Meet Our Contributors



RaeAnne Fredrickson is mama to Samuel Evan, and married to her loving husband, Bryan. She is the creator of All That Love Can Do. She runs the Facebook page and private groups for All That Love Can Do. She writes for Still Standing Magazine. Samuel's story is on her blog, The Love We Carry, in the book Still Standing: Because They Lived, and the upcoming book, Invisible Mothers. Her precious son, Samuel, was carried with all her love for 35 weeks, and lived for 4 hours after birth. Every moment of his life was filled with love, and she wants to help other families experience the joy of carrying their babies to birth and the peace that comes from saying goodbye in the best way possible. She speaks openly about the grief of living without her son, and the lasting impression his life has made on this world. She is also the co-founder of Still Mothers, Childless Living After Loss, which provides support to mothers with no living children (coming Mother's Day, 2015). She firmly believes all life is precious, even a short one.

Megan Coker carried Eden Olivia to birth in June 2015 after receiving a diagnosis of a severe Congenital Diaphragmatic Hernia in the Bilateral form. Eden lived for 40 minutes. Megan is Ryan’s wife and together they follow his Army career. She has found a way to honor Eden’s short life in capturing the beautiful moments of others through starting her photography business, Eden’s Garden Images. Each day has its new challenges for both Megan and Ryan but they are learning to lean on each other through it and work steadily on strengthening their marriage. Megan finds healing through writing about Eden and remembering their beautiful time together





Bethany Conkel lives in Ohio and is married to her wonderful husband, Eric. She is the mommy to two amazing children – one who is in heaven, the other here on earth. Bethany carried her precious son, Amalya Nathaniel (meaning: “work of the Lord”, “given by God”) to term after receiving the diagnosis of anencephaly when she was 11 weeks pregnant. Amalya lived for 1 hour and 20 minutes before taking hold of the Lord’s hand. After he passed, his liver, pancreas, and whole body were donated to scientific research. Bethany has since created a website about neonatal organ, tissue, and whole body donation called Purposeful Gift to help other families explore the option of donation. She is also a certified Birth and Bereavement Doula through Stillbirthday.com and serves with Sufficient Grace Ministries.



Jenna Gassew is from outside Philadelphia, Pennsylvania. She is a graduate of Rosemont College with a degree in Mathematics. She is the mother to a beautiful little boy in heaven, Shane Michael Haley. Shane was diagnosed with Anencephaly at 13 weeks gestation. Jenna and Shane’s father, Dan, decided to create a bucket-list on which they took Shane to various places such as Phillies games, New York City, and Ocean City, Maryland. Shane was born October 9, 2014 and lived for four precious hours where he spent his whole life loved. She continues to bring awareness to Anencephaly in honor of her son. More about Jenna, Dan, and Shane’s journey can be found on  their facebook page, “Prayers for Shane.”


Alex Hopper is a writer in North Carolina. She is married to her beloved, Trent, and mommy to her angel, Cyrus. Cyrus was diagnosis with a fatal birth defect in the womb at 12 weeks. He was carried with love until he was born at 33 weeks on November 25, 2013. He lived for 1 hour and 9 minutes. His life was short, but his legacy lives on.






Heather Kimble lives in the Philadelphia area. She is married to her best friend, Jason and is mommy to Hannah Sue Kimble. Hannah is her only child. Heather carried Hannah after receiving a fatal diagnosis and was told to terminate. Heather was told to terminate based on the serious risk to her own personal health. She doesn't believe in termination and chose to carry Hannah with love. Hannah passed away and was born sleeping on December 23rd, 2013. Heather and Jason treasure every moment they had with Hannah during pregnancy and after delivery. Hannah has inspired a nonprofit started by her parents to help others and to help break the silence by sharing their journey of baby loss. Visit her blog, Hannah's Heart and Love, and follow her page on Facebook.


Christine Russo is a wife to an amazing, supportive husband, and a mommy to Angel Gianna Marie, her first child. She carried Gianna after receiving a fatal diagnosis halfway into her pregnancy. Through the love and spirit of their special daughter, who means the world to them, they wish to help support other families who have to say goodbye to a piece of their heart.







Kayla Schacht is a writer from Utah. Her youngest princess lives in the clouds after living for 48 minutes after birth, all which were in her daddy's arms. Elly Jae was diasgnosed with a fatal birth defect at 13 weeks gestation. She spent 31 weeks and 5 days safely in her Mommy's womb where she was cherished every second. Elly Jae has changed not only her parents and sisters lives, but lived of complete strangers. Find them on Facebok, at  Prayers for Little Elly Jae.







Jessi Snapp resides in Indiana where she is pursuing her master’s degree in social work. She is married to her wonderful husband, Karl, and she is a mother to one living child and three in Heaven. After enduring two losses to miscarriage, Jessi became pregnant with her son Silas Edison who was diagnosed with Trisomy 18 at 20 weeks gestation. Silas was born and passed on August 20, 2014. Though his life was brief, he is loved for a lifetime. In Silas’ memory, Jessi turned his nursery into an art studio where she creates custom memorial art for other babies gone too soon. You can find her heart-centered work at LuminousLightStudio and on Facebook.







Kellie Soper lives in Arizona and is wife to her amazing husband, Jason. Together they have two beautiful children, one on earth and one sweet, perfect soul in Heaven. Ted is a wild, silly, and rambunctious toddler. Their sweet Lily Frances was born sleeping on November 12, 2014. They learned at their 18 week ultrasound that Lily had a fatal neural tubal defect the doctors said was "incompatible with life." Kellie and Jason both knew Lily was not a "decision", but their precious daughter and they believe her life was of value, no matter what. She carried Lily with love for 42 weeks and 2 days. They miss her every single day, but are grateful for the honor and privilege of being her parents. You can read more about their family on Kellie's blog, Life and Love.

0 comments:

Post a Comment

Powered by Blogger.
 
Design by Luminous Light Studio | All Rights Reserved