Alex and Maddy

Alex and Maddy

Wednesday, August 31, 2011

Doing Great

I cannot believe we have only been here for two days! We have been BUSY!!! Alex and I arrived safely on Monday afternoon. Although I was worried I was able to juggle my Bug, a suitcase, a car seat, a wheelchair and two carryons and safely make it onto a monorail to the rental car center and then drive the 30 min to our hotel! Needless to say we were happy to arrive at our hotel. But WOW I was not prepared for the beauty of Northern California. I truly enjoyed the scenic drive from the airport to our hotel. Buggy just wished I would stop telling him to check out the scenery. Shortly after arriving we were able to visit with one of my good friends (Erin) since high school who made the trip up from Southern Cal to visit!

Tuesday I wasn't sure what to expect. All I knew was that we were supposed to meet at the clinic at 9 with Dr. E (the geneticist in charge of the study) and his clinical coordinator, Katherine. After a LARGE starbucks to help propel me through the day, we were off. I must say I have been thrilled with how nice and accomodating the staff here has been. Katherine met us in the waiting room and immediately took us back to a room. We were in clinic for 2 and a half hours! The first little bit was going over Alex's meds and allergies. Then we went over his history. Finally, Dr. E explained the trial and let me ask as many questions as I had. Last he examined/videotaped Bug. I was impressed with how patient they were with both Alex and I and how willing to answer all of our questions. Dr. E also asked us about participating in a few other studies he is doing and offered some possible suggestions to help his liver. After finishing in clinic we headed downstairs to run labs. Then we had a quick hour break to grab a bite to eat before we were off to the hospital for an EKG and Echocardiogram of Bug's heart. We finally finished up for the day at 2:45. We hurried back to the hotel to meet up with our dear friends the Spry's. I have blogged many times about the special friendship Mariah and I have. Mariah and I met online when we thought the kids "just" had food allergies. Her twins (who are just 2 weeks younger then Alex) and Alex were diagnosed with eosinophilic disorders, got tubes and were diagnosed with mito within months of each other. Mariah and I have buoyed each other through 6 years of this journey, but have rarely gotten to see each other in person. Luckily they were able to spend a few hours with us yesterday. We are hopeful that we will have more time together on subsequent trips. Then Erin and I were able to spend more time grabbing dinner and chatting late into the night before she had to head back home. I was so blessed to have these two special friends take the time to come to Stanford to make this trip easier for Alex and I.

This morning we had to be at the hospital at 8 for a special test called a Brain Spect. It was difficult for Alex. I was so proud of him as he did a GREAT job. We had been told to prepare for him to have to lay still for 25 min. however, they failed to mention the first part of the test. Alex and I were taken into a holding room. he had to lay on a bed with the lights out for 30 min as still as possible and he wasn't allowed to talk to me or me to him. Then they injected him with the radioactive tracer before he had to lay still and quiet for another 30 min. Finally he was taken to the scanner room where he was strapped to a table and unable to move at all for the final 25 min while they did the scan. Well, anyone who knows Alex and I knows being quiet for an hour and a half is NOT easy!!! While this wasn't a painful or scary test, it was hard. I was so proud of my mature, brave boy who did fantastic. When that first scan was done, we had a break until 1, when we had to be back to repeat another 25 min scan (but did not have the hour lead up). I was lucky to get to spend some time talking to the radiologist who pioneered this test and the use of studying the function of the mitochondria in the brain. Once again he was so nice and forthcoming and willing to answer ALL my questions. Once the second scan was done, Alex and I came back to the hotel and crashed! We were still tired after waking up and decided to get room service instead of going out to eat.

Tomorrow is the big day! It will once again be quite busy. He has his first dose of the medication, 3 separate sets of labs throughout the day and another EKG of his heart.

I have been very happy with the care here and excited for the prospects of what is to come. I have felt you all lifting us up this week as I have been calm and at peace throughout. We are so lucky to have so many friends and family who say faithfully love us and pray for us. I ask specifically for prayers tomorrow that Alex does not have an allergic reaction to the medication. I will update tomorrow to let you know how he does!


  1. Thanks for the update, Ali - I'm so glad Alex has been able to handle everything well so far. Praying he continues to do great!!
    Love & hugs,
    Natalie Furman

  2. SO glad you guys made it safely AND can actually enjoy the scenery some!! I am SOOOOO proud of your big boy!! What a hero!!! Praying everything continues to go smothly!!!

  3. Hi,
    I found your blog from my churchs prayer request. Have you seen this video before?

    Check out it. In the meantime, we are praying.