Saturday, July 16, 2011
Summertime
I really do not enjoy Summer in Tucson. My poor children don't see much of the sunshine June-August, but every once and awhile.... :-)









Tuesday, July 5, 2011
Dear Everyone, Just Enough of Special. Sensory Integration/Processing Disorder
I am SO grateful that for the most part, when Tenley grows up (and even now), she will pretty much do everything that everyone else does. There is hardly anything in her every day behavior that would suggest to a passerby that she has "issues", in fact to most people it appears that she is a normal three year old that is just overwhelmed, most would just think she just needs a nap.
This is a blessing, but it is also a curse. I'll tell you why.
Recently I had a pretty invalidating experience where someone said "I'm sure the Dr's know what they are talking about, but Tenley seems fine sometimes..." and they went on to suggest that her problems stemmed from my lack of consistency.
It wasn't the first time I'd heard the "but she seems normal" or "I know so and so with an SPD or Autistic kid, she doesn't behave anything like that" verbage. I try not to take it personally. I know people have a picture in their heads of what a child with Sensory Integration Disorder or an Autism Spectrum Disorder behaves like. They picture kids rocking themselves, shouting, never ever making eye contact, and memorizing the TV guide.
They don't picture anyone like Tenley.
I try not to take it personally, but it gets to me after awhile. It makes me second guess myself constantly. I think to myself, "Am I trying to fill some desperate need for attention of my own that I am so willing to accept an erroneous label of Special Needs on my child?", or "Have I failed THAT horribly at establishing a routine that I caused these behaviors, these behaviors that are slow to change or unchangeable, in her?". I am, of course, faulted as a parent. I am aware that I am less than organized and have pretty inconsistent self motivation. But the answer to those questions I ask myself is, of course, no.
I then remember the things that brought us hear. I remember marveling at how many words this smart little less than two year old knew, only to see her in pieces not ten minutes later over something she couldn't tell me because she couldn't access the ability to communicate effectively. This didn't just happen on occasion, it happened all day long and seemingly with little to no provocation. I could see it in her eyes, she was fearful and frustrated. I remember the nights I laid awake thinking of new strategies, new ways to tweak her schedule, meal times, what is in her meals, order of activities such as bath and book and play, new ways to help her recognize bed time or other pieces of a good daily routine. I remember notebooks full of logs and lists and brainstorming sessions. I remember watching Happiest Baby on the Block, reading the No Cry Sleep Solution, logging countless hours in parenting forums, several trips to the pediatrician, and scouring Google on sleep training advice. I remember keeping sleep logs in my phone of when she slept and woke. I remember trying to enforce all of these methods and routines with surprising militancy considering my own tendency to check out when things get rough in my own life. I also remember throwing my hands in the air, giving up the militant diet and stopping all of the forcing her to into things she obviously was not going to do. At some point you just have to say, ok this isn't working. Clearly, we have a unique situation on our hands.
I know that I am less than go-getting, but let me assure you, if this were as simple as being home for a specific nap time and reading Goodnight Moon every night at 7pm sharp and keeping the house dark and quiet all night, I'd be all over that like white one rice. But it is not, it won't ever be.
So-
Well intentioned family, friends, and onlookers, while I appreciate you and your concern and support, I have this to say to you:
If you cannot refrain from the "Maybe if you (insert one of many tried and true obvious solutions found in nearly every parenting resource known to man here) it would help", then just please don't talk to me. It sounds harsh but I'm that serious. I am so TIRED of trying to validate our situation to you, I don't have the energy, and more importantly I don't have it in me emotionally. It takes a lot out of me. I hardly have any patience left and I don't need to be spending what is left of it doing THAT. I will probably just stop talking to you, and that's the gospel truth.
However if you are willing to follow our journey with an open mind and compassion, I invite you to, whole heartedly. There are a lot of families with children with mild forms of developmental disorders, and it's more of a tricky place to be than you would think. I would love to be one to help spread awareness so that the world may become more sensitive the varying degrees of these disorders and the attention and heart they require.
