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I have a 6 year old with AS, some sensory issuea, etc. When he was

having trouble keeping his place when reading and writing, and when

catching a ball, we took him to a developmental optometrist for an

eval. Turned out after an $ eval he has tracking and depth

perception problems, etc These are developmental delays and will

improve with age but it is hard for them in the classroom in the

mean time so we signed up for the $ vision therapy.

After 2 weeks my son developed a HORRIBLE eye tic that was so

disturbing. I immediately stopped the therapy and the tic stopped

in about 6 weeks. Just remember that vision therapy is neurological

retraining. They stress the visual system to bring about change but

you can stress it to much and cause a tic! The Dr doesn't even do

the therapy, a technician does. Since kids on the spectrum can be

prone to tics it makes sense to me how it could have happened.

There is no negative press on vision therapy, its all glowing so I

just wanted to share my experience. We are in the Philadelphia area.

Thanks,

Debra Melamed

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Fight more for OT and PT. He has propriception difficulty. He

needs swinging, jumpimg, spinning, joint compression to help

stabilize his body. My daughter was very clumsy and her vision and

hearing were fine. She had a lot of therapy in the gym and that

helped. The gfcf diet plus supplements helped more.

>

> Hi everyone,

>

> OMG, since school started in July, we have been busy. has

> been doing OK in 1st grade. I like his teacher. Not fond of his

> aide. There is a more severe child in class and she always tends

to

> her and at times is very mean to . I have complained but

> nothing will change. She is also the PTO president and my co-

worker.

> I comfronted her and said I think your great as a person but as

> 's aide, I do not. Just because he looks normal, doesn't mean

> he is.

> has been having too many accidents this month and this

> prompted us to check his vision. got his hand caught in the

> car door, then at a birthday party, he tripped and went head first

> into a picnic table-7 stitched above his eye. Then at another

> birthday party he knocked out his front tooth. It was loose but

not

> ready to come out. I did talk to his OT at school, which has not

> been doing much with him. It seems he is the ONLY child in our

> entire school that needs OT. (he has sensory dysfunction) and

there

> is no one to give it to him. So I am doing most of it and

sometimes

> that can be a huge battle with him. The OT recommended that

> see a developmental opthalmologist. (I didn't know they existed).

> We have an appointment for December. She feels he uses his

perifial

> (spelled wrong) vision instead of his focus vision, causing him to

> always be walking into things. I did take him to get his regular

> vision checked and it is 20/15. Better than perfect. I don't get

it.

> He talks very loud-take him to get his hearing checked 2X and

> perfect hearing, hears better than me. Now his vision but yet he

> constantly is getting hurt and walking into things. But we will go

> to the developmental doctor and see what they say.

> Other than that- has had 1 exceptionally good week that, he

was

> chosen for student of the week. Usually he gets that the last week

> of school. LOL!!!

> We are now ending our two week break from school and I am not

> really looking forward going back. I just feel, they don't give a

> sh**. His IEP, we found out is all messed up. He is supposed to

> receive sensory and does not. Then he gets sent to another

classroom

> because he doesn't raise his hand when he has the answer. I have

> explained that he can not do two things at once. He needs

> redirection not punishment. But do they do this-no because, WHY!!!

> He looks normal. I don't know-I am at my wits end. ARGGGG!!

> Thanks for letting me rant. I needed that.

>

> Cori

> mom to 6, AS and SD

> and to ph 9, Left clubfoot

>

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OT addresses visual issues without the intense retraining that was

descibed. We do activiies all day during selfcare, school, and play

that require depth perception and tracking. Keep the activities

meaningful and the child will not overload.

>

> I have a 6 year old with AS, some sensory issuea, etc. When he

was

> having trouble keeping his place when reading and writing, and

when

> catching a ball, we took him to a developmental optometrist for an

> eval. Turned out after an $ eval he has tracking and depth

> perception problems, etc These are developmental delays and will

> improve with age but it is hard for them in the classroom in the

> mean time so we signed up for the $ vision therapy.

