April, Hi, I'm glad you sent this, I dont get to read the Star Ledger very often, I'm glad you sent this, It is very interesting!! I hope it will turn out to be beneficial for our kids and families. I hope your kids are doing great and enjoying the summer! Diane
April Larsen <ALarsen65@...> wrote:
State sued on special ed student separation Thursday, June 28, 2007 BY JOHN MOONEY Star-Ledger Staff A coalition of advocacy groups has filed a
federal lawsuit against the state that contends thousands of special education students are being wrongfully educated in segregated classes, bringing to court a long-running sore point for New Jersey.
The groups say in the 40-page complaint filed in federal District Court in Newark that New Jersey's policies and funding allow, if not encourage, districts to serve a majority of their disabled students in separate classes and schools.
The state serves about 43 percent of its children with disabilities in predominantly general education classes, well below the national average of about 55 percent, according to the most recent data.
More glaring is the 10 percent who are placed in separate schools altogether, by far the nation's highest rate. And the lawsuit contends the use of separate classes or schools is especially high among some students, including those in preschool, black and Hispanic children.
"If New Jersey approached the national average (for separate classrooms)," reads the lawsuit, "almost 13,000 fewer children would be in segregated placements."
They would include those like a girl cited in the complaint who was denied mainstream preschool after the district told her parents "that it did not offer inclusion unless so ordered by the courts." Other districts said they couldn't afford such programs.
The plaintiffs in the case are New Jersey Protection & Advocacy Inc., Education Law Center, the Statewide Parent and Advocacy Network of New Jersey and the Arc of New Jersey. The defendants are the state Department of Education, state Education Commis sioner Lucille Davy and the state Board of Education.
For years, the advocate groups have fought for more mainstream education, or "inclusion," for the state's 230,000 students with disabilities.
Backing them up is state and
federal law that demands students be served in "least restrictive environment" that is appropriate, and advocates and families have maintained that such mainstream classes are critical for their children to learn and to socialize.
Yet New Jersey has struggled meeting these demands, especially in sending thousands of students into separate schools altogether. New Jersey has nearly 400 such schools, public and private, and it is not rare that families clamor to get into these programs when they are dissatisfied with those in the district.
State officials have recently been aggressive in pressing districts to provide more inclusive programs, setting broad goals for bringing down the separate- placement numbers in the next five years. Nearly $19 million was earmarked this year for in-district programs as well.
Still, officials have acknowledged that for all their efforts, they have yet to see much progress in
the overall numbers. Yesterday, they would not comment on the lawsuit, other than to say they re main committed to inclusion.
"We stress the need for special education students to be educated alongside their non-disabled peers," said state spokesman Jon Zlock.
The advocates maintain the state must back up its words with tougher actions, and they hoped the lawsuit would force its hand. They acknowledged the difficulty of overseeing 600-plus districts, but said too often, the state still won't act forcefully.
"When they do find a problem," said Joseph Young, deputy director of New Jersey Protection & Advo cacy, "there is a lot of carrot kind of responses and not enough sticks."
Others said the state has clearly stepped up its efforts, but they are not enough.
"Nothing they have promised will happen meaningfully within the academic lifetime of children now in school," said Ruth Lowenk ron,
an attorney with the Education Law Center. "This lawsuit was the only way for something meaningful to happen."
And they stress that it is not just about shifting the numbers to more inclusion, but also providing appropriate supports and other programs for children once they are in mainstream classes.
"We don't want to just be moving from no inclusion to more inclu sion without the services these children need," Lowenkron said.
April L. Larsen Certified Natural Childbirth Educator, AAHCC The Bradley Method www.bradleybirth.com?L315
"Changing the world; one natural birth at a time"
Luggage? GPS? Comic books?
Check out fitting gifts for grads at Yahoo! Search.
State sued on special ed student separation
Thursday, June 28, 2007
BY JOHN MOONEY
Star-Ledger Staff
A coalition of advocacy groups has filed a federal lawsuit against
the state that contends thousands of special education students are
being wrongfully educated in segregated classes, bringing to court a
long-running sore point for New Jersey.
