Progressing Everyday

The doctors and therapists continue to be amazed by Paxton. The can’t relate his MRI pictures to how he looks clinically. His hemorrhage was very large and will take at least another month until we can actually see what’s under there and find the potential cause.

Pax is super interested in learning about his stroke and the effects of different parts of the brain. They have printed out a bunch of his images from the MRI to explain it to him. He loves looking at all the different views. He said I could share one of these images so people could see what happened. He also hopes it helps everyone understand why he speaks differently and walks a little uneven. There’s rumors we are getting out soon and he’s nervous to see people for the first time.

As you can see the bleed is very large and is right over the speech center of his brain. He will continue therapies at home, his recovery is far from over. We are so proud of his hard work and determination. We should know by tomorrow what the new discharge date is.

Paxton spent the day in between therapy appointments with Brandon. His schedule is so busy but him and Brandon were able to hang out and even continued the ice cream tradition.

Bray and I spent the day at the Denver Zoo. The weather was great and we got to see a lot of the animals up and roaming around. I promised I would take Pax when we come back for one of our many follow up visits.

Hopefully Brandon and Bray will be able to fly out tomorrow without too many delays or complications. Pax has another full day of therapies plus our meeting with his team to discuss coming home. We will keep you posted.

Thanks for the continued love, support, and prayers. We are so grateful for all the kindness.

Janell

Comments

Denver

Yesterday Pax had his MRI and angiogram. They found a small AVM that caused the bleed. This abnormal vessel will need to be removed. It happens to lie right on the pronunciation speech center of his brain. There is a risk of him have temporary or permanent set backs in his speech with the removal. The neurosurgeon is consulting with other specialists to determine the best way to remove it. The vascular neurosurgeon said it’s close to the surface, which is good. We aren’t sure when the surgery will take place, but it doesn’t sound like this trip. I have a mixture of emotions. On one hand, I’m glad we know the cause and it can be fixed, but the risks are scary. Of course we’ve gotten ice cream since we’ve been here. He was thrilled to see they had Cookie Butter this week. We have an appointment with the rehab doctor today so I’m sure we will be getting more ice cream today. Thanks for keeping us in your thoughts and for all the love and prayers. I will update the blog when I know mo...

Quick Update

He’s done. Took about 10.5 hours. It was MUCH more complicated than anticipated. They say he's doing good. We are headed up to the icu now to see him. Thanks for all the support. I will update more tomorrow.

Christmas Miracles

We have some great news…Paxton started walking on his own! He literally went to PT in the morning being helped by his therapists and a hour later came walking back without assistance. He is literally blowing everyone away. So many people have told me that he is the hardest worker they’ve ever had. We are so incredibly proud of him. We kept the secret from Brandon and when he got here tonight, Paxton got up from his wheelchair and walked to give him a hug. Lots of happy tears were shed. He fatigues really quick and still has some work to do to perfect his stride, but he’s crushing it! I tried to upload the videos but I can’t get them to work. I will keep trying. My favorite response is from Eva and Nellie. They sent an awesome video in response, but I can’t get it to upload either. Grrr Bray and Pax were so excited to see each other. They hugged and were so sweet to one another. Bray and I cried as soon as we saw each other. I have a feeling these next few days will go by much too ...

Paxton's Progress

Search This Blog