Marissa Bishop's guest appearances

Marissa Bishop

Lady Business Radio with Jessica Kupferman

Once Upon A Gene

The Young Perspective

Elon Musk

Kamala Harris

Michele PW

Laura Roeder

David Solomon

Nicole Antoinette

Becca Piastrelli

Natalie Eckdahl

Jenny Shih

Ilise Benun

Alexandra Franzen

Scott Stratten

Michelle Fetsch

Christina Rasmussen

Andrea Owen

OwlTail

Today Marissa Bishop breaks down her opinions on the recent leaked draft my Justice Alito that may overturn Roe V Wade in the coming months. Find more of us at http://theyoungperspective.netInstagram: the_young_perspectiveEmail: ejtheyoungperpspective@gmail.com 

Today Marissa Bishop breaks down her opinions on the recent leaked draft my Justice Alito that may overturn Roe V Wade in the coming months.  Find more of us at <a href="http://theyoungperspective.net" rel="nofollow" target="_blank">http://theyoungperspective.net</a> Instagram: the_young_perspective Email: ejtheyoungperpspective@gmail.com

Roe V Wade With Marissa Bishop 

ONCE UPON A GENE - EPISODE 127Building a Different Kind of Motherhood Experience Than We Had Anticipated with CDKL5 Deficiency Disorder Mom and Founder of Art For Hope Love Cure, Marissa BishopMarissa Bishop's son Gregory was born with CDKL5 Deficiency Disorder (CDD), a rare neurological disease that causes a variety of symptoms including seizures and cortical visual impairment. Marissa is a board member for the International Foundation for CDKL5 Research (IFCR) and started Art For Hope|Love|Cure to raise money for CDKL5 Deficiency Disorder research.EPISODE HIGHLIGHTSCan you tell us about Gregory?Gregory is almost 6 years old and my only child. He's handsome, laid back and a great snuggler! He lives with CDKL5 Deficiency Disorder (CDD), which is a developmental and epileptic encephalopathy. His brain is missing a protein essential for healthy brain function. Being his mom has challenged me in ways I never could have imagined, but he's a wonderful little boy.How did you connect with the rare disease community and get involved in advocacy?I asked our early intervention provider to help me connect with other moms who had kids that weren't typically developing. CDKL5 has a support group for parents on Facebook and I've been able to find friendships there with other moms who have sons that are Gregory's age. Can you share about Art For Hope|Love|Cure?Gregory doesn't have a lot of functional finger skills or function vision, so doing toddler crafts wasn't practical, but what worked best to be creative was painting on canvas. I began using Gregory's creations to raise awareness and fundraise for CDKL5. I started Art For Hope|Love|Cure on social media, took the artwork to craft shows which helped me talk to people about CDKL5. The creative endeavor has been fun and has served multiple purposes- giving Gregory and I something special we do together, raise awareness and raise funds. I'm always in search of ways to embrace Gregory's rare disease and bring richness to our lives and this has brought a lot of joy to me.CONNECT WITH MARISSAArt For Hope|Love|Cure Websitehttps://artforhopelovecure.wixsite.com/cdkl5Instagram @artforhopelovecurehttps://www.instagram.com/artforhopelovecure/?hl=enFacebook @artforhopelovecurehttps://www.facebook.com/artforhopelovecureLINKS &amp; RESOURCES MENTIONEDCDKL5 Parents Support Grouphttps://www.facebook.com/groups/CDKL5/International Foundation for CDKL5 Research (IFCR) https://www.cdkl5.com/Beyond the Diagnosishttps://www.beyondthediagnosis.org/NORD (National Organization for Rare Disorders)https://rarediseases.org/ONCE UPON A GENE - EPISODE 056 - Rare Leader Patricia Weltin, CEO, Beyond the Diagnosishttps://effieparks.com/podcast/episode-056-patricia-weltin-beyond-the-diagnosisNAC Rare Caregivers Guidebookhttps://drive.google.com/file/d/1ucr96wjmFGDFYqaKzrlkpDi_SAK4M7lA/view?usp=sharingTUNE INTO THE ONCE UPON A GENE PODCASTSpotifyhttps://open.spotify.com/show/5Htr9lt5vXGG3ac6enxLQ7Apple Podcastshttps://podcasts.apple.com/us/podcast/once-upon-a-gene/id1485249347Stitcherhttps://www.stitcher.com/podcast/once-upon-a-geneOvercasthttps://overcast.fm/itunes1485249347/once-upon-a-geneCONNECT WITH EFFIE PARKSWebsitehttps://effieparks.com/Twitterhttps://twitter.com/OnceUponAGeneInstagramhttps://www.instagram.com/onceuponagene.podcast/?hl=enBuilt Ford Tough Facebook Grouphttps://www.facebook.com/groups/1877643259173346/