The groups say in the 40-page complaint filed in federal District
Court in Newark that New Jersey's policies and funding allow, if not
encourage, districts to serve a majority of their disabled students
in separate classes and schools.
The state serves about 43 percent of its children with disabilities
in predominantly general education classes, well below the national
average of about 55 percent, according to the most recent data.
More glaring is the 10 percent who are placed in separate schools
altogether, by far the nation's highest rate. And the lawsuit
contends the use of separate classes or schools is especially high
among some students, including those in preschool, black and Hispanic
children.
"If New Jersey approached the national average (for separate
classrooms)," reads the lawsuit, "almost 13,000 fewer children would
be in segregated placements."
They would include those like a girl cited in the complaint who was
denied mainstream preschool after the district told her parents "that
it did not offer inclusion unless so ordered by the courts." Other
districts said they couldn't afford such programs.
The plaintiffs in the case are New Jersey Protection & Advocacy Inc.,
Education Law Center, the Statewide Parent and Advocacy Network of
New Jersey and the Arc of New Jersey. The defendants are the state
Department of Education, state Education Commis sioner Lucille Davy
and the state Board of Education.
For years, the advocate groups have fought for more mainstream
education, or "inclusion," for the state's 230,000 students with
disabilities.
Backing them up is state and federal law that demands students be
served in "least restrictive environment" that is appropriate, and
advocates and families have maintained that such mainstream classes
are critical for their children to learn and to socialize.
Yet New Jersey has struggled meeting these demands, especially in
sending thousands of students into separate schools altogether. New
Jersey has nearly 400 such schools, public and private, and it is not
rare that families clamor to get into these programs when they are
dissatisfied with those in the district.
State officials have recently been aggressive in pressing districts
to provide more inclusive programs, setting broad goals for bringing
down the separate- placement numbers in the next five years. Nearly
$19 million was earmarked this year for in-district programs as well.
Still, officials have acknowledged that for all their efforts, they
have yet to see much progress in the overall numbers. Yesterday, they
would not comment on the lawsuit, other than to say they re main
committed to inclusion.
"We stress the need for special education students to be educated
alongside their non-disabled peers," said state spokesman Jon Zlock.
The advocates maintain the state must back up its words with tougher
actions, and they hoped the lawsuit would force its hand. They
acknowledged the difficulty of overseeing 600-plus districts, but
said too often, the state still won't act forcefully.
"When they do find a problem," said Joseph Young, deputy director of
New Jersey Protection & Advo cacy, "there is a lot of carrot kind of
responses and not enough sticks."
Others said the state has clearly stepped up its efforts, but they
are not enough.
"Nothing they have promised will happen meaningfully within the
academic lifetime of children now in school," said Ruth Lowenk ron,
an attorney with the Education Law Center. "This lawsuit was the only
way for something meaningful to happen."
And they stress that it is not just about shifting the numbers to
more inclusion, but also providing appropriate supports and other
programs for children once they are in mainstream classes.
"We don't want to just be moving from no inclusion to more inclu sion
without the services these children need," Lowenkron said.
April L. Larsen
Certified Natural Childbirth Educator, AAHCC
The Bradley Method
www.bradleybirth.com?L315
"Changing the world; one natural birth at a time"
Right not on all but on some - my friend does therapy at a few of the
elementary schools and assists taking the children off the bus - again
depends I guess on the need, age, district, etc.
Have a good day,
A
Hi April, We actually had a brainstem auditory invoked potential test done when my son was 6 months old. It confirmed his hearing loss is neurologic in nature, and the result said that it should only afftect certain tones, not ones that are involved in human speech, at that time. We cant do that test very often, it requires sedation, but the regular auditory exams that we have been doing as a follow up at JFK in Edison show improvement. It was about 3 months after that test under sedation that we found out about his epilepsy and Benign External Hydrocephalus. His ENT specialist told me that treating the Epilepsy might improve his auditory exams, and I was a little skeptical then, but, I am not complaining!!! Improvement is a beautiful thing, and an answer to our prayers!!! I've been to St Peters audiology department, and our ENT prefers JFK's audiology department. I'm not sure
why, because he is on staff at both. I have even had two of the audiologist we have seen in both places at different times. It's certainly a small world. DIane
April Larsen <ALarsen65@...> wrote:
Diane - I am not sure about EI but for our son who was three when tested last we went to St. Peter's. He is not due to be tested again until this fall but we are having that done at Kean University. We have also requested a screening for central auditory processing by one of the
leading professors at Kean. I can keep you posted.
