Monday, 21 July 2008

The Beginning

Note: This entry is not meant to be depressing or make people feel sad. It is an honest account of how I felt at the time to help other parents who might be going through a similar experience.



We did not know about Daniel's condition until he was born. It was not picked up on the ultrasound because the sonographer only measured one femur, the left one.

After 27 hours of labour, we were handed our beautiful, tiny (5lb 5oz) boy. We were so excited to finally meet him. After some cuddling time, we handed him over to the midwife to bathe him. I will never forget the words of the midwife, "Let's show your Mum something". Our overwhelming joy and excitement turned to despair.

Daniel and I were wheeled to the maternity ward at about 4am. Shane tried to stay but security told him he had to leave and couldn't come back until 8am. It was the longest 4 hours of my life. I couldn't sleep thinking about whether my baby would ever be able to walk and what had I done to cause this. I didn't want to talk to anyone except Shane.

The pediatrician came to see us the next day to check over Daniel. Daniel was otherwise healthy and he referred us to a pediatric orthopaedic consultant.

The months afterwards were of mixed emotions. We had so much love for Daniel. He is such a beautiful baby. But there were days where I cried and cried. I felt so much guilt and so much fear for his future. I felt like I was in a dark hole and would never be able to get out of it.

Doctors don't know what causes PFFD and over the last year the feelings of guilt have minimised. I am still fearful for what lies ahead for Daniel but he has such a great personality and is loved by everyone who meets him so I know he will do okay. I think he will be an inspiration to a lot of people including myself! Daniel is a very determined little man and there was no way he was going to let me stay in that dark hole.

There is a story called "Welcome to Holland" which really helped me in my darkest time. It has helped a lot of parents who have had a child born with a disability.


Welcome to Holland
By Emily Perl Kingsley


I am often asked to describe the experience of raising a child with a disability - to try to help people who have not shared that unique experience to understand it, to imagine how it would feel. It's like this......

When you're going to have a baby, it's like planning a fabulous vacation trip - to Italy. You buy a bunch of guide books and make your wonderful plans. The Coliseum. The Michelangelo David. The gondolas in Venice. You may learn some handy phrases in Italian. It's all very exciting.

After months of eager anticipation, the day finally arrives. You pack your bags and off you go. Several hours later, the plane lands. The stewardess comes in and says, "Welcome to Holland."

"Holland?!?" you say. "What do you mean Holland?? I signed up for Italy! I'm supposed to be in Italy. All my life I've dreamed of going to Italy."

But there's been a change in the flight plan. They've landed in Holland and there you must stay.

The important thing is that they haven't taken you to a horrible, disgusting, filthy place, full of pestilence, famine and disease. It's just a different place.

So you must go out and buy new guide books. And you must learn a whole new language. And you will meet a whole new group of people you would never have met.

It's just a different place. It's slower-paced than Italy, less flashy than Italy. But after you've been there for a while and you catch your breath, you look around.... and you begin to notice that Holland has windmills....and Holland has tulips. Holland even has Rembrandts.

But everyone you know is busy coming and going from Italy... and they're all bragging about what a wonderful time they had there. And for the rest of your life, you will say "Yes, that's where I was supposed to go. That's what I had planned."

And the pain of that will never, ever, ever, ever go away... because the loss of that dream is a very very significant loss.

But...if you spend your life mourning the fact that you didn't get to Italy, you may never be free to enjoy the very special, the very lovely things...about Holland.


Posted By Kristen (Daniel's Mum)

17 comments :

ASMO said...

Hi Daniel,

I love your new blog! You are very lucky to have a mum who can write so beautifully about you and what she and your dad are going through.

And it's true that everyone who meets you loves you... but me especially! Your Constance

Anonymous said...

Kristen and Shane

I'm sorry to hear of Daniel's condition but I pray that he will walk tall and strong. Thank you for keeping us updated. You are great parents and Daniel is absolutely gorgeous.

I know it's hard but try not to despair. Daniel is going to be okay and you will rejoice when he takes his first steps.

Unknown said...

The blog is a great idea, Thanks Kristen it will be a great way to keep track of things.

Anonymous said...

Kristen, Shane & Daniel,

This blog you are sharing with us is inspirational.

It is so beautiful how you can express your love & emotion - feelings & fears so frankly and openly.

As a new father myself (Kasey Cross born 28 May 2008) I can understand the all consuming love for a child and the raw emotion of those first hours/days/weeks together.

As happens with many newborns Kasey needed to leave mum and go straight into neonatal care in the minutes after birth due to breathing difficulties.

Having to leave Sherryn on the operating table was so tough and during the next few hours I was so torn. I was allowed to spend every minute with Kasey, but nobody else was, including Sherryn. But I could only imagine how Shez was feeling alone in her ward bed.

Kasey's breathing calmed down after 4 hours but that time was just surreal, up and down the lift between Shez & Kasey. Keeping our parents and immediate family members updated but with them not able to visit. It was very different from the few hours of our first son Kyle, but no less special.

