We want to dedicate this site in remembrance of Raina and her spirit. We would like to invite you to join us.
Raina cared deeply about helping people. Her friends and family were always on her mind. At the end, she wanted to leave us all with “a good memory”.
Please visit the blog and add your comments or an anecdote about her. You are welcome to contact us and send us a picture or a memory we can post on the site.
We can make a difference if we care.
In honoring Raina, we especially want to remember her kind spirit. We have developed a foundation that can provide scholarships for students in need. We will also seek to help people understand rare diseases and its impact and seek to make difference.
Raina passed away from a rare cancer called histiocytosis. Becasue histiocytosis disorders are rare, it is extremely difficult for those battling these cancers. Raina cared about those like her and hoped something would be learned from her personal battle. She was courageous and never wavered in fear. If you want to help “Take Action”. We are working with the Histiocytosis Association and the Erdiheim Chester Disease Global Alliance to fight histiocytosis disorders. We have formed the Raina J Evans Foundation.
