Skip to main content

Busy Sunday

 I just want to start out by thanking everyone who has called, text,  private messaged, donated, commented, and prayed. We are seriously overwhelmed (in a good way) by the support we have received from friends, family, neighbors, and strangers. It made me realize there’s still a lot of good in people even though we are living in crazy times.

Pax had a pretty good day. We started out early with PT this morning. He got to go to the therapy gym for the first time. They have tons of amazing equipment. Today’s therapy was a game of Jenga with dad. This helped his core strength and using his arm. Dad won, but we are all pretty confident he cheated.

After PT we did feeding therapy. Paxton was able to eat 2 veggie straws, up from 1 goldfish yesterday. He was able to swallow a little water as well. The therapist gave us permission to try ice cream! There is a little gelato shop in the lobby of the hospital. We loaded him up in his wheelchair and went on an ice cream run. He got hazelnut flavor and LOVED it. He probably ate 4 spoonfuls which is significantly more than he’s eaten up to this point. 

Paxton also got to take his first shower today. It’s a learning curve for both of us, but I’m sure with time we will have down to a science.

Bray and Pax were able to play Roblox together today online. Pax smiled the entire time, and Bray was so sweet and patient with him.

Sounds like the real work starts tomorrow. They have a pretty rigorous therapy schedule during the week. We are excited to get going on it all.

We snuggled in his bed and watched some TV this evening.  We were both exhausted. He got his IV out, which is a huge step in the right direction. Pax gets frustrated but still laughs when I’m guessing what he’s trying to tell me and I’m way off base. He’s still the sweetest boy ever. I’m so proud of him and want nothing more than to take away his pain and frustration. He is my hero.

Love to you all.

Janell 

Comments

Post a Comment

Popular posts from this blog

Feeling Better

 Pax is doing much better today. His silly personality is back. ❤️ He’s still a little swollen but much better. His jaw hurts a little less so he’s eating more. He crushed it at PT yesterday, and can’t wait to go back to the rehab gym later today. His angiogram is first thing tomorrow morning. He hates being sedated and can’t get up and move for 4 hours after the procedure. They will keep us overnight tomorrow for monitoring, and if all goes well he will be discharged Thursday. We had an appointment with the Acquired Brain Injury Clinic on March 24th and they were able to move it to this Thursday. This is a huge relief, the flights are exhausting and expensive. I don’t think we have to come back for 3 months…wahoo! He’s seriously so brave, strong, and had such a positive attitude. His attitude is the only thing that’s kept me so positive. I’m beyond proud of him and am striving to be more like him. Thank you all so much for all the support. We are so grateful for each and every per...

Long Overdue Update

 I'm not sure if anyone even checks this anymore since I kind of stopped doing updates. I apologize for the gap in time. To be honest, I've been struggling with some depression over Milton's death and PTSD about Paxton. I am working on both of these and hoping to start feeling better. Enough about me. Paxton is doing AMAZING! He is done with PT. He crushed all his goals and they said there wasn't much more they could do for him. He is still in OT 1x week, mostly working on fine motor skills with his right hand. He currently does any writing or drawing with both hands. He continues with speech therapy twice a week. Speech is still his biggest deficit, but he has come so far. He struggles with bigger words or saying longer sentences. He communicates great and everyone knows what he is saying.  School is going great. They just completed state-wide testing and he surpassed all the goals that were set at the beginning of the year before his stroke. We are all so incredibly p...

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...