The main thing I learned with speech and hearing is that they don't want the kids to memorize the test which is why they ask for yearly testing or they can administer a different type of test to evaluate. YOu don't want to bias the study results.
April
Boardwalk for $500? In 2007? Ha! Play Monopoly Here and Now (it's updated for today's economy) at Yahoo! Games.
Hi everyone,
I wanted to make sure that we are all being judicious in our postings
and replies to one another.
This site is a venue for parents and educators to communicate their
experience, share resources and yes to vent and ask for help when we
need it. Bearing that in mind, I ask that everyone please use the
following school of thought when postings:
1. Please refrain from using language or expressions that elude to
inappropriate or unneccessary actions.
2. Talk about YOUR experiences as your own instead of telling others
what they should and should not do. Remember that some of us are
more experienced with the system than others and although our posts
may seem to be helping that person by telling them what they should
do, unless we have the whole story or take the time off line to do so
than we may be setting that family up for a situation that they
cannot handle on their own, thus making the situation more difficult
for them.
3. If a chat continues back and forth on a "personal level", please
take it off line. This is a wonderful opportunity to make new
friends and develop relationships and it also frees up the rest of
our members from recieving 15 emails back and forth on your personal
exchanges (ie: "thanks Joe", "ave a nice weekend", or 10 people
responding to the same question with the same answer).
Lastly, please remember that while their are some inadequate service
providers, resources and people within the system for our children
that their are ALLOT of really good ones and some of them happen to
be members of our site. Making consistent derogatory comments about
professionals in a general way may be misinterpeted by others and
paint an unclear and biased point of view which is not what we are
about.
In my experience, I have found that trying to support the process of
the professionals (such as the school or EI providers) with a
positive and rational point of view is the best way to advocate for
our children. This does not mean that you have to give in to
everything they offer but often it means that you might have to pick
your battles carefully because it is a system. A system that most of
us have no choice but to be a part of, but how we interact within
those parameters will pave the way for how THEY react to us and other
families after us.
I always say, if there is a problem lets fix it not just for
ourselves but for others that will come after us. Make the difference.
Thank you for your participation and support.
Sincerely,
Tina Rear
Care-to-Share Support Network
Founder
Colleen, It's like the syms commercial, an educated consumer ..... I am convinced that my little guy will be in school when he is 3, so I will probably be picking your brain one of these days about the special ed stuff. I went to a couple of spann meetings, hell, at least it's free! If my son does to into school in special ed, I will be one of those educated consumers! Have a great day, I hope your family has a great summer! Diane
Colleen Bain <colleenbain@...> wrote:
Diane:
:-) I like the flames comment. EI - my kids are 8 and 10 so I was thinking of all the special ed acronyms we use and EI was not one of them in present conversations... thanks for the information.
Subject: Re: [Care-to-ShareSupportNetwork] On a much lighter note!!!!
Hi Colleen, I'm sorry, EI or EIP stands for Early Intervention, or Early Intervention Program. In NJ it's for children under three, after the age of three, the kids can get into the school system, either by an early intervention referral, or by the parents request for services, I think the municipality's have child study teams who determine eligibility once the request is made. The early intervention system in NJ is broken down by the county, and each county has a phone number to call to request an evaluation from Early Intervention. Also, the therapies are provided in
the child's home, or daycare, and there is a sliding scale for the cost based on the family's gross income. It is a good thing that we have it at all, but, of course, if your child is in early intervention, the parent must make themselves an educated customer, I also find that little flames about three and one half to 4 feet high (the height of one's buttocks!) also work quite well to motivate the people to get their job done!!! LOL Sorry, a little sarcasm goes a long way!!! Diane
Colleen Bain <colleenbain@patmedia.net> wrote:
Hi,
What does EI stand for? I'm an occasional reader
to the forum and trying to catch up on emails. Thanks
Subject: [Care-to-ShareSupportNetwork] On a much lighter note!!!!
