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Danielle Bean
Danielle Bean, a mother of eight, is editor-in-chief of Catholic Digest and Faith & Family. She is author of My Cup of Tea, Mom to Mom, Day to Day, and most recently Small Steps for Catholic Moms. Though she once struggled to separate her life and her …
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Rachel Balducci
Rachel Balducci is married to Paul and they are the parents of five lively boys and one precious baby girl. She is the author of How Do You Tuck In A Superhero?, and is a newspaper columnist for the Diocese of Savannah, Georgia. For the past four years, she has …
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Lisa Hendey
Lisa Hendey is the founder and editor of CatholicMom.com and the author of A Book of Saints for Catholic Moms and The Handbook for Catholic Moms. Lisa is also enjoys speaking around the country, is employed as webmaster for her parish web sites and spends time on various …
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Arwen Mosher
Arwen Mosher lives in southeastern Michigan with her husband Bryan and their 4-year-old daughter, 2-year-old son, and twin boys born May 2011. She has a bachelor's degree in theology. She dreads laundry, craves sleep, loves to read novels and do logic puzzles, and can't live without tea. Her personal blog site …
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Rebecca Teti
Rebecca Teti is married to Dennis and has four children (3 boys, 1 girl) who -- like yours no doubt -- are pious and kind, gorgeous, and can spin flax into gold. A Washington, DC, native, she converted to Catholicism while an undergrad at the U. Dallas, where she double-majored in …
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Robyn Lee
Robyn Lee is a 30-something, single lady, living in Connecticut in a small bungalow-style kit house built by her great uncle in the 1950s. She also conveniently lives next door to her sister, brother-in-law and six kids ... and two doors down are her parents. She received her undergraduate degree from …
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DariaSockey
Daria Sockey is a freelance writer and veteran of the large family/homeschooling scene. She recently returned home from a three-year experiment in full time outside employment. (Hallelujah!) Daria authored several of the original Faith&Life Catechetical Series student texts (Ignatius Press), and is currently a Senior Writer for Faith&Family magazine. A latecomer …
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Kate Lloyd
Kate Lloyd is a rising senior, and a political science major at Thomas More College of Liberal Arts in New Hampshire. While not in school, she lives in Whitehall PA, with her mom, dad, five sisters and little brother. She needs someone to write a piece about how it's possible to …
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Lynn Wehner
As a wife and mother, writer and speaker, Lynn Wehner challenges others to see the blessings that flow when we struggle to say "Yes" to God’s call. Control freak extraordinaire, she is adept at informing God of her brilliant plans and then wondering why the heck they never turn out that …
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Wayyyy off topic here, but it’s “today” that I’m dealing with this so I’ll see who can write then I’ll repost probably next week.
We’re 23 weeks pregnant with our fourth child and have just been to two specialists confirming a mild heart defect in the baby - good news is surgery will not be until 3 or 4 or so.
The hardest part has been one of the appts. was with a genentic specialist that looked and looked and found a shortened nasal bone and says one other thing looks suspicious of a “soft marker” of Down’s Syndrome. I know it’s not a diagnosis, but the heart doctor mentioned it too to “prepare” us. I’ve done too much internet looking and you know how that goes.
I was wondering from you two things: I’m having a very hard (embarassingly hard) time getting peace with this. It’s only been a few days so it’s all pretty raw. But how do you just “accept” the news a child may have a disability? I love my other children unconditionally but they are all healthy and this is just new and unfamiliar.
Second, would you suggest I go ahead and mentally/emotionally prepare for Down’s? Would you read a book? Anyone have any suggestions or experience with this? Where do you start? I have serious postpartum depression usually so this is all pretty overwhelming. Amnio is absolutely a no and I think more ultrasounds would be just more speculation.
What do you all think? Thank you for your prayers for peace.
Staceymvanderbent.blogspot.com. found out her daughter was downs in the.delivery room. Christian mom talking about what she went through and how having beautiful daughter has changed her ability to love. She just started the blog.
Barbara Curtis has a website -
http://mommylife.net/archives/down_syndrome/
Her 8th child has Down’s syndrome. They had another biological child and then adopted 3 more children with Down Syndrome. She has a lot of info as well as links to resources.
Please don’t beat yourself up for being taken aback. You’re not rejecting your child by being confused and, perhaps, frightened. Even Mary didn’t readily understand what was being asked of her…she said yes but also still pondered it in her heart. Seems to be that you’re following her example.
