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Double Rare: A Mother's Path With Two Rare Diseases


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  • 9. We get to go to Disney?? what??

    15:45||Season 1, Ep. 9
    Talking about good things happening obviously :) I mean....vacation for a medical family? enjoy our info and our podcast? leave a review please!
  • 8. We drove 5 hours to see a Nuero Genetic Dr to discuss UBTF

    28:42||Season 1, Ep. 8
    On this episode i discuss what happened during my trip to Winston Salem as well as Carters MRI experience. Carter got to see the pulmonologist and an allergist.
  • 7. DC Leukodystrophy Research Trip Update(UBTF)

    29:30||Season 1, Ep. 7
    During our trip to Washington, DC for medical research related to my son's Leukodystrophy gene mutation (UBTF), we stayed at the Ronald McDonald House for accommodations. In addition to focusing on medical appointments and research, we took the opportunity to visit family members, including his grandparents (nono and yaya) and aunt. We also enjoyed attending a lively Greek festival together, immersing ourselves in the cultural experience. The trip was rounded off with a pleasant brunch shared with our relatives, combining both the pursuit of medical insights and cherished family moments in our nation's capital.
  • 6. Sick Policies and what's coming up

    39:53||Season 1, Ep. 6
    In this Episode I will talk about our son being discharged from therapies and what appointments we have coming up
  • 5. A Little Life Update

    28:17||Season 1, Ep. 5
    In this episode we will give a little life update. Stay tuned for some news!
  • 4. Mental health along with diagnosis

    33:35||Season 1, Ep. 4
    On todays episode we dive into the mental health aspect behind a diagnosis