Ordinary Family, Extraordinary Circumstances

Posted on

We are just an ordinary family.  A dad, a mom, some kids, and the token yellow lab.  We live in a normal house and do normal things.

And yet, in June 2011, the most abnormal thing happened to us that changed our lives forever.

I found out I was pregnant again by the end of January 2011.  Of course I was a nervous wreck until we reached that 12 week mark, because of my miscarriage that previous Fall, but luckily my OB was very supportive and even gave me an ultrasound at 13 weeks so I could see that everything was perfect.  From that point on, we were flying high with the excitement of a new baby and were looking forward to our 20 week scan.  No matter how many times we’d been through it, those ultrasounds were so incredible each and every time.  Little did I know,this 20 week scan would be different than any other I’d had.

When we arrived the morning of the ultrasound, we were very excited.  We had chosen to keep the sex of the baby a surprise again, and were looking forward to seeing all his/her perfect parts and the profile of our newest baby.  The scan went great, but at the end the Tech told us “I’m going to have to send you to a Specialist because the baby has some fluid in the brain and you will need to be monitored. Your baby hassevere Fetal Hydrocephalus.

Enter: Knife in heart.  What? What did this mean?

This news would send us on a whirlwind of emotions, research, and a journey into the unknown.  So much unknown, that we decided to go ahead and find out the sex of the baby… it was another girl. We chose to name her Meagan Theresa.

After having a few days to digest the diagnosis and do hours of research on our own, we had adjusted…well, as much as you can adjustWealways felt open to whatever child was sent into our life, so we just had to pick up our pieces, and keep going.  The diagnosis had a name – but we soon realized the prognosis was completely up in the air.  We had found several helpful websites, and through those, found other Hydrocephalus parents’ blogs.. who then invited us into a private Hydocephalus message board online.

We gained a wealth of information and knowledge. We found out that her brain was being squished by the fluid against the back of her skull… that there was nothing we could do for her while in utero … that she would need brain surgery after birth to insert a shunt (“fake” drain) into the area her body had failed to form correctly.. that she would need this device for life… and that there is NO guarantee or predictor as to how our daughter would be when she was older. Some kids have multiple surgeries because of the failure rate of the shunts… some get lucky and have one.  Some kids are slow to ‘catch up’ but then are ‘normal’ by age 4 as long as the shunt keeps functioning… some kids have severe special needs…from eating, to gross motor skills, to mental issues.

There was literally no way to tell what we would be dealing with until we actually lived through it.

We had to see a Perinatologist due to our daughter’s condition.. One of the first things we were asked upon our first ultrasound with their office was… “And would you like to continue this pregnancy?” It really shocked me.. I was 21 weeks pregnant – were they serious?  And yet, we were asked again by the doctor, “I just have to ask this to do my job…but are you thinking of terminating the pregnancy?

This initial appointment really stung.  The words of the doctor and genetic counselors hung over me like a black cloud. Why would they ask this of parents ONE day into a devastating diagnosis…and how exactly is asking “just doing his job?

Isn’t the Specialist’s job to treat my baby in the womb… not offer to abort her like she’s worth nothing?

Isn’t she his patient?

I’ve always been a pro-life woman.  But now it was personal…and it really got me thinking about the issue.  I couldn’t believe I had been asked to terminate my pregnancy at all…let alone at 21 weeks. And that’s not even the worst. I was asked again at 23 weeks, 25 weeks, and 28 weeks pregnant.  Abortion takes women in my situation, a distressing, devastating diagnosis of a child, and preys upon the woman’s emotions before there is any time for logical and rational digestion of that issue.  Too many lives are lost to abortion due to these ways that the industry ‘attacks’ women.  The apathy surrounding the abortion issue doesn’t help either.  When people say “I would never have an abortion, but it’s not my choice to make for others,” it disregards any human responsibility we have for compassion towards others and valuing our fellow human citizens.

As we continued our journey, I read more and more stories of mothers contemplating termination for a Hydrocephalus diagnosis.  Without trying to sound insensitive, I didn’t understand this logic.  For us, our options to “deal” with a pregnancy (good or bad) ended when we became pregnant. I’m not disregarding the fact that a diagnosis such as our daughter’s was tough… it still is.  It is devastating, sad, and uncertain.  It can (and frankly, should) make us, as her parents, upset, worried and even angry at the world. However, how.. HOWdoes this translate into thinking it is then ok to end her life? What if my oldest daughter, born perfectly normal and healthy, was in a biking accident at 8 years old and had severe brain damage? Would we end her life because it would be “better for her?” How is this any different than Meagan, who happens to have a condition from birth? The answer is, there is no difference.

This is why I hate the term that was thrown around so casually to us … “Termination for Medical Reasons.” That isn’t mercy – it is a nice way of saying “I chose to kill my child  because I did not want to deal with the hardships she may bring to MY life.”

I know it sounds blunt, but, it is the TRUTH.

Why are we teaching our children of this and the next generation to give up on difficult situations?

Or that life with hardship means that life is not worth experiencing?

What kinds of lessons do we give our children and grandchildren?

How will they handle life, then, when it DOES get hard?

How can we expect good children…when from the beginning we tell a mother it is ok to kill her child?