Check out http://www.prenatalpartnersforlife.org It was started by a wonderful Catholic mom from our parish who received an adverse diagnosis before her son was born 7 years ago.
This is from the site:
“If you have come to this site because you or someone you know has received an adverse or negative prenatal diagnosis, you have come to the right place. We are parents who have gone through similar circumstances and we want to offer support. Most of the stories on this site are of families who have carried to term after receiving an adverse diagnosis. We are here to help you. You are not alone! “
Praying for peace for you and your family.
In addition, there’s a new book by Leticia Velasquez called “A Special Mother is Born.” (I think she sometimes posts here at F&FL;, too—check thru some of the feature articles?)
Here’s a link to a nice interview with her about her book, and about Down Syndrome & diagnosis in general:
http://www.ewtn.com/vnews/getstory.asp?number=116879
Michelle, I will pray for your peace of mind, heart & body. I will pray for your sweet baby, too. I will ask the Holy Spirit to guide you *only* to the information that you need to hear & read, and shield you from anything harmful or anxiety-provoking. What is it the priest now says after the “Our Father”? “...Deliver us, Lord, we pray, from every evil, graciously grant peace in our days, that, by the help of your mercy, we may be always free from sin and safe from all distress….” That’s *ALL* distress, Michelle!
God bless you.
I’ve had two babies now with soft markers for DS. The first time I had a very hard time with it. It pretty much ruined the pregnancy. We have pictures immediately after the birth where I look like I am just intently gazing at my baby, I know that I was looking for markers of DS. By the time the next baby rolled around and the markers showed up and the blood tests were concerning (which I did because one hospital had a NICU, one didn’t-turned out that baby did need a week long NICU stay), I was completely at peace with it and blessedly so were my doctors. No one mentioned amnio but once and then the subject was dropped for the duration. BTW, both of those babies were 100% chromosomally normal.
You have already been given lots of great resources. I’d also recommend calling your local chapter of the DS Society. See what is available in your area in regards to support. I’d wager they have a list of people willing to talk to families with a prenatal diagnosis or possible diagnosis.
There is one other blog I recommend. http://www.kellehampton.com
She had a little girl, Nella, with DS in late Jan almost 2 years ago. They didn’t have a prenatal diagnosis and didn’t find out until birth. The birth story is told with text and pictures and is very raw. Kelle was extremely honest about her feelings. She has continued to blog about her life and Nella and Nella’s sister and her journey from shock and fear to the absolute joy she has found. She is a professional photographer and the pictures she takes of her girls are beautiful.
Having a child with DS isn’t the end of the world but you will have to find a new normal. A wonderful normal but different and that is OK. Don’t let this ‘if’ consume the next few months. If your baby has DS there is nothing you can do to change it, there is nothing you did to cause it. You will love this little one no matter what, everything else will come with time.
Michelle - Prayers for you and your family in this challenging time. Please don’t be embarrassed that you are having a difficult time coming to terms with this. I know I felt the same way just thinking that something might be wrong with a child in my womb (which is always a possibility, and even more scary when tests come back with suspicious results). I have always worried that I would love a child less if it wasn’t within my definition of “normal.” Now I realize that it is only the unknown which is truly frightening. While we don’t have a child with Down’s, we too had to deal with a difficult “possible” diagnosis of brain damage after our fourth child had a significant episode of birth hypoxia. However, once the child was “outside,” and I got to meet this sweet soul in person, I could have cared less what the diagnosis or possible future problems might be. I loved this child as fiercely as the 3 God gave me before this sweet soul, and I truly think you will be given the grace to feel this way too, no matter what the diagnosis. God provided us with a miracle, and our sweet baby has seemed to make a complete turnaround, for which I am truly grateful. But what I was most relieved to discover was that it really didn’t matter if my child didn’t match up to my own narrow idea of normal. God prepared me to love this soul no matter what lay in store for the future. I pray this will be your experience too!
I forgot to hit submit earlier and what i wrote pretty well echoes what you’ve already received but here goes: I just lifted you up in prayer! As for advice, i wonder about reading some blogs of families who have kids with Downs and experiencing their joy. Pondered in my heart is one that comes to mind. A family from my hometown had a baby with Downs several years ago and i remember the dad reading a book and getting super excited about a part where it discussed a technique of teaching math to a child with Downs while mom was still pregnant. I guess all that was to say to focus on what the baby can do, and wait to find out how he or she will adjust to do what others think he or she can’t. I wish you well… Please keep us posted!
