The beginning of a new work week...
Today was the beginning of week 3 of work at the Haven. I have worked in B. Weave’s feeding group, Kara’s toddler group and this week I am working with Dr. Tullos’s toddler and special needs group. Each group has it’s own advantages and has been very exciting. During the first few days we all did diagnostics and determined who would be in which group. The first week I was a part of the feeding class. We used different things to stimulate the babies into eating better. We sang songs, did stretches on each of the babies and just loved on them. The second week I was part of Kara’s group, which is for the older toddlers. These children enjoy running around and making you chase them! We sang more songs, read to them, and still loved on them. This week I am working with the younger toddlers and a child with cerebral palsy, Rita. During the morning we work with Kara’s group in Haven 2 and then have the younger toddlers in Haven 1. Today all the children were cranky because they had a big change this weekend--Haven 2 needs an estimated $10,000 worth of maintanence done and they had to move the children out of the house. The boys went to Eric’s house and the girls moved into Haven 3. Our groups may have started a little late today but it was because we had to chase down the kids in the different houses! After lunch our group had special group one-on-one time. Charissa had Kritz, Ashley had Jonathan, and I had Rita. Dr. Tullos stated that the last couple of weeks they have been trying to elicit any verbalization from her but they have not had any luck. I brought three toys, four books, and the knowledge of some kids songs because I knew that I was going to be bombarding her with language. During one of the books that I read, she maintained focus on the book the entire time, which Dr. Tullos said that she had not been maintaining for long periods before. So at the end of the session I read this book again and she maintained focus on it for the entire book again! It was a pretty good day.
Tonight has been a very relaxed night for all of us. We did not leave to go to the soccer football field tonight, nor did we go to the neighbor who sews for all of us, Mrs. Moono. We all stayed in the girl’s house (the Mann house) and played games. It is the last night of just this group. Tomorrow new people come, including the guys that will be making a documentary and Dr. Weaver’s daughter, Reagan, an OT. We are excited to have new people but will miss the Pharmacy group when they leave on Wednesday. We also realize that our time is winding down and in less than three weeks we will be home.
Much love to everyone,
Naiveen

That is really sad about their building! How will thrifty the money to fix the buildings how d they come up with enough space to hold all of the children in the other places?? Btw, it's Great to here from you!
ReplyDeleteWhat was the book that you read to Rita? Maybe you can read others to her from the same series or author. Do they have the money for the renovations?....how long will their construction displace the children in other homes?
ReplyDeleteThat is so sad! Have they raised the money or how do they get it? Also... what documentary is taking place? I am so excited that Reagan will be there! Do you know what she is planning to do/ will you guys get to have a group to learn about OT in combination with ST? I think that would be fascinating! I'm trying to find out what the OTs at my placement do, and how I can help them in my therapy. It sounds like so much is changing! I am so proud of you and Rita! (by the way, I don't think I ever asked...are any of the children in a wheelchair?)
ReplyDeleteIt sounds like you guys are having so much fun! I really do love reading all of your blogs.
ReplyDeleteWhat all different progress has Charissa and Ashley's kids made?
That is so exciting your little girl was able to stay focused during the whole book.
I have a 20 month old in clinic who is completely non verbal and shows zero interest in anything. Today I read Brown Bear Brown Bear book and he sat there and listened to me the whole time.
Have fun!!
Hey mom. I'm glad to hear your having fun.. Last day of school was today.. I'm glad to hear that stuff about Rita.. It would be so cool if I could have seen that. About the maintenance thing.... Would me donating that $50 help a little bit?? I'm willing to help in any way I can.... The picture that Ashley posted was SO CUTE!! Can you send me a picture of Pamela?? I wanna see what she looks like. Well, we miss you and love you. Can't wait for you to get back home..
ReplyDeleteWow, that is such rewarding work, Naiveen! Does the child with cerebral palsy use crutches or any other device to walk?
ReplyDeleteI am absolutely loving reading everyone's blogs!!! I have a questions about Rita? Does she make a lot of nonverbal gestures?
ReplyDeleteHey Naiveen! It's good to hear from you!! I'm happy that you got to see so much progress with Rita. How severe is her cerebral palsy? There is no way my child with cerebral palsy could focus on an entire book :) Keep up the great work!
ReplyDeleteNaiveen!!! Are yall doing any stretches with the little girl with CP? If so, what?
ReplyDelete