If you or someone you know has been recently impacted by GBS, be sure to check out her article: Tips for families of those recently diagnosed with Guillain-Barré syndrome. 

Holly After GBS

Holly created “Holly After GBS” to reach others who had been through GBS. To contact Holly directly by e-mail or on social media, click Contact Holly.



The GBS/CIDP Foundation improves the quality of life for individuals and families affected with GBS, CIDP & Variants. Holly actively volunteers with the foundation, organizing awareness events and provides support to those who need it. Along with her mother, she has visited many patients in the hospital, providing encouragement, advice and hope to patients and their caregivers.

For more information on GBS and its variants, to receive support, or to donate to the foundation, please visit the GBS Foundation Website.


Online Support Groups are a way for people affected by GBS and CIDP to connect with others all around the world. They are a great place to share stories and ask questions. GBS/CIDP may be rare, but these support groups remind us that we are not alone.  To find FB support groups, search GBS, Guillain-Barre, and/or CIDP in the search bar of Facebook.


The Gimpy Girl Who Could.





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