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The KIS Foundation — Raising Awareness of Sickle Cell Disease

Home
About Us
The KIS Foundation, Inc.
Our Mission Statement
The Founder
Board Of Directors
Advisory Board
Sickle Cell Disease
By The Definition
In The News
In The Community
Hindsight Series
Programs & Events
The Crisis Care Package Program
Upcoming Events
Past Events
Resources
Applications & Materials
Press
Photo Gallery
Donate & Give
Make A Donation Now
Give Gifts From The Heart
Volunteer Your Time
Contact Us
KiKi Shepard
January 11, 2018

Sickle Cell Patients, Pain and Pneumonia

KiKi Shepard
January 11, 2018
Sickle Cell Patients, Pain and Pneumonia

One day, while advocating for a patient diagnosed with Sickle Cell, a Respiratory Therapist shared with me and the patient so much about the relationship of Sickle Cell Patients, Pain and Pneumonia!

KiKi Shepard
November 5, 2017

Learning About Leg Ulcers

KiKi Shepard
November 5, 2017
Learning About Leg Ulcers

A patient had listened extensively to the guest physician at a Sickle Cell Adult Group Meeting raving about Hydroxyurea, the wonder drug that stopped people from having pain crisis!  The patient still had doubts, so they went on with life! In hindsight, the patient & spouse realized that they should always...

MadeByKenni™
September 8, 2017

The Story Behind The “Sickle Cell in Hindsight” Series

MadeByKenni™
September 8, 2017
The Story Behind The “Sickle Cell in Hindsight” Series

In my years of advocating for Persons Diagnosed with Sickle Cell, I've heard, and seen much first hand, as well as learned from others! 

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