01/06/2024
My mom had a beautiful Requiem Mass. please continue to pray for her soul.
Shout My Story (www.shoutmystory.org) is a social media campaign of Pro-Life Champions, a tax exempt
(5)
My mom had a beautiful Requiem Mass. please continue to pray for her soul.
March is Trisomy Awareness Month. And Sajjona is 6 1/2! Her mom wanted to give an update:
"Sajjona is a ROCK STAR! She will be 6 1/2 on April 3. That's a far cry from only surviving 2 weeks as the medical professionals predicted. We chose life for Sajjona and followed God's plan. This past summer we took her to the top of Cannon Mountain in New Hampshire. Sajjona loved it! Her oxygen levels were amazing up there! We went glamping at Yogi's Campground. Sajjona loved the water park! She had a blast! Her life is rich and filled with adventure and with her family that knows how to care for her. Sajjona is developing quite nicely...she is learning how to walk! And she is taking short steps with help! She can sit by herself and she loves her gait trainer.
Sajjona is saying words and she understands what is said to her. One day she called "Girls! Girls!" She was calling her sisters because she needed her diaper changed. She says several words including "Dada, momma, ayge (for her sister Sayge), p**p, baby and girls," She shakes her head "yes" or "no" to questions like "Do you want to go to bed?"
Sajjona was recently featured in a Born Abel book called "Leary the Leprechaun." These books are written to educate people that kids with complex medical conditions have value and worth.
Sajjona has a love of art and music. She is very capable of using her hands and can hold a crayon or paintbrush. Pretty impressive since she was never supposed to be able to use those "clenched hands."
We were devastated when Kate Cox terminated her Trisomy 18 child. We don't always get what we want, but God sends us exactly what we need. Sajjona has helped us all become stronger people. Her siblings have more compassion and love for those with disabilities.
Sajjona may not follow the "typical child" and she fits right in with us because we aren't the typical family. She does everything on her own time. She has a story to tell and we let her tell it her way."
You can follow Sajjona on her page:
March is Trisomy Awareness Month!
Sajjona is now 6 1/2! Her mom gave me an update:
Sajjona is a ROCK STAR! She will be 6 1/2 on April 3. That's a far cry from only surviving 2 weeks as the medical professionals predicted. We chose life for Sajjona and followed God's plan. This past summer we took her to the top of Cannon Mountain in New Hampshire. Sajjona loved it! Her oxygen levels were amazing up there! We went glamping at Yogi's Campground. Sajjona loved the water park! She had a blast! Her life is rich and filled with adventure and with her family that knows how to care for her. Sajjona is developing quite nicely...she is learning how to walk! And she is taking short steps with help! She can sit by herself and she loves her gait trainer.
Sajjona is saying words and she understands what is said to her. One day she called "Girls! Girls!" She was calling her sisters because she needed her diaper changed. She says several words including "Dada, momma, ayge (for her sister Sayge), p**p, baby and girls," She shakes her head "yes" or "no" to questions like "Do you want to go to bed?"
Sajjone was recently featured in a Born Abel book called "Leary the Leprechaun." These books are written to educate people that kids with complex medical conditions have value and worth.
Sajjona has a love of art and music. She is very capable of using her hands and can hold a crayon or paintbrush. Pretty impressive since she was never supposed to be able to use those "clenched hands."
We were devastated when Kate Cox terminated her Trisomy 18 child. We don't always get what we want, but God sends us exactly what we need. Sajjona has helped us all become stronger people. Her siblings have more compassion and love for those with disabilities.
Sajjona may not follow the "typical child" and she fits right in with us because we aren't the typical family. She does everything on her own time. She has a story to tell and we let her tell it her way."
You can follow Sajjona on her page:
This is Jessica's story.She is a survivor of forced prostitution and abuse. She was given support by a stranger and it completely changed her life and the li...
All links are to SPL content unless otherwise specified. You can also search our blog containing 1000s of non-religious pro-life articles.
In the past few reels, we shared Karina’s powerful story of choosing life and how her family came beside her. Listen to the full story through link in bio!
Read Dana’s full story through link in bio
•
•
•
•
•
I posted this meme last year and it proved to be popular. Sadly, this year the message is still just as important so I'm posting it again. Say no to prejudice. 🚫
They said “ Your daughter Sajjona will be nothing but a vegetable”…She is nothing but a carrot top they were partly correct🥰Our little Red head proving them so wrong! Cider Hill Farm!
What are your thoughts? Write in the caption ⬇️
Thoughts from a pro-life foster mom: "Implying the world would be better if children like my son, or the other incredible children I’ve met in foster care, didn’t exist is a HORRIBLE thing to say. It’s not the moral high ground people think it is. He is loved. He is valued. He is valuable."
https://secularprolife.org/2023/04/a-foster-mom-speaks-up-my-son-is-loved-he-is-valued-he-is-valuable/
No matter the situation… we have a duty to speak up for the vulnerable.