ONCE UPON A GENE - EPISODE 127Building a Different Kind of Motherhood Experience Than We Had Anticipated with CDKL5 Deficiency Disorder Mom and Founder of Art For Hope Love Cure, Marissa Bishop Marissa Bishop's son Gregory was born with CDKL5 Deficiency Disorder (CDD), a rare neurological disease that causes a variety of symptoms including seizures and cortical visual impairment. Marissa is a board member for the International Foundation for CDKL5 Research (IFCR) and started Art For Hope|Love|Cure to raise money for CDKL5 Deficiency Disorder research. EPISODE HIGHLIGHTS Can you tell us about Gregory?Gregory is almost 6 years old and my only child. He's handsome, laid back and a great snuggler! He lives with CDKL5 Deficiency Disorder (CDD), which is a developmental and epileptic encephalopathy. His brain is missing a protein essential for healthy brain function. Being his mom has challenged me in ways I never could have imagined, but he's a wonderful little boy. How did you connect with the rare disease community and get involved in advocacy?I asked our early intervention provider to help me connect with other moms who had kids that weren't typically developing. CDKL5 has a support group for parents on Facebook and I've been able to find friendships there with other moms who have sons that are Gregory's age.  Can you share about Art For Hope|Love|Cure?Gregory doesn't have a lot of functional finger skills or function vision, so doing toddler crafts wasn't practical, but what worked best to be creative was painting on canvas. I began using Gregory's creations to raise awareness and fundraise for CDKL5. I started Art For Hope|Love|Cure on social media, took the artwork to craft shows which helped me talk to people about CDKL5. The creative endeavor has been fun and has served multiple purposes- giving Gregory and I something special we do together, raise awareness and raise funds. I'm always in search of ways to embrace Gregory's rare disease and bring richness to our lives and this has brought a lot of joy to me. CONNECT WITH MARISSA<a href="https://artforhopelovecure.wixsite.com/cdkl5" rel="nofollow" target="_blank">Art For Hope|Love|Cure Website</a><a href="https://artforhopelovecure.wixsite.com/cdkl5" rel="nofollow" target="_blank">https://artforhopelovecure.wixsite.com/cdkl5</a><a href="https://www.instagram.com/artforhopelovecure/?hl=en" rel="nofollow" target="_blank">Instagram @artforhopelovecure</a><a href="https://www.instagram.com/artforhopelovecure/?hl=en" rel="nofollow" target="_blank">https://www.instagram.com/artforhopelovecure/?hl=en</a><a href="https://www.facebook.com/artforhopelovecure" rel="nofollow" target="_blank">Facebook @artforhopelovecure</a><a href="https://www.facebook.com/artforhopelovecure" rel="nofollow" target="_blank">https://www.facebook.com/artforhopelovecure</a> LINKS &amp; RESOURCES MENTIONED<a href="https://www.facebook.com/groups/CDKL5/" rel="nofollow" target="_blank">CDKL5 Parents Support Group</a><a href="https://www.facebook.com/groups/CDKL5/" rel="nofollow" target="_blank">https://www.facebook.com/groups/CDKL5/</a><a href="https://www.cdkl5.com/" rel="nofollow" target="_blank">International Foundation for CDKL5 Research (IFCR) </a><a href="https://www.cdkl5.com/" rel="nofollow" target="_blank">https://www.cdkl5.com/</a><a href="https://www.beyondthediagnosis.org/" rel="nofollow" target="_blank">Beyond the Diagnosis</a><a href="https://www.beyondthediagnosis.org/" rel="nofollow" target="_blank">https://www.beyondthediagnosis.org/</a><a href="https://rarediseases.org/" rel="nofollow" target="_blank">NORD (National Organization for Rare Disorders)</a><a href="https://rarediseases.org/" rel="nofollow" target="_blank">https://rarediseases.org/</a><a