Friday, July 31, 2009
Surrogacy questions, enough.
I think about our surrogacy journey all the time. How amazing it was. It gets better and better as I think about it. Since we decided to go this route, we did not encounter one wrinkle, one obstacle, seems like we have enough of those in everyday life Martin and I. Getting listed for transplant has been one thing after the next, but getting Scarlett into our lives was perfect. I feel like she is my miracle. Her presence in this house has lifted up all of us more than we expected. Not that we're miserable people, we're not, but she just brings so much love and happiness to us. I can be in the worst pain in the morning, and my mom will bring her down for me to see and feed, and I just melt. How can I not smile. She does her little lazy stretches as I change her diaper and I kiss her little feet and face and she makes my morning.
The connection that I have with my daughter is not arbitrary. It's not because she's here and I have her, so I will love her. I loved her from the second that I saw the top of her head coming out during labour. I looked at her and I felt it, she was my daughter, Martin's daughter. It was instinctual, it was spiritual, it was biological. When we decided to go with surrogacy, I contended with the fact that I might lose some connection due to the fact that I was not carrying. But I had no choice, and I was okay with that loss. I had no idea how it would all go. Neither did Beth I don't think. But both Beth and I learned so much about that connection. Beth felt physically pregnant, but not emotionally. I did not feel physically pregnant, but emotionally I was more and more pregnant as the weeks and months went on. By the time Scarlett was in my arms, I was ready for her and she fit into my arms as if she just came out of my uterus. I knew what to do, she was happy to be in my arms, and I knew right then that I lost nothing and gained everything. I know that people don't understand that, not everyone has to, and that the most common question about all that we went through now that we have our daughter is about Beth's connection to Scarlett and her ability to give her up....I just wish people would stop asking me that. I try to explain, but people don't want to hear it. The people that ask seem to want me to say that I had to rip Scarlett out of the arms of our surrogate, and that I felt no connection to my daughter. That's what people seem to want to hear. It is not the truth, and when you listen the stories of other mothers that used surrogates, they will tell you the same thing. It's incredible, and they know they're children immediately and they love their children immediately. It's an incredible thing.
I am not insecure about it. I will never lie about it. I am proud of Beth and I. I am proud of Martin and Don. I am proud of all of it. But now that Scarlett is here and we're taking care of her and growing with her, I wish people would stop asking questions that are made to question the process, or myself, or Beth and her family. I am waiting for the day that I lose my patience. And of course I don't want to do that, with anyone.
On a totally different and much lighter note, we had a photographer take Scarlett's pictures last weekend and I cannot wait to get them back. I will post them as soon as I have them. This lovely lady has also agreed to help me document my transplant journey from start to finish. Something that I am very excited about. Both for my blog, as well as an album that I will put together about the process. I will then print the blog and the pictures for Scarlett (and us) for the future. This project will be amazing I think. I want it to be as detailed as possible when it comes to the medical aspect of the tx and the recovery. I think Jenn will do a great job!
Tuesday, July 28, 2009
Scarlett's getting bigger, I'm getting smaller...
I have some pain killers and anti inflammatory drugs for my hands, and these help the symptoms. I have also been able to do extra physio and masks to allow me to breathe better, since I have had a pretty rough go during the last few days. Things seem to be stable again. But I certainly see that things can get much worse within a day or two, and my breathing gets frighteningly shallow and panicked.
Today I also had to go to TGH and do my final blood work. The vaccines are all done, and looks like those results should be in soon. Once they are, I'll get an appointment with a surgeon and get listed. Phew, that's all I want right now, to get listed. The pain, from my lungs, my back and my joints is getting to be too much for me, and I am ready to say goodbye to these lungs.
Friday, July 24, 2009
Growing, eating, changing. The first week.
We have had many visitors to see baby Scarlett, and many gifts from people that have never met her, but only know us through my blog. I have sent out thank you cards to everyone, but would like to say thank you again here, thank you everyone for your support. How amazing is it that there are so many special people out there thinking of us. Thank you.
