Holly created “Holly After GBS” social media pages to share her life after GBS, to connect with others, and to provide support/information to those who’ve been through GBS or CIDP.
“Holly After GBS” can be found on Facebook, Instagram, and YouTube.
If you or someone you know has recently been diagnosed with GBS, be sure to check out the article:
TIPS FOR FAMILIES DEALING WITH GBS.
Holly’s book is also a wealth of knowledge:
“Happily Ever After : My Journey with Guillain-Barre Syndrome and How I Got My Life Back.”
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 providing support to those in need. Along with her mother, she has visited many patients in the hospital, providing encouragement, advice and hope to patients and their caregivers.
In 2017, Holly was recognized for her passion to give back to the GBS/CIDP community and awarded the Walter Keast Award from the Foundation.
For more information on GBS , CIDP and their variants, to receive support or to donate to the foundation – please visit the GBS/CIDP Foundation Website.
GBS/CIDP Support Groups are an incredible way for people affected by GBS and CIDP to connect with others 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. For Facebook support groups, search Guillain-Barre, GBS, and/or CIDP in the search bar on FB. The GBS/CIDP Foundation website also has an online chat forum and a list of upcoming support groups across various locations.
GBS/CIDP Foundation Publications