Thank God baby Mikey is doing better!!! On a much lighter note, Joe-Joe had an evaluation from someone at the Arc in Manville, for his physical therapy needs. She agreed that we need to boost his PT time by one hour per week!!! She is a Physical Therapist who has not worked with grown ups in 15 years!! She noted how he is almost crawling, and he showed off how he can pull himself up to standing, and hold on to stuff, and creep around. She also agrees
with me that this extra time towards PT will probably be needed for a temporary basis, because once he learns how to get around more, ha ha ha, look out Amanda, and lookout Michael (our dog!) So, it is a huge thing to me because Joe is actually getting more help, and I didnt have to fight!!!! I was all ready, had my boxing gloves on and everything, but I was able to take them off and save my energy for something else. It was wonderful to have someone from EI see things from Joe Joe's point of view and actually make a recommendation that is good for him. Thank you Tina, and everyone at the last Care to SHare meeting, I would not have pursued this if it was not for your encouragement. Even our regular "interventionist" from the Arc/early intervention is impressed at how easy this one was, and she is happy too!!! I was all ready to go over some people's heads, again, but, this time was better!!! I will see you on Thurs
nite!!! Love, Diane (PS Joe Joe said thank you too!!!)
:-) I like the flames comment. EI - my kids are 8 and 10 so I was thinking of all the special ed acronyms we use and EI was not one of them in present conversations... thanks for the information.
Subject: Re: [Care-to-ShareSupportNetwork] On a much lighter note!!!!
Hi Colleen, I'm sorry, EI or EIP stands for Early Intervention, or Early Intervention Program. In NJ it's for children under three, after the age of three, the kids can get into the school system, either by an early intervention referral, or by the parents request for services, I think the municipality's have child study teams who determine eligibility once the request is made. The early intervention system in NJ is broken down by the county, and each county has a phone number to call to request an evaluation from Early Intervention. Also, the therapies are provided in the child's home, or daycare, and there is a sliding scale for the cost based on the family's gross income. It is a good thing that we have it at all, but, of course, if your child is in early intervention, the parent must make themselves an educated customer, I also find that little flames about three and one half to 4 feet high (the height of one's buttocks!) also work quite well to motivate the people to get their job done!!! LOL Sorry, a little sarcasm goes a long way!!! Diane
Colleen Bain <colleenbain@patmedia.net> wrote:
Hi,
What does EI stand for? I'm an occasional reader to the forum and trying to catch up on emails. Thanks
Subject: [Care-to-ShareSupportNetwork] On a much lighter note!!!!
Thank God baby Mikey is doing better!!! On a much lighter note, Joe-Joe had an evaluation from someone at the Arc in Manville, for his physical therapy needs. She agreed that we need to boost his PT time by one hour per week!!! She is a Physical Therapist who has not worked with grown ups in 15 years!! She noted how he is almost crawling, and he showed off how he can pull himself up to standing, and hold on to stuff, and creep around. She also agrees with me that this extra time towards PT will probably be needed for a temporary basis, because once he learns how to get around more, ha ha ha, look out Amanda, and lookout Michael (our dog!) So, it is a huge thing to me because Joe is actually getting more help, and I didnt have to fight!!!! I was all ready, had my boxing gloves on and everything, but I was able to take them off and save my energy for something else. It was wonderful to have someone from EI see things from Joe Joe's point of view and actually make a recommendation that is good for him. Thank you Tina, and everyone at the last Care to SHare meeting, I would not have pursued this if it was not for your encouragement. Even our regular "interventionist" from the Arc/early intervention is impressed at how easy this one was, and she is happy too!!! I was all ready to go over some people's heads, again, but, this time was better!!! I will see you on Thurs nite!!! Love, Diane (PS Joe Joe said thank you too!!!)