Since I'm already thanking people, I might as well thank the people that are sucha help right now. My mom has been amazing. Little Scalrlett is very lucky to have a babcia like her!! My dad, John and Angie are my amazing family. They are wonderful. Martin's family has been very supportive too. Visiting little Scarlett and welcoming her to the Ritchie family. Our pedietrician Dr.L has been to the house already once (and at the clinic once for her first check up), when we called her about Scarlett's umbilical cord. It's fine by the way, we're just crazy parents!! She is amazing! We love her. She has a good laugh at us, being first time parents, but is just so valuable to us. We are excited to have her in our life. Other than that, we literrally have dozens of people that I think of and want to thank every day. It seems like people are reaching out so much, and being so kind and excited for us, that it feels like many people out there have been waiting for Scarlett to arrive. I love that. I will make sure she knows it when she's older, how much she was wanted.
Above anything and anyone else, my friend Beth is still primary on our mind. My dad and I were talking about her and her family the other day, we think so much of her. We are still in awe of her, and will continue to be, when Scarlett is 1 month, 1 year, or when she is all grown up.
Tuesday, July 21, 2009
5 day old baby Scarlett
Scarlett 5 days old
http://www.facebook.com/photo.php?pid=2712921&l=01862d095f&id=541641274
Sunday, July 19, 2009
We've got ourselves a sleeper.....so far =)
First off, I have to say, we have a good baby. and when I say good baby, I don't mean good baby, mean GOOD baby. We're slightly freaked out by it. She sleeps. eats like a little monster, and then sleeps more like she just ran a marathon. We're all resting lots. My mom is here for night duty. Martin and I are days. Marty is super dad, I knew he would be, but it's still great to see. He's a pro?! I think he's been practicing all these months!!
So I need to write down how Scarlett came into this world. I will try my best to capture what it was like. It will be hard to do any justice to it all.
We were supposed to induce July 21st. That was the plan. But I was nervous about it. Not because I didn't want Scarlett to be born out of town, I did not care, but because I am so dependant on IV's, oxygen, meds, blah blah blah.....near home I can function. Away, I fall apart. So when it got close to the induction date, I started to panic a bit. I didn't sleep well, called my oxygen company and had a hard time communicating to them what I needed from them. Tons of things. Then on Thursday, Beth emailed me that she was at the OBGYN in St.Thomas and she said that she was 4cm dilated. Cervix was hard, but still 4cm?! That totally made me panic.
Beth and I decided that I was going to call Martins dad (who's an OBGYN at Mt.Sinai) and ask him what to do. Should be go in early? So I did call, and Dr.Ritchie called our doctor, Dr.S and we went from there. After some conversation and the panic that everyone heard in my voice, and that I certainly heard from Beth (who was worried that she would go into labour and we would miss it) we all decided that Beth and her husband Don were going to come to Toronto that night! What?! We were so excited!!
They arrived July 17th at 1am, and we all made our way to Mt.Sinai. I was just relieved that Beth was in Toronto, we were all there, so far so good. By 2am we were in our delivery room (a large lovely room where we would all make ourselves at home for quite some time!) and ready to go. Well, not really. Dr.S started the induction, and well, we just hung out. Soon they rolled in a bed for me to sleep on (though I did not sleep at all but I gave my back a break) and large chairs for Martin and Don to lounge in. Martin got some sleep, Don too. But generally we were all awake. Nothing was happening. Beth got an epidural super early, and she was having contractions within a few hours. She felt nothing, except for slight pressure and cramping, and was loving the epidural, and we were thrilled for that!! I was so thrilled!! I did not want to see her in pain.
I did go home at 6am to do some Iv's, and returned to the hospital for 8am. Beth was about 5cm then, and progressing nicely. But generally this was not visible labour. Beth was speaking normally and in and out of a restful half sleep.
At this point in time, our doctor went home (which we were a little disappointed about since he was the one that saw us in clinic and I knew him from my pre-pregnancy infertility days) but we knew the staff there were amazing. The doctor that we got was delightful!! We thought we loved Dr.S, but Dr. W was so kind, so sweet! We just loved him. He took Martin and I aside at one point when we were out in the hallway after a quick meal, and told us that it will be a magical experience. That it will be 'magical, so lets all go in there and make it happen, it will be special'. We were moved by his ability to understand that we were not only having a baby, we were about to experience a dream that Martin and I never thought would happen. He saw this in our faces and I thought the pep-talk was special.
