by Remember The Girls | Jul 19, 2022 | Community
Mom and Manifesting Carrier Written by Beth BauerPosted 07-19-2022 It was November of 1993 when my first son, Alex, was born. He was diagnosed with Myotubular Myopathy (MTM). In meeting with the geneticist, I was told that I was “just” a carrier and would never have...
by Remember The Girls | Jan 18, 2022 | Education
Our Thoughts on Noninvasive Prenatal Screening (NIPS) Written by Remember The GirlsPosted 01-18-2022 Remember The Girls is a nonprofit organization that supports carriers of rare, genetic X-linked conditions, and advocates for greater access to affordable and...
by Remember The Girls | May 26, 2021 | Community
Carrier Connections: Interview with Barbara Machado Written by Remember The GirlsPosted 04-26-2021 Carrier Connections is a Remember The Girls program where we feature a different X-linked condition each month and interview female in the condition community. In the...
by Remember The Girls | Nov 16, 2020 | Community
Legally Blind With X-Linked Retinitis Pigmentosa Written by Tia Mc’DanielPosted 11-16-2020 The day after Christmas 2018 I started experiencing flashes of light in my peripheral and I instantly knew something was wrong, I made an appointment with an eye...
by Remember The Girls | Jul 11, 2020 | Community
Kisses and Cream: A Story of X-Linked Ichthyosis Written by Hillary ChristiePosted 07-11-2020 It all started with “I’ve never heard of this before, I just got off the phone with the children’s hospital, this is all the information I have and I know...
