Tuesday, July 27, 2010

Pictures of the girls

Belinda told me that I needed to post more pictures of the girls, so here you go:

Here is Andi (in red) and Bella back in June.














Here's another of the twins playing in our cool pool (Andi is standing)















And here are a couple of Piper.  Just chillin'

Thursday, July 22, 2010

Last season on "All You Need is (Young) Love"

(if you want the full effect with music, turn up your volume, right click the "Soundtrack" link below, and select "Open in new window"

Soundtrack

When we last left our fearless family, we had just sold our house and were settling into a palatial 900 sqft apartment waiting for construction to finish on our new home.  Things have been moving pretty fast since then.  Andi and Bella have learned how to walk, are starting to jabber it up, and are learning how to manipulate their parents.  Ah, the good times.  Nothing like an infant that cries as if they've been shot in the foot, who is suddenly the happiest baby in town after being picked up by mommy (I'm looking at you Andi).  They've also learned how to poo four times a day.  Must be some kind of record.  I mean seriously, put a plug in it.  There will be plenty of time for that tomorrow, and the next day, and the next day...  I why must you scream bloody murder when I try to change your diaper.  Hello!  I'm not doing this for me.  How about a thank you next time.

Tuesday, May 25, 2010

And then the other shoe drops...

How does it go, "The good Lord giveth and the good Lord taketh away."  Well, I guess in our case, the good ole government giveth and the good ole government taketh away.  Or more appropriately, the FDA giveth and taketh.  What the heck am I talking about?  Well, we got a call from our doctor at Stanford (we'll call him Dr. A) last week and he informed us that because we didn't have an official "genetic" diagnosis for Piper, the FDA is not going to allow her to participate in the drug study.  Needless to say, we were not happy with this news.  Now I'm going to get into some of the scientific mumbo-jumbo to explain this more in detail, so if science gives you tired head, then all you need to take away from this, before you skip to the next paragraph, is that the FDA is a bunch of lazy assed, incompetent, pencil pushers who are more interested in collecting their union pension than doing their job and probably can't find their F'ing DA from a hole in the ground.

Tuesday, May 18, 2010

On the surprise ending

Well, it looks like my definition of "tomorrow" and yours is probably different, but here is the news you've all been waiting for.  About 3-4 weeks ago, Belinda posted about Piper's condition on a website where you can post questions and Dr's will read and provide input/answers to your questions.  So after Belinda posts a question about Piper, she is contacted by a doctor at Stanford University who is researching mitochondrial diseases (including Leigh's.)  One thing leads to another and it turns out he is leading a trial for a new drug that is showing some promise helping children with Piper's condition.  After talking with him some more, he tells us he want to include Piper in his study.  Now from what we've been told, they had another, unofficial study with about 1/2 dozen patients that showed "remarkable" progress as they went through the study.  This time around they are an official FDA approved study including about 3-5 children and Piper will be one of those.  We are still working out the details, but hopefully in the next couple weeks Belinda and/or I will start taking weekly flights to Stanford to begin treatment.  We're not getting our hopes up (at lest not a whole lot) but it is wonderful to at least have a way to fight back.

On a somewhat related note, without the tireless efforts of researchers like our Dr. at Stanford and Dr. Pascual (our specialist here in Dallas) these potentially life saving treatments would not be possible.  If you want to be part of the team striving to find a cure, you can help by visiting www.childbrainfoundation.org, a non-profit organization run by Dr. Pascual and his wife Albertina helping to raise money for research.

Wednesday, May 12, 2010

We're back!

Hello all!  Sorry for the long absence, but with apartment living, crazy work schedules and even crazier babies, I haven't had all the time I've wanted to keep the blog updated.  So, I'll give you a quick recap on our latest events (with a surprise ending.  ooohhhhhh!)

Thursday, April 22, 2010

It's a Festivus miracle!

We've finally gotten our TV and internet setup, so we can be back on the blog. The move to our spacious 2 bedroom, 2 bath, 900 sqft, resort style apartment has been excellent. And by resort style, I mean last resort. Andi and Bella have one room, Piper has the other, and Belinda and I have the living room/master suite all to ourselves. That's right, we've got our bed in the living room. But hey, it's cheap.

Wednesday, April 14, 2010

Just checking in

We have finished up the move, but don't have TV, phone or internet, so posting will be a bit spotty until we get that setup. Move went as well as could be expected (thanks to all that helped).