"The real problem of blindness is not the loss of eyesight; it is the misunderstanding and lack of information that exist." NFB Welcome to our exciting journey with Ellie Grace. Ellie was diagnosed with Septo Optic Dysplasia (SOD) and Optic Nerve Hypoplasia (ONH). These diagnoses mean her optic nerves/discs are under developed causing significant vision impairment (what degree is not known yet). Her pituitary gland is under developed too which creates hormone inbalances.
Saturday, January 7, 2012
Wednesday, January 4, 2012
Starting the year off right!
Over the holidays we got to spend extra time with the lil
miss which was absolutely GREAT! She liked it too because when I did have to
take her back to daycare she cried when I gave her to the provider. (Hurts my
heart but it’s good to know she’s going to miss us too.) Anyway, extra time
with her meant extra activities and in-home therapy sessions with mommy and
daddy. She got to relax and lounge with us and then we played (therapy
activities) too. Man, what a great time!... Anyway...
She’s starting to get bursts of energy, I can imagine
that these little spazes (that’s what I like to call them) would normally
result in a toddler running around or being rambunctious, but she has mobility
limitations so she just tenses up and screams with excitement.* We’re engaging
her more at home so I can really tell a difference in how she’s acting and
exploring more and doing more things and so last night this little girl pushed
up on her legs supporting all of her weight by herself! Super proud but thought
it was one of those things like the first time she rolled over... she rolled
but didn’t know what she did; it took her another 3-4 or months to do it again.
Well tonight when Dusty was working with her not only did she stand ALL BY
HERSELF! (with daddy behind her) she did it multiple times and at one point it
lasted about 10 seconds.
There’s woman “the mom” from Uncommon Sense Blog who
basically explained this time is when hope moves to reality. That we are moving
from hoping that she’ll stand to knowing that she will one day and it’s not too
far off. We hoped that she would stand and walk but quite frankly, I was
preparing myself for wheel chairs.
Then, just when I thought I just witnessed the best thing
of my day, week, and possibly month Dusty came up with an idea to try whip
cream when feeding her.** So, he tried the whip cream and what an excellent
idea! It has texture, solid without being too thick to make her sick, and she
should gag that bad because it will water down quickly. She did GREAT! It was
awesome and amazing and was eating it up! She didn’t gag or fuss! She ate a lot
and did great.
Proud doesn’t even cover tonight!
-------------------------------------------------------------
As for daycare and therapy... well I sent the therapists and email with alternate therapy methods and told them hand-over-hand isn't effective and it's time to try something else.... and daycare, well it's time for me to get out of the military. We talked and made a list and decided it's time for Ellie. It's scary to 1/2 our income but it's Ellie, she's need people who know her needs. Now it's just a matter of finding a reserve position open for me (I don't want to completely throw away 10 years in the military).
*Yes it’s really excitement; she’s not over stimulated or
any of that stuff.
** Yeah, I know what you’re thinking, “But you’ve got to
be worried about her teeth and you’re giving her sugar?” The answer is yes and
we will continue because if we don’t move past the feeding issue then she’ll
have teeth for no reason that will rot out anyway.
Thursday, December 29, 2011
New Year Resolutions
This is Ellie's blog, but she's not old enough to type or write, or even talk yet so I'll tell you my new year resolutions.
1) Not to accept anything less then the best. This goes for Ellie's medical care, her daycare, her therapists, her clothes and toys. This is the least I can do for her. She has been through more in her life then she deserves, as have most special needs kids, so that is what I can do for her.
2) To do the best I can. I work full time and take a full load of classes and take care of the house (ok so that's mutual between me and the husband but still). Dusty and I have a lot going on in our lives, we have our own wants and desires and we have ones that we want and desire for Ellie. She take precedence but that doesn't mean that we won't take time for ourselves. We will do the best that we can for her and ourselves. (Luckily I have a husband who makes me take time for myself! We're good for each other like that.)
3) To make progress. Heck yes I want her to eat, even baby food. I want her to stand and talk and walk and twist and turn like she's supposed to. BUT that may or may not happen in the next year, who knows! What I do know is that she will make progress, little by little she will do something better today then she did yesterday and that's all we can expect and ask for.
4) To learn! We will go to the The MAGIC Foundation's Convention in July again. It's great to be around people who understand or know about your daily struggles as a parent of a child like Ellie. It's also educational, even if we learn just one thing new, it's completely worth it! And just like not settling for anything less then the best we will be on par with the doc's and their terminology. In order to get the best care it's nice to have two people speaking the same language.
