Mi Vida... My Life.
About a year before David was born, Mabel and I were in a restaurant. A few tables down, there was a mother with her young child. Probably about 3 or 4 years old. When we got there they were eating quietly. About 5 minutes later her child had to go to the bathroom, but the way she addressed her wittle one stuck in my head. She called her "Mi Vida" (My Life).

When she said it, I noticed. Never heard that statement before referring to people. Growing up in a working class, it usually came from co-workers complaining about their back breaking and cursed lives. At the time I remember thinking, WOW she really adores her wittle one.

Now I've always loved children, I even remember changing my younger brother's diapers, so it was easy to become googly-eyed over David.

It's only natural to love ones' kids, but with careers and expenses we sometimes can't stop to enjoy all the subtle phases of child development. So David's first 6 normal months flew by in such a blur. Inbetween, there were regular pediatric visits, first 5 vaccine shots, middle-of-the-night feeding times, late work nights, and new child care.

When David was 3 months old, Mabel were back to work and her mother Naty stayed with him during the day. Besides getting her settled into our apartment and lives we began house hunting. At that point we lived in a 2 bedroom apartment and we shared our bedroom with David. We wanted him to have his own wittle space.


(ABOVE; David and his dada posing in one of the Beardsley Zoo cutouts.)

(ABOVE; David and his dada going over some sitting exercises and positions.)
From David's 6th month, is when I began to take notice. As his medical problems began and his situation complicated, the bond grew. With each of the IVs, bloodwithdrals, sour medications, and overnight bed stays came an emotional drain. Any pain David felt physically, was emotionally magnified in us.

We also understood that when he was on heavy medication the first few initial months (12-15 months of age) that he was slightly sedated and probably felt minor pain, but it was very tough to see a wittle suffer so.

Clearly he wasn't comfortable at that time, feeling restless, itchy, thristy, and with little or no appetite.

I have to also mention the mommy factor. I feel that Mabel basically saved David's life. As a daddy, I would've tried my best to get David the proper specialists and doctors, but being a nurse-and from the health industry-Mabel was better able to focus our efforts.

As a RN, Mabel knew more of David's proposed medications and their side effects. She had actual first-hand accounts of these meds and their drawbacks. She knew of neurological specialists and successful practices in her field. Her schedule, working longer shifts to total less days, left more full days to reserach and meet the doctors. Her insurance gave us a broader network of doctors.

Looking back, it was definitely a joint effort to get through the last year and a half. It was always about David, but parents usually need each other to feed off of and remain positive. Especially when doctors speak about technicalities and harsh facts. True the body has limits, but its healing power can be what you make it.


(ABOVE; David not wanting to go to bed.)
With each passing day, I thank god for truly blessing me/us with such a beautiful and wonderful wittle boy. He has changed my life and all those around him. Before him I didn't know what it meant to live or truly love. David is my every breath, my love... and my life.
one amazin' wittle boy l mama l dada l meme l play dates l school l home
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