Who are we to decide what quality is when it comes to life?

The job of being a mother, I have learned, is not to make it as easy on us as possible.  It is not to alieviate our child’s suffering by ever crossing those deep moral boundaries of taking an innocent life.  It is simply to LOVE the childPeriod. End of story.  Anything else that comes along with it is just part of being human.  It is part of our humanity to have human suffering. As mothers, this is difficult to see when it is our own children – but – we must understand that it is not ours to take into our own hands.  That is why we must try our hardest to accept what we have been given, and help our children in whatever hand they have been dealt, because, ultimately, we are trying to get our children to heaven.  We cannot accomplish this by hiding behind the “termination for medical reasons” excuse.

WE do not decide if and when our children enter heaven.  We need to accept them, hold them in our arms, and walk the path withthem no matter how hard. This is how we are truly fulfilling motherhood – as Mary did on Jesus’ path of suffering. This is how we truly help our children to reach heaven and live God’s intended promise for their life.

I believe I was chosen for a reason to have a child who will need me so much.  God knows that women like me, who go through such devastation of a bad diagnosis/prognosis, are stronger than the “what ifs” and the negatives.  He has looked upon us and said “YES! You are strong and loving. You can do this, so I will give you this special child.” I think about this everyday and thank God that Meagan was given to us…because with another family, she may not have even made it to her birthday. They may have chosen to “terminate for medical reasons.”  She is here now – with her ups and downs, and worries and scares. And she is not even 3 weeks old. But I wouldn’t have it any other way. There is a woman who was contemplating aborting her Hydrocephalus baby who came across my blog and then decided to keep her baby girl. Meagan is already changing and saving lives…and she doesn’t even know it yet.  We cannot continue to let doctors scare women out of being what they already are with that child in their womb: a mother.

Our whole situation with Meagan made me think of one of my favorite quotes, from one of my favorite people: Mother Teresa. I think she sums up best the attitude we should all strive for, especially in such times of despair:

“Please don’t kill the child. I want the child. Please give me the child. I am willing to accept any child who would be aborted…”


**You can follow Molly’s online journal of Meagan’s story at Priceless Little Pearl**


8 Replies to “Ordinary Family, Extraordinary Circumstances”

  1. All I can say is “AMEN!” I hear your righteous anger, and it is well justified. Key phrase: “Abortion takes women in my situation, a distressing, devastating diagnosis of a child, and preys upon the woman’s emotions before there is any time for logical and rational digestion of that issue.” Every abortion, regardless of medical diagnosis, does just that–takes a woman in a distressing situation who feels trapped/powerless/threatened/scared–and gives her the illusion of an “easy” solution. Doctors who present abortion as an option, even obliquely, though their hands are not “dirty” with the act of abortion, are complicit in the deaths of untold numbers of babies. It is shameful! Shameful!

    God bless you and your precious baby. You are powerful witnesses to LIFE!

  2. God Bless you Molly and all your family, especially your little angel, Meagan Theresa. You will all be in my daily thoughts and prayers.

  3. Thank you for sharing your story and congratulations on the birth of your beautiful daughter! I loved reading this and am pregnant myself so it was an emotional story for me. God bless you and your sweet family.

  4. This is a beautiful post! I loved the point you made about how you wouldn’t kill your 8- year old if an accident left her with brain damage, yet somehow it’s supposed to be okay to kill a baby with the same problem.
    I will keep Meagan and your family in my prayers.
    God bless!

  5. Molly, God has blessed you and Meagan and your whole family with lots of love and you are so gracious in sharing it. Thank you for choosing life for God’s beloved child, Meagan and her siblings. Your Uncle Pat shared your blog with me. Congradulations on your new baby girl. May your family continue to be blessed as you venture on your new unfamiliar course. Love will guide you. There is a website you may be interested in: http://www.benotafraid.net

  6. Molly — I just clicked over here from your blog — wow, what a piece!!!!! Great great job!

  7. I realize this is an older post, but just wanted to say thank you. My son was diagnosed with hydrocephalus at 6 months old, and our conversations wtih the doctors were, of course, all about how to treat him – it’s amazing to think that if his diagnosis had been at 6 months gestation, the conversation would have been so different. He’s now a completely “typical” 2.5 yr old, and is our constant joy. Love and prayers – LMM.

  8. When I was pregnant with my first they suspected hydrocephaly, so for 2 weeks we walked around knowing that was a possibility. Thankfully our second ultrasound revealed he was fine, no hydrocephaly, simply a large head in general. My cousin’s wife received the same scare, but got different news. Her son had severe hydrocephaly and was already quite bad off. She ignored the doctors’ repeated attempts to get her to abort her baby and she carried him to term knowing he would die. He was born by c-section about a month early and lived about 10 days. Instead of choosing an abortion she nurtured her son in her womb as long as she could, then she and her husband welcomed him into the world and nurtured him as best they could once he was out. He received reasonable medical care, food by tube, and a lot of comfort care and was held and loved for those 10 days. His parents got to meet him and say hello and goodbye all at once. I can’t imagine how she must have felt but I greatly admire her strength and dignity in caring for her child no matter what. She gave him 10 days full of what life should be full of…love, care, and faith.

Comments are closed.