The elevator to success is out of order. You'll have to use the stairs...one step at a time. ~Joe Girard

Spreading Awareness

My purpose in writing this blog is to spread awareness and provide support to parents of children with and without special needs. I have one child with a Learning Disability, more specifically, a Visual Processing Disorder including Dysgraphia and another child with a disease called Eosinophilic Esophagitis, an allergic white blood cell disease that attacks the esophagus.

Tuesday, May 18, 2010

Eos Awareness Week: Day 3


Did you know that all of the funding for Eosinophilic Disorder Research comes from private providers. The National Institute of Health currently provides $0 in funding for research for these diseases that are rapidly on the rise.

Today is the day to PARTICIPATE in Eos Awareness Week. A few suggestions given by apfed.org are:
*VIRTUAL WALK – Encourage those in your community to participate in APFED’s

National Eosinophil Awareness Virtual Walk. Get together some friends or your local
support group, Register online, collect pledges, and then meet at local park for a
“Walk” and social event.
*SIGN UP: Take the day to commit to participating in an APFED event, like

attending the conference this summer. Get registered at: APFED 2010 Conference
*ATTEND A LOCAL APFED EVENT: Check the Fundraising Page of the APFED

website to see what events are planned in your area and show your support by
attending. The list will be updated as events come in.
*WEAR YOUR APFED SHIRT: A simple way to participate is by wearing your

APFED t-shirt. If you don’t have one, you can purchase one by visiting the APFED
Store.

2 comments:

  1. Thank you for supporting APFED

    Thank you for raising awareness

    ReplyDelete
  2. Anytime! It's the least I can do for children suffering from these horrible disorders and their families.

    ReplyDelete