Reagan had her 4 month follow up with Dr Love last Wednesday.
She is now 11lbs 10oz and 23 inches long. Dr Love was very happy with her
weight and we are switching her to “regular” formula (20 calorie) from Neosure,
which is 22 calorie. She no longer has a blocked tear duct and her umbilical
hernia is looking much better. During the appointment, we received a call from
Dr Jeff regarding Reagan’s apnea monitor download results. We put him on
speaker phone so Dr Love could hear everything he had to say. He said there
were no events with the last download and he is comfortable with Reagan not
wearing the monitor anymore. He did say that by her wearing the monitor is what
alerted us to her having rsv which is true. The alarm was going off multiple
times every hour. We agreed that we would feel comfortable if Reagan wears the
monitor only at night for one more month. That should get us through most of
the cold/flu season and she can still go to daycare because she won’t be
wearing it during that day. We were so happy that she doesn’t have to wear it.
Now she can wear cute outfits instead of a sleeper with snaps all of the time.
We had Avery’s parent teacher conferences last Thursday. I am
not going to lie. We were dreading going there because we thought for sure they
were going to ask why Avery isn’t wearing her hearing aids at home, etc. When
we walked in, her teacher told us she was so excited to see us because she had
good news. She said she really sees improvement in Avery. She has been
saying/trying to say more words, asking for help when she needs it and playing
with(instead of alongside) her peers. She did agree that Avery has plateaued
when it comes to potty training. She used to not want to sit on the potty. Now
she sits but nothing comes out. I told her we have had Avery sit on the potty
at home for 45 minutes at a time and still nothing. Even after bribing her with
fruit by the foot, icecream, Chuck E Cheese…still nothing. We need to take one
weekend and really work with her on it.
The teacher then said that on days Avery doesn’t wear her
hearing aids (whether we forgot to pack them, dead battery, etc) that she
doesn’t notice a difference in Avery’s response to sound. Thank you Jesus,
someone else who sees Avery almost every day and doesn’t believe she has
trouble hearing. I will be mentioning this to her pediatrician, ENT and
audiologist. (We go to see the Cleft palate clinic in June so we will discuss
it then)
Me and my bestie Aria
Happy baby
Special Valentines I made with my handprint for special people
Look at all of my Valentine's Day candy!!!
Reading to my sister
My sister is a chunker
Two of my faves
More smiles
Momma and Reagan