Let me just say Tenley is on 50mg of a medicine that her developmental pediatrician thought would knock her out completely back at 12.5mg and then be weaned from six months after beginning. The 50mg dose not only doesn't knock her out, the only purpose it serves is to keep her asleep through *most* of her night terrors, and keep her nightly sleep length somewhat consistent. It has been over a year.
Tenley goes to a special pre school program and her IEP showed that in the best areas she has only made a 20% move toward our goals for her in the best areas, and in some areas she has shown no progress at all. The goals aren't even aimed at what her peers are doing, they are Tenley specific small goals.
Anyhow, I could go on all day, as this has been something that has really been on my mind lately.
This is a great article called "Why Mild Matters", that illustrates what I am trying to say much better than I can.
http://www.sensory-processing-disorder.com/why-mild-matters.html
This is a blessing, but it is also a curse. I'll tell you why.
Recently I had a pretty invalidating experience where someone said "I'm sure the Dr's know what they are talking about, but Tenley seems fine sometimes..." and they went on to suggest that her problems stemmed from my lack of consistency.
It wasn't the first time I'd heard the "but she seems normal" or "I know so and so with an SPD or Autistic kid, she doesn't behave anything like that" verbage. I try not to take it personally. I know people have a picture in their heads of what a child with Sensory Integration Disorder or an Autism Spectrum Disorder behaves like. They picture kids rocking themselves, shouting, never ever making eye contact, and memorizing the TV guide.
They don't picture anyone like Tenley.
I try not to take it personally, but it gets to me after awhile. It makes me second guess myself constantly. I think to myself, "Am I trying to fill some desperate need for attention of my own that I am so willing to accept an erroneous label of Special Needs on my child?", or "Have I failed THAT horribly at establishing a routine that I caused these behaviors, these behaviors that are slow to change or unchangeable, in her?". I am, of course, faulted as a parent. I am aware that I am less than organized and have pretty inconsistent self motivation. But the answer to those questions I ask myself is, of course, no.
I then remember the things that brought us hear. I remember marveling at how many words this smart little less than two year old knew, only to see her in pieces not ten minutes later over something she couldn't tell me because she couldn't access the ability to communicate effectively. This didn't just happen on occasion, it happened all day long and seemingly with little to no provocation. I could see it in her eyes, she was fearful and frustrated. I remember the nights I laid awake thinking of new strategies, new ways to tweak her schedule, meal times, what is in her meals, order of activities such as bath and book and play, new ways to help her recognize bed time or other pieces of a good daily routine. I remember notebooks full of logs and lists and brainstorming sessions. I remember watching Happiest Baby on the Block, reading the No Cry Sleep Solution, logging countless hours in parenting forums, several trips to the pediatrician, and scouring Google on sleep training advice. I remember keeping sleep logs in my phone of when she slept and woke. I remember trying to enforce all of these methods and routines with surprising militancy considering my own tendency to check out when things get rough in my own life. I also remember throwing my hands in the air, giving up the militant diet and stopping all of the forcing her to into things she obviously was not going to do. At some point you just have to say, ok this isn't working. Clearly, we have a unique situation on our hands.
I know that I am less than go-getting, but let me assure you, if this were as simple as being home for a specific nap time and reading Goodnight Moon every night at 7pm sharp and keeping the house dark and quiet all night, I'd be all over that like white one rice. But it is not, it won't ever be.
So-
Well intentioned family, friends, and onlookers, while I appreciate you and your concern and support, I have this to say to you:
If you cannot refrain from the "Maybe if you (insert one of many tried and true obvious solutions found in nearly every parenting resource known to man here) it would help", then just please don't talk to me. It sounds harsh but I'm that serious. I am so TIRED of trying to validate our situation to you, I don't have the energy, and more importantly I don't have it in me emotionally. It takes a lot out of me. I hardly have any patience left and I don't need to be spending what is left of it doing THAT. I will probably just stop talking to you, and that's the gospel truth.
However if you are willing to follow our journey with an open mind and compassion, I invite you to, whole heartedly. There are a lot of families with children with mild forms of developmental disorders, and it's more of a tricky place to be than you would think. I would love to be one to help spread awareness so that the world may become more sensitive the varying degrees of these disorders and the attention and heart they require.
