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      How many pALS, caregivers or loved ones of pALS have reached out to their local ALS Association Chapter? Were they helpful? What types of resources and services did they provide?

      They have an entire online series of publications for pALS and caregivers starting with important information when you are diagnosed, health insurance issues and much more. There are 11 publications in all that provide detailed information to assist pALS.  This is just one of the resources they provide. Have a look at the publication topics and let our forum members know what you think of the information

      Also, please share any resources that you have found helpful! The more information we share the better.

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