowledge, acceptance, understanding and research of Autism and ASD.
My doctor isn‘t interesten in finding out whats wrong with me.
The mission of r/epilepsy is to provide a community forum for people who are affected by epilepsy. We exist to share ideas about the direction of epilepsy research, available treatment options for all seizure disorders, SUDEP, and to overcome the challenges and stigma created by epilepsy through lively discussion in a safe supportive environment.
Weird preception of music getting slow and distorted.
The mission of r/epilepsy is to provide a community forum for people who are affected by epilepsy. We exist to share ideas about the direction of epilepsy research, available treatment options for all seizure disorders, SUDEP, and to overcome the challenges and stigma created by epilepsy through lively discussion in a safe supportive environment.
I‘m going to be mute for 6 weeks. I need advice.
This is a subreddit for people with difficulties speaking, whether its partial or total loss of their voice. Anyone is welcome to post here, please be respectful of all members. Questions are encouraged