Sunday, June 21, 2015

a father's day

A special guest post by Joan's Dad.


How many kids do you have?  That should be an easy enough question.  It’s a question that really seems like a throw away, like, “How was the drive (or flight)? Or “How was the food?”  It’s a softball.  The kind of question that’s more to fill time and either keep a conversation going or start it.  It’s a warm-up swing question.  There should be nothing wrong with it.  Except.  Except when the real answer is a bit more painful than recounting the number of children you’ve gotten out of diapers.  In that case it can detonate the conversation like someone out for a stroll stepping on a mine in a dormant battlefield.  It’s just so unexpected.
How do I answer?  My most common answer is to use some permutation that we lost our first daughter and her little sister is at home driving her mommy crazy.  Why do I answer that way when I know that it can make people uncomfortable or clam up?  I answer that way for a few reasons.  First, it’s the truth, and nothing in the truth is linked to comfort of anyone, A is A.  Whether it gives you chills or a warm and fuzzy.  Joan is my daughter and she’s gone, but my love for her is not.  Secondly, I’m a parent.  Parents talk about their children.  I want to talk about mine.  Not at length, but for a second in conversation, I’ll mention the children that I love just like any other parent would.  Third, there is nothing in me that has any desire to disconnect with my daughter or her memory.  Ever.
Father’s day is an odd one.  I appreciate the sentiment of it, but I always view it through the prism of my life and that means that Father’s Day is about my dad, not me.  Father’s day is also when you get asked about your children the most by people who are generally well-meaning.  They understand that as a father you want to talk up your children, and they are giving you a chance to do so.  Queue my answers and the ensuing gallery of stranger’s faces from lack of recognition to genuine sadness and all stops in between.
The Father’s day while we were waiting for Joan was specifically difficult.  We knew about the diagnosis, we knew statistically what we were facing and most outside of our inner circle only knew that we were pregnant.  There were a lot of things that I couldn’t say but wanted to.  It was a challenge, and I just laid low and let it pass.  Since that first father’s day, I’ve felt largely the same.  I know that there are traditions with ties or ceramic ash-trays that I am sure we’ll go through with Vivian, but we’re just not at that stage.
As Father’s day is a pseudo holiday there is some level of giftery. Hmm. I think that I just made that up.  I’m fine with having made up that word, and I can’t believe it hasn’t been made up previously.  Giftery brings us to another classic question, “What do you want?”  This has become the easiest question I can ever answer.  
I’m a bereaved parent.  Like every other bereaved I’ll want the same thing every time I am asked that question until my last breath & I’ll want it fully knowing that I can’t and won’t ever get it.  

I’m not unique, I just miss my daughter.  It’s that simple and that complex.


My little girl was a fighter

Wednesday, March 18, 2015

Trisomy Awareness

On more than one occasion I have received comments like these from various doctors, both while pregnant with my daughter, Joan, and since losing her to Trisomy 18:


Those babies don't survive.

Your baby will never be normal.

Your baby will never be able to communicate with you.

Your baby won't be able to eat normally.


Your baby will never smile at you.


I distinctly remember a conversation I had with a doctor not long after we lost Joan.  When I told him that I had a daughter that passed away from Trisomy 18 at full term, he asked if I knew about the politician, Rick Santorum, who had a then 4 year old daughter with Trisomy 18.  For a second I was hopeful, thinking he was not going to be like other doctors.

Until he continued with, "She doesn't have full Trisomy 18.  It must be a less severe partial trisomy.  Babies with full Trisomy 18 don't survive.  You know your baby would not have been like a normal baby."

To this doctor, and many others... Bella Santorum is now 6 years old, living with full Trisomy 18.  Bringing joy to her family and many others.

While survival statistics are bleak for children with disorders like Trisomy 13 and 18, some do survive and thrive.  Their physical and intellectual disabilities should not determine the value of their life.

Let's raise awareness together.

