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Tuesday, April 11, 2017
Last Monday, I received a call from the District Attorney’s office stating they did not have enough evidence to file criminal charges of any kind against my rapist. I literally collapsed on the floor upon hearing the news. The wind was knocked right out of me. That wasn’t enough, however. The story of my rape, pregnancy, and birth of my child made a lot of local news headlines because of my demands for justice, so when the DA made the nine page memo describing why he wouldn’t pursue any criminal charges against my rapist public, the media had a field day. Within a couple hours, my face was once again splashed all across the television and social media.
The reaction on social media was nothing short of disgusting and devastating. Sure, I had support from friends and family, even from strangers who have been following my story, but the nasty comments were hard to ignore.
I read things like:
“Your credibility went out the window when we found out you had a bunch of different kids with a bunch of different fathers.”
“You’re a known drunken whore.”
“You are a liar.”
“You belong in jail.”
But the worst was:
“I feel sorry for that poor baby. I hope the father will finally get to see his baby.”
Immediately, I began to pray. I pleaded that God would protect my child. In the state of
Wyoming, telling your rapist “No” is not
enough to prosecute a rape. In Wyoming, being
incoherent, drunk, or drugged is not enough for a rape conviction. Further, a rapist has total access and
ability to exercise his parental rights to his child conceived in rape without
a conviction. In other words, it's open season on women.
My mind wandered to a dark place. I thought about the fact that, had I just snuck out of town and had an abortion, no one would’ve ever known about the rape. My rapist wouldn’t be able to fight for custodial or visitation rights. No one would be calling me a liar or a whore.
I wanted to slap myself. I sobbed and looked down at my beautiful little girl and I thanked God for her. I am so thankful God protected her, and I didn’t kill my precious and innocent baby with an abortion. How dare I let my mind even consider such horrible thoughts, just because of the cruelty of others. I refocused and praised God.
Having my beautiful daughter, finding my voice, giving hope and inspiration to other women who have been victims of sexual assault, and advocating for victims' rights was worth whatever public backlash I was receiving via social media and within my community. I was being labeled a liar and a whore. I was being told I made the entire thing up just so a "potentially loving father" wouldn’t get to see his baby -- never mind the fact that he never sought to see her. So despite all of my public advocacy for my rights, for rape victims and victims' rights, I learned I have a long road ahead of me with the news of the DA not being willing to file charges.
My fight is just beginning. I am so thankful for the people who continue to support me and who continue to stand beside me. I am proud of the choice I made to keep and parent my baby conceived in rape. I will continue to fight tooth and nail to ensure my rapist cannot exercise parental rights to her. With the help of social justice advocates and local legislators, I hope to achieve legislation that will actually protect babies like mine.
If a woman is brave enough to report her rape, give birth to a child conceived in rape, and speak out against a flawed legal system, the last thing she should ever have to worry about is her rapist having access to her child. No wonder so many women are forced into silence and feel as if they are forced to abort. What a nightmare to be faced with the potentiality of having to co-parent with a rapist!
I am so thankful for the legislators who have reached out to me and offered support to pass a bill in the state of Wyoming which will include language to prevent rapists (even without a conviction) parental access to the child conceived in rape -- The Rape Survivor Child Custody Act. I hope other legislators will see our laws are flawed. Rape is almost impossible to get an arrest, let alone to convict in my state. Loving mothers who become pregnant by rape shouldn’t be further victimized by being forced to subject their innocent children to rapists. Our laws need to be fixed. Rapes need to be easier to prosecute; police need to be given all the tools to investigate a rape swiftly; and children conceived in rape need protection from their mother’s rapist.
Please keep my family and my beautiful baby in your prayers. I declare God will protect my child -- a precious blessing He bestowed upon me.
Thank God for protecting her and loving her. I pray He continues to do so.
BIO: Aimee Kidd is a mother of 6, self-employed, in Casper, Wyoming, and is a pro-life blogger for Save The 1. Her first piece written for our blog is found here: http://savethe1.blogspot.com/2016/12/she-has-no-part-in-any-of-ugliness.html and her second piece is found here: http://savethe1.blogspot.com/2017/01/raped-pregnant-and-determined-to-abort.html
Labels: Aimee Kidd, Conceived in Rape, pregnant by rape, pro-life blogger, Rape Survivor Child Custody Act, Save the 1 | 0 comments
Friday, March 10, 2017
Are You Planning on Supporting the March of Dimes this Spring? Think Twice- Their History of Eugenics May Surprise You
Are You Planning on Supporting the March of Dimes this Spring? Think Twice- Their History of Eugenics May Surprise You
It's the beginning of March- spring is almost here, and some of us welcome the image of snow melting away and flowers in bloom once again.
