Thursday, February 13, 2014

Finding grace in an unlikely place


In our house we've had our share of serious talks with the kids.  Especially over the past 18 months.  Today we had a grace conversation in the bathroom while oldest was getting ready for school.  

Hey buddy, you've been in here awhile...you ok?  

Yes, Mom.  I'm just brushing my teeth.  Can I have a hug?  Lots of hugs? 

Sure, what's up?  

Well, I've been doing lots of bad things and I just need forgiveness.

Buddy, we're just trying to teach you.  We love you.  And if we have forgotten to tell you, we do forgive you when you don't do what you're supposed to.  But guess what?  The Bible tells us that we are not good people who sometimes do bad things, does it?  

No, we are sinners.  What does that mean again?

It means that we think mostly of ourselves and want to be in charge and not let God be in charge.  And because we are sinners we can't do good without His grace, Him helping us.  And when we sin we can know that He forgives us too. Want to pray together?  

After we prayed, as we drove to school, we did a familiar morning routine, saying, "This is the day the Lord has made. Let us rejoice and be glad in it! Rejoice!"  Followed by a regular line in our house: Remember today that Mommy and Daddy love you forever and ever, no matter what. And Jesus does too

These moments that I have shared with each of my three kids, telling them about Jesus, are the ones I tuck away in my heart and memory to treasure forever.  These are the moments that really matter.

Monday, February 10, 2014

Birthday Boys

We just finished the birthday marathon week.  Gabe and Zach's birthdays are five days apart so it makes for a busy week.  I still haven't figured out our traditions so it can get a bit busy especially since there are two celebrations back to back.  We made pancake breakfasts for both of them and then we celebrate at dinner with a dinner of their choice and cake.  This year, I tried to make small cakes for them this year so we don't have a ridiculous amount of cake that we "have" to eat!  We were supposed to have a party for them both but it will be in a few weeks since Zach ended up with a fever on his big day that lasted through the weekend.

For whatever reason, this year, both boys were really into their birthday and the fact that they were so much older.  The morning after Gabe's birthday he said many times, out of the blue, "Oh! I'm six.  I almost forgot I was six because I'm new at it!"  And Zach kept reviewing all the things he will now do since he's a "big boy"--go potty, clean up after himself, etc.  All stuff he does anyway so I'm not sure what his definition really is.  It was also good to see Zach so confident and excited about his birthday.  He called everyone to the table for his cake--"My cake is here.  Everyone sit down!"  And before we were halfway through singing Happy Birthday, he calmly blew out the candles and was asking for the candles out so we could eat.

Gabe will be starting piano lessons now that he's six and Zach will be taking a t-ball class.  I look at them and I do wonder where the time has gone.  I love seeing them each growing up, learning new things, being such good friends and loving Jesus.  I love being their mom, sorting out the fights, teaching them, playing with them, learning more about their personalities, cuddling them when they need extra hugs or when they are sick.  Being a parent is hard work, and even though I sometimes grumble about the messes or piles of paperwork around my house, I wouldn't trade the messes for anything else.    

Monday, December 23, 2013

shattered glass

We have been getting ready for Christmas and the season has been filled with all the usual traditions of baking cookies, parties, Christmas music and movies, and decorations. We also started a new tradition of going to a nearby town's Christmas parade.  I started that by accident--last year I convinced Pat that we should all go since I thought going to a parade would be fun.  It was ok and I didn't plan to bring it up this year.  But the boys brought it up and were adamant that we all needed to go.  It was freezing that day, literally in the teens, and we lasted about halfway before they were ready to go.  Overall the season has been filled with laughter and good family time which is exactly what we wanted this year.

Yesterday we went to the hospital where Sarah lived to bring some beautiful dresses that many have made for their bereavement program.  We had a chance to talk with a nurse who holds a special place in our hearts since she very lovingly gave us a dress on Sarah's last day.  She explained how helpful these dresses are since there are approximately 200 families a year who say goodbye to their little ones.  She is expanding the bereavement program at the hospital to be more than just mementos and to include bereavement training for staff to better support families who are losing someone.  Our heart is in this program that supports families because we cherish the kind words and gestures the staff gave us. We regularly look at the pictures, blanket, teddy bear and other mementos they gave us.

