I've been thinking all day about how I have not been writing in this blog much and sharing Reagan's story as I have in the past. It is not because I don't want to share and really didn't realize until today how infrequent I was posting or reading Rett related stuff. I think my subconscious forced me to take a break from all things Rett Syndrome. Obviously that excludes taking care of my sweet daughter that has Rett.
I not only stopped blogging over the past several months, but I also stopped reading the blogs. I feel like maybe I had an emotional shut down in regard to Rett and had to take a step away from all of it to get a clear head again. There is no doubt about it that having a child with Rett Syndrome can be (and usually is) overwhelming most of the time. There are the medical issues and concerns due to the multiple disabilities, there is ensuring that she is getting a fair and proper education, there is tending to her basic needs which are extensive since she is fully dependent on an adult for all of her needs. I didn't want to write about all the struggles we are facing and how overwhelmed I feel. I didn't want to read a close friend's blog and hear of the struggles that they are facing and feel so helpless that my Rett family is hurting. I shut it all out and stayed in a bubble.
But, now I am missing expressing myself, posting update and not knowing all that my Rett family is facing, the good and the bad.
Quick update - Reagan has started the night screaming spells again last month. They usually start around 2am and she can not go back to sleep afterwards. We are running a couple of gastrointestinal tests on Friday to start the process of elimination because the previous explanation/reason is no longer applying and it makes me so sad to see her in pain every night. Second, Reagan continues to love going to school and her therapists are working with her diligently on using eye gaze and switches. I am so thankful for the people that believe in her and continue to encourage her to do her best. Lastly, she also continues to get upset when we go out in public. I have concluded that she feels insecure in her wheelchair so we have ordered her a different type of wheelchair that is more similar to the past stroller that she used before the screaming fits in public started. Please keep your fingers crossed because we really miss going out as a family.
Abby's first visit to Boston for the IGF-1 Trial
3 years ago