How to handle doctors visits with special needs kids like a boss! or our trip to U of M
I am going to dive right into this one as I am excited to share the news.
The reason for the doctors visit is Bella has 80% hypers-nasal speech means when she speaks air goes up her nose is what the test showed at the last doctors visit.
In Aug, in fact, we were scheduled to go ahead and correct this issue she has with air by fat graphing which involves fat from some part of Bella (I wasn't sure where they were going to find any fat on her) I was wondering if we should wait it out until she passes puberty or just go ahead and do it now and get it over with.
The speech doctor at the clinic had to perform her speech test on Bella by asking Bella to say funny sounding sentences. Bella had to say words while pinching her nose, followed by the breath o her breathing on(magic mirror thing a ma jigger) I am not sure what it was called but it goes under Bellas' nose and you can tell if there is air in the mirror if it clouds up or not. Bella had no air on the mirror this time. Last time the mirror was all cloudy.
Bella then had to sit with a fun looking space helmet on her head and speak into a sensor while she said the same funny worded sentences. Bella scored a perfect normal on the test. 4 times. Normal from 80% is something only short of a Miracle.
I don't even think it sunk in yet. Bella was thrilled and thankful that Bella did not have to have a camera go down her nose into the back of her throat. It was a shock to both of us no surgery needed Bella will go back for a team visit soon as they can fit us in to talk to the team about our next treatment plans.
Below is some info on what Velopharyngeal or for short Vpi is
Bella playing in the play area on the 8th floor after to burn off her energy before we headed home
I know I asked all of you to visit my website to hear about this trip because it is such great news it was difficult to talk to 100 different people and I can not keep up with that many questions. If you do have any questions feel free to leave a comment on the blog in the comment section below.
Thank you for reading. Bella looks forward to seeing your likes, comments, and shares and she said she is super excited she does not have to have surgery. Bella is a 10-year-old girl with 22q and cerebral palsy. I am a mom who also has 22q. This is our journey and I am sharing to help others out there not feel so alone. Don't forget if you like it subscribe (Purple button top right of the homepage)
Until next time take one second at a time.