Heather Figueroa's guest appearances

Heather Figueroa

The Mike Wagner Show

Bradon Nave

Brent Michael Phillips

Michael Boyd

Peter Block

Matt Wagner

Nick Turner

Renee Casteel Cook

Michelle Kopalski

Amora Coffee

Zachary Hudson

Gianna Harris

Tim Bakken

Fuller French

Fem Founder

Asher Laub

OwlTail

Mike Wagner

A special edition with New Hampshire resident Heather Figureoa and her story of her young son Branson with a rare skull condition called craniosynostosis and in need of a second surgery requiring to go to a specialist in Texas. Heather talks about the rare condition and the story behind of how it all got started..and is also asking for support to raise $50,000 for the process at https://www.gofundme.com/f/help-for-bransons-surgery-and-travel?utm_source=customer&amp;utm_campaign=p_cp+share-sheet&amp;utm_medium=copy_link-tip !

A special edition with New Hampshire resident Heather Figureoa and her story of her young son Branson with a rare skull condition called craniosynostosis and in need of a second surgery requiring to go to a specialist in Texas. Heather talks about the rare condition and the story behind of how it all got started..and is also asking for support to raise $50,000 for the process at <a href="https://www.gofundme.com/f/help-for-bransons-surgery-and-travel?utm_source=customer&amp;utm_campaign=p_cp+share-sheet&amp;utm_medium=copy_link-tip" rel="noopener nofollow" target="_blank">https://www.gofundme.com/f/help-for-bransons-surgery-and-travel?utm_source=customer&amp;utm_campaign=p_cp+share-sheet&amp;utm_medium=copy_link-tip</a> !

It's a very special Mike Wagner Show talking about the Branson Figueroa Craniosynostis fundraiser with Heather Figueroa!

A special edition with New Hampshire resident Heather Figureoa and her story  of her young son Branson with a rare skull condition called craniosynostosis and in need of a second surgery requiring to go to a specialist in Texas. Heather talks about the rare condition and the story behind of how it all got started..and is also asking for support to raise $50,000 for the process at https://www.gofundme.com/f/help-for-bransons-surgery-and-travel?utm_source=customer&amp;utm_campaign=p_cp+share-sheet&amp;utm_medium=copy_link-tip!--- Send in a voice message: https://podcasters.spotify.com/pod/show/themikewagnershow/messageSupport this podcast: https://podcasters.spotify.com/pod/show/themikewagnershow/support

A special edition with New Hampshire resident Heather Figureoa and her story  of her young son Branson with a rare skull condition called craniosynostosis and in need of a second surgery requiring to go to a specialist in Texas. Heather talks about the rare condition and the story behind of how it all got started..and is also asking for support to raise $50,000 for the process at <a href="https://www.gofundme.com/f/help-for-bransons-surgery-and-travel?utm_source=customer&amp;utm_campaign=p_cp+share-sheet&amp;utm_medium=copy_link-tip" rel="nofollow" target="_blank">https://www.gofundme.com/f/help-for-bransons-surgery-and-travel?utm_source=customer&amp;utm_campaign=p_cp+share-sheet&amp;utm_medium=copy_link-tip</a>!--- Send in a voice message: <a href="https://podcasters.spotify.com/pod/show/themikewagnershow/message" rel="nofollow" target="_blank">https://podcasters.spotify.com/pod/show/themikewagnershow/message</a> Support this podcast: <a href="https://podcasters.spotify.com/pod/show/themikewagnershow/support" rel="payment nofollow" target="_blank">https://podcasters.spotify.com/pod/show/themikewagnershow/support</a>