Been busy couple of weeks. Back from Chicago. Hanging out in Boston or New Hampshire. Otherwise, going to work, keeping the kids safe and trying to make sure that we remember to do basic needs. :-)
But in the past 2 days, we've been quite busy. Jessica had her follow-up 6month review for Early Intervention. She still qualifies for EI, and here are her scores (she should be all at 25months-her current age): Self care 20months, gross motor 23months, fine motor 21months, social 27months, cognition 26months, receptive language (listening and using her hearing to do things): 23months, expressive language 12months. So basically Jessica is caught up in most all areas except now she's 12months behind her age in EXPRESSIVE LANGUAGE (that is talking). It isn't great news, but it "jives" with what we observe, which obviously means we agree. We will continue Early Intervention and hope that her increasing time in daycare will help her improve in this area.
Today, we had 2 sets of appointments for Alexis. First in Boston for 8am, then in Waltham for 10am. A bunch of silliness if you ask me. But at least we got to both appointments in time. The first appointment was to meet with the Neurology/Sleep Clinic doctors about Alexis' sleep apnea. The doctor was in a seminar until 9am, so that was a real trail on my patience. Otherwise, he wants us to follow-up with an EEG (to check abnormal spikes he sees in her brain activity), follow-up with CPAP usage/fittings, follow-up with Craniofacial doctors at Children's, and probably something else that for sure we can't remember and hope that his report will come out to us quickly so we can do all of the things right.
The second appointment was with Dr Terrell Clark, she is a psychologist that works with Hearing impaired kiddos. She helped to get Alexis in her right placement by describing the educational environment that would be ideal for Alexis. So, this was our return visit (9months later) to see how everything was going. She and Denise (SLP) are hoping that Alexis will develop some more pretend play and symbolics for more than just toys (like using pictures to choose foods, choose what she wants to do, etc). Yep, yep. And it was HOT today.
Alexis and I came home and literally rolled around on the floor after those appointments.
Now both girls are exhausted (already in bed for nearly 1 hour) and I'll be joining them very very soon.
Take good care,
Catherine, Alexis, Jessica & Matt (and the two hot furry cats that were sunbathing in the sun to get even hotter... silly cats)
Tuesday, August 18, 2009
Sunday, August 2, 2009
Where have we been?
Well, it seems that we are quite late in posting anything to the Blog!
We went to Chicago for Charge Conference. The Charge Conference was basically 700+ people that are either have CHARGE Syndrome, are the parents of someone with CHARGE syndrome, family of someone with CHARGE Syndrome or professionals (teachers, doctors, researchers) affiliated with CHARGE Syndrome.
It was an action packed weekend!
For the parents, action packed days of lectures / information sessions.
For the kids, action packed days of play group.
Meals were provided and a ton of entertainment! One night they had a social hour, another night CHARGE Idol, another night Carnival / Dance Party (and Rachel Coleman from Signing Times).
It was all-around-exhausting!
The kids sort of adjusted to the time zone but they were asleep about 2 seconds after they were put in their pack-n-plays each night. And Jessica HATES sleeping in a pack-n-play and there were no complaints from her. Exhausted!
Many people have asked why we went to this conference....
It a lot of ways it's probably confusing and in other ways, it makes perfect sense.
1. Most of you know already that Alexis is "undiagnosed," genetically speaking that is.
2. Alexis has a lot of similarities to the kids with CHARGE (deaf-blindness, limited mobility, food/eating problems/swallowing difficulties, g-tube feedings, kidney difficulties, etc)
3. Alexis' parents (us) have a lot of similiarities to the parents of CHARGE kiddos (dealing with educational issues, medical issues, teaching a toddler how to eat, teaching a toddler how to walk when they don't balance well, teaching a toddler how to talk even though they don't understand clearly).
4. Alexis' family is the whole world. Meaning, there is a popular saying, "It takes a village to raise a child." Well, for Alexis, "It takes the whole world to raise a CHARGE child".
So over the past 6-9 months I've been on the CHARGE email list. It truly has been a source of strength and family network beyond anything that I have ever found otherwise. Mostly made up of mothers, these mothers have been through EVERYTHING. Unfortunately, more trials and tribulations than normal people should go through. But fortunately, they are a wonderful group of ladies that want to make sure others can learn from their experiences. As well, there are many people with CHARGE on the email as well, which is a major source of inspiration. So, these folks are my WHOLE WORLD, helping me navigate the path for Alexis.
So, what did we get out of the conference? (I probably won't do this justice)
1. Face-to-face contact with my other CHARGE families. I have followed many of them on their family blogs, it was GREAT AWESOME SPECTACULAR to hug them and meet their beautiful children!
