The Faces of Rare Connection

At Rare Connection, our team is a blend of dedicated professionals and passionate advocates, each contributing unique expertise and personal experience to our mission. From seasoned medical experts and researchers to committed community support specialists, every member plays a crucial role in advancing our work.

Joanna Ball

Founder & CEO
Joanna is a Rare Disease patient with Homocystinuria, Joanna has been fundraising since childhood when she went door to door to collect donations for March of Dimes Walk America. In 1983 Joanna's lungs were colllapsing so she had to have scoliosis surgery, which involved putting a Herington rod in her back.. Because of the surgery she missed most of the 6th grade and was home schooled for most of that year. During the surgery she had to have a major blood transfusion (7 pints of blood). This was at the height of the AIDS epidemic. She later did the AIDS walk again raising funds door to door. People were ignorant at the time and thought it was caused by homosexuals primarily. They thought you could get it just by exchange of saliva. It was a lot harder raising funds for AIDS then, but Golden Gate Park where they held it was beautiful. After moving to Oregon in 1991, Joanna started volunteering for the American Red Cross. This lasted for about 3 years when her father gave her a recommendation to go to take classes to become a CNA. She was told that she was to slow at making beds and that she wouldn't pass the test. Determined, Joanna gave up after 4 attempts, and decided to build her skills working for a local residential care facility. Whereas she never passed, the information would come in handy following a major stroke in 2005 that paralyzed her left side entirely. She was able to gain everything back and she had her father walk her around on a gate belt until she learned to walk. Joanna is now a Home Care Worker/Personal Care Attendant for the Oregon Home Care Commission, She also hosts the Rare Connection Podcast, and does cooking videos on YouTube. She is also in a clinical trial for Homocystinuria that looks promising.

Rebekah Parrish

Treasurer & Co-Founder Rebekah brings a rich background from her 20-year U.S. Army career and a dedicated focus on family life and advocacy. In her role as a Global Compensation Analyst, she applies her strategic and problem-solving skills to complex issues, aligning well with the foundation's goals. Rebekah’s personal experience as a mother of a child with Hypohydrotic Ectodermal Dysplasia drives her commitment to improving resources and support for families dealing with rare conditions. Her unique blend of professional expertise and personal dedication makes her an invaluable asset to the board. To connect with Rebekah, email her at rebekah.l.parrish@gmail.com.










Susan Needleman

Secretary, & Co-Founder Susan's has been working for nonprofits since 2017. She is currently the secretary and outreach coordinator for the New England Connection for PKU and Allied Disorders. She has been the editor for the Maple Syrup Urine Disease Family Support Group since 2021 and She is also the MSUD Chair for Canada PKU. With the wealth of knowledge that Susan has and her dedication Rare Connection is lucky to have her. Susan is also a MSUD patient.

Joanna Ball

Founder & CEO

My Name is Joanna. I have a rare condition Homocystinuria. Homocystinuria is an Inborn Error in Metabolism affecting 1 in 200,000 to 335,000 World wide. It is commonly misdiagnosed as Marfan’s Syndrome because it looks like it outwardly. Unless the lenses dislocate it is often missed even though it is on the newborn screening. I was diagnosed when I was 3 years old in California. I had rubbed Trisodium phosphate into my eyes, and I happen to see a substitute doctor that day. She told my mother that it was either Marfan’s Syndrome or Homocystinuria. I was tested and the rest is History. Because no doctor took the time to look things up and I didn’t know anyone with it or even any vegans (we follow a low protein diet AKA the PKU diet and take a medical formula without methionine in it) I was didn’t believe in the condition. I have been through 2 strokes because of noncompliance and several seizures. I became compliant after my second stroke caused left sided paralysis. I made a full recovery and today the only thing you may be able to see if you look closely is a slight droop on the left side of my mouth. Today I am a caregiver by trade and I also have a YouTube channel that I film a podcast and several cooking videos many of which use medical foods that aren’t sold in stores. Since not all vegan foods are low in protein and not all low protein foods are vegan, this diet is harder to follow. I have a tolerance of 30 grams a day which is considered to be high.

Rebecca Parrish

Board Member, Rare Connection

Rebekah Parrish, a board member of Rare Connection, brings a rich background from her 20 year US Army career and a dedicated focus on family life and advocacy. In her role as a Global Compensation analyst she applies strategic and problem solving skills, aligning well with the foundation’s goals. Rebekah’s personal experience as a mother of a child with Hypohidrotic Ectodermal Dysplasia, drives her commitment to improving resources and support for families dealing with rare conditions. Her unique blend of professional expertise and personal dedication make her an invaluable asset to the board. To connect with Rebekah email her at rebekah.l.parrish@gmail.com

Joel Mushagasha

Co-Founder & COO of Endurant Healthspan

Joel Mushagasha is a leader in the field of rare disease management, serving as the Co-Founder and COO of Endurant Healthspan. With a robust background in computational biology and biomedical engineering. His academic journey began at Virginia Tech, leading to significant research roles at the National Institutes of Health (NIH) and Carnegie Mellon University, where he contributed to groundbreaking studies in bioinformatics and regenerative medicine. Joel’s expertise in machine learning and AI, combined with his strategic leadership, drives his passion to serve the rare diseases community.