PatientsLikeMe : Real-world treatment and symptom information from ALS (Lou Gehrig's Disease) patients like you

Search this site
FAQ

Select a community: ALS including PLS and PMA; Find out more about the PatientsLikeMe
ALS Community

All Communities
Neurological Conditions
MS (Multiple Sclerosis)
Parkinson’s Disease
ALS (Amyotrophic Lateral Sclerosis) / MND (Motor Neuron Disease)
PLS (Primary Lateral Sclerosis)
PMA (Progressive Muscular Atrophy)
PSP (Progressive Supranuclear Palsy)
CBD (Corticobasal Degeneration)
MSA (Multiple System Atrophy)
Devic’s Neuromyelitis Optica
Epilepsy
Neuroendocrine Conditions
Fibromyalgia
CFS (Chronic Fatigue Syndrome) / ME (Myalgic Encephalomyelitis)
Mood Conditions
Anxiety
Bipolar
Depression
Obsessive-Compulsive Disorder
Post-Traumatic Stress Disorder
Immune Conditions
HIV/AIDS

Home > ALS (Lou Gehrig's Disease) Patients

You appear to have JavaScript disabled in your browser. PatientsLikeMe relies on JavaScript and Cookies to deliver the best possible experience to you. How do I enable JavaScript?

Showing 1 patient who stopped taking Hyoscyamine because of Did not seem to work

Status			Hyoscyamine info	Profile

1 member have decided to share their profiles only with other members of the PatientsLikeMe ALS Community. To see these profiles matching your search criteria, Join now!

Report Back to Hyoscyamine report

PatientsLikeMe ™