Hi Colleen, I'm sorry, EI or EIP stands for Early Intervention, or Early Intervention Program. In NJ it's for children under three, after the age of three, the kids can get into the school system, either by an early intervention referral, or by the parents request for services, I think the municipality's have child study teams who determine eligibility once the request is made. The early intervention system in NJ is broken down by the county, and each county has a phone number to call to request an evaluation from Early Intervention. Also, the therapies are provided in the child's home, or daycare, and there is a sliding scale for the cost based on the family's gross income. It is a good thing that we have it at all, but, of course, if your child is in early intervention, the parent must make themselves an educated customer, I also find that little flames about three and one half to 4 feet high (the height
of one's buttocks!) also work quite well to motivate the people to get their job done!!! LOL Sorry, a little sarcasm goes a long way!!! Diane
Colleen Bain <colleenbain@...> wrote:
Hi,
What does EI stand for? I'm an occasional reader to the forum and
trying to catch up on emails. Thanks
Subject: [Care-to-ShareSupportNetwork] On a much lighter note!!!!
Thank God baby Mikey is doing better!!! On a much lighter note, Joe-Joe had an evaluation from someone at the Arc in Manville, for his physical therapy needs. She agreed that we need to boost his PT time by one hour per week!!! She is a Physical Therapist who has not worked with grown ups in 15 years!! She noted how he is almost crawling, and he showed off how he can pull himself up to standing, and hold on to stuff, and creep around. She also agrees with me that this
extra time towards PT will probably be needed for a temporary basis, because once he learns how to get around more, ha ha ha, look out Amanda, and lookout Michael (our dog!) So, it is a huge thing to me because Joe is actually getting more help, and I didnt have to fight!!!! I was all ready, had my boxing gloves on and everything, but I was able to take them off and save my energy for something else. It was wonderful to have someone from EI see things from Joe Joe's point of view and actually make a recommendation that is good for him. Thank you Tina, and everyone at the last Care to SHare meeting, I would not have pursued this if it was not for your encouragement. Even our regular "interventionist" from the Arc/early intervention is impressed at how easy this one was, and she is happy too!!! I was all ready to go over some people's heads, again, but, this time was better!!! I will see you on Thurs nite!!! Love,
Diane (PS Joe Joe said thank you too!!!)
That is not actually true - Piscataway school district has an aide on
each bus for the disabled (preK - third grade) and many other school
systems do as well such as E. Windsor, W. Windsor, Wayne and Middlesex
town. Our friends are special ed teachers. Even Bridgewater has a bus
aide for school bused kids on pre-k. Two of the Moms that go to Kean
with me are from Union and Elizabeth and they have an aide as well.
Perhaps it depends on your district.
April
Contact SPAN to find out the codes and the rules!
Diane - I am not sure about EI but for our son who was three when
tested last we went to St. Peter's. He is not due to be tested again
until this fall but we are having that done at Kean University. We
have also requested a screening for central auditory processing by one
of the leading professors at Kean. I can keep you posted.
The main thing I learned with speech and hearing is that they don't
want the kids to memorize the test which is why they ask for yearly
testing or they can administer a different type of test to evaluate.
YOu don't want to bias the study results.
April
Subject: [Care-to-ShareSupportNetwork] On a much lighter note!!!!
Thank God baby Mikey is doing better!!! On a much lighter note, Joe-Joe had an evaluation from someone at the Arc in Manville, for his physical therapy needs. She agreed that we need to boost his PT time by one hour per week!!! She is a Physical Therapist who has not worked with grown ups in 15 years!! She noted how he is almost crawling, and he showed off how he can pull himself up to standing, and hold on to stuff, and creep around. She also agrees with me that this extra time towards PT will probably be needed for a temporary basis, because once he learns how to get around more, ha ha
ha, look out Amanda, and lookout Michael (our dog!) So, it is a huge thing to me because Joe is actually getting more help, and I didnt have to fight!!!! I was all ready, had my boxing gloves on and everything, but I was able to take them off and save my energy for something else. It was wonderful to have someone from EI see things from Joe Joe's point of view and actually make a recommendation that is good for him. Thank you Tina, and everyone at the last Care to SHare meeting, I would not have pursued this if it was not for your encouragement. Even our regular "interventionist" from the Arc/early intervention is impressed at how easy this one was, and she is happy too!!! I was all ready to go over some people's heads, again, but, this time was better!!! I will see you on Thurs nite!!! Love, Diane (PS Joe Joe said thank you too!!!)