5) VIDEO'S! I bought a small and easy video camera last year for the convention and thought, sure I'll use it again... well I just got it out of storage. I also bought a small (and portable) tripod to get better videos.
Here are some new and old videos from the video camera for you to enjoy.
1) Not to accept anything less then the best. This goes for Ellie's medical care, her daycare, her therapists, her clothes and toys. This is the least I can do for her. She has been through more in her life then she deserves, as have most special needs kids, so that is what I can do for her.
2) To do the best I can. I work full time and take a full load of classes and take care of the house (ok so that's mutual between me and the husband but still). Dusty and I have a lot going on in our lives, we have our own wants and desires and we have ones that we want and desire for Ellie. She take precedence but that doesn't mean that we won't take time for ourselves. We will do the best that we can for her and ourselves. (Luckily I have a husband who makes me take time for myself! We're good for each other like that.)
3) To make progress. Heck yes I want her to eat, even baby food. I want her to stand and talk and walk and twist and turn like she's supposed to. BUT that may or may not happen in the next year, who knows! What I do know is that she will make progress, little by little she will do something better today then she did yesterday and that's all we can expect and ask for.
4) To learn! We will go to the The MAGIC Foundation's Convention in July again. It's great to be around people who understand or know about your daily struggles as a parent of a child like Ellie. It's also educational, even if we learn just one thing new, it's completely worth it! And just like not settling for anything less then the best we will be on par with the doc's and their terminology. In order to get the best care it's nice to have two people speaking the same language.
5) VIDEO'S! I bought a small and easy video camera last year for the convention and thought, sure I'll use it again... well I just got it out of storage. I also bought a small (and portable) tripod to get better videos.
Here are some new and old videos from the video camera for you to enjoy.
Sunday, December 18, 2011
Lazy Dayz
This is our second lazy weekend. Lazy in our world means no therapy. I hate the guilt that I feel for not doing tummy time or feeding time. It should be easy to just feed a child or put them on their stomach to play or push up, especially at 15 months but it's not. It takes work and persistance and some tears and time. In order to do it we have to plan feeding just right. She can't have just ate, she can't be thirsty, it has to be just right. Tummy time, well we should just do that anyway but I feel like she gets beat up enough during her one 30 minutes OT session and 45 minutes PT session once a week that I don't want to put her through it at home when we can just have an enjoyable time together.
I know we need to do these things to help her not be so difficult during therapy. I swear though, I just want to hold down her therapists, blind fold them, and shove their hands out into the unknown and touch things they don't know. She cries from discomfort and frustration just about the whole time and it's starting to wear on this mommy. I just keep quite until her cries go from discomfort to meltdown and then I intervene. My other job there is to cheer her on when she does things that she doesn't normally do or like. Luckily feeding therapy is less tramatic, we try to prevent the crying there. And her sensory issues with things touching her mouth and going inside are doing much better! She'll let me get a spoon in there now but she doesn't exactly swallow. She'll just leave it in her mouth until she can't anymore and then either swallow or spit it out. But she doesn't throw a fit when her lips are touched with a spoon so that's progress.
For the mommies out there with kids with no issues. Be thankful when they roll over... it took a lot of work and 9 months before she did it for the first time. For the mommies out there with kids who lock their legs and try to stand at 5 months be thankful, Ellie still doesn't. I'm not bitter, or down, I'm thankful for every moment, for her licking her lips for the first time a month ago, for the first roll, and for the first twist to pick up a toy.
Tomorrow and the next day and every following day we'll do better... we have to. We want her to progress and that's going to take work.
I know we need to do these things to help her not be so difficult during therapy. I swear though, I just want to hold down her therapists, blind fold them, and shove their hands out into the unknown and touch things they don't know. She cries from discomfort and frustration just about the whole time and it's starting to wear on this mommy. I just keep quite until her cries go from discomfort to meltdown and then I intervene. My other job there is to cheer her on when she does things that she doesn't normally do or like. Luckily feeding therapy is less tramatic, we try to prevent the crying there. And her sensory issues with things touching her mouth and going inside are doing much better! She'll let me get a spoon in there now but she doesn't exactly swallow. She'll just leave it in her mouth until she can't anymore and then either swallow or spit it out. But she doesn't throw a fit when her lips are touched with a spoon so that's progress.