>

> After 2 weeks my son developed a HORRIBLE eye tic that was so

> disturbing. I immediately stopped the therapy and the tic stopped

> in about 6 weeks. Just remember that vision therapy is

neurological

> retraining. They stress the visual system to bring about change

but

> you can stress it to much and cause a tic! The Dr doesn't even do

> the therapy, a technician does. Since kids on the spectrum can be

> prone to tics it makes sense to me how it could have happened.

> There is no negative press on vision therapy, its all glowing so I

> just wanted to share my experience. We are in the Philadelphia

area.

>

> Thanks,

>

> Debra Melamed

>

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, what supplements are you talking about?

> >

> > Hi everyone,

> >

> > OMG, since school started in July, we have been busy.

has

> > been doing OK in 1st grade. I like his teacher. Not fond of his

> > aide. There is a more severe child in class and she always tends

> to

> > her and at times is very mean to . I have complained but

> > nothing will change. She is also the PTO president and my co-

> worker.

> > I comfronted her and said I think your great as a person but as

> > 's aide, I do not. Just because he looks normal, doesn't

mean

> > he is.

> > has been having too many accidents this month and this

> > prompted us to check his vision. got his hand caught in

the

> > car door, then at a birthday party, he tripped and went head

first

> > into a picnic table-7 stitched above his eye. Then at another

> > birthday party he knocked out his front tooth. It was loose but

> not

> > ready to come out. I did talk to his OT at school, which has not

> > been doing much with him. It seems he is the ONLY child in our

> > entire school that needs OT. (he has sensory dysfunction) and

> there

> > is no one to give it to him. So I am doing most of it and

> sometimes

> > that can be a huge battle with him. The OT recommended that

> > see a developmental opthalmologist. (I didn't know they

existed).

> > We have an appointment for December. She feels he uses his

> perifial

> > (spelled wrong) vision instead of his focus vision, causing him

to

> > always be walking into things. I did take him to get his regular

> > vision checked and it is 20/15. Better than perfect. I don't get

> it.

> > He talks very loud-take him to get his hearing checked 2X and

> > perfect hearing, hears better than me. Now his vision but yet he

> > constantly is getting hurt and walking into things. But we will

go

> > to the developmental doctor and see what they say.

> > Other than that- has had 1 exceptionally good week that, he

> was

> > chosen for student of the week. Usually he gets that the last

week

> > of school. LOL!!!

> > We are now ending our two week break from school and I am not

> > really looking forward going back. I just feel, they don't give

a

> > sh**. His IEP, we found out is all messed up. He is supposed to

> > receive sensory and does not. Then he gets sent to another

> classroom

> > because he doesn't raise his hand when he has the answer. I have

> > explained that he can not do two things at once. He needs

> > redirection not punishment. But do they do this-no because,

WHY!!!

> > He looks normal. I don't know-I am at my wits end. ARGGGG!!

> > Thanks for letting me rant. I needed that.

> >

> > Cori

> > mom to 6, AS and SD

> > and to ph 9, Left clubfoot

> >

>

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My daughter takes Brainchild Spectrum Support 11 (High level

multi-vitamin)

Cod Liver Oil (has DHA for brain support)

Transdermal glutathione for detox

Calcium supplent because of the diet

probiotic for good bateria in gut

zyme prime enzyme for digestion

> > >

> > > Hi everyone,

> > >

> > > OMG, since school started in July, we have been busy.

> has

> > > been doing OK in 1st grade. I like his teacher. Not fond of his

> > > aide. There is a more severe child in class and she always tends

> > to

> > > her and at times is very mean to . I have complained but

> > > nothing will change. She is also the PTO president and my co-

> > worker.

> > > I comfronted her and said I think your great as a person but as

> > > 's aide, I do not. Just because he looks normal, doesn't

> mean

> > > he is.

> > > has been having too many accidents this month and this

> > > prompted us to check his vision. got his hand caught in

> the

> > > car door, then at a birthday party, he tripped and went head

> first

> > > into a picnic table-7 stitched above his eye. Then at another

> > > birthday party he knocked out his front tooth. It was loose but

> > not

> > > ready to come out. I did talk to his OT at school, which has not

> > > been doing much with him. It seems he is the ONLY child in our

> > > entire school that needs OT. (he has sensory dysfunction) and

> > there

> > > is no one to give it to him. So I am doing most of it and

> > sometimes

> > > that can be a huge battle with him. The OT recommended that

>

> > > see a developmental opthalmologist. (I didn't know they

> existed).