It seems like so long ago now (7 weeks) but it felt very much like the story of Welcome to Holland, thankfully in our case it was more of an unplanned stopover than change of destination.

I hope that by documenting the journey you will be able to capture and reflect on the powerful, life changing moments you have experienced and will experience in the future in a tough but inspirational journey.

Thanks so much for sharing it with us.

Adam, Sherryn, Kyle & Kasey Cross

Anonymous said...

Kristen and Shane,
With two positive parents I know Daniel will be in great hands.

It is clear the love you have for Daniel will never faulter. No matter what he will grow up to be a beautiful and handsome young boy just like his parents.
Our thoughts are with you all
Pen and Chris Savage

Anonymous said...

Kristen and Shane

Thanks for the courage to share your personal experience with everyone.

The story about Holland is very relevant, but I am reminded that humans are resiliant and adaptive creatures and you will be amazed how much Daniel takes this in his stride, probably even to the point where he would say why did you want to take me to Italy when Holland is my home?

Take care and all the best
Andrew & Alyson

Unknown said...

Hi Shane & Kristen:
And hello to you little Daniel

Oh how I wish I was able to be there for you guys. maybe offer some form of support. I feel so useless.

Believe it or not I have been there Kristen when mothers get handed over these beautiful bundles of joy and in between all the excitement they get told there is something we did not pick up. The despair and hurt seen on these mothers faces is enough to make any man break down.
I do not know much about the condition, but hopefully the trusted medline search can enlighten me.
This is a great idea to let us all know how he progresses.
I just want to add one thing. Doctors do not like to paint the best possible scenario that often as it may not happen, but I very much doubt anyone would think of amputation as a problem solving way.
Good luck and please let me know how things progress.
Thinking of you all and god bless.
bj

Anonymous said...

hello baby daniel
my names is michael i am nine and i have pffd
i have so far had my leg lengthened 20cm and i use an extension prosthesis in between surgeries
i will keep reading your blog and hope when you are older we can be friends
michaelmckenzie619@hotmail.com

Anonymous said...

Hi Kristen, Shane & Daniel,

This blogger is such a good idea, and i'll follow the little man's progress with interest.

I have bpffd and only half my left arm, and i was born approx. 3 months premature weighing 2 lbs. I'm also a through knee amputee since 9 yrs old. I used to wear prosthetic legs & an arm, but since 12 i'ved just used a wheelchair, with an arm socket.
With loving, caring parents like yourselves Daniel will be absolutely fine in life.
Holland is a nice enough place to be. I think Italy's probably over rated, never been there myself! ;)

Dave

Anonymous said...

Hi Guys, What a great idea to have this blog to keep us all updated. Good luck on your trip to the US and give Daniel a kiss and tickle from us.

Dagmar xx

Anonymous said...

Hi Kristen, Shane and Daniel

Thank you so much for sharing this blog and giving us and insight into the progress of your precious baby boy.

Reading your experience and emotions following the birth brought a tear to my eye as I have recently given birth myself and can only imagine what you must have felt. But your son is so lucky to have parents as special as the two of you and I'm sure he will have lots of support and love to help him though.

I look forward to reading more about your experiences.

Shez Cross
x

Anonymous said...

Daniel looks very proud of himself standing up against those bars, and so he should be! What an amazing little man who is so lucky to have such amazing parents! We look forward to seeing you guys in March for Jemma's wedding and meeting Daniel.
Love
Kelly, Dylan and Ali.

Unknown said...

Daniel is a beautiful boy. Thank you for sharing your story. We look forward to seeing more pictures of him.

Unknown said...

Daniel is a beautiful boy. Thank you for sharing your story. We look forward to seeing more pictures of him.

Anonymous said...

Hi came here via STEPS and just wanted to say the piece about Holland is so true. Our daughter Emily was born in may and diagnosed with DDH at 5 dyas old and like yourselves we have found it heartbreaking at times but have learned easily to appreciate all the wonderful things about our little piece of Holland. Daniel is gorgeous, thank you
Dawn & Emily xx

Anonymous said...

My daughter is 2 months old(8-20-09) and has pffd in her right leg. Reading the story "welcome to Holland" just made me cry because the feelings are so true. I actually hope to share that story with my daughter when she is older. You son is so handsome and I love seeing how well he gets around and how happy he is. It gives me such hope for my daughters future.

Amber said...

I just discovered your blog today. My own daughter, who is seven, was also born with PFFD.

First, I want to thank you for taking the time to create your blog.

I scrolled all the way to the beginning and will eventually read every post. I do not know your family, but at the same time I feel like I do.

Your "Welcome to Holland" made me cry. It's exactly how I've felt. I've never heard/seen it expressed so well.

I am in Holland.

Sometimes it's hard seeing all the people enjoying all that Italy has to offer, but I am seeing the beauty of Holland more and more each day.

Best wishes to you and your family!