The People Behind The Disease
Very grateful to GeneFo – A Social Medical Platform for asking to interview Life as a Zebra Foundation for the The Huffington Post. Please read and share: The People Behind The Disease
Very grateful to GeneFo – A Social Medical Platform for asking to interview Life as a Zebra Foundation for the The Huffington Post. Please read and share: The People Behind The Disease
August 2016 Update from Dr. Kenneth Hensley:
I have been working with one of Dr. Grubb’s student residents Dr. Ruzieh Mohammed to teach him the immunoglobulin pull-down assay in my lab. We have performed some technical variations to determine how the assay might be modified. Our hope is to continue to try to identify novel immunoglobulins in POTS sera.
Please see below for the latest update on Dr. Grubb and his team’s progress on the groundbreaking research project they are currently doing on Dysautonomia that Life as a Zebra Foundation has helped fund.
Did you know that you can benefit the Life as a Zebra Foundation every single time you shop at Amazon.com? Amazon will donates 0.5% of the price of your eligible purchases to the charitable organization of your choice. To learn more about how you can support the Life as a Zebra Foundation every time you shop, click here.
For the third year in a row, both the Michigan Senate and House of Representatives unanimously adopted a resolution formally declaring the week of May 22, 2016 to May 28, 2016 as “Invisible Illness Awareness Week” in Michigan. The goal of the week is to raise awareness of invisible illnesses among the general public and medical community, while reducing stigma surrounding these illnesses.
Senate Resolution 0063 (2016) was adopted on May 19 following similar action by the House of Representatives. Senator Curtis Hertel, Jr. introduced Katie Dama-Jaskolski, co-founder of the Life as a Zebra Foundation, to the Senate floor.
The 2016 Invisible Illness Awareness Week was themed “Making the Invisible Illnesses; Visible Hope” to reflect the widespread scope of the issue and to create a forum to share the stories of people living with invisible illness.
Dama-Jaskolski commented:
“We have shined the light on invisible illnesses throughout the years, but it’s still not enough to erase the stigma many people feel, and to bring more early diagnoses to these conditions,” Dama Jaskolski said. “It’s great to have advocates like Representative Schor and Senator Hertel in the Michigan Legislature to bring this issue to the forefront. The person right beside you could be suffering from an unseen illness, and in need of compassion, care and understanding.”
Throughout Invisible Illness Awareness Week, “zebras” from around the country shared their stories about living with various invisible illnesses on social media. They are written with bravery, honesty, and inspiration. Check out our Facebook page to read the stories, or to share your own.
The 5th annual Zebra Day at Wexford Montessori Academy was a success! Wexford’s staff and students came together to dress in their favorite zebra gear. Foundation co-founders Katie Dama-Jaskolski and Allie Dama Affandy gave presentations to children from kindergarten through eighth grade about invisible illnesses and the importance of having empathy, and compassion for others and of living a life of fulfillment despite adversity.