Wednesday, December 24, 2014

META-MOURN-PHOSIS

I wrote this the first Christmas after we lost Joan  just 2 short months after our firstborn baby died and was born.  I remember the agony of receiving daily Christmas cards with the adorable smiling faces of the children of everyone we knew, while there would be no first Christmas card with a photo of our new baby girl.

For any newly bereaved parent navigating this first Christmas after the loss of your precious baby, you are not alone.  I hope this is a reminder to treasure the small joys in life and hold on to hope…



I fear that this traumatic life event  the devastating loss of our beloved daughter Joan  has turned my husband into Martha Stewart.  He has been perusing recipe books, commandeering my Better Homes and Gardens magazines, baking up a storm... and now, the ultimate proof... He announced that he is going to try decoupage. Decoupage. Seriously.  I don’t even bake very often, let alone decoupage.  If you know my husband, you know that he is far from the domestic or crafty type, which makes this all the more unexpected.

In all seriousness, this post is intended to bring humor in a difficult situation.  And also to encourage those of you going through a similar grief experience, to find the things that bring you joy and embrace them.  Whether it’s discovering your inner homemaker or training for a marathon.  Start a new hobby if you feel a calling, or rekindle an interest that you haven’t found the time for in a while.  Just make sure it is not a potentially dangerous or destructive pastime.  Be kind and gentle with yourself.

While my husband is morphing from a man’s man to into a domestic goddess, I have found small joys and healing in other things.  Here are a few:
  • Reading whatever interests me at the moment (at first it was infant loss websites and self-help books about grief, then light romance novels with happy endings only, we’ll see what’s next…)
  • Journaling
  • Eating out at a favorite restaurant
  • Savoring a chai tea latte or jasmine green tea
  • A quiet walk near the beach with the afternoon sunlight glistening off the water
  • Creating photo books with pictures of Joan and inspiring quotes
  • Finding creative ways to donate to charities that are meaningful to us
And though our house has been in a nearly constant state of renovation for the last 4 years, with many projects partially completed and now sitting idle, I no longer care.  I am content to watch my husband bake and then enjoy eating some of the best cookies I have ever tasted.  I don’t even care about the additional pounds (caveat: to a certain degree.  I am a big proponent of everything in moderation, and we have also been conscious to make time to exercise since it helps with grief.)  Ironic how many new mothers are preoccupied by losing the baby weight quickly, while I now see how trivial that is in the grand scheme of things.  (But that is a post for another time – the many ironies of infant loss.)

For now, find your joy – even if it is only for a few minutes a day. Happy decoupaging.

Thursday, October 9, 2014

3 Years



Be still.


Close your eyes.


Breathe.


Listen for my footfall in your heart.


I am not gone but merely walk within you.


- Nicholas Evans



In loving memory
Joan Louise
October 9, 2011


Tuesday, May 27, 2014

Providing Resources


When we received Joan's Trisomy 18 diagnosis we were immediately referred to a genetic counselor.  That was a very good first step.  I wanted as much information as I could get about the disorder, our situation, and what comes next.  In addition to much discussion, the genetic counselor had a few booklets that we could read, but said, "I'm sorry, these are my only copies so you can't take them with you."

I remember sitting in the crowded waiting room after our appointment trying to read through the material and soak up whatever I could.  Let me tell you, shortly after receiving a terminal diagnosis for your child you are mainly in shock and cannot focus on much of anything.  So we wrote down the titles, went home and ordered copies of a couple of booklets from Amazon.  When they arrived I began reading one and noticed that several pages in the book were blank.  Pages of text were missing right in the middle.

Really?  Is it too much to ask for some resources and information to guide us through these terrifying uncharted waters?  This is unacceptable.  Maybe that's when the spark of Joan's Reach first ignited.

Secondly, the brief booklets focused mainly on difficult decisions -- in other words deciding whether or not to end your pregnancy.  Then they stopped.  What happens next??

There were some support group resources listed for pregnancy termination.  But the continue your pregnancy route seemed lacking in guidance, resources and information.

