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Amyotrophic Lateral Sclerosis Type 13
An amyotrophic lateral sclerosis where a mutation that is caused by the ATXN2 gene on chromosome 12 contributes to suscepitbility.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
When to seek help
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
If you are experiencing a medical emergency, contact your local emergency services immediately.
Overview
An amyotrophic lateral sclerosis where a mutation that is caused by the ATXN2 gene on chromosome 12 contributes to suscepitbility.
Resources
Join the Amyotrophic Lateral Sclerosis Type 13 community
Talk with people who understand, share what helps, and find support from others living with amyotrophic lateral sclerosis type 13. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.