For the mommies out there with kids with no issues. Be thankful when they roll over... it took a lot of work and 9 months before she did it for the first time. For the mommies out there with kids who lock their legs and try to stand at 5 months be thankful, Ellie still doesn't. I'm not bitter, or down, I'm thankful for every moment, for her licking her lips for the first time a month ago, for the first roll, and for the first twist to pick up a toy.
Tomorrow and the next day and every following day we'll do better... we have to. We want her to progress and that's going to take work.
Saturday, December 17, 2011
Resolution?
Well I talked to daycare and I felt like I got brushed off by the program director. BUT something has changed or clicked. She's been changed at daycare two days in a row and they are writing down her daily activites now. She was changed because she has a faucet of drool coming out of her mouth and it's soaking her shirt... to save on clothes we're going to have to get some bibs! I also randomly went into daycare this week. I told them I was going to do it but didnt' exactly tell them when. As for the daytime provider... I think we're on the same page and we understand eachother a little better. She doesn't have kids of her own which makes me nervous but my cousin and friends have worked at a daycare and they don't have kids of their own and they love the babies, so maybe that is a feeling that isn't valid and I just need to get over.
Ellie has a cough that has been going on for a few weeks now. Partly because of a runny nose, partly because she was sick a couple of weeks ago. Either way, I hope it goes away soon. Each cough is like a dagger in my heart. She was getting melatonin to help her sleep through the night but she'd still wake up at 2 or 3, so one night she didn't get it and slept through the night, she hasn't gotten it for a week and has been doing better at sleeping through the night. (Yes, melatonin is not exactly normal for children to get to help them sleep but when you can't see day or night you can get a little mixed up on sleeping times.) I think melatonin has jump-started her normal sleeping pattern, I just hope it continues.
She's still not eating food, but since she started feeding therapy her mouth is a little less sensative... baby steps right? And she has teeth! 4 on top, 4 on bottom and 2 coming in on the sides (random premolars). Anyway, it's time to hit the books before my deadline comes and goes. Have a great weekend!
Ellie has a cough that has been going on for a few weeks now. Partly because of a runny nose, partly because she was sick a couple of weeks ago. Either way, I hope it goes away soon. Each cough is like a dagger in my heart. She was getting melatonin to help her sleep through the night but she'd still wake up at 2 or 3, so one night she didn't get it and slept through the night, she hasn't gotten it for a week and has been doing better at sleeping through the night. (Yes, melatonin is not exactly normal for children to get to help them sleep but when you can't see day or night you can get a little mixed up on sleeping times.) I think melatonin has jump-started her normal sleeping pattern, I just hope it continues.
She's still not eating food, but since she started feeding therapy her mouth is a little less sensative... baby steps right? And she has teeth! 4 on top, 4 on bottom and 2 coming in on the sides (random premolars). Anyway, it's time to hit the books before my deadline comes and goes. Have a great weekend!
Sunday, December 11, 2011
Dear God, I'm at work but I need you at daycare please
Let me start by saying, we are very
thankful for the healthcare that we have gotten since moving here to Ohio. Work
is a struggle for Dusty and I; he's learning a new portion of his job, and I'm
getting back into the heart of mine for the first time in years.
Anyway, Ellie's daycare has her PT,
OT, and feeding therapy. (That's right, she's getting feeding therapy! Onto
that later...) Dropping her off the first day was incredibly scary, as with any
child. She's still in the infant room since it's safer then the toddler room
where kids are running around not paying attention. She had her adjustment
drinking so she was getting DDAVP more than normal which interfered with her
drinking and it was a vicious circle. After about a month and a half she got on
a routine, and I grew to really appreciate the daytime care provider. I had my
worries about the afternoon care provider.
With all of that said since her
daytime care provider quit less than two weeks ago Ellie has come home with a
wet shirt on two occasions, and Friday... well that’s why I’m praying. I’m
praying for patience and understanding because I want to know WHY Ellie came
home with her shirt smelling like puke, front AND back. I don’t have the
patience not to go in there fuming. I forgot about it yesterday and honestly
that’s best because my blood boils too hot when I think about it, and tonight
before I started typing I had to have two glasses of wine (all I needed was an
excuse).I’ll do my best to update quicker but until then I’ve got to sign
off...
Please look below and see the link
to our family photos. Yes, we’re cute/awesome/loving and any other adjective
you can think of ;) And I know, they both look exactly like Dusty... damn those
genes are strong, let’s hope my nose gene is stronger ;) just kidding, I don’t
notice those things. (haha, although weight I do...)
Anyway, more to come later...
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