Subject: [Care-to-ShareSupportNetwork] On a much lighter note!!!!
Thank God baby Mikey is doing better!!! On a much lighter note, Joe-Joe had an evaluation from someone at the Arc in Manville, for his physical therapy needs. She agreed that we need to boost his PT time by one hour per week!!! She is a Physical Therapist who has not worked with grown ups in 15 years!! She noted how he is almost crawling, and he showed off how he can pull himself up to standing, and hold on to stuff, and creep around. She also agrees with me that this extra time towards PT will probably be needed for a temporary basis, because once he learns how to get around more, ha ha ha, look out Amanda, and lookout Michael (our dog!) So, it is a huge thing to me because Joe is actually getting more help, and I didnt have to fight!!!! I was all ready, had my boxing gloves on and everything, but I was able to take them off and save my energy for something else. It was wonderful to have someone from EI see things from Joe Joe's point of view and actually make a recommendation that is good for him. Thank you Tina, and everyone at the last Care to SHare meeting, I would not have pursued this if it was not for your encouragement. Even our regular "interventionist" from the Arc/early intervention is impressed at how easy this one was, and she is happy too!!! I was all ready to go over some people's heads, again, but, this time was better!!! I will see you on Thurs nite!!! Love, Diane (PS Joe Joe said thank you too!!!)
Thank God baby Mikey is doing better!!! On a much lighter note, Joe-Joe had an evaluation from someone at the Arc in Manville, for his physical therapy needs. She agreed that we need to boost his PT time by one hour per week!!! She is a Physical Therapist who has not worked with grown ups in 15 years!! She noted how he is almost crawling, and he showed off how he can pull himself up to standing, and hold on to stuff, and creep around. She also agrees with me that this extra time towards PT will probably be needed for a temporary basis, because once he learns how to get around more, ha ha ha, look out Amanda, and lookout Michael (our dog!) So, it is a huge thing to me because Joe is actually getting more help, and I didnt have to fight!!!! I was all ready, had my boxing gloves on and everything, but I was able to take them off and save my energy for something else. It was
wonderful to have someone from EI see things from Joe Joe's point of view and actually make a recommendation that is good for him. Thank you Tina, and everyone at the last Care to SHare meeting, I would not have pursued this if it was not for your encouragement. Even our regular "interventionist" from the Arc/early intervention is impressed at how easy this one was, and she is happy too!!! I was all ready to go over some people's heads, again, but, this time was better!!! I will see you on Thurs nite!!! Love, Diane (PS Joe Joe said thank you too!!!)
Thank you for passing the information along. We can always use more resources.
Tina
From: Care-to-ShareSupportNetwork@yahoogroups.com [mailto:Care-to-ShareSupportNetwork@yahoogroups.com] On Behalf Of Diane Lang-LaMorticella Sent: Tuesday, June 26, 2007 11:24 AM To: care-to-sharesupportnetwork@yahoogroups.com Subject: [Care-to-ShareSupportNetwork] Fwd: Info for Support Group
Tina, I have found another local support group for families of those affected by Hydrocephalus. "Hydro" for short, is a condition where there is too much fluid (Cerebro spinal fluid) in the brain, part of my sons medical issues include a form of this, where the fluid is not in the ventricles, but in the external layers of his brain. We were very lucky, he has not needed surgery or shunts put into his brain for this. Could we include a link to this group on the Care to SHare site?? We have a lot in common, these children have developmental delays, and usually need combined types of therapies like you have worked so hard to get for your son. I'm looking forward to seeing you on Thurs nite, my best to your husband too. Diane
Hi Tracy, We actually have been very lucky, the audiology exams have been done every three months for about 9 months now, we go to JFK in Edison. They participate in our insurance, and we go there with the prescription from Dr Sabin, ENT. I have been happy with this combination so far, but of course, I couldnt help but ask when I was told that the audiologist at Summit is so good. I will check and see if there is a possibility of using our insurance to go there for the next audiology exam. Another good thing is that my son's audiology exams have actually improved since he has been on Phenobarbital for his Epilepsy, Dr Sabin told me that might happen, and I was a little skeptical, but so far so good!!! Like they say, dont pray for a nickel!! I also feel fortunate that my son "failed" the hearing screen at birth, I have a friend who had a child with severe hearing loss by age 2, and she
initially passed at birth, so it took the pediatrician a long time, 6 months, to decide to check her hearing, in that time, the pediatrician told the mother she was just comparing the child to her siblings too much. Advocacy is a full-time job!!! Will you be at the seminar on Thurs nite?? I hope to meet you in person!! I wonder what it would be like without the computer, having pen-pals like this is wonderful!!! Have a great day, Diane
upezme <upezme@...> wrote:
Hi Diane,
I was told from my EI experience last fall that the state used to provide audiology exams, but since state funds are low, they've eliminated that luxury. However, I do know that the audiologist at Summit Speech School is not only excellent, she works with special-needs toddlers on a daily basis. She seems to know what's behavioral "not listening" and what's actual hearing loss. She is worth the out of pocket expense. Did you go through your insurance co. yet?