href="https://effieparks.com/podcast/episode-056-patricia-weltin-beyond-the-diagnosis" rel="nofollow" target="_blank">ONCE UPON A GENE - EPISODE 056 - Rare Leader Patricia Weltin, CEO, Beyond the Diagnosis</a><a href="https://effieparks.com/podcast/episode-056-patricia-weltin-beyond-the-diagnosis" rel="nofollow" target="_blank">https://effieparks.com/podcast/episode-056-patricia-weltin-beyond-the-diagnosis</a><a href="https://drive.google.com/file/d/1ucr96wjmFGDFYqaKzrlkpDi_SAK4M7lA/view?usp=sharing" rel="nofollow" target="_blank">NAC Rare Caregivers Guidebook</a><a href="https://drive.google.com/file/d/1ucr96wjmFGDFYqaKzrlkpDi_SAK4M7lA/view?usp=sharing" rel="nofollow" target="_blank">https://drive.google.com/file/d/1ucr96wjmFGDFYqaKzrlkpDi_SAK4M7lA/view?usp=sharing</a> TUNE INTO THE ONCE UPON A GENE PODCAST<a href="https://open.spotify.com/show/5Htr9lt5vXGG3ac6enxLQ7" rel="nofollow" target="_blank">Spotify</a><a href="https://open.spotify.com/show/5Htr9lt5vXGG3ac6enxLQ7" rel="nofollow" target="_blank">https://open.spotify.com/show/5Htr9lt5vXGG3ac6enxLQ7</a><a href="https://podcasts.apple.com/us/podcast/once-upon-a-gene/id1485249347" rel="nofollow" target="_blank">Apple Podcasts</a><a href="https://podcasts.apple.com/us/podcast/once-upon-a-gene/id1485249347" rel="nofollow" target="_blank">https://podcasts.apple.com/us/podcast/once-upon-a-gene/id1485249347</a><a href="https://www.stitcher.com/podcast/once-upon-a-gene" rel="nofollow" target="_blank">Stitcher</a><a href="https://www.stitcher.com/podcast/once-upon-a-gene" rel="nofollow" target="_blank">https://www.stitcher.com/podcast/once-upon-a-gene</a><a href="https://overcast.fm/itunes1485249347/once-upon-a-gene" rel="nofollow" target="_blank">Overcast</a><a href="https://overcast.fm/itunes1485249347/once-upon-a-gene" rel="nofollow" target="_blank">https://overcast.fm/itunes1485249347/once-upon-a-gene</a> CONNECT WITH EFFIE PARKS<a href="https://effieparks.com/" rel="nofollow" target="_blank">Website</a><a href="https://effieparks.com/" rel="nofollow" target="_blank">https://effieparks.com/</a><a href="https://twitter.com/OnceUponAGene" rel="nofollow" target="_blank">Twitter</a><a href="https://twitter.com/OnceUponAGene" rel="nofollow" target="_blank">https://twitter.com/OnceUponAGene</a><a href="https://www.instagram.com/onceuponagene.podcast/?hl=en" rel="nofollow" target="_blank">Instagram</a><a href="https://www.instagram.com/onceuponagene.podcast/?hl=en" rel="nofollow" target="_blank">https://www.instagram.com/onceuponagene.podcast/?hl=en</a><a href="https://www.facebook.com/groups/1877643259173346/" rel="nofollow" target="_blank">Built Ford Tough Facebook Group</a><a href="https://www.facebook.com/groups/1877643259173346/" rel="nofollow" target="_blank">https://www.facebook.com/groups/1877643259173346/</a>

Building a Different Kind of Motherhood Experience Than We Had Anticipated with CDKL5 Deficiency Disorder Mom and Founder of Art For Hope Love Cure, Marissa Bishop

Marissa Bishop is the VP of a top NYC marketing firm, has a marketing consultancy of her own AND is beginning a new venture to help the rest of us start our own side businesses while working full time. In this episode she offers us the key to getting it ALL done as well as how to turn off the brain as well. Served with a side of Long Island charm.

Marissa Bishop is the VP of a top NYC marketing firm, has a marketing consultancy of her own AND is beginning a new venture to help the rest of us start our own side businesses while working full time. In this episode she offers us the key to getting it ALL done as well as how to turn off the brain as well. Served with a side of Long Island charm.

Marissa Bishop - Getting It On The Side