Something else happens in March, which most people are probably aware of, but don't pay mind to. The March of Dimes steps up its fundraising campaigns, utilizing the warm weather (great for walking), the fact that people are financially recovering from their Holiday shopping, and the name of the month for inspiration.
Those of us who advocate for the non-typical child may see friends posting information about their personal walks. My family participated the first year after losing our daughter, Beatrix and raised a small bit of money. However, upon taking a more detailed look into the March of Dimes we decided that it wasn't for us.
Who could speak out against an organization which has the sole purpose of saving the lives of babies?
Over the years the March For Babies has come to symbolize all that's good about public contribution to modern medicine: it's most likely the closest many people come to actively working towards ending birth defects. It gets people together to work for the most worthy cause of all: saving lives.
Unfortunately the March of Dimes has a decidedly eugenic, pro-abortion history.
Originally founded by FDR to combat polio, the March of Dimes moved on to "birth defect prevention" after successfully curing polio in the US, via funding research for Jonas Salk's polio vaccine.
During the early 60's, when they switched gears and began working to prevent birth defects, prenatal testing became their main focus. The purpose of this testing was to figure out how to detect anomalies in order to terminate pregnancies where they were found. The researchers employed, educated, and/or supported by the MOD pioneered the use of amniocentesis and chorionic villi sampling to prenatally detect disorders such as Downs Syndrome. The MOD claim this testing is necessary to "prepare" parents for a child with special needs, yet over the decades it's become apparent that the tests are used for search and destroy missions against genetically atypical children. For example, in the US we know that 90% of children with Trisomy 21 (DS) are aborted after a positive genetic test. For more serious Trisomy disorders, the percentages of abortion are even higher. In addition, for those babies who are allowed to progress full-term, the prenatal testing which identified their syndrome can be used to deny life-saving medical care. Their "quality of life" becomes an issue, as does the concept of "futile" care, leaving many parents without the legal ability to advocate for their children's lives (1) (2). Genetic testing has become the means by which a human being can legally be denied medical care, and that genetic testing was developed through the MOD.
While the March of Dimes claims this to be an unfortunate byproduct of their research, and to be a neutral party to the abortion debate, they have a history of supporting the studies of eugenic physicians, utilizing aborted fetal tissue in fetal experimentation, (1), and relying on exceptionally gruesome fetal experimentation- including experimentation on living fetuses- which far surpasses anything we've heard on videos from current times. While we can't draw a direct line from their research into prenatal diagnosis to abortion, the connection is abundantly clear for any who choose to search for it -- although, you must search through archived internet articles because they've "scrubbed" many of the documents supporting abortion which they previously authored and offered. (please see note below regarding links).
The March of Dimes, far from being a premier supporter of the rights of babies with disabilities, currently uses their clout to secure funding and donations which are used to develop even more specific testing. While claiming to have "conquered" a number of genetic disorders, the record shows that many of their "successes" comes from ever-earlier prenatal testing and abortion, rather than finding cures for genetic disorders which affect children.
We urge pro-life individuals to refrain from donating to this organization.
For those who wish to contribute to research into prenatal diagnosis and complimentary treatment for children with disabilities, there is an alternative organization you can donate to: the Lejuene Foundation (named after Jerome Lejeune, the physician who discovered the cause of Down Syndrome). The Lejeune Foundation is a life-affirming research group which studies genetic disorders with the aim of helping individuals live better, fuller lives within the context of their disabilities. Jerome Lejeune was horrified when his discovery of a third chromosome 21, as the cause of Down Syndrome, was used to target affected unborn children for the purpose of ending their lives. He spent the later part of his life fighting for the rights of all children to live to the best of their ability.
If you would like to give to this organization (or any other pro-life organization which helps individuals and families meet the challenges of an atypical life), we have included a few links below. All of these organizations are decidedly pro-life, and will satisfy both the desire to help families, and the desire to encourage them to keep their babies.
From their website:
From their website:
"Support information & encouragement for carrying to term with an adverse prenatal diagnosis and support for raising your child with special needs after birth."
From their website:
"The mission of the Jerome Lejeune Foundation USA is to raise and disburse funds in order to provide research, care, and advocacy to benefit those with genetic intellectual disabilities in accordance with the medical and ethical standards of Dr. Jerome Lejeune, the father of modern genetics. This is carried out by conducting, promoting, and funding therapeutically oriented research; by assisting in the development of healthcare services for these individuals; and by serving as their advocate in a spirit of respect for the dignity of all human persons."
(Note: Much of the information available is only accessible via print, so sources linked above may not be varied enough to satisfy some readers- please feel free to research individual claims on your own, and if you find discrepancies or current links, please comment below so we can correct the information. Unfortunately the Pro-Life clearinghouse for MOD info, The Michael Fund, is no longer in service, and adding each individual link rather than articles referencing them would mean an excessive number of outbound links.)