We want to read your answers in the comments!!
… and we still have a long way to go to ensure equal protection for all humans!
What will you do to help end abortion in America?
•
•
•
•
Samuel Wade Wardrop was a loved and cherished 3-year-old, who was full of joy and s***k. In his short life he overcame many prejudices and medical challenges. So, who would have imagined that the very medical professionals and equipment his life depended on would have been slowly killing him?
You see, Samuel was born with a 47th chromosome, a condition similar to Down syndrome, but known as Trisomy 18 (or Edwards syndrome). Despite being wanted and valued by his parents, the medical community considered him “incompatible with life.” Thus, his parents were forced to advocate for his every care, even to the point of going out of state for life-saving heart-repair surgery, at the tender age of ten weeks old.
Thanks to the wonders of modern medical technology, Samuel was able to receive the hydration, nutrition, and oxygen necessary for life, growth, and healing, through a feeding tube and ventilator. However, it was his ventilator that ultimately caused his death, over a period of 10 months of neglect and misuse by the very medical professionals tasked with his care.
After about a year of successful ventilator use, Samuel’s Respiratory Therapist switched him to a ventilator that was NOT prescribed by the doctor. Two months later, a new Respiratory Therapist, who had admittedly not been trained on this particular ventilator, assumed care of Samuel. Thus, without securing doctor’s orders specific to the new ventilator, he blindly inputted the settings prescribed for the previous ventilator. This error went unchecked for an additional eight months, at which time the Pulmonologist made every effort to correct the consequences. However, the ventilator was also found to have a software defect and the damage to Samuel’s lungs (from receiving adult ventilator volumes for 10 months) was irreversible, so he ultimately succumbed to pulmonary hypertension and pulmonary hemorrhage.
Now, you would think that in a society which highly values “choice,” that parents’ “choice” to value and cherish their own flesh and blood child would be respected and upheld at all cost. But, such is NOT the case!!! In fact, not only was Samuel’s life cut short by medical prejudice and neglect, but his family is also being denied the satisfaction of a legal inquiry, because even in death he is considered “unworthy.”
Samuel’s family has 10 days left on the statute of limitation, so if you are or know of an attorney, licensed to practice in the state of Utah, who is willing to defend Samuel’s value and dignity to life, THEY NEED YOU NOW!!!
Maybe you think you’re too small to make a difference
Maybe you think you don’t have a story significant enough to share
Maybe you just need a little more motivation..
Click the link in bio, watch stories of brave women who chose life, and consider sharing with your friends and family. You have incredible potential to make a difference!
•
•
•
•
•
•
Knowing where your priorities lie.
Want to know how? Watch our videos through link in bio to see how other women have exercised their bravery :)
•
•
•
•
•
•
•
Everyone… in every country… deserves the right to LIFE!
•
•
•
•
•
•
Can we get an “Amen?”
•
•
•
•
•
•
•
•
•
The Pro-Life Movement is the most important human rights movement of our time.
•
•
•
•
•
•
•
As Mother’s Day approaches, let’s be grateful that our moms chose life and watch the beautiful videos of brave women who also chose life through the link in bio.
•
•
•
•
•
•
Listen tomorrow from 6-8 am central!
20 Years of Bringing Christ to the World: Morning Air - Relevant Radio
Dena celebrated her 40th birthday! See her story here: https://youtu.be/lsU-2PuUWng
Incredible victory! Go to the link in bio to see stories of women who also, bravely, chose LIFE!
•
•
•
•
•
•
Be the first to know and let us send you an email when Shout My Story posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.
Send a message to Shout My Story:
"The phrase “incompatible with life” is not a medical diagnosis: Doctors use it to pressure women to have an abortion when their child is diagnosed with a life limiting condition. "My message to doctors is to tell the other side of the story."---Nancy BInger, Executive Director of Gigi's Playhouse. This film will educate and challenge the medical community to change the way they view pre-born children who are diagnosed with a disability or life-limiting condition. It will also give women faced with this challenge to choose life for their child. Help up complete this 30 minute inspiring film! Donate here: https://transaxt.com/Donate/GTFDD3/The40Film/
Pro-life champion Ryan Bomberger, Co-Founder of The Radiance Foundation on why Shout My Story. #ShoutMyStoryorg #whywemarch
Dan and Deborah FioRito share why the story of miracle Baby Thomas needs to be seen across our nation. Thomas is one of the youngest babies ever to be born in our country at 22 weeks. He's a living testament to life who overcame a million to one odds. Visit our webiste at www.ShoutMyStory.org
Want your business to be the top-listed Media Company?
Pro-Life Champions, producers of the 40 film, introduces the Shout My Story campaign. Shout your video, audio and print stories of choosing life in difficult situations at www.ShoutMyStory.org #ShoutMyStoryorg