Alex and Maddy

Wednesday, August 10, 2011

More Pics and Good News

As you can see we have been having fun in the pool! I will let the pics speak for themselves. We also got Alex's 7 year pics done. I posted a few so you could see a preview! Look closely, something is missing!

The next few weeks are going to be CRAZY!!!!! Sometime next week Alex will be admitted to the hospital in Houston. There is some concern for how skinny he is and how puny he has been acting. We will be inpatient for 4-5 days while we try and come up with a plan to get him back to baseline.

Then on August 29th, Alex and I will fly to California to begin the new medication. We are so thankful to the team at Stanford and in Dr. K's office for working so hard to get Alex in the trial and set up so quickly. We will be at Stanford for 3 days (and travelling for 2). In that time Alex will have a clinic appointment, a heart eval, 2 brain scans and get his first dose of medication. Assuming he does well we will fly home on Friday and continue the medication. The next few months will be a whirlwind of travel back and forth between home, Houston and california, but we are so hopeful we will see good results from this medication and it will all be worth it.

Thank you to all who continue to pray so fervently for us.
Ali









































We went on a dolphin watching cruise and saw a ton of dolphins!



















Wednesday, August 3, 2011

Not Feeling Great, But Still Having Fun

I haven't updated in a week so I thought I would give a quick update on the last few days and some pics!


Alex is still not himself! He has been pretty puny. Mostly wanting to stay in bed and watch videos and play his Nintendo DS. Mimi and I have been "forcing" him to get out and have some fun the last few days with lots of quiet time in between. We have seen friends, been swimming and riding go-karts. I'll let the pics tell the story.






Alex and his Cousins





Want some Seaweed?




Sand Monster




Beach bum








At the creamery with Mimi and PopPop




Mommy's Angel





Buggy and Cayman







PopPop and Bug leading the Race





Buggy DID NOT like driving himself!




Win #2




Where Bug has spent most of his time!




In some other exciting news....I had mentioned a clinical trial for a new medication they are using with some Mito patients. We just got word today that Alex has been accepted into the trial. Thank you for all who prayed for us. We are very hopeful for what this may mean for our Bug!




Ali
























































































































Saturday, July 23, 2011

Balancing fear and life

Keeping living and fear balanced is not an easy thing to do these days. How do I let Alex be a carefree little boy and keep my Mommy's heart from stopping him because I am scared of the outcome? Not an easy feat these days. Despite tubes, ports, medications, etc I have always let Alex LIVE. But after 4 years of NEVER pulling out a tube, we have now pulled out 2 in 6 months time. And both times have been somewhat traumatic. He has to be hooked up. It is his only source of nutrition and fluids. BUT he also needs to play. So 1000 times a day he has to hear me say "be careful of your tube". It is not something I have ever worried about before. I am hoping I can find some peace and we can get back to "normal".

This week in the hospital was not one of our easier weeks. There is a level of frustration because all of the doctors and myself are sure something isn't right. The problem is that NOBODY can put their finger on what it is. The most likely cause and our biggest fear is that his liver has taken a turn for the worst. BUT his liver numbers are ok. We know those are not always accurate so we just wait and watch. Alex continues to run low grade fevers as he has for a month. We continue to struggle to control his Ammonia levels. (Although an increase in meds has definitely helped which is promising), we continue to keep his clotting numbers in range, we struggle to keep his blood counts normal and his color is TERRIBLE. Yet despite it all he is back to acting more like himself.

After how awful he looked and acted on Tuesday we figured out he was in a good deal of pain. He was a little better Wednesday. The plan was to finish antibiotics Wed. night and be discharged first thing Thursday Morning. Unfortunately, we woke up to labs that were not great Thursday morning and prompted a little scrambling before we could leave. Alex's blood counts and more importantly coags were off again despite intervention over the last few weeks. It was decided we needed to see Hematology before we could leave. They ordered some extra labs which confirmed what they thought was the problem. Some of your clotting factors are produced in the liver and need Vitamin K to work. One of those factors was very low (It has been low in the past, but was considerably lower this time). So Alex is receiving 5 days of Vitamin K injections in the hope of getting his clotting back to normal. Luckily we were able to be discharged Thursday, but we didn't get out until 4:00. I sure was happy to hit my bed when we got home. Poor Bug must have been exhausted, I woke him up at 9:00 yesterday morning!

Thank you once again for all of your prayers. You, our family and friends, lift us up when we are down. When I don't have the strength to put one more foot forward I know there will be someone to carry me. For that I am eternally grateful.
Ali