Let me just say Tenley is on 50mg of a medicine that her developmental pediatrician thought would knock her out completely back at 12.5mg and then be weaned from six months after beginning. The 50mg dose not only doesn't knock her out, the only purpose it serves is to keep her asleep through *most* of her night terrors, and keep her nightly sleep length somewhat consistent. It has been over a year.
Tenley goes to a special pre school program and her IEP showed that in the best areas she has only made a 20% move toward our goals for her in the best areas, and in some areas she has shown no progress at all. The goals aren't even aimed at what her peers are doing, they are Tenley specific small goals.
Anyhow, I could go on all day, as this has been something that has really been on my mind lately.
This is a great article called "Why Mild Matters", that illustrates what I am trying to say much better than I can.
http://www.sensory-processing-disorder.com/why-mild-matters.html
Sunday, June 26, 2011
Baby Brudda
Congratulations!
Tonight the Turners welcomed a beautiful baby boy into their lives.
Welcome to the world little man,
we are going to spoil the crap out of you!
Saturday, June 25, 2011
Inspiration
As I said earlier this week I am focusing on foreground framing,
and I've been perusing the internet and using Pinterest to round up some inspiration.
I pinned this yesterday at Heather San Photography and had to share.
I pinned this yesterday at Heather San Photography and had to share.
Such a gorgeous photograph and a rich use of foreground framing.
Credit to Heather San Photography, Utah.
Labels:
composition,
foreground framing,
inspiration,
photography
Friday, June 24, 2011
Photo Challenge to Myself: Foreground Framing
I'm going to try to give myself some kind of photo skill or technique or neat little thing to focus on each week.
This week I'm going to try foreground framing.
Foreground framing is a compositional technique in which you use something in the foreground between you and your intended subject to frame the subject,
adding depth, complexity, and/or whimsy and leading the viewers eye to your subject in an interesting way.
Next Friday I will post my practice shots.
Wednesday, June 22, 2011
remembering
This morning I'd been reminiscing about Tenley and thinking how adorable it is when little children misunderstand, mis hear, and mispronounce everything, and how bittersweet it is when they finally get it right.
Today she was walking on the sidewalk, wheeling her fuschia/multi-colored, tot sized, Dora the Explore suitcase behind her saying, "See? I got my soup-case! I got my soup-case Mommy!"
I melted.
And not just because it was 110 outside.
Today she asked me to draw her smiley faces, and I couldn't remember when she stopped calling them "happy bubbles".
Raising growing babes is so bittersweet.
And exhausting.
And wonderful.
And at times when people don't understand what you are up against,
extremely invalidating.
But I love it all the same,
I love being a Mom and I love my girls.
Today she was walking on the sidewalk, wheeling her fuschia/multi-colored, tot sized, Dora the Explore suitcase behind her saying, "See? I got my soup-case! I got my soup-case Mommy!"
I melted.
And not just because it was 110 outside.
Today she asked me to draw her smiley faces, and I couldn't remember when she stopped calling them "happy bubbles".
Raising growing babes is so bittersweet.
And exhausting.
And wonderful.
And at times when people don't understand what you are up against,
extremely invalidating.
But I love it all the same,
I love being a Mom and I love my girls.
Friday, May 27, 2011
Karen's Birthday Character Breakfast
A Character Dining experience at Disneyland is something I always wanted to do as a kid.
So in honor of her graduation and birthday,
Karen and I did the Minnie and Friends Character breakfast.
If you're going to do Character dining (unless you have little ones DEAD SET on having the princesses there) this is the most bang for your buck as far as both food goes and the character to diner ratio.
There was so much to choose from as far as the breakfast feast and it was all buffet style so you definitely get your $$ worth.
They had bacon, ham, sausage, hash browns, biscuits and gravy, mickey waffles, pancakes, french toast, assorted muffins, fresh fruit, breakfast cereals, oatmeal, even a made to order omelet station.
Plus about every non alcoholic beverage you could think of.
Karen even got a cute kiddie princess birthday chest. :-)
I have so much Disneyland Vacation wisdom that I would love to share with y'all.
Seriously, if you want to do Disney on a budget, tips on how to stay on that budget, and how to squeeze the most out of your Disney experience- Let me know!
Refer me some followers so I don't feel like I'm wastin' time!
I'll deliver, I promise!
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