Musings of a Marfan Mom

December 1, 2011
by marfmom
7 Comments

Sarah’s Story

Sarah is a reader turned friend I’ve been corresponding with via email for months. I really appreciate her insightful comments and was delighted when she agreed to guest post here.

Marfan first entered my family’s vocabulary when I was three months old, and it had just killed my father.

Our understanding of it grew as I did, through my misshapen bones and the failed childhood surgeries to repair them, through the genetic screenings and loose joints and floppy heart valves, through my teenage denial and eventual acceptance of a part of me to be neither loved nor loathed.

My truce with Marfan lasted until the eve of my 30th birthday, when my biological clock became a time bomb. I both ached for a child and feared losing it to Marfan like I’d lost my father. I simply couldn’t take that chance.

Geneticists offered few options. I could get pregnant and then use my family’s mapped mutation to test the baby before birth. But my soul would not have survived extinguishing a life whose only wrong was to be too much like me.

I could adopt. I knew many families joined by love and not blood. But I desperately wanted the joy of creating a life, of being pregnant and giving birth to a child no one could question was my own.

The only road left was to use fertility treatments and genetic screenings to ensure any baby I became pregnant with would not have Marfan.

For weeks I ingested, inhaled and injected myself with hormones, slowly losing my grip on reality as the pharmaceuticals took control. However, luck was with us. We fertilized 20 eggs, creating a veritable army of future infants to fill my empty arms.

At three days old, a single cell from each of my would-be babies was shipped from my home in western Canada to Detroit Michigan to be tested. The results took my breath away.

Fourteen of my embryos had Marfan. Another four were weak and likely not to survive. I had just two healthy embryos to create my family. TWO. And there was no guarantee if we froze one of these embryos for later that he or she would make it.

So we did the only thing we felt we could. We put all our eggs in one basket and held our breath.

Six weeks later I was staring at an ultrasound of my babies – both of them.

Overjoyed to be pregnant, it took mere seconds to realize that my high-risk pregnancy had just become doubly complicated. I’d aimed to be one of a handful of Marf-mom’s to give birth in my city. I was now the only expecting twin Marf-mom in my zip-code.

Undaunted, I marshalled my medical troops. A high-risk obstetrician was enlisted and my cardiology team supplemented with a trio of physicians who would monitor my blood pressure, joints and skeleton monthly. Even my Marf-specialist eye doctor was brought in to consult on how labour could affect my retinas.

Desperate for information I surfed the web, stumbling on this Marf Mom blog and taking solace in all the guest postings of women who had their own families. For as my waistline expanded, so did my dread. Something felt wrong.

Exhaustion plagued me every second of the day. Soon staircases were too much for me, and a simple walk in from the parking lot felt like a marathon.

Twenty-five weeks into my pregnancy, my cervix disintegrated and I went into labour.

For 48 harrowing hours we tried everything to keep my twin boys inside me. But the time for bed rest and drugs was past. And this March, my sons came into this world three and a half months too soon.

Baby W was born weighing 1 pound 11 ounces. His brother Baby D arrived one minute later weighing 1 pound 15 ounces. They couldn’t breathe on their own, eat on their own and their eyes were fused shut like kittens. They were rushed to incubators, too fragile to even be held up to my face for a few seconds before heading to the NICU.

I felt broken. Betrayed by my body, my boys were clinging to life inside an artificial womb instead of in me.

In the following days, I watched my eldest undergo heart surgery and my youngest fight off a deadly infection. They would both be pumped full of countless drug and blood transfusions. But my miniature men seemed as hell bent on being part of this family as I’d been to make them. They fought.

Everything came slowly for us. I held my firstborn for the first time when he was seven days old, fed the twins for the first time at eight weeks old and waited 102 days before I could have both my boys come home from hospital. But they did come home.

There are plenty of challenges ahead for us. At nearly nine months old, my twins may be nearly 20 pounds each but they are still trying to come off oxygen supports. And with compromised immune systems they must be kept isolated for fear that a simple cold could devastate their fragile lungs. But with each day they grow stronger. And with all their antics, giggles and cuddles it is easy to forget how close we came to losing them.

Lately, caught up in the whirl of diapers and feedings and bouncing baby boys, I’ve forgotten all about Marfan. Because when my twins were born they brought a new phrase into our vocabulary – micro-preemie — and we will learn what that means as they grow up, just like I did.

November 30, 2011
by marfmom
4 Comments

First Birthday Party

Although Baby J’s birthday isn’t till next week, we celebrated this past weekend so we could have our extended family present. It was a Very Hungry Caterpillar themed party.