good luck.....
~Tracy
To: Care-to-ShareSupportNetwork@yahoogroups.com From: dianelanglamorticella@yahoo.com Date: Sat, 23 Jun 2007 07:00:43 -0700 Subject: [Care-to-ShareSupportNetwork] Audiology Exams???
Hi Everyone, I have
heard that the EI kids can get an Audiology eval once a year from Summit Speech School. Does anyone know if this sounds correct? Of course, I did NOT find this out from my "service coordinator" my son has had problems on his audiology exams, and we have a good ENT for him, but I have heard that the audiologist at Summit Speech School is very thorough, and does a really good eval. I will be calling my "service coordinator" on Monday, and let her know that my son needs this, I guess she didnt hear me tell her that he has already been diagnosed with some mild hearing loss!! Gee, I only told her in December, and I told the two women who did his EI Eval on March 1, I have also given them copies of his previous audiology evals. DING, ring the bell, the next boxing match will begin!!! thank God I have the strength and a big mouth to use for my son!!! LOL I hope everyone has a great weekend! Diane
Allison DiGiovanni <allie08520@yahoo.com> wrote:
Diane We had our IEP meeting and they do provide transportation, just not an aid unless you have a medical need. Just becuase my son can not speak according to the district it does not qualify for an aid. My husband and I are going to pursue this. We will see where it gets us. Thanks Allison --- Diane Lang-LaMorticella <dianelanglamorticella@yahoo.com> wrote:
> Allison, You should DEMAND a IEP meeting to get > this worked out. They want you to take over the > transportation to save them the money!!! You > should also keep track of the mileage, I have heard > that if the township makes you drive, that they have > to reimburse you for the mileage. Use a
reason, not > a want, to communicate the need for a bus aide, ie > if you child has speech problems and cant > communicate with the bus driver, then a bus aide is > needed!!! In Montgomery, they just voted on a $57 > million dollar budget for the next school year, so > it's not that they dont have the money, that is > BOLONEY!!! They are also required to provide > transportation, It needs to be stated clearly and in > detail in your child's IEP. I hope it works out > well for you and your family! Diane > > Allison DiGiovanni <allie08520@yahoo.com> wrote: > Kim > Thanks for responding that is what I am being told. > We have no medical reason, so I guess I will be > driving my son, as I do not think a bus driver can > do > both jobs. > Allison > --- Kim Szeremeta <three2many2000@yahoo.com> wrote: > > > Allison, > > The only way the district will put an aide on the > > bus is through your IEP. You have to have it > written > > in your IEP an it will have to be a good reason, > not > > just because your child is young and you would > feel > > more comfortable knowing someone is taking care of > > them on the bus ride to school. Most school > > districts won't buy that, I believe every school > bus > > should have an aide on the bus, it should be the > > law, but it is not. It is absurd to think the bus > > driver can do both jobs. Good luck. > > Kim > > allie08520 <allie08520@yahoo.com> wrote: > > I was wondering does anyone know for sure, > > are aides or monitors
> > required on buses for the preschool disabled > > programs? > > We are being told by our district that they do not > > have aides, but it > > sounds absurd to us. Any answers or where I can > turn > > to find this out > > for sure? > > Allison > > > > > > > > > > > > > > --------------------------------- > > Get the free Yahoo! toolbar and rest assured with > > the added security of spyware protection. > > __________________________________________________________ > Moody friends. Drama queens. Your life? Nope! - > their life, your story. Play Sims Stories at Yahoo! > Games. > http://sims.yahoo.com/ > > > > > > >
> --------------------------------- > Ready for the edge of your seat? Check out tonight's > top picks on Yahoo! TV.
