Skip to content

The E.WE Foundation

A Global Advocacy Network for Families with Rare Diseases and the Professionals Who Serve Them

  • Home
    • PRIVACY POLICY
  • ABOUT
    • OUR STORY
    • OUR TEAM
  • TRISOMY 18
    • TRISOMY AWARENESS
    • TRISOMY 18 COALITION
    • RARE DISEASE DAY
  • PROGRAMS
    • LEAP PROGRAM
    • ZEBRA PROGRAM
    • STRIPE PROGRAM
  • SERVICES
    • E.WE LEARNING
    • GET CERTIFIED (YMHFA)
  • RESOURCES
    • PROFESSIONAL COUNSELING
    • MENTAL HEALTH
  • RESEARCH
    • RARE PATIENT VOICE
    • TRIS PROJECT
  • POLICY
  • EVENTS
  • MEDIA
    • PODCAST
  • PARTNERS
  • DONATE
  • CONTACT
    • SCHEDULE A CALL
  • PORTAL

Me and Mom

Posted byewefoundationJanuary 22, 2021February 24, 2021Posted inElijah

❤..

Related

Posted byewefoundationJanuary 22, 2021February 24, 2021Posted inElijah

Published by ewefoundation

The E.WE Foundation is a global healthcare advocacy organization providing resources and support to families impacted Trisomy 18 (Edwards Syndrome) and other rare diseases. View more posts

Post navigation

Previous Post Previous post:
Eating From A Spoon
Next Post Next post:
Trending..
  • Facebook
  • Instagram
  • X
  • LinkedIn
  • Spotify
  • YouTube
  • Mail
Follow The E.WE Foundation on WordPress.com

The E.WE Foundation | PO Box 6391, Huntsville, AL 35813 | IRS approved 501(c)(3) | EIN 84-2765554 | Copyright ©2019-2025. All Rights Reserved.

The information provided by the E.WE Foundation is for educational and informational purposes only and is not intended to replace the advice of a physician or other qualified medical or social service professional.

The E.WE Foundation, Create a website or blog at WordPress.com
  • Subscribe Subscribed
    • The E.WE Foundation
    • Already have a WordPress.com account? Log in now.
    • The E.WE Foundation
    • Subscribe Subscribed
    • Sign up
    • Log in
    • Copy shortlink
    • Report this content
    • View post in Reader
    • Manage subscriptions
    • Collapse this bar
 

Loading Comments...