I have been reflecting over the past year and how different it is from last Christmas.  We were still in a fog, focused on getting through the holidays and didn't really enjoy them.  This year has been so full of joy.  I'm thankful that so many gifts we often take for granted such as laughter, smiles, and dreaming are back in our lives.

The other day, a friend was talking with me about a friend of her's who had just lost a baby prematurely. She wondered what she could do to help.  The best analogy I thought of is this--Our life before had been like a glass vase but when she died it was as if the glass had been shattered.  When we lost Sarah we also lost all the dreams we had for her and for our family.  We had looked forward to knowing her, seeing the relationships form with her brothers, and growing as a family. The past year we have been picking up the pieces and putting them back together knowing that the vase will never look the same again.   Who I am today, who our family is today, is not who we were sixteen months ago.

What can you do to support someone who has lost a child?  Know that you can't fix it or make it better.  Nothing can--our lives will forever be different because of what we experienced.  You can help the person pick up the pieces, help them sort through the emotions and figure out what the "new normal" is.  Ask parents questions about how they are, acknowledge difficult anniversaries, don't shy away from us.  Yes, we may cry, but love us enough to give us safe space to do that.  Others' presence as well as mementos help the healing process.  Some loving co-workers and another family gave us gifts of flowers so that each spring when they bloom we will remember Sarah. And we will remember their love and support of us as well.

Its the small gestures of support that mean a lot to families going through this process.  Yesterday, we learned how special the dress fund has been.  We really had no idea so many of you would support it, and we are grateful that those gifts are bringing comfort to grieving families.

Thanks for being on this journey with us and for helping us put the pieces back together.

Merry Christmas!





Sunday, December 22, 2013

kid stuff

The boys have been saying and doing some silly things lately that has kept us all laughing:

Gabe at the table on Thanksgiving after we explained how a wishbone works: "If I get the big part, I want to become a duck.  Don't tell anyone."

Gabe after school: "Mom!  I was skipping today.  And I'm really good at it even though I'm not a girl!...Why are you laughing?"

Zach, responding to Gabe saying some mean words to him: "Dad!  Gabe's voice is being bad.  Take it away, dad!"  (with the tone of an announcer)

And we've been getting firmer with Zach (our picky eater) about what he eats.  He's down to one PB sandwich a day (from 5) and then has to eat whatever we give him.  Today he ate his first ever grilled cheese.  But first demanded that we put salad on it.  I never thought I'd have to beg a child to eat a grilled cheese.  At least he likes salad.  Last week he at pasta for probably the 3rd time in his life.  He needed PB to dip the noodles.  Baby steps...

Zach also has resisted showing us that he is learning things like his letters.  We will ask what a letter is and he will start being silly.  We've wondered if he's having trouble learning or what's going on.  Well, it seems he's learning just fine.  He wrote his full name, ZACH, last night without asking for help.  The only letter he acknowledges knowing is Z.  So, we've been tricked.  We believe he may even have a book written and ready to be published.





Tuesday, November 5, 2013

Transitions and moving forward

This blog was started as a way for us to quickly share information with so many who were caring for us when Sarah was in the hospital.  After she died, it was a place for me to share how we were doing but also for me to write about our grief process.  I wrote publicly for two reasons--first, I think that death (especially death of a child) is a topic that is understandably avoided.  I get it--losing a child is probably every parents' worst nightmare, its hard to know what to say to someone who is grieving since you really can't fix it, and maybe we worry that we will say or do the wrong thing.  But so many people lose babies and grieve in silence.  Perhaps people think it should be "easier" to lose a child since we didn't really know her, but that made the pain worse for me since I lost her along with all the dreams I had of what our relationship might be.  My hope is that those who lose babies will feel the support that they need, to know that others are around them, to be asked how they are doing.  And my hope is that we may all feel strengthened to reach out to parents who are grieving.  Because miscarriage and infant death are a lot more common than we all probably realize.

I'm off my soapbox now.

The second reason I wrote was because even in the initial fog I was in I knew that our family would make it and I wanted to document our journey.  It wasn't about "getting past" it or "putting it behind us"--that won't happen.  Sarah and her death changed us as individuals and as a family.  I wanted, and still want, to see how we would be changed as we pulled together, moved forward, let God heal us and figured out what our new normal was.