Hungry Caterpillar Birthday Party
party punch
4 liters 7-Up, 1 pack lime kool-aid mix, and lime sherbert
Hungry Caterpillar food
baby eating chips
Baby J wouldn’t eat his food, but he did reach behind him to grab his great-gradmother’s chips off her plate!
Baby who hates birthday cake
J is rather texture sensitive and really hated the cake at first.
baby eating first birthday cake
He warmed up to it later, but only for a few bites. Then, it was back to crying.
baby hates cake

November 28, 2011
by marfmom
1 Comment

Learning from Each Other

I’m excited to have my friend Erin guest posting today. Erin and I met in graduate school. She is very active in the Type 1 diabetes community and was a big help when Mark was diagnosed with it. Erin blogs over at The Insulin Crowd. Please head on over and say hello, especially since November is Diabetes Awareness Month!

Hello Marfmom.com readers! I was excited and honored that Maya asked me to guest post on her blog this month. In all honesty, I’m nervous! I read her blog, and the comments from all you readers regularly, so I know what an amazing group of people you are! I hope that I can say something here that will be worth the time you take to read it.

Maya has given me virtually free reign over what I should write about, so I think I’ll stick to what I know (and hopefully a little of what you all know, too). I have Type 1 diabetes. I’ve had it since I was 11 years old, and without getting into too many boring specifics about what that all entails, it means I’m a life-long member of the exclusive chronic illness club, along with Stacey from the Babysitters Club, Wilfred Brimley, B.B. King and Brett Michaels. And Joe Jonas. But that’s a post for another day. I digress.

From the little I know about Marfan syndrome that I’ve gleaned from knowing Maya and reading her blog, Marfs (am I allowed to use that word, or do I have to be a Marf to do so? hopefully I haven’t offended anyone . . .) are members of this chronic illness club, too. So, I thought I’d commiserate here a little about this club of ours. Specifically, I want to talk about how reading about you all has illuminated my own journey through life with a chronic illness. There are a lot of things that you all do that have allowed me to see myself and what I do more clearly.I feel like reading about you all, even though we have distinctly different chronic conditions, has made me better understand and relate to my own.

Doctors & Patients
One of the things that has impressed me so much is how much it seems physicians and patients in the Marfan community work together. I was so impressed when I first read about your NMF conference and the physicians that are a part of that group. It seems, at least from an outsiders perspective, that they are so invested in you all. And the fact that at your conference there is a clinic that you can attend was very impressive to me. If there’s one thing I would wish for the diabetes community (other than a cure, of course), it would be that the physicians would work with us and not just tell us what we should and shouldn’t do. Now, I’m sure not everything in your Marf-world is all butterflies and roses all the time, but I do think my Dia-world could take a few lessons on doctor-patient interaction from you all.

Advocacy
I love reading Maya’s posts about the NMF Conference you have every year. And while I know that not every single person with Marfan syndrome is attending the conference, or maybe even knows about it, I think it is amazing that you have something like this. We have a few things like this in the diabetes world, too. We have the American Diabetes Association (ADA) and the Juvenile Diabetes Research Foundation (JDRF-they specifically focus on Type 1 diabetes). I think they both have some kind of annual conference, although interestingly enough, I don’t think they’re as patient-oriented, but more like conferences for researchers, physicians and pharmaceutical companies. I know that there is a “Children with Diabetes” Conference that goes on every year at Disney World, or some place equally as fun, that is much more patient-oriented. Aren’t these kind of events amazing? I think the diabetes patient community is starting, ever-so-slowly, to come to the table at these kinds of conferences and demand a voice. And I love that that is happening. And I love seeing that happen at your NMF conference.

Community
I reach out to members of the diabetes community, via the internet, all the time. If there’s one thing we PWDs (persons with diabetes) are doing really well these days, it’s creating a few on-line hubs for a place to connect with other PWDs. There is a great website called tudiabetes.org that is basically like Facebook for diabetics, only instead of passing around annoying internet memes, you can ask questions of your fellow PWDs and get amazing advice. There are several other sites like this floating around out there in cyberspace, and they are a treasure trove of helpful information. I hadn’t realized how much I actually rely on these sites until I read some of the comments here at Marfmom.com, and Maya’s tweets. I see you reaching out to each other for support and advice (I especially love when Maya updates about a sale on tall jeans), and it makes me realize what an important piece of living with a chronic illness that is and how much I depend upon it!

Any way, those are just a few of the things I’ve been thinking about lately, especially when reading Marfmom.com. There’s so much we can learn from each other, and I love coming here and feeling accepted and like I can relate to you all on some level, even if we are members of different “chapters” of the chronic illness club!