Part of what we are doing with Joan's Reach is trying to fill this gap.  We provide bags full of resources and information that parents can take home with them.  To look through when the shock has dulled a bit.  Enough information to make informed decisions for their family.  As well as contacts and resources to guide them throughout the pregnancy and beyond.

Sunday, May 11, 2014

Mother's Day

Three years ago was my first Mother's Day.

I was pregnant with our first child.

Just a few days earlier we were told the unimaginable.

The baby you are carrying is not going to survive.

We, like many parents in this situation, were essentially offered one solution.  Terminate the pregnancy.

The alternative -- carrying to term -- was viewed by the doctors as doing nothing.  As in, why torture yourself like that?

It's not doing nothing.  It's the furthest thing from doing nothing.

It's the most important thing I've ever done.


Carrying your baby to term, knowing she will not live long is...

... loving, protecting, and providing for your child's needs -- even if it means providing a peaceful life and death.

... allowing her to have the natural life, and natural death, she was intended to have.

... recognizing that the grief will be there, and will be complicated, regardless of the choice.

... filling each day with gratitude and cherished memories of your much loved and wanted child.


People have told me it is brave.

For me, it was just necessary.  I got to spend nine months with my daughter, see her and hold her in my arms.

Wednesday, October 9, 2013

The Brave Little Soul

In loving memory of our brave little soul
Joan Louise
October 9, 2011

Not too long ago in Heaven, there was a little soul who took wonder in observing the world. She especially enjoyed the love she saw there and often expressed this joy with God. One day however, the little soul was sad, for this day she saw suffering in the world. She approached God and sadly asked "Why do bad things happen, why is there suffering in the world?"

God paused for a moment and replied, "Little soul, do not be sad, for the suffering you see unlocks the love in people's hearts." The little soul was confused. "What do you mean?" she asked. God replied, "Have you not noticed the goodness and love that is the offspring of that suffering? Look at how people come together, drop their differences, and show their love and compassion for those who suffer. All their other motivations disappear and they become motivated by love alone."

The little soul began to understand and listened attentively as God continued. "The suffering soul unlocks the love in people's hearts much like the sun and rain unlock the flower within the seed. I created everyone with endless love in their heart, but unfortunately most people keep it locked up and hardly share it with anyone. They are afraid to let their love shine freely, because they are afraid of being hurt. But a suffering soul unlocks that love. I tell you this - it is the greatest miracle of all. Many souls have bravely chosen to go into the world and suffer to unlock this love - to create this miracle - for the good of all humanity."

Just then the little soul got a wonderful idea and could hardly contain herself. With her wings fluttering, bouncing up and down, the little soul excitedly replied, "I am brave, let me go! I would like to go into this world and suffer so that I can unlock the goodness and love in people's hearts! I want to create that miracle!"

God smiled and said, "You are a brave soul I know, and thus I will grant your request. But even though you are very brave, you will not be able to do this alone. I have known since the beginning of time that you would ask for this, so I have carefully selected many souls to care for you on your journey. These souls will help you create your miracle: however they will also share in your suffering. Two of these souls are most special and they will care for you, help you and suffer along with you, far beyond the others. They have already chosen a name for you."

God and the brave little soul shared a smile, and then embraced. In parting, God said, "Do not forget little soul that I will be with you always. Although you have agreed to bear the pain, you will do so through my strength. And if the time should come when you feel you have suffered enough, just say the word, think the thought and you will be healed."

Thus at that moment, the brave little soul was born into the world and through her suffering and God's strength, she unlocked the goodness and love in people's hearts. For so many people dropped their differences and came together to show their love. Priorities became properly aligned. People gave from their hearts. Those who were always too busy, found time. Many began new spiritual journeys - some regained lost faith - many came back to God. Parents hugged their children tighter. Friends and family grew closer. Old friends got together and new friendships were made. Distant families reunited and every family spent more time together. Everyone prayed. Peace and love reigned. Lives were changed forever. It was good. The world was a better place. The miracle happened. God was pleased.

The Brave Little Soul
By John Alessi