To say this family LOVES New York is an understatement. So you can imagine how lucky we feel to have found the most amazing doctor for Juliana (Dr. Djukic at the Montefiore Rett Clinic) right here in New York. We don't get to come too often, but when we do, we really try to enjoy our time there.
We were fortunate enough to find a room at the Hilton, right by Radio City Music Hall. Here we are the first day, walking around the town.
Here were my awesome camera skills. You can really see Juliana behind her computer screen, right?
The next day our driver Rick picked us up as usual, bright and early to get us to the Bronx on time. Unfortunately we did not take any pictures with her amazing doctors. We learned a ton in our time with Dr. Djukic. Have I mentioned how much we LOVE this lady. She is truly incredible. So, here are some of the highlights:
The Good News:
- She was so impressed with how well Juliana is communicating with her computer. While we were there Juliana let us know she had to use the restroom. I had just taken her and nothing. We get in the room and she starts with "Bathroom". I'm thinking, really!? We just went. So I asked her, "Are you sure, because we just went to the restroom?" She said - YES! So I excused ourselves and took and guess what, she really had to go. She also repeatedly thanked Dr. Djukic and said I love you. I think she started showing off when she saw how excited Dr. Djukic was.
- Her lower extremities are in great condition. She is doing very well with bearing weight and initiating steps. Really the only thing lacking is balance.
- Dr. Djukic is very happy about Juliana's school situation and that she is in a mainstreamed class room. She is even going to hold a conference call with all of Juliana's school team to give some advice and answer any questions they may have.
- We met with GI doctor because she has been throwing up again and it seems we have not increased the dose of her prevacid since she was two years old. We upped it a bit and it seems to be doing the trick!
- Her arms are very tight. She always has them bent into herself, it's kind of like her comfort position. This is very bad because it is very difficult for her to extend her arms now, especially the left arm. This will only get worse if we do nothing and eventually she will have little to no range in her arms. So the plan - Botox. Who knew. She will get Botox injections in her arms which apparently loosens the muscles that she is holding so tight. Then we will get arm braces that she will wear through out the day, off and on to maintain that range.
- We have been noticing Juliana kind of "checking out" for about a minute at time several times per week. We weren't sure if these were "Rett Episodes" or possibly seizures. We were hoping for "Rett Episodes" because they weren't anything like her other seizures. She isn't stiff or holding her breath, her eyes don't roll back like in other seizures. She just kind of stares off and is pretty much non-responsive for about a minute and then she's back. Fortunately she one of these episodes while we were with Dr. Djukic and she did feel like this was a seizure. So the plan - up her meds again. We are trying this for about two weeks, if we see improvement then great, if they keep happening we need to do a follow up EEG to (1) confirm that they are seizures and (2) discover what kind they are and if a different med might be more effective.
- And finally, the one that probably scared me the most is her back. We had x-rays done six months ago here in Dallas to confirm that she had a scoliosis. She did and it was measured at about a 25 degree curve. Now, just 6 months later, we had x-rays done and it has progressed now to a 30 degree curve. She has gone through a bit of a growth spurt which could have caused it to worsen at a much faster rate, but at any rate, it was highly recommended that we brace her back in an attempt to slow it down. I know many people in the Rett community are torn about this method and many have not seen too much of an improvement with bracing. But here's our thought - it's a brace. At the end of the day, if we see no improvement or it is so uncomfortable and she hates it, we can always take it off. The alternative to bracing is waiting until it gets so bad and we have to have surgery where they will fuse her spine together. So I think at this time we are opting for bracing in combination with some serious PT/weight bearing/stretching/exercises.
So we headed around town.
We ended up buying them some New York scarves because it was much colder than what we packed for. Here are our city chic girls!