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Transitioning Young Adults With Sickle Cell
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The Sickle Cell Community Consortium powers the VitaminSC3 Podcast. Today's show is brought to you by the Caring is Giving segment with Elle Cole.
During this episode, I spoke with Francine Baker, a wife, mother, caregiver, and student. In episode 12, Francine spoke with me transparently about the highs and lows of parenting a child with sickle cell disease. Francine has two children who are living with sickle cell disease. Her son and daughter are now young adults who have gone through the transition process.
Transition is when pediatric patients move from pediatric care to adult care. Sometimes this change means the patient receives new doctors and a unique team of healthcare professionals. Francine helps moms and dads understand that the role of a parent is not just to be a caregiver, but they should also be an advocate, supporter, listener, and at times healthcare coordinator. She also spoke about the shift students who enter college must take when they are away at school and have to learn a new team. Sometimes getting the college and home healthcare team to communicate with each other can be challenging, but Mrs. Baker shared what works well for her and her daughter to make it a seamless process.
If you have additional questions about this episode, please let us know so we can answer your questions.
We want you to stay connected with the sickle cell community and the VitaminSC3 podcast, so please visit our VitaminSC3 Instagram page. Send us a direct message and let us know what you think about the Podcast.
Follow Elle Cole
Instagram: @CleverlyChanging
Website: https://CleverlyChanging.com
Twitter: @CleverlyChangin
Facebook: @CleverlyChanging
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Did you enjoy listening to this episode? If so, please consider donating to keep this podcast going. Donations are tax deductible and are made to the Sickle Cell Community Consortium.
The next episode of the Vitamin SC3 Podcast drops on Monday
Please tune in next week for a new episode we will hear from the Essential RX segment with Dr. Lametra Scott.
Do you want to become a Sickle Cell Community Consortium Partner?
Become a Sickle Cell Community Consortium member by clicking here to learn more.
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