Sunday, April 19, 2009
2 month checkup
This past week was another busy week for the G-man and the Gibbs family. Several weeks ago we searched out a local chapter of the Spina Bifida Association here in Grand Rapids and on Monday we had the opportunity to meet with the group. Not really knowing what to expect we headed downtown to the Mary Freebed Hospital and after a few wrong turns made our way into a conference room. WE honestly had no idea what it would be about or how many people would attend, but we thought we'd give it a shot. What we discovered was what seemed like a once healthy and flourishing support group, that today seemed burned-out and in need of some help. The information we got was at times helpful but at other times not relevant to us at this time. The members all had boys with SB age 15-22, so although it was nice to hear that these boy are doing well today, we have a long way to go to get to some of the issue they are dealing with. I feel the idea of a "support group" has changed dramatically, especially with our generation. For one, this blog acts as a great support group for Leigh and I. Leigh also is involved in a wonderful online support group consisting of mainly new moms with SB children. So after the meeting we had mixed feelings about it, but feel its to early to bail on it at this point. Perhaps the group needs to be shaked up a bit and maybe we can help with that :)
Greyson also had his 2 month check up on Friday and he's doing great!
The G-man now weighs 12lbs 7oz and is 23 3/4 inches long. He's growing right on track. Greyson also needed his 2-month shots and as strange as it sounds we were hoping the little guy would scream his lungs out when those shots went into his legs!! Something I think only a parent with an SB baby would understand. Although Grey didn't cry when he got his shots his little leg shot up so fast! Which means he has some feeling in his legs! His hips also appeared to bother him the rest of the afternoon, especially when we pressed on the sore spot. I know, doesn't that seem horrible, pressing down on your child's shot "wound" and then smiling when we reacts to it. Again, I think any SB parent could relate.
So our boy keeps getting bigger and cuter everyday, we give thanks for him and how happy and content he is. We pray everyday that his shunt continues to work properly and continues to get stronger.
love to all,