Musings of a Marfan Mom

June 27, 2009
by marfmom
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My Life With Marfan, Part 2

Nothing happened for a while. Months and months went by, and my doctor didn’t answer my letter. Finally, towards the end of 7th grade, nearly a year after I mailed it, I received a response. A hospital social worker had been forwarded my letter and was letting me know of a Marfan support group in the area. The group included a 13-year-old girl! However, even though I had waited so long for a response, I didn’t jump on it right away.

Now, I didn’t usually participate in PE class. I was at a small private school, preschool thru 8th grade, and my teachers allowed me to work with the kindergartners during my phys ed time. [For awhile they had tried to make me teach myself yoga using a video in an empty classroom, but I axed that idea once one of my male classmates accidentally walked in on me with my legs over my head and my bum facing him. That was pretty mortifying for a middle schooler!]

Anyway, in 7th grade we got a new teacher, and he took it upon himself to try to get me more involved in gym. This particular day, he told me he’d re-worked the rules of kickball so that I could participate. I don’t remember much of the game, but it ended with my team blaming their loss on my lack of athletic prowess and me being scorned off the field. That was the moment I decided I’d had enough, and that evening I called the mother of the girl my age to learn more about the support group.

Luckily for me, they were having a meeting a few weeks later, in early June. I was excited to go, but my father was upset about it. I didn’t understand it then, but he was remembering other types of support groups that he’d been to and the negativity that could occur. He didn’t want me to be frightened. The Sunday of the support group meeting, my mom took my siblings and me to church. My dad was supposed to pick me up early so I could make the meeting on time, but Mom had warned me that he might not show up. I sat in the lobby and prayed and prayed that he would come. I needed to go to this meeting and for the first time meet people like me. Luckily, Dad came through.

When we got there, he stopped me in the parking lot. “Maya,” he said, “I want to warn you. Some of the people here, they might be pretty deformed. They might be really sick. Do you think you can handle it?” I replied, “I am one of these people, Dad.”

By the end of that meeting, I was so grateful to Mom for suggesting I send that letter to my cardiologist.  S. was the girl my age. She and I left the adults at the meeting and went to talk. It was like we’d known each other our entire lives! I had never felt such an immediate connection with a person like that before, or since. We both loved dancing and pushing the limits that our doctors set. We were active in our church youth groups. S.’s health was worse than mine, but she kept such a good attitude. At the end of 3 hours our parents had to drag us away from each other. For over a month, we emailed each other nearly every day, and made plans to spend the day at the pool together.

At the end of July I asked Mom permission to invite S. to the pool for the following week. Mom said no, that it wasn’t a good time for me to call. She was distracted all day long. In fact, coming home from a church activity that night we almost got into a car accident because of it. After family prayers my siblings were sent to bed and I was told to stay behind. “Am I in trouble?” I asked. “Maya,” Dad said, “S. died last night.” I didn’t believe him at first. Anyone who knew Dad knows he had an offbeat sense of humor. I thought it was the start to a sick joke. Then all I could think about was that in my last emails to her I had complained about my new scoliosis diagnosis and the silverfish I’d found in my bed and how her last thoughts of me must have been that I was dumb. Mom said, “don’t worry Maya. Just because S. died doesn’t mean you’re going to die too.” My pediatrician had told her to say that. I knew I wasn’t about to die. I knew her Marfan was worse than mine. As I sobbed away the entire night, all I could think about was that it wasn’t fair that someone so knowledgeable and optimistic, someone who was doing everything to take care of herself, should die.

And then I decided I had better do something about it.


This picture of our local Marfan group was taken a little over a year after S. died. It almost doubled in size over that year.

The rest of the story: Part 1, Part 3, and Part 4

June 24, 2009
by marfmom
6 Comments

My Life with Marfan, Part 1

I’m not quite sure where my story starts, but I suppose the Coolest Thing to Ever Happen to an 8 Year Old is as good a place as any.

Ever since my parents first used me to get them free candy, I’ve wanted to be in a parade. I used to beg my dad to paint his ugly pickup truck magenta and hang streamers from the ladder racks and let me ride in the back, tossing candy to the other kids. (My mother is eternally grateful that the year Dad offered to indulge me in this fantasy, he missed the deadline to register his truck by a couple of days.)

Finally, when I was 8, I was set to increase my cool factor by 110% by riding on the Girl Scout float in the Pataskala Street Fair parade. It was a hot day and all of us Brownies had to wait a while for the start of the festivities. I don’t remember much of what happened, but at one point I woke up in the gravel next to an ambulance (how convenient!). I didn’t know it then, but it was the first of many fainting spells. Someone fetched my mother and soon I was riding home in Dad’s ugly pickup, instead of standing atop the Girl Scout float in all my 8 year old glory.

Shortly thereafter, Mom took me to my pediatrician’s to find out why I had fainted. In retrospect, I wonder why she didn’t just chalk it up to the heat and me locking my knees and leave well enough alone. But she didn’t, and my doctor knew my family well enough to know to take mom seriously. He looked through my chart for a while, bustled around taking some measurements, and said “I’m sorry, I really should have caught this earlier.” And then he told my mom about Marfan.

The doctors at Childrens’ Hospital confirmed the diagnosis, which sent my family into a tailspin. I understood that Abraham Lincoln had had the same illness, which I thought was pretty awesome. I wanted to tell everyone at school. I mean, having the same illness as a dead president had to make me famous by association, right? However, Mom suggested that my diagnosis might be something better kept a secret.

For the next 4 or 5 years, I just sort of existed in this awkward place where I didn’t really understand what Marfan meant, and neither did my parents. They meant well, but were at times suffocatingly overprotective, and I began to rebel. Mom finally suggested I write a letter to my doctor and ask if he had any other patients with Marfan that I could talk with.

That letter changed my life.


My first (and last) equestrian competition, taken about a month after I was diagnosed with Marfan

You can read the rest of my story here: Part 2, Part 3, and Part 4