At 1:30pm, we got really tired and kinda lost momentum. Things were not changing that much. We were at 6-7cm, but still far. My family was all trying to hold off from coming right away, but eventually they could not stand it any longer, and we thought it was a good time to have some lunch downstairs. Don and Beth encouraged us to go, and said that they would call if anything happened. So off we went. We met my mom, John (my brother) and Angie (sister-in-law) and had something to eat. We were all very excited. Just when we were done eating, Don called. "The show is about to start" he said. We rushed upstairs. It was 2:30pm
When we walked passed the nursing station, the electronic chart on the wall, flashed "10cm" next to Beth's name. That was fast!! We were ready to go.
When we got to the room, Beth was visibly uncomfortable. The doctor was at the foot of her bed, and there were three nurses mulling around. They told us to move close, we were ready to push.
The rest is a bit of a blur for me. For all of us for sure. When we first looked, Scarlett's head was already there, showing. Martin and I were captivated. I started to sob. Martin moved next to me and held me, we held on tight. Don coached Beth through a series of pushes. I can't tell you if it was 2 in total, or 3, but it was not many. Little Scarlett slid right out, 2:58pm. Emotional and exhausted, Beth looked at me and said, "she's beautiful!" and I said "I know!!" Beth was crying, we were so connected in that moment. I will never forget it. In that split second Beth understood my pain. All of it. In her eyes she understood my pain due to infertility, due to missing out on carrying my child, and she understood the years of pain that CF has been. And somehow, she took it all away from me. With one look, Beth gave me Scarlett, and took my pain away.
Scarlett was at the foot of the bed, crying and pink! So pink! She was big too!! Perfect. Martin and I cut the cord like a couple would cut a wedding cake. Together. The staff then wrapped her up, and I sat down in the lounger and held her. She was marvelous! A little Narty! (I know, it's silly, but she is, a Nat-Marty!!)
We then took her over to weigh her and check her out. 8lbs. 10 oz! Yup, we were expecting a big baby! She stopped crying then, and has yet to really let out a cry. She just stared at us for the next little while, or slept. And we marvelled at her. Beth was taken care of by Dr.W, who told us that he had to really make sure that Beth was okay before she went home, since she's birthed 7 babies. He took his time, and Beth was well. She looked so happy, and content, and just watched us in delight.
After a few hours, after my family came and just could not get enough of our newest family member (especially my dad!), the nurse came in and told me that my room upstairs was ready. It was kinda neat, to feel like a mommy that just delivered her baby. I got a hospital bracelet that matched Scarlett's, and a gown, and was wheeled upstairs holding my bundle of joy. The nurse pushing me whispered to me at one point..."it looks just like you gave birth to her....only all the other mom's are jealous at how thin you are!!" She was a sweet woman, that wanted me to have the full experience. When rolling through the halls, people glanced my way, and looked at my baby, and smiled. It was cool. I was happy.
From there, things went well. Scarlett had to stay an extra night under the light for elevated jaundice levels. But they were fine the next day. Martin and I fumbled around with the car seat, and Scarlett looked at us warily, but that was our only pitiful parent moment....other than that it's been quite smooth.
Details will come to me here and there. This is what I remember now.
I am filled with love, and happiness. I am filled with hope, strength, and gratitude. I believe anything can happen, even when things don't go as planned. I believe she was meant to be my daughter, my little Scarlett, and she was meant to come into this world as she did, not birthed by me, but by Beth. I believe that life has to be as it is, filled with the horror of illness and sadness, in order for such moments of love and serenity to exist. At least it had to be that way in my life, and I am grateful for that. It's okay with my now. It never has been before, but now it is okay. God wanted me to have it all, but in order to give me everything, I had to have CF and go through what I have. Today I would not change a thing. Not a thing. In time, I will be listed for transplant, and I will get my new lungs, and that will be my next chapter. But today, I would not change a thing.
Saturday, July 18, 2009
Scarlett Anna Ritchie
Friday, July 17, 2009
She's coming!!
She's coming!!
Keep us all in your thoughts and prayers!! Especially Beth that is doing a fantastic job!
Thursday, July 16, 2009
Just a few more days

Sunday, July 12, 2009
Not feeling that well.
