One thing all mothers share, special needs or not…our constant companion waiting behind every decision big or small:
Today was a perfect example. I have not been feeling well all week, dealing with a virus that is giving me painful, swollen glands, sore throat, headaches, body aches and fatigue. By the time I left work this afternoon I wasn’t sure I could even stay awake another hour. So, I decided to take a nap. M was home from school due to a power outage, so I had her take a nap as well. A was supposed to take a nap, but I couldn’t drag her away from her baby dolls & didn’t have the energy to try too hard. But it was a difficult, emotionally painful decision. The house was a mess after a hectic Halloween, and I felt I should spend the time doing something special with the girls since M was home. On the other hand, I knew I would be very irritable & even more tired if I chose another option. And this is how a mother thinks and weighs every scenario in a day. It turned out fine, after nap we picked up K, ran to the grocery store which was *mostly* a nice experience together & cleaned the house while listening to Christmas music. (Shhh…don’t tell my husband. He has a “no Christmas before Thanksgiving” philosophy 😉 ) But I know I will still second and third guess myself next time I try to prioritize, especially if I put myself first.
I also know I am long overdue to update you all, so here goes:
A: nothing to report, as usual. She is very happy in preschool. She did have her 3 year well child, where she was a very big, brave girl and earned her chocolate milk and cheeze-its. She is in the 87% height & weight (thus why she & M almost share clothes) & the doctor was delighted with her language & cognitive abilities, stating she is right on track for a 4 year old, actually. (No surprise to me.)
K: The mono is still kicking her butt a little, but so far she has only missed half a day of school, though she has to take Ibuprofen throughout the day to dull her awful headaches. I am praying it is over soon, and that she doesn’t catch any other virus in the meantime. She is excelling in her gifted program at school, especially science, her passion. She has a FLL Robotics tournament next weekend, and she is taking the SAT next month to secure a spot in an even more advanced, rigorous program for next year.
M: She is still progressing on the meds. We did end up increasing her dosage a little to twice per day. She still struggles with changes in routine, some sensory issues and other areas, but overall what a huge improvement! Everyone who knows her on any level has commented on how different she is. She is HAPPY. She smiles and laughs. She has stopped hissing and growling at other children and plays more, with other children and with her toys. The biggest thing is, she is more verbal. Instead of an immediate meltdown she will tell me (in a loud tense voice) “I’m feeling anxious!” So we can remedy it before it escalates. She still stims, but not as often. She still has her obsessions, but they don’t over shadow everything. I can listen to something other than Taylor Swift on the radio!! 🙂 She still has not given me that hugging-me-and-telling-me-I-love-you-Mommy moment, but she has given me a couple of kisses & lets me hug her somewhat more often. Today there was unexpectedly no school, and I got that sick in the pit of my stomach feeling that comes when I know she is going to lose it. She was fine! Overall a bit more tense and anxious today, but not terribly. She was happy to get to wear whatever she wanted today (they have uniforms)! Her therapist even noted the enormous difference, and said she had never seen anything like it before. It proved that it was not lenient parenting (she had been pushing for me to be more strict) & she noted how remarkable that one thing in her brain was so far off that this medication could transform her so. The brain is such a mysterious thing! She even finally won her BeyBlade…a reward we put in place over 3 months ago for a week of good behavior!
We had a great Halloween trick or treating for the first time, with Kaity’s best friend. There was very little anxiety from M. She was amazing. So was A, for being only 3! They won’t eat much candy but it sure was a fun experience!