0
Skip to Content
RUNX1 Research Program
RUNX1 Research Program
For Patients
For Researchers
For Clinicians
Take Action
About RRP
English
DONATE
RUNX1 Research Program
RUNX1 Research Program
For Patients
For Researchers
For Clinicians
Take Action
About RRP
English
DONATE
Folder: For Patients
Back
Folder: For Researchers
Back
Folder: For Clinicians
Back
Folder: Take Action
Back
Folder: About RRP
Back
English
Back
DONATE
  • Patient Stories,
• 4/2/24

Melissa & Ethan's Story

Melissa and her son, Ethan, share how his diagnostic journey helped her finally receive the correct testing, and how they are moving forward as a family with this rare disease.

Previous

The Berg Family

Next

The Manch Family

You Might Also Like

Related Embedded Video Item Thumbnail Crosstalk Between Transcription Factors, Methyltransferases and Tyrosine Kinases
Related Embedded Video Item Thumbnail RRP Patient Meeting 2023: RUNX1 PDH Update Nov 2023 - Dr. Amanda Eggen, RRP
Related Embedded Video Item Thumbnail Hereditary Hematologic Malignancies: Not That Rare
Related Embedded Video Item Thumbnail Inherited Thrombocytopenia (ITP): What Is It, Whom To Test and How To Test?
Related Embedded Video Item Thumbnail RUNX1 Deficiency in Megakaryopoiesis: Discovering Therapeutics for RUNX1 Haploinsufficiency
Name *
Thank you!

Sign up to receive the latest RRP news and updates.

Stay In Touch

Email RRP

Newsletter

Policies

Privacy Policy

Cookie Policy

Accessibility Statement

Site Resources

News & Updates

Calendar of Events

DONATE
SHOP