> > > We have an appointment for December. She feels he uses his

> > perifial

> > > (spelled wrong) vision instead of his focus vision, causing him

> to

> > > always be walking into things. I did take him to get his regular

> > > vision checked and it is 20/15. Better than perfect. I don't get

> > it.

> > > He talks very loud-take him to get his hearing checked 2X and

> > > perfect hearing, hears better than me. Now his vision but yet he

> > > constantly is getting hurt and walking into things. But we will

> go

> > > to the developmental doctor and see what they say.

> > > Other than that- has had 1 exceptionally good week that, he

> > was

> > > chosen for student of the week. Usually he gets that the last

> week

> > > of school. LOL!!!

> > > We are now ending our two week break from school and I am not

> > > really looking forward going back. I just feel, they don't give

> a

> > > sh**. His IEP, we found out is all messed up. He is supposed to

> > > receive sensory and does not. Then he gets sent to another

> > classroom

> > > because he doesn't raise his hand when he has the answer. I have

> > > explained that he can not do two things at once. He needs

> > > redirection not punishment. But do they do this-no because,

> WHY!!!

> > > He looks normal. I don't know-I am at my wits end. ARGGGG!!

> > > Thanks for letting me rant. I needed that.

> > >

> > > Cori

> > > mom to 6, AS and SD

> > > and to ph 9, Left clubfoot

> > >

> >

>

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  • 4 years later...

>

> I have now been on Bees diet for over a year now and I feel so much better

than I have in the past six years. My weight finally normalized after what

seemed to be forever. I'm basically at the point where I eat almost no carbs

whatsoever. Been kind of away from the group for awhile and was checking in.

However I'm still having specific issues that continue to bother me. Every time

I squat and then rise my legs get a extreme itchy burning sensation, I still

have urinating issues with " The Sudden Urge, " if you know what I mean which I

can't seem to shake. Itchy in other places like my ears as well. I've also began

to think my Hiatal Hernia has a lot more to do with my problems than I've ever

thought. When it's not in place I tend to have barely any bowel movements

whatsoever, which I can now tell seems to be a precursor to other pains in my

digestive track. I am extremely happy, but it really seems that these pains are

never going to end. I don't really stress about them too much, but I do realize

that the situation has yet to improve, which makes me wonder if there is

something else I should be doing? Thoughts? Basically my diet consists of

eggs,meat, ghee, coconut oil, sea salt, and saurkraut.

+++Hi there. What is your name please?

Just to ensure you understand, all plant foods are carbs, so that includes

sauerkraut, so carbs include vegetables, spices, herbs, grains, nuts, seeds,

legumes (peas and beans from pods), fruits, etc. In other words any foods that

aren't classified as protein or fat.

I do have an all Meat & Fat Program, which you should be following if you are

only going to consume proteins and fats:

http://www.healingnaturallybybee.com/articles/meat5.php

You will have less stool when you aren't eating many plant foods, so the urge to

go will be less. You need to take time every day to move your bowels. If they

are sticky or slow you probably need more fats as in my all meat and program.

Having a hiatal hernia wouldn't affect your bowel movements, but the stress it

causes can, since your body will be running on its fight/flight nervous system.

In order to switch your body over to running on its more healing nervous system

do deep breathing exercises whenever you have the hiatal hernia or are under

stress (body or mental):

http://www.healingnaturallybybee.com/articles/breath4.php

Itching and burning sensations are caused by toxins, so they too will get better

as you progress.

The sudden urge to go will also lessen as you progress. When your cells are

strong and healthy, you won't have loose weak muscles and tissues in that area.

Of course if you've had any of those issues in the past your body will be

retracing them as it heals itself, which takes 1 month for every year - see this

article:

http://www.healingnaturallybybee.com/articles/heal10.php

I hope that helps.

Bee

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