So here we are.  It has been a year since Sarah's birth and death and our grief isn't  as raw.  We are healing.  We will always have a scar across the picture of our family but instead of trying to hide it, we just know it is part of us.  We are still on a journey of letting God shape us and I've decided that I'd like to keep journaling.  At least for a bit.  I've learned to slow down and appreciate the small stuff and I'd like to record the small joys, lessons learned, and struggles dealt with.  And probably some goofy things the boys do.  Because they are goofy kids.

If you'd like to continue to follow along on our family's journey, it would be an honor.  And I hope to hear from you as well.  Let us know how we can help carry you in prayer or in tangible ways as you've done for us this past year.

Monday, August 12, 2013

Letter from Sarah's nurse & the NICU dress fund

Today we received a beautiful letter from one of Sarah's nurses.  R. was working the last night when we were called in when Sarah went in for emergency surgery.  She was with the Drs. when they came to tell us that things were bad and that Sarah was very likely going to die.  She stayed past the end of her shift and worked with another nurse to help us understand all that was happening and offered support as we made decisions. When we asked for a photographer they called one and R. asked if we wanted a dress to put on Sarah.  At first I said no-despite the face that the drs. had said she had a 0% chance at surviving more than a couple days, I was clinging to hope and didn't want to disturb our fragile girl.  A bit later, she asked again and we decided to just lay the dress on Sarah and tuck it around her so as not to move her much.  It was a beautiful white crocheted dress with a pink rosette and was just what I had envisioned for her baptism dress.  Later, after pictures, I asked about it and if they had lots of dresses--I assumed there was a closet-full.  R. said that she had been given the dress awhile ago and told to give it to a family who needed it. For whatever reason, she felt we were the right family.  That kindness shown to us and our daughter took a bit of the rawness out of the day.  Our girl was "dressed up" for a bit and we got to have sweet pictures taken as a family.

We started a fund to provide dresses to families whose premies are in the NICU where Sarah was.  Much more was generously given that we ever thought.  The letter says that the donations given in Sarah's name "have currently purchased over 75 beautifully handmade layette sets for infants and their grieving families."  Additionally one of their knitters "is from England and her profits from our [the hospital's] purchases all go to a charity known as Love Light Romania which supports children affected by disease and poverty in Romania." 

We are humbled to know that children and families are being cared for because of Sarah and so many generous people.  


Sunday, August 11, 2013

Celebrate Sarah's birthday with us!

We will never know the extent of who was praying for and supporting us a year ago as our daughter, Sarah, was born prematurely and died nine days later.  As her birthday approaches, please help us

  • celebrate her life,
  • honor the wonderful Drs and nurses who fought for her life with us, and
  • honor the wonderful family and friends who have supported us  
We believe that all life is precious--an infant who was on earth a short time as well as every person we are surrounded with each day.  All life is special and no one should ever be taken for granted or feel unimportant.  


Additionally, in our family birthdays are special and the first birthday is always a celebration of our child but also of our survival through that first, sleep deprived year!  This year was filled with its own struggles as we’ve grieved individually and as a family and...we’ve made it.  


From August 14-23 (the days of Sarah’s life with us), please do something to recognize and honor life--such as take time to listen to someone, offer assistance to someone in need, call or write to someone who may be lonely.  Focus on showing value and love to someone’s life.  If you’d like to leave a message of what you’ve done on our blog (below), that would be great.  If you’d like to stay anonymous, that’s fine too.  And if you'd like to donate to the NICU dress fund we started at Royal Oak Beaumont hospital, the information is below.  

Thank you for celebrating with us!


You are loved,
Patrick and Heather


http://sarahs-baby-steps.blogspot.com/

NICU Dress fund
Donations can be made to “William Beaumont Hospital NICU” in memory of Sarah Shaw.  Before she passed away, her nurses gave her a dress so we could dress her once and take some pictures as a family to help us remember her.  We would like to provide dresses in Sarah’s memory for other families who have to say goodbye to their little girls-this is a fund we started to support families in their grief. Checks or micro-preemie dresses (button or closures in the back, please) may be sent to William Beaumont Hospital 3601 W. Thirteen Mile Rd. Royal Oak, MI 48073-6769  Attn: Mara Sipols) Please put "Sarah Shaw" in the memo of checks so your donation goes to the right fund.  Thank you!