2. Adhoc interaction with leading medical researchers in CHARGE to help determine if Alexis has a genetic syndrome (there was one vote for 18q deletion and another vote for "not-CHARGE" based on looking at her hands, "she doesn't have CHARGE hands".)
3. Whether or not Alexis has a different genetic syndrome, we are STUCK with CHARGE. These people are our family, they get us, they understand our struggles, they cherish our children, they support our dreams, they believe in us and know how difficult each day is. So, we are happily STUCK with CHARGE, because the family reunions are awesome.
So, when is the next CHARGE Conference? 2 YEARS from now! In July, In Orlando Florida. It will be even more AWESOME than this year, because we will get Alexis ready for her live performance (I don't know what she'll do, she plays a mean piano and does a great boogie). Also, it'll be even more AWESOME than this year because every 2 years when they have the conference, it seems that it's grown by 20-25% each year. So, there will be even more families at the conference. And FRIENDS AND FAMILIES are welcome to attend.
So, I will get to bed now because I have to work tomorrow.
P.S. Alexis is out of school for the month of August -- so PARTY TIME for Alexis!!! She did get her Progress Report from Perkins, she hasn't been expelled yet (just kidding!!)
Love to you all,
Catherine
We went to Chicago for Charge Conference. The Charge Conference was basically 700+ people that are either have CHARGE Syndrome, are the parents of someone with CHARGE syndrome, family of someone with CHARGE Syndrome or professionals (teachers, doctors, researchers) affiliated with CHARGE Syndrome.
It was an action packed weekend!
For the parents, action packed days of lectures / information sessions.
For the kids, action packed days of play group.
Meals were provided and a ton of entertainment! One night they had a social hour, another night CHARGE Idol, another night Carnival / Dance Party (and Rachel Coleman from Signing Times).
It was all-around-exhausting!
The kids sort of adjusted to the time zone but they were asleep about 2 seconds after they were put in their pack-n-plays each night. And Jessica HATES sleeping in a pack-n-play and there were no complaints from her. Exhausted!
Many people have asked why we went to this conference....
It a lot of ways it's probably confusing and in other ways, it makes perfect sense.
1. Most of you know already that Alexis is "undiagnosed," genetically speaking that is.
2. Alexis has a lot of similarities to the kids with CHARGE (deaf-blindness, limited mobility, food/eating problems/swallowing difficulties, g-tube feedings, kidney difficulties, etc)
3. Alexis' parents (us) have a lot of similiarities to the parents of CHARGE kiddos (dealing with educational issues, medical issues, teaching a toddler how to eat, teaching a toddler how to walk when they don't balance well, teaching a toddler how to talk even though they don't understand clearly).
4. Alexis' family is the whole world. Meaning, there is a popular saying, "It takes a village to raise a child." Well, for Alexis, "It takes the whole world to raise a CHARGE child".
So over the past 6-9 months I've been on the CHARGE email list. It truly has been a source of strength and family network beyond anything that I have ever found otherwise. Mostly made up of mothers, these mothers have been through EVERYTHING. Unfortunately, more trials and tribulations than normal people should go through. But fortunately, they are a wonderful group of ladies that want to make sure others can learn from their experiences. As well, there are many people with CHARGE on the email as well, which is a major source of inspiration. So, these folks are my WHOLE WORLD, helping me navigate the path for Alexis.
So, what did we get out of the conference? (I probably won't do this justice)
1. Face-to-face contact with my other CHARGE families. I have followed many of them on their family blogs, it was GREAT AWESOME SPECTACULAR to hug them and meet their beautiful children!
2. Adhoc interaction with leading medical researchers in CHARGE to help determine if Alexis has a genetic syndrome (there was one vote for 18q deletion and another vote for "not-CHARGE" based on looking at her hands, "she doesn't have CHARGE hands".)
3. Whether or not Alexis has a different genetic syndrome, we are STUCK with CHARGE. These people are our family, they get us, they understand our struggles, they cherish our children, they support our dreams, they believe in us and know how difficult each day is. So, we are happily STUCK with CHARGE, because the family reunions are awesome.
So, when is the next CHARGE Conference? 2 YEARS from now! In July, In Orlando Florida. It will be even more AWESOME than this year, because we will get Alexis ready for her live performance (I don't know what she'll do, she plays a mean piano and does a great boogie). Also, it'll be even more AWESOME than this year because every 2 years when they have the conference, it seems that it's grown by 20-25% each year. So, there will be even more families at the conference. And FRIENDS AND FAMILIES are welcome to attend.
So, I will get to bed now because I have to work tomorrow.
P.S. Alexis is out of school for the month of August -- so PARTY TIME for Alexis!!! She did get her Progress Report from Perkins, she hasn't been expelled yet (just kidding!!)
Love to you all,
Catherine
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