Friday, March 2, 2012

One Step at a Time


The next 6 months were spent focusing on food trials. Rosie had a blood test done to test for traditional allergies, which all came back negative (and the Allergist labeled her ‘Protein Intolerant’…off to find a knowledgeable GI!) At first we were doing week long food trials. Rosie was eating sweet potatoes, raspberries, blueberries, avocado, apples, peaches and some sweet potato puffs. At first she seemed fine with these things as we added them in... but slowly her good spirits started to fade. She developed a constant crusty eczema rash on her face that didn’t respond to any cream. She went from sleeping pretty consistently at night to being wide awake for hours at a time, to waking up screaming. I knew something wasn’t agreeing her, but the question was what.

The only way to find out was to pull ALL of her food. So we started back at square one with sweet potatoes. They went well for a few weeks, I had high hopes. But her eczema started to flare, then she got these cold symptoms, then she started vomiting after her meals. As soon as we pulled the food, her symptoms disappeared. And the same thing happened with white potatoes. Accidental ingestion of a serving of apples gave Rosie the worst case of crusty, oozing eczema I had seen on her.

And so it went. Food fail after food fail. Pears were our last trial and arguably the worst. I pulled them before she got to the vomiting stage, but even so, Aurora had 15 days of diapers filled with mucus and blood. This was right before her first birthday.

So by the time my Rosie turned a year old she had failed 11 foods and had nothing safe to eat, except Elecare formula. Instead of a cake for her first birthday (which was a BIG deal to me, my older son wouldn’t touch his cake at ANY of his birthdays!) I made her a giant box cake-out of hat boxes decorated with fabric and filled with toys. She LOVED it!! And seeing her chubby little face light up at the cake that was bigger than her was just overwhelming.

A few weeks after her birthday we made the trek to Kansas City again, to the new GI. She was finally formally diagnosed with FPIES. What a relief. To finally have the confirmation that I’m NOT crazy was overpowering- it was EMPOWERING. We were told to stop all food trials for 3-4 months to give her insides sufficient time to heal.

So here we sit, just waiting. Rosie is now 14 months old with still no food she can safely eat. Truth be told, it is nice to have this break of not worrying about feeding her something that will make her sick. It’s a terrible feeling, knowing you’re trying to nourish your child and instead causing them extreme pain. I do have to be very careful and watch her very closely…that cheerio her brother dropped? That piece of corn she snuck off the table? The tiny raisin she found under the couch? More damage to system, more nights of screaming and cramping.

It’s been a long year but we have learned a lot. My autistic son learned compassion and patience with his baby sister. My husband learned that doctors don’t know everything but if you keep pushing and fighting, eventually someone will listen to you. And I learned that as a mother I am equipped to face anything life throws at me. But I think we have all learned from little Rosie that no matter what you’re dealt in life, take it with a smile and keep a dance in your step because life is too sweet to take for granted.



4 comments:

  1. It makes me so sad for her and you guys but you are all soo strong! I hope soon she can find her safe foods!
    Hugs!!

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  2. Stopping over from the fpies group. So sorry about this awful journey. Hang in there, it does get better. My 2.5 year old flies kid is down to just under 8 trigger foods. :)

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