Help young Erin rage against ALS and offer support

This fundraiser is for Erin Taylor.   Erin was diagnosed with ALS at 23 years of age. Fresh out of college she began wondering why she was becoming increasingly weak. 

ALS is a terminal disease of which there is no cure or effective treatment. Erin was given 3 to 5 years to live. Since her diagnosis in 2023 she is now dependent on a wheelchair and has lost her voice. 

Even though her abilities are fading, she hasn’t stopped her work of creating awareness for ALS and letting those who will listen that even young people can get ALS.  

This past year using AI technology, opened for Lenovo Tech World, represented ALS for the first time at the UN during Zero Project, was the feature story on the national news in Austria. She also made a keynote speech at the Los Angeles ALS Network walk and has been featured in many stories online regarding ALS and using AI as a communication device 

We are raising funds to assist Erin with her immediate and long term needs. ALS is a relentless disease that requires mobility aids, home modifications, treatments, transportation, caregiving.  All donations go directly to Erin to meet her needs and is greatly appreciated and accepted with a humble heart

You can follow Erin’s journey as she posts on Instagram as @unsteadyandready