Wright Family support

I'm starting this fundraiser for my bonus son Derek and daughter in law Cassie to help ease some of the upcoming stress they may have...back in March my oldest granddaughter Isabelle fell off her papa's bed (a blessing in the long run) and hurt her neck...several Dr visits, ER visits and a stupid amount of phone calls finally got her an MRI this last week.....below is Cassie's most recent update about everything...Donations will be used to help w gas, bills, food, things for the kids, to cover loss income so Derek can miss work and not stress over that...please share, donate if you can and keep our family on your thoughts and prayers...feel free to reach out to me questions or to pass messages on to them

August 1st Isabelle had an MRI. I went in the back with her to get her all situated. They gave her a cute pink tablet she was so excited. I talked to the anesthesiologist and signed more paperwork while Isabelle was playing on the tablet. After that it was time to put the iv in so I held onto her while they did it and she did an amazing job didn’t even cry, she said ouchie that hurt then I got her back on the bed and she got to pick out a prize. Then it was time for the medicine and she was out, I gave her some kisses and she was off. They said about an hour an 30 minutes. I went back out to the car and waited with Derek and phoenix. She called me and said they wanted to add contrast and take more pictures and get everything our dr needed. She calls me again and said 15-20 more minutes which then turned into an hour later. She called me again and said they are taking Isabelle back to the room so I walked back to the room and as I’m walking back our dr from PMC called me and said they will probably want you to go to the emergency Pediatric unit, because they found something. I’m bawling my eyes out texting Derek to come. We got into the room for the neurologist to come in and talk to us about what they found. Isabelle has several brain tumors. That are all connected. The big one they found is non-operable if they operate it will leave her brain dead. Two of the Drs that we have talked to (which we have talked to several people) think it is NF1. We don’t know what kind it is, or how aggressive it is. They are working so hard to try and find the best and safest way possible to help my baby. They are getting opinions from California neurologist and everywhere. He said to keep her being a kid and continue doing what we are doing. We will know in a week about the next steps. They are talking about doing a brain biopsy to test it and figure this out they are worried about doing that as well because of the location. They also don’t want to put her through more stuff. They are being very thorough. This explains everything that Isabelle has been going through. With her speech, how she acts and walks and her eyes She is on medication that she has to have every 6 hours. Please please please pray for her. The Drs are absolutely amazing amazing people. They truly do care about the children and families.Made my sweet girl feel so welcomed and happy. She has an Eye drs appointment on August 16th In Portland. Please send Positive thoughts and prayers for our sweet girl. I will keep everyone updated as soon as we know.