Beth has been tired, and has had pain. She feels that the cramps she's experiencing are earlier than when she was carrying her kids, and this worries me. Will she be able to hold out (or will Scarlett be patient) for another week and a bit. The 21st is very close, but not if you have had enough with being pregnant!! Needless to say Beth is being great. She's doing such a great job, and will soon get relief! But I do really want things to work out for the 21st. Especially with my not doing all that well right now. I hope that is just a result of the new meds, and things will settle down. I just need a few more days for that to happen.
So, 10 days. It's hard to believe. All of a sudden she can be here any minute. Hard to believe we got here.
I'm just going to try to rest, and hope things go to plan. But if they don't that's ok, we'll figure it out. I just want to be well enough to enjoy it.
Wednesday, July 8, 2009
My hero
The book by Lance Armstrong and Sally Jenkins, called "It's Not About the Bike: My Journey Back to Life" is still one that I have, and one that I have re-read many times. The life that Lance has lead outside of his cancer battle and cycling career, does not change how I view the man. It does not change his struggles, and his victories. I could not care less about who he dates, how many children he fathers, or how many women he marries. I love his story. It's a story of overcoming tragic and debilitating illness. Though I am not an athlete, and certainly do not have cancer, it was my story when I read it. I would recommend this book to anyone. It's remarkable.
So, 2009 rolls around and Lance is back. They say he won't win the Tour with year, that he isn't even trying to win, but I don't care, I am still hoping he does, and cheering for him.
When I got out of the hospital those many years ago, after those months of being so sick, and so defeated, I came home to nothing. I was unable to work. I was depressed. I watched all my friends start their careers (as this was just after my finishing University) as I was just happy to be alive. I almost died. My doctor reminds me of this when I feel like I can't take it any more. She says to me, '....after seeing what you went through, I will always bet on you. You're tough. You were really really sick. I was worried. I don't often get worried.' That was years ago, and I know that it was bad, since I don't remember most of it. But I do remember that when I finally got discharged, I faced such a staggering depression. I was alone, I was very thin, I had the lowest lung function that I ever had, and I just didn't know how to cope. That first summer, I literally did nothing. I think back to the person I was and the person that I am now, and I can't believe that was me. But it was a long time ago, and I had to learn how to cope. I had to learn how to accept CF in my life. So, that summer, all I remember is watching the Tour de France. It was my only enjoyment. But as I watched for the 2 weeks, loyally, jumping up and down at every win, crying when Lance overcame climbs and time trials, I was lifted up. After having read what he went through (much like the hell that I went through the months before) and then seeing him rise above it all, and win and win and win over and over, well I was sold. I was also convinced that there was more for me. So what if I could not pursue the career that I wanted, or the life that I had planned for. There was so much more out there. Life was waiting for me.
It was in the months ahead that I began to live life. Since I could not work full time, I volunteered at an art gallery, and ended up curating there later on. I met some amazing people, some of which Martin works with now, and just came alive. I applied for disability to help me along, and I was okay with the fact that I had to do what I had to do to make life work. And I was okay with it. I was no longer moping about all that I lost.
Within 6-12 months, I was loving life at the gallery. I was having fun, going out, really enjoying the things that I thought I had lost. My lung function began to rise, and soon it was back up to the 50s. I was active, and happy, and I always, ALWAYS thought Lance taught me to be that person. He often talked about the fact that after the cancer, after the chemo and the treatments, he was different, both physically and mentally. As a result he was angry and depressed. He didn't want to be different. He wanted to be the same, as he was before the cancer. He didn't understand why so much was taken away from him. That's how I felt. But once he got it, he changed the world! The world of cycling, of cancer awareness, and most importantly he changed himself. Something that is always the first and hardest step to take. The hardest change to make.
In the years to follow, I met my future husband, and, well the rest is history. Though I know Lance won't read this, I want to him to know that he changed and continues to change lives. Lance you certainly changed mine!
Below are my favourite Lance ads out now, they're amazing!!
http://www.youtube.com/watch?v=MIl5RxhLZ5U
http://www.youtube.com/watch?v=ph6Gd2Cg4gc (my favourite!)
http://www.youtube.com/watch?v=oXAleHsmgEg (Healthy Lungs, Just Do It)
This may sound strange, but I don't think it's a coincidence that Lance is back when I need hope again! Ok, yeah, that does sound strange. But I believe it!
Lucky 13 again....