__________________________________________________________ Bored stiff? Loosen up... Download and play hundreds of games for free on Yahoo! Games. http://games.yahoo.com/games/front
I was told from my EI experience last fall that the state used to provide audiology exams, but since state funds are low, they've eliminated that luxury. However, I do know that the audiologist at Summit Speech School is not only excellent, she works with special-needs toddlers on a daily basis. She seems to know what's behavioral "not listening" and what's actual hearing loss. She is worth the out of pocket expense. Did you go through your insurance co. yet?
good luck.....
~Tracy
To: Care-to-ShareSupportNetwork@yahoogroups.com From: dianelanglamorticella@... Date: Sat, 23 Jun 2007 07:00:43 -0700 Subject: [Care-to-ShareSupportNetwork] Audiology Exams???
Hi Everyone, I have heard that the EI kids can get an Audiology eval once a year from Summit Speech School. Does anyone know if this sounds correct? Of course, I did NOT find this out from my "service coordinator" my son has had problems on his audiology exams, and we have a good ENT for him, but I have heard that the audiologist at Summit Speech School is very thorough, and does a really good eval. I will be calling my "service coordinator" on Monday, and let her know that my son needs this, I guess she didnt hear me tell her that he has already been diagnosed with some mild hearing loss!! Gee, I only told her in December, and I told the two women who did his EI Eval on March 1, I have also given them copies of his previous audiology evals. DING, ring the bell, the next boxing match will begin!!! thank God I have the strength and a big mouth to use for my son!!! LOL I hope everyone has a great weekend! Diane
Allison DiGiovanni <allie08520@yahoo.com> wrote:
Diane We had our IEP meeting and they do provide transportation, just not an aid unless you have a medical need. Just becuase my son can not speak according to the district it does not qualify for an aid. My husband and I are going to pursue this. We will see where it gets us. Thanks Allison --- Diane Lang-LaMorticella <dianelanglamorticella@yahoo.com> wrote:
> Allison, You should DEMAND a IEP meeting to get > this worked out. They want you to take over the > transportation to save them the money!!! You > should also keep track of the mileage, I have heard > that if the township makes you drive, that they have > to reimburse you for the mileage. Use a reason, not > a want, to communicate the need for a bus aide, ie > if you child has speech problems and cant > communicate with the bus driver, then a bus aide is > needed!!! In Montgomery, they just voted on a $57 > million dollar budget for the next school year, so > it's not that they dont have the money, that is > BOLONEY!!! They are also required to provide > transportation, It needs to be stated clearly and in > detail in your child's IEP. I hope it works out > well for you and your family! Diane > > Allison DiGiovanni <allie08520@yahoo.com> wrote: > Kim > Thanks for responding that is what I am being told. > We have no medical reason, so I guess I will be > driving my son, as I do not think a bus driver can > do > both jobs. > Allison > --- Kim Szeremeta <three2many2000@yahoo.com> wrote: > > > Allison, > > The only way the district will put an aide on the > > bus is through your IEP. You have to have it > written > > in your IEP an it will have to be a good reason, > not > > just because your child is young and you would > feel > > more comfortable knowing someone is taking care of > > them on the bus ride to school. Most school > > districts won't buy that, I believe every school > bus > > should have an aide on the bus, it should be the > > law, but it is not. It is absurd to think the bus > > driver can do both jobs. Good luck. > > Kim > > allie08520 