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My daughter has apraxia and sensory problems also. She can tolerate

lots of things when she is well rested, but if she is tired she gets

overly sensitive to everything. She cannot tolerate PM school

because it is just way too much for her in the afternoons. It's a

lot of stimulation, and she is too tired at that time of day.

Good luck!

Suzi

> hi everyone,

> I'm writing to ask a question about somethings I've noticed lately

about my daughter. Gwen was diagnosed by speech therapist at two

and half and is now almost four.

> When she started treatment she had less than 50 words and was very

sensitive about being touched, having her hair brushed, etc. After

being in the program for less than a year she loved hugs and started

to request them, and still does, and is talking nonstop! She

tolerates her hair being brushed, but is still a picky eater.

> She spent the summer in an integrated setting with several other

children and now seems to be having sensory issues again. She won't

take a hot/warm bath. The water needs to be almost ice cold before

she will get in. She won't take a shower, where as before she loved

having her hair washed this way. Her teachers report that she isn't

eating, but crying at lunch time. She's stopped talking to them as

well. She won't tell them about our trip to disney world/seaworld.

> Her class meets in the pm and last yr and the summer program were

both am. The teachers are all the same, except a student teacher

that is done with her requirements. (She was only in summer

program. I am at a lost. Has anyone else thought they made it over

sensory issues and they have resurfaced?

>

> Sorry so long, not many of my friends understand why I am

upset......, mom to Cain (almost 7) and Gwen (almost 4 -

apraxia)

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My son has apraxia and sensory issues too, but my problem is getting

him to sleep. We have tried everything and nothing seems to work. We

had him in AM kindergarten but because he was over tired and over

sensitive we moved him to afternoon school because he can sleep in

and is more rested. Do you have problems with bedtime and sleeping

also or any ideas?? Thanks, Crystal

> > hi everyone,

> > I'm writing to ask a question about somethings I've noticed

lately

> about my daughter. Gwen was diagnosed by speech therapist at two

> and half and is now almost four.

> > When she started treatment she had less than 50 words and was

very

> sensitive about being touched, having her hair brushed, etc. After

> being in the program for less than a year she loved hugs and

started

> to request them, and still does, and is talking nonstop! She

> tolerates her hair being brushed, but is still a picky eater.

> > She spent the summer in an integrated setting with several other

> children and now seems to be having sensory issues again. She

won't

> take a hot/warm bath. The water needs to be almost ice cold before

> she will get in. She won't take a shower, where as before she

loved

> having her hair washed this way. Her teachers report that she

isn't

> eating, but crying at lunch time. She's stopped talking to them as

> well. She won't tell them about our trip to disney world/seaworld.

> > Her class meets in the pm and last yr and the summer program were

> both am. The teachers are all the same, except a student teacher

> that is done with her requirements. (She was only in summer

> program. I am at a lost. Has anyone else thought they made it

over

> sensory issues and they have resurfaced?

> >

> > Sorry so long, not many of my friends understand why I am

> upset......, mom to Cain (almost 7) and Gwen (almost 4 -

> apraxia)

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I have a 4 year old son who was diagnosed with apraxia at 2 and also has the

sensory problems. He was having a difficult time sleeping also until we

tried a few different things. We discovered that one problem was his pajamas.

We had him try all different kinds until he found one that he loved the feel

of. He still won't sleep with a top on, but we also found a blanket and bed

sheets that he liked. We just kept trying different fabrics until he told us

what felt good. Now he sleeps great!

We also have a 2 year old daughter who has apraxia and has really bad sensory

issues with the water. Our OT just helps us tremendously. We take it in small

steps each day, always doing some sort of water " game. " Letting her get used

to the feel of it in different environments and different temps has helped.

She doesn't have such violent reactions to water anymore, but still has

hesitancies. Once she learned that it wasn't always a bad thing, she started

to be more open to try new things with the water.

Good Luck!

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One child I have done therapy with seems to go in cycles...a few weeks the SI

issues seem almost non-existent, and then almost suddenly the SI issues start up

again. I have noticed this and wondered what triggers the phases.

[ ] Re: sensory issues

My daughter has apraxia and sensory problems also. She can tolerate

lots of things when she is well rested, but if she is tired she gets

overly sensitive to everything. She cannot tolerate PM school

because it is just way too much for her in the afternoons. It's a

lot of stimulation, and she is too tired at that time of day.

Good luck!

Suzi

> hi everyone,

> I'm writing to ask a question about somethings I've noticed lately

about my daughter. Gwen was diagnosed by speech therapist at two

and half and is now almost four.

> When she started treatment she had less than 50 words and was very

sensitive about being touched, having her hair brushed, etc. After

being in the program for less than a year she loved hugs and started

to request them, and still does, and is talking nonstop! She

tolerates her hair being brushed, but is still a picky eater.

> She spent the summer in an integrated setting with several other

children and now seems to be having sensory issues again. She won't

take a hot/warm bath. The water needs to be almost ice cold before

she will get in. She won't take a shower, where as before she loved

having her hair washed this way. Her teachers report that she isn't

eating, but crying at lunch time. She's stopped talking to them as

well. She won't tell them about our trip to disney world/seaworld.

