Help Spread Awareness
#ALSLooksLikeMe
The lifetime incidence of ALS is estimated to be 1 in 400, and it can impact anyone. We need your help to spread awareness of how differently ALS impacts individuals.
How to Participate:
  1. Complete the short questionnaire below to share how ALS impacts you as a person living with ALS, or answer on behalf of a friend or loved one who is living with/lived with ALS.
  2. When you submit the questionnaire, ALS TDI will email you your personalized image (be sure to check your spam folders).
  3. Download your image and share it using #ALSLooksLikeMe.
We know that the impact of ALS on individuals and families goes far beyond what is conveyed here – but we hope that these short snapshots can help to increase awareness and understanding of the disease.
Start your questionnaire
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A name is required
A symptom is required
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An ability lost is required
50 character limit
An ability not lost is required
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Only fields marked with an asterisk (*) are required. None of these fields will be displayed on your image.
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Stay informed
We'd love to keep you updated about our research to discover treatments and cures for ALS. We'd also like to let you know how you can help by donating or fundraising to fuel our lab.
By generating a shareable image, you will automatically receive ALS TDI's monthly newsletter. You may choose additional email options below. You may unsubscribe or change your preferences at any time.
Share our Posts On Social
We need your help to spread awareness about ALS!
Throughout the month of May, ALS TDI will be sharing posts about ALS and spreading awareness that the disease can impact anyone.
How can you help? Follow us on social and share our posts throughout the month.
• Be sure to tag @ALSTDI when posting on different social sites so we can share your photos/videos/blogs.
• You can use hashtag #ALSLooksLikeMe, #ALSAwarenessMonth, and #ALSFacts in your posts to spread awareness.
Follow Us to See All of Our ALS Awareness Month Posts!
#ALSLooksLikeMe
1 in 400 people may be diagnosed with ALS, and no two cases are the same. See the hundreds of badges from our ALS community below and create your own #ALSLooksLikeMe badge to join the movement.
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