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Saturday, June 9, 2012

The Free tutoring offer

Some history:  At the beginning of January 2012 we got the diagnosis of dyslexia for our daugther.  I immediately began searching for a tutor (thinking that we were going to stay in the small Catholic school we attended at the time).

She could barely read. She was getting one hour of tutoring from a supposedly Orton Gillingham trained tutor (who was really doing reading recovery which doesnt work for dyslexic kids).  It was not  helping.  I read with her every single night so I would have known.

It was first grade but in her classroom of 25 kids there was a sink or swim attitude from her teacher who had, in our first conference of the year called her inattentive, unable to complete her work etc etc (all very personally critical of our daugther).

This prompted the testing since of course I didnt believe this teacher who I really saw as trying place as much blame as possible on my daughter with no regard to teaching methodology. (Plus remember my family had been through this when I was growing up with my brother- lots of staying in at recess and punishments).

I worked for the whole month of February as hard as possible trying to find a tutor once I knew it was dyslexia.  

One of the places which is free is run by the Masonic Temple and in my town is called the Children's Dyslexia Center.  I submitted all the necessary paperwork as quickly as possible. 

It's June.  They now have a free tutor for my daughter starting this fall.

This is good of course but my point here is that none of this is fast enough. 

An ENTIRE YEAR would have passed had I been in the position to have to wait for this assistance for my child. 

That is an ENTIRE YEAR of:

being berated by her teacher,

not being able to keep up with her lessons,

working 4 times harder in class than a non-dyslexic student,

being called ____ (you name it) by peers who would have no inkling about learning differences,

having her self esteem challenged by a read-as-fast-as-you-can overly competitive society.

None of this is okay.

Will we take the free tutoring?  I dont know. 

So far I have paid for many other options and my child is reading (thanks to the Orton Gillingham based instruction at her private school) at a grade appropriate level now.  Still, none of this should be about how much our family can pay!  

I say my prayers every single day that God bless those children who I know are blaming themselves for their learning difference.  Most of them dont even know they have a learning difference. 

I can get really worked up about this very quickly.

On the good side for me I just had our daugther privately assessed again by a private tutor who didnt even think her dysgraphia was too bad (and this tutor has seen a lot over the years).

So I'm feeling pretty good about our current situation although I am pressing hard for another year at the overly expensive private school.  Saying my prayers she can be there another year.  We shall see.

 

Dyslexie font notes

Here are a few of the things that the new dyslexie font does to help dyslexic people read easier.

1. Increase openings of the letters
2. Make the start and finish of a word bold
3. Use larger punctuation
4. Slant some of the letters (tipping)
5. let gravity emphasize the difference
6. lenghten or descend letters

since so many letters look similiar any way of making them different is helpful to a person with dyslexia.

The problem is that, well,  you of course have to pay for this.  It's not like it's a font that has been freely given to the public for the use of people with dyslexia. 

It's sort of like charging a toll for the wheelchair ramp.

That is the sort of thing that disgusts me about our society.  People see a need and their minds go to"cha ching".  Is'nt there any such thing as altrusism anymore?  Good grief.

Friday, June 8, 2012

Reading/Art

Summer has begun and, well, there is a lot of homework.  Math (which is my daughter's strong area), reading (lots) and in the mix things like telling time etc. 

They say the kids "lose" a lot of what they learned during the year over the summer if they don't practice.  It seems to me like an awful lot falls onto the parents and students in this line of thinking and I don't quite trust it.

Not to be too critical but it seems to me like kids need this break in the summer.  Certainly we will read but I plan to (secretly) not be too hard on her.  Summer is time to breathe.  We all need that and it seems like these days kids need it more than ever. 

This morning when I woke up the thought that I need to go and get a bunch of washable markers and some drawing paper entered my head.  We don't have enough art supplies around here.  We have crayons and coloring books but I think they need some color saturation (that markers are best at) and some paper (to make their own pictures- not something an artist has already drawn for them). 

I read the book Drawing On The Right Side of The Brain (revised version) a couple of years ago and the author pointed out that she believed early reading got in the way of art.  Language became how things were described rather than an illustration of them. 

Also I read Daniel Pink's book (cant remember the name right now) where he pointed out that he believed artistic ability will become more sought after in the future - many can write, not many can make art type of thinking.

So here I am, on the one hand being given a lot of busy work for my daughter to do over the summer but on the other hand thinking we need a light touch here. 

Sunday, May 20, 2012

Labels

There is a lot of resistance to labels (aka diagnosis) dislike of labels is often claimed as an excuse to not take action.

Teachers warn against labels if it suits their agenda to.  Parents claim to not like labels in an effort to cover up their denial that there is a learning difference.

I do understand this thinking.  But the slight weight a label carries is not heavier than the weight of not dealing with a potential diagnosis. 

A wise parent will want to know and understand as much about the way their child's brain works as possible.

I remember in the 1970's the classes in elementary school labeled classes L. D. (for learning disabled).  As with many things about education at that time it was ridiculous in retrospect to single out children, putting them in a separate room with all different behavioral issues and a teacher who may or may not have been qualified to work with them (I'm not talking about official credentials, I'm talking about personality traits that make one able to succeed at working with learning differences).  A lot has changed (thankfully). 

Mainstreaming,  putting children with learning differences in a regular classroom for the most part, is not always in everyone's best interest but I do agree that children need to be exposed to all different types of people, this is part of the goal of education.

Still, I see the way my daughter is being taught and I know that 1 hour a day of the Orton Gillingham method with a tutor who may or may not even be using a proven method would not have ever really been enough.  he would not have been reading at grade level by the end of the year with only that to help her.

One of the statisics I have heard about dyslexia is that the dyslexic child is working 4 times harder in the regular classroom than everyone else.  So if you are taking them through this, getting the 1 hour or so a day and then putting tutoring on top of that, by the fifth grade they are burnt out.

I believe this.

Dont be afraid of the diagnosis.  It is more than a street sign, it is a map to take your child to a place where they can succeed.



Thursday, May 3, 2012

Cost Section

Although I have sometimes alluded to it I have never set down and written out what all of this costs. 

Again, with the hope of being helpful to someone somewhere I would like to share the costs of what we have done since discovering our child was struggling in school last fall (the beginning of first grade).

Private tutor evaluation                                                                                                              $60.00

Private evaluation with pediatric neuro-psychologist                                                            $1,500.00

Lexia Learning computer program                                                                             (roughly) $200.00

Official Annual cost of dyslexia school (they have income-based discounts though)               $20,000

School testing fee                                                                                                                         $250.00

Child Advocate                                                                                   $400 retainer and $80.00 per hour

Summer camp for language run by our school which she will attend                                      $1,800.00

Tutor we hired who specializes in dysgraphia                                                                $75.00 per hour


The school provided all new school supplies so we didn't have to run out and buy those again. 

Also they gave me free uniforms so we didn't have to pay for those.

I'm not including the gasoline price we now have to pay to drive 20 extra miles per day (when we were walking to school before) but I guess that comes with the territory.

This is not a complaint, simply a list of how our family has chosen to use our resources in order to help our child with her dyslexia in a world that seems to lack understanding of how to teach a dyslexic child.





Wednesday, May 2, 2012

A Climate of Distrust

I did not personally create the climate of distrust with our current school and the public school professionals. 

I do, however, respond to what has happened thus far and I'm not certain how to move past any of this or if I even should. 

Some background: 

Knowing what we all know about the Catholic Priest Child Molestation Scandal (I'm calling it that I don't know any other way to put it).  The Catholic Church and School Systems have gone above and beyond being proactive in terms of protecting the children of the present and future. 

My husband and I went through a class when our daughter first became a part of the Catholic School that was called "Protecting God's Children".  It was highly informative and I was glad to be educated this way.  We were also fingerprinted and I will say too that we were closely watched until people got to know us.  This was all fine by me.

So when we left the Catholic School System in order to go to the "best school in our area for dyslexia" we left the safety measures that have been instituted by the Catholic Church.

At our first parent/teacher conference at our new school I was already actively pursuing the IEP for our daughter to qualify for the scholarship that was attached to it.  I had already had an initial meeting which I had thought went okay. During that conference I asked about the IEP process (how little I knew). 

At that point no one from the office had called me back so I was hoping to talk to someone face to face. The teachers directed me to the School Psychologist.

My husband and I walked over, introduced ourselves and I asked my questions. 

As soon as he heard them he rudely wouldn't let me talk and proceeded to put it bluntly, verbally rip me up one side and down the other about how busy they all were. 

He went on about how (since we were new)  we were last on the long list and so on. 

I was astonished that someone could be so mean the first time they met a us.  It was all very unpleasant.
Later, I mentioned this incident to the school counciler who was also supposed to be working on helping us get our IEP.  She was unhelpful to me.  But at least she wasn't mean and nasty like Mr. School Psychologist.

When I heard three more times from three other school professionals that my daughter did not qualify for an IEP (yes, even after a pediatric neuro-psychologist had clearly defined her with dyslexia).  Our family had to hire a Child Advocate (PTL: I have resources).

 Hence, a climate of distrust.

Because of all that had transpired at that point I did not want my daughter in the same room alone with the Mr. School Psychologist so at our (second) initial IEP meeting we discussed that the school would call our family if there was any reason for our young daughter to be alone in a room with any male professional. 

Everyone was understanding and the female speech teacher even volunteered to be present with my daughter if there was ever such a need.  Also, I offered to come to the school and be present or sit outside the door if there was a need for a male professional to be alone in a room with my daughter.


Since I see the potential for a witch hunt type situation here (and I am not an unfair person) I will say that Mr. School Psychologist was not in that (second) initial IEP meeting.  So potentially he did not know about this agreement. 

Our request for a chaparone It was also never put into an email format by myself.

(Side note: I didn't have a working email address for Mr. School Psychologist until I had to ask for one specifically and was given what seemed to be a private email address.  Also, let me remind the reader that he works a dual position for both the Public School System and our Private School, which seems unclear to me).

The other day a parent friend told me a story that happened at a meeting where Mr. School Psychologist was overtly rude to a wonderful teacher that we all know well.  I had not even mentioned him or my incident to her.  My friend brought it up but I knew immediately exactly what she was talking about based on my own experience with him.

As we walked in to our combined ETR/IEP meeting the other day he greeted us.  I quickly pulled the Child Advocate to the side and told her to expect Mr School Psychologist to try to take a bite out of one of us during the meeting.

He was all sweetness and niceness during the ETR meeting where he blabbered on with some unhelpful charts attempting to show where our daughter stood in terms of her learning difference and norms.  Personally, I thought he was wasting our time and kept waiting for him to take his bite.

At the very end he wanted us to sign off on something that our Child Advocate pointed out was not correct.  I said I would not sign it.   He did go above and beyond (she said later) when he reprinted that page for us to sign.

Thankfully, he did not need to be part of the IEP meeting portion so we went on. 

Incidentally, the IEP still need to be corrected so it isn't signed as of now but I think it's okay enough.  Our advocate (who sees IEPs all the time in school districts all over our state) wasn't especially impressed but for our present purposes it was good enough with a few changes.  More about this later.

I stayed at the school to pick up my daughter who told me as soon as she had gotten into the car that Mr. School Psychologist had pulled her out of her Math class to talk to her.  Alone.  In a room with the door shut.

Apparently, he asked her some routine questions. 

The next day the school counciler spectulated that he maybe hadn't ever assessed her (so why was he even conducting our ETR meeting?)

I had gone into the office and told the secretaries (with my daughter present) that my daughter was to go to the office if any adult male tried to be in a room alone with her. They seemed to be understanding and hadn't known any of this beforehand.  

Also, I sent an email reminding everyone (including Mr. School Psychologist) about our previous meeting and what had been discussed.

But..........

There is a deep distrust here now--- due to all of these incidents.

In the climate of our society (after the Catholic Church scandal and the Penn State Football camp scandal) school professionals MUST BE TRANSPARENT. 

Mind games, temper fits and acting in any way untrustworthy sets off my personal warning flags.

At this point our child is in the hands of STRANGERS and anything that causes me to question them is going to be an issue.   

For the record I'm not accusing anyone here of anything other than perhaps forgetting our family's request. 

Still, I hope my daughter catches on to all the Orton Gillingham quickly so that we can move out of this school which in some respects seems a bit too loose for me and back into a Catholic School situation (where yes the children are miserable and bored but at least I feel like they are for the most part safe).









Tuesday, May 1, 2012

Future Planning Statement

In our state there is a section in the IEP that the parents must fill out called THE FUTURE PLANNING STATEMENT.  (I'm yelling that in jest because it seems like such an overly big deal). 

Really it's a good idea to have such a thing.  Here is the area where you talk about the plans for your child, what you would like to see.

While I think it's a little bit presumptous to assume we know where our children will be at the end of high school graduation (at least when they are as young as my child is) I dont think it's a bad idea to be thinking ahead. 

What path are we going to want our child to walk?  Can we start to encourage that now?  After all isnt that what it means to raise a child, we instill ideas about their future into their sweet little heads, we teach them which way to go and we hold on to the back of their proverbial bicycle seat until they are ready to pedal for themselves.

I want to share our FUTURE PLANNING STATEMENT with you, keep in mind that our daughter is 7.  The point here is to simply to give a glimpse of what we have written. Here it is:

Mary Miller will attend college, most likely at The Ohio State University where she will be encouraged to use her strenghts in a Math/Science related major. She will also be strongly encouraged to pursue an advanced degree perhaps in a medically related field.

In the short term, daily action will be taken in order to manage her learning differences and pursue educational achievement in spite of her dyslexia and dysgraphia. With the goal of reading and writing at age/grade appropriate levels, her family will be utilizing the various local educational professionals, opportunities and forms of educational technology available in order to achieve these goals.