Preview Mode Links will not work in preview mode

Insight with Lise and Nichole

Jun 19, 2020

Todd Simms received his diagnosis and now has to wait for the next step. The global pandemic has changed things a little. 

We will have to wait to hear the next part of the Simms' family story.


If you have a Pheochromocytoma or a Paraganglioma story you would like share, we would love to hear from you.


Jun 12, 2020

Diagnosis Discovery of a Rare Disease

For maybe the first time in the history of the Simms family, cancer has become a very good thing. They finally got a name for the mystery disease that they have been struggling with all this time. pheochromocytoma.


A pheochromocytoma (fee-o-kroe-moe-sy-TOE-muh) is...

Jun 5, 2020

Part of the story you will hear in the episode.


"There were lots of times when his energy levels would, would come and go, and he wouldn't have seen a pattern. I always would say to him, you're in the middle of it. So sometimes you Can't see you're just experiencing and reacting and responding and being and me a bit...

May 29, 2020

This is the first full episode of the mini series.

The Simms' family share what life was like before diagnosis. 


The music in this episode is by Grant Boyer Music. 

If you have a story to share, please contact us.  We would love to hear from...

May 22, 2020

In this new mini series, we explore what it's like to live with a rare disease.

The Simms' family will share what life was life before the diagnosis, the process as well as finally getting a diagnosis.

The music in this series is by Grant Boyer Music

If you have a story to share, we would love to hear...