So let me introduce am Jake and I have Functional Neurological Disorders or FND for short for over 10 years now I live in Sheffield. I Want to use this podcast to talk to other people with FND, Medical people in the area of Functional Neurological Disorders. To try and get more awareness on FND and to show people that you are not alone with it but to create a support system for other people suffering from FND.
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So let me introduce am Jake and I have Functional Neurological Disorders or FND for short for over 10 years now I live in Sheffield. I Want to use this podcast to talk to other people with FND, Medical people in the area of Functional Neurological Disorders. To try and get more awareness on FND and to show people that you are not alone with it but to create a support system for other people suffering from FND.
Balancing Parenthood, Creativity, and Chronic Illness: A New Year's Reflection
The It’s Me It’s Me It’s FND Podcast
6 minutes 40 seconds
10 months ago
Balancing Parenthood, Creativity, and Chronic Illness: A New Year's Reflection
Welcome to the kickoff of 2025! As we step into the new year, our host reflects on the challenging yet rewarding journey of the past year. Juggling the demands of parenthood, creative ventures, and personal health issues, such as dealing with migraines, has not been easy.Despite the hurdles, there's a strong desire to improve and develop a structured plan for future podcast episodes. Our host discusses the difficulties of managing time effectively, especially with additional commitments and the new responsibilities of being a parent for the second time.As we welcome 2025, join us in looking forward to new possibilities and hoping for a year of growth and achievement.
The It’s Me It’s Me It’s FND Podcast
So let me introduce am Jake and I have Functional Neurological Disorders or FND for short for over 10 years now I live in Sheffield. I Want to use this podcast to talk to other people with FND, Medical people in the area of Functional Neurological Disorders. To try and get more awareness on FND and to show people that you are not alone with it but to create a support system for other people suffering from FND.