We were in a similar situation about two years ago. I had a level 2 ultrasound that revealed our second baby had three soft markers (heart issue, cysts on the brain, and he refused to open his hands!) for Trisomy 18, a chromosome issue that is usually fatal. Against medical advice, we declined all further testing. I gave birth to a very healthy baby with a mild heart murmur
Please do keep reminding yourself (I know it’s hard) that soft markers are not a diagnosis. They tell you about them to keep you informed and also to cover themselves.
I read absolutely everything I could about Trisomy 18, then figured out that I was making myself more anxious rather than reassured, and gave it up to God. I truly believe that we get the grace to deal with these types of things in the moment, not in the months before. Prayers for a peaceful pregnancy and healthy delivery!
Only you know you. At birth, my son was diagnosed with spina bifida. At first, all I could do was read read read read about SB. I joined support forums, read blogs of other moms with SB babies… the whole nine yards. It became my life for awhile. Afterall, at the time I knew nothing about spina bifida & also only had a fuzzy sense of how serious my son’s current condition is/was. So it was kind-of like I had to immerse myself in the world of SB to be emotionally, mentally, and knowledge-based-ly prepared for anything. Once tests started being done & facts about my son’s actual situation started coming up & we could talk with people who not only knew about SB in general but about my son’s particular case… I was suddenly able to let go of all the books and websites (though who knows—I may need them again in the future!) I just share this to say that whatever you feel you need to help you get through NOW may not be what you need tomorrow or next week… so just go for what feels helpful to you now & let later take care of itself—even if you realize that may mean there are no “issues” later. Just do what you need to do to heal NOW. The news of possible handicaps is its OWN issue for YOU to “heal through” even if it turns out to be unfounded. Seek support!!
Also, please give yourself time to warm up to your baby & the possibility of the struggles he/she (and your whole family) may face. Pain, struggles, heartache… you are not “supposed to” be able to just embrace all that right away! I KNOW it feels nasty to not fall in love right away with your little life inside you… but just be at peace that it WILL happen. I have a dear friend whose daughter has various health issues (deafness, inability to sit or walk, etc.) and my friend said it took two solid years to “fall in love,” but now she can’t imagine life without her dear one!
I know those may not have all been the words you were hoping to hear. Some rough patches on the road of life are rough for awhile & it is never nice to have to drive through them on and on and on. But whatever the future holds for your little one and your family please remember that
a) you will FALL IN LOVE with this child over time
b) you will adjust to your child’s special needs and soon they won’t feel unusual but simply part of your normal routine and your child will stop feeling “handicapped” to you
I recommend you name your baby as soon as possible!! It helps the falling in love part…
I am currently going through pretty much the exact the same thing…I am currently 25 weeks pregnant with my second daughter, and am anxiously awaiting an appointment with the pediatric cardiologist.
Everyone has given great advice, but I would just like to add- I know this is hard to process. By the time my daughter arrives, we will have been struggling with the many different feelings that come with this diagnosis for about 6 months. Just today in my “research” I came across this article http://abcnews.go.com/blogs/lifestyle/2012/01/target-ad-with-down-syndrome-boy-helps-dad-blogger-raise-awareness/ that links to a dad’s blog about his son’s story: http://noahsdad.com/story/
The article points out the reoccurring statistic that “90 or 92 percent of of parents who learn through prenatal screening that they have a relatively high chance of having a child with Down Syndrome abort the pregnancy.” Personally, I was HORRIFIED, and I believe that we have been chosen to carry and love this child because we are NOT that 90 to 92 percent. We will choose to bring this child into the world confident that they are perfect in the eyes of God who created them. This doesn’t mean it won’t come with struggles and fear, but I believe that He knows what both our children and us need. Keep praying, you’ll be in mine, and update us if you feel like it!
My brother in law has Down Syndrome, and my beloved mother in law told me about a simple short story called “Welcome To Holland”. If you google it you can find it. It is a beautiful analogy for learning to accept the initial heartbreak and confusion that comes with learning about a disability, and the joy that can be found when you rearrange your expectations. Please check it out!! I will pray for you, your baby and your family.
Yes, do read Welcome to Holland!