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.
All content for The It’s Me It’s Me It’s FND Podcast is the property of itsmeitsmeitsfnd and is served directly from their servers
with no modification, redirects, or rehosting. The podcast is not affiliated with or endorsed by Podjoint in any way.
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.
Welcome to "It's Me, It's Me, It's F&D." In this episode, we delve into the complexities of dealing with the Personal Independent Payment (PIP) form, a crucial yet challenging part of life for many.
Our host shares their personal struggles with the PIP review process, discussing the anxiety and difficulties faced, from gathering evidence to the nerve-wracking waiting period. Hear firsthand how dealing with non-medical professionals and bureaucratic hurdles can turn a necessary procedure into a nightmare.
Whether you're familiar with the PIP system or learning about it for the first time, this episode offers valuable insights and practical advice on navigating this daunting process while managing your health and well-being.
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.