Wednesday, February 22, 2017
My name is Jennifer Frey. I would like to share a piece of my heart here with you, and her name is Faith Elizabeth.
Before I get there, I would like to confess, I haven’t always been pro-life. In fact, I was very much pro-choice until my children came into my life. I remember in high school writing my senior paper on the topic of abortion. Being the naive teenager that I was, I thought for sure those extreme cases of rape, or health of the mother/baby were valid reasons for abortion.
I hadn’t thought much about the topic of abortion until I had children -- in particular, my second born baby. All of my children have changed my life, but she is the one who changed things deep in my heart.
While I was pregnant with my second born baby, at my 20 week ultrasoundcame some devastating news. Our baby was promptly diagnosed with anencephaly. Words I had never heard before -- “incompatible with life” -- were used.
The doctor refused to show us any more pictures of the baby, as to "not hurt our feelings." They did not tell us the gender and they sent us on to a specialist. I left feeling like my baby was already dead.
At the appointment with the specialist, they confirmed the diagnosis. They told us over 95% of families with this diagnosis have an "early termination." They told us it was okay to do, that it was too difficult to carry the baby to term just to watch it die. We were told the baby wouldn’t make it much past birth or could pass away in utero. The doctors offered no support for choosing life. It was never given to us as an option.
I will admit right now, I believed them. I was a beginner Christian, a fairly new mom (my oldest was 3) and was still unsure about abortion. The doctors did a really good job of making it seem like termination was the best choice.
Without making any decisions at that appointment, my husband and I went home, barely able to talk to each other, let alone cope.
We were leaning towards early termination. I thought that there was no way I would be strong enough to carry the baby to full term, just to watch the baby die. I had even made the appointment for the termination. By the grace of God, we ended up cancelling the termination the day before my appointment. Something stirred in my heart to love my baby, and I regained my mother's heart for my child which was almost stolen by lies and deceit -- not just from the doctors, but by our country's opinion of babies with adverse diagnoses.
We carried our baby -- our daughter -- to full term. We named her Faith Elizabeth. During the remainder of the pregnancy, she lay breech in my womb, her head right up under my left rib cage, close to my heart -- the symbolism of which I hold very dear.
We included our older daughter, Julianna in all the planning so she could always remember having a part in her sister's life.
On December 27, 2010, Faith Elizabeth was born. We were told to expect theworst, that she would be deaf, blind, mute, and probably unconscious. From what they could see on ultrasound, she had a severe case and seemed to only have use of her brain stem.
Faith was born, and she defied all expectations! She was alive, alert, eyes open, making noises and responding! We spent the day with her, introducing her to family and friends.
She lived for 18 hours, and died in my arms. She was here only a short time in our lives, but the impact she made in my life is continuous and ongoing.
While it is a sad, bittersweet memory of mine now, there is also an enormous Joy that goes along with it. Her life changed mine. And when I think back about being in that place of finding out her diagnosis, wondering if it would be easier to terminate or not -- I find myself so thankful for choosing life. I imagine I would have been filled with regret had I chosen to terminate. But now I am thankful to have given her the best chance at the longest life possible for her. I will never regret having met my daughter and seeing my oldest who was wise beyond her years cradle her baby sister.
My family and I are now a solid pro-life family. We stand for life, we fight for life, we help others going through situations like our own because we KNOW how precious life is. We have learned that life is sometimes short, but sweet, and to enjoy the time we have together. It is so worth it to choose life every time -- whether in your womb or in your heart. You won't regret it!
I've been doing my own research on abortion ever since I've had Faith and it always felt like there was a portion of the discussion missing because abortion is often associated with clinics like Planned Parenthood, there wasn't much talk of the abortions that happen in hospitals due to medical influences there. It's a whole hidden agenda that most people aren't aware of, and so many babies are killed by abortion each year as recommended by doctors, at hospitals, because of a disability.
When I was pregnant with my firstborn, it was suggested that we do genetic testing and they said our daughter had a high chance of Down Syndrome. We were offered "options." And then again, same thing with our 3rd born child. She had measurements which were "off" and they were talking about doing more testing so I could have "options." Today, all three of my living children are completely healthy. Had I taken the advice of my doctors, I would have aborted three children and have only one living child today!
Thank you to Save The 1 for bringing awareness to this sneaky area of abortion. I am available and would love to help in any way!
BIO: Jennifer Frey is a wife, mother of four, photographer and pro-life blogger for Save The 1.
Labels: anencephaly, babies with adverse diagnoses, carry the baby to term, early termination, incompatible with life, Jennifer Frey | 0 comments