Well, yesterday was 14 days until induction. 2 weeks. Today 13 days. Wow, can you imagine?! I'm happy that nothing happened while I was in there this time. I would have had a hard time leaving in the middle of an ICU treatment. I just try not to think about it. But I am thrilled that that's all over. I have my new meds, and I can stay on them until tx. Which is amazing. I also found out that my friend Amy is doing really well, a few weeks after her tx, and that another lady (a 54 year old with CF) just got her call a few days ago. The 3 ladies were waiting while I was at the hospital in March, and I cannot believe they are all with their new lungs now, doing well. Wait time 4 months, 1 month, and 3 weeks. Amazing. The ward as a result is quite empty, and that is a rare thing! It's good!!
So today lucky 13. I have always had good thing happen to me on the 13th of the month, or the 13th time....it's just always been a lucky number for me. In fact we found out that we were expecting on November 13th.
Hang in there Beth!! We're almost there!
Monday, July 6, 2009
Got a bed for the desensitization!
I will not have my laptop in the hospital, just too much packing that I don't want to do, so no posting until then. I'm bringing my iPod and my baby book. I have important things to keep reading about!!
Everything is going to plan, so I am trying to keep my cool and let time unfold. We're juggling lots of things with my health and Beth and planning and hoping everything will come at the right time. Let's all keep our fingers crossed that happens!!
Sunday, July 5, 2009
We're so close, and waiting.
Aside from that, we are counting down the days. Our little Scarlett will be here so soon, and it's hard to believe as each day passes that we are in fact so close. After all this time, after all that we've been through, it's just such a blessing.
I don't have a lot to say these days. I'm ok, Martin is great, and we're still waiting for Scarlett. We're in no hurry, we want her healthy and strong when she arrives to be with us. Beth is doing well, but is ready to have this baby! But she's always telling me that's it's well worth the struggle to know that Martin and I will have our little girl with us soon. That's why we love Beth, she's such a great woman.
16 days. Hang in there Beth. Scarlett, mommy and daddy cannot wait to have you home with us. Finally!
Wednesday, July 1, 2009
Happy Canada Day.
I became a Canadian 20 years ago. I love this country. Everything about it! I can get into how much I love the East and the West, and Toronto, and all that's in between. How much I love the freedom that we enjoy. How much I love the endless possibilities that Canada offers. Or that we tend to gravitate towards peace, not war, and guns. I love Canada since it's so beautiful. So beautiful. Or that in Toronto I can get authentic Thai, Japanese, and Indian food within a walking distance of one another. I love that we encourage diversity, but at the same time were so patriotic. I love so many things about Canada.
But the fact is that I owe my life to this country. What would have been of my life in Poland I do not know, but statistically I would not be alive any more. I got great care here, at Toronto's Sick Children's Hospital until I was 18. And I got it without ever seeing one bill. In fact Sick Kids often takes kids from all over the world when they have no more hope, and provides free care, and saves lives. There are so many of those stories. I am so proud to live in a country where we value life and care over the all mighty dollar. And even though people complain about the system all the time. About the fact that people do take advantage of it, and that there is waste within the system, I love that as a country we have decided to choose life, choose hope, and choose love, and providing medicical carefor all!! I'm sure many people would rather a private system, but I think most Canadians are proud of the country that we are, and what we can do when we pool together our funds and make things happen.
So on the days that I complain about clinic, and this and that (and may be I've just had enough of CF more than the system, may be I'm just tired of being sick all the time for all these years) I try to think about the day that I came to Canada. The first time we went to the CF clinic at Sick Kids, and the care that we got. How quickly we were able to start me on all those wonderful meds that changed my life so dramatically. I remember my mom and I getting all those meds, without what we had to endure in Poland, and it was amazing.
Now that I near transplant, I think the same thing. How lucky I am, to have a system in place that will work to save my life, no matter what. The fact is, Canada is one of the only places in the world with such a premier facility, that does it all for free. I know, I know, it's not free, we pay more taxes than most places in the world, but you know what I mean. When it comes down to it, I am glad that those taxes are taken away. They provide me with the insurance to know that if Scarlett ever needs anything medically, we will find what we need and we will not have to pay for it. Since all Canadians pay into it every day.
That is why I love Canada. There are things I don't like about it.....things that I love the States for more, or many other countries (so don't get angry at me people!!), but this is my Canada Day post, so I will say only the beautiful things.
Canada, your Candians love you!!