> Her class meets in the pm and last yr and the summer program were

both am. The teachers are all the same, except a student teacher

that is done with her requirements. (She was only in summer

program. I am at a lost. Has anyone else thought they made it over

sensory issues and they have resurfaced?

>

> Sorry so long, not many of my friends understand why I am

upset......, mom to Cain (almost 7) and Gwen (almost 4 -

apraxia)

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`Our Ot said that was the case in my son. STacy

> Could illness or allergies be the reason that sensory issues are triggered

or

> reappear? That is my humble opinion. Carolyn

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The only time I have problems with bedtime is if my daughter has

taken a nap. If she has a nap, she's not sleepy at 8 and will

usually want to stay up to 9 or 10.

Unfortunately, some days she'll fall asleep in the car when we pick

up my son from school. Other days, if she is having tantrums right

and left, I'll put her in her room for a nap. I'd rather her stay

up late and be in a good mood then put up with a fussy kid for 3 or

four hours.

I think in a year or two we won't have any problems in the

afternoons. As she gets older, she keeps on being able to handle

staying up more.

actually is pretty good at going to sleep. It's one of her

best attributes. Our babysitters always comment about how good both

of my twins are about going to sleep.

I also think it is a twin thing. When you have twins, you can't

rock them to sleep when they are babies. If they had been fed and

had their diapers changed, they got put in their cribs. Most of the

time they were asleep in 15 minutes. They also have always had

their sister around. If they are having a bad night, they just

climb in bed together and sleep that way.

Good luck!

> > > hi everyone,

> > > I'm writing to ask a question about somethings I've noticed

> lately

> > about my daughter. Gwen was diagnosed by speech therapist at

two

> > and half and is now almost four.

> > > When she started treatment she had less than 50 words and was

> very

> > sensitive about being touched, having her hair brushed, etc.

After

> > being in the program for less than a year she loved hugs and

> started

> > to request them, and still does, and is talking nonstop! She

> > tolerates her hair being brushed, but is still a picky eater.

> > > She spent the summer in an integrated setting with several

other

> > children and now seems to be having sensory issues again. She

> won't

> > take a hot/warm bath. The water needs to be almost ice cold

before

> > she will get in. She won't take a shower, where as before she

> loved

> > having her hair washed this way. Her teachers report that she

> isn't

> > eating, but crying at lunch time. She's stopped talking to them

as

> > well. She won't tell them about our trip to disney

world/seaworld.

> > > Her class meets in the pm and last yr and the summer program

were

> > both am. The teachers are all the same, except a student

teacher

> > that is done with her requirements. (She was only in summer

> > program. I am at a lost. Has anyone else thought they made it

> over

> > sensory issues and they have resurfaced?

> > >

> > > Sorry so long, not many of my friends understand why I am

> > upset......, mom to Cain (almost 7) and Gwen (almost 4 -

> > apraxia)

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I know it does happen with my daughter. It's one of the first signs

that she is sick, and the sensory issues usually linger longer even

after she is well.

> Could illness or allergies be the reason that sensory issues are

triggered or

> reappear? That is my humble opinion. Carolyn

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Stacey,

Graham also has the bowl type hair cut! He is 4.8 and it is the only

haircut he will let anyone cut. if it looks any different he cries

uncontrolably! As if haircuts aren't bad enough! So we just let him have,

as he calles it ,His Grammy hair.

Our OT suggested to let him play with shaving cream in the bathtub to help

clean his finger nails. At first he hated it but now he likes it. I think

because, he knows if he plays with the shaving cream I don't have to clean

out his nails, which he hates worse.

Our son has always worn hats. Since birth! He was so fair, I was always

afraid he'd burn.

> does this. In the last couple of days, he has taken to

wanting to put on a hat. I was truly amazed. We live in hairbrushing hell

usually around here. The child is starting to look like one of the Beatles

with his bowl like hair. Everynow and then he will take spurts where he can

handle certain things better than usually.

>

> Just a note on the bath- we tried using some of those bathtub crayons and

we have found that he tolerates the bath better now. The other bath toys

don't do much for him except for the cups. ( fill em up - empty em out)

>

> Stacey

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My daughter has a short page-boy haircut. That's what she wants, and

I'm happy to let her have short hair. She hates to have her hair

brushed, and the short hair usually always looks neat.

> Stacey,

> Graham also has the bowl type hair cut! He is 4.8 and it is the

only

> haircut he will let anyone cut. if it looks any different he cries

> uncontrolably! As if haircuts aren't bad enough! So we just let

him have,

> as he calles it ,His Grammy hair.

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  • 3 years later...
Guest guest

Good advice, Katy. :-)

Also, folkes should be aware that there are basically THREE types of " foam " ear

plugs on the market.

- Cylindrical (E-A-R brand in yellow)

- Cone

- Hexagonal

Personally, I have found:

- the CONE shape to be the best fitting, easiest to manipulate, and highest in

noise reduction rating (NRR).

-the Cylindrical E-A-R brand to be a bit rough in texture and awkward insert and

extract (Hint: Know where your tweezers are kept).

- the Hexagonal to be just gimmick.

Hope this helps (HTH). :-)

Regards,

Sharafanowich

-- Katy Harandi <katyh@...> wrote:

My daughter started screaming a year ago and we have found that earplugs reduce

her screaming significantly. We use the foam kind you find at drugstores. She

seems so much more relaxed with them on.

Katy

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