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      The ALS Association publishes an ALS guide along with other free resources for pALS and care givers. https://portal.alsa.org/  Check out the ALS Association portal to order and see what other resources that are available.

      My family has been very fortunate to have worked closely with the St. Louis Chapter. They helped with medical information and coordination of services, devices and family and patient support.

      Has anyone been helped out by their local ALS Association Chapter?  What kind of assistance have the provided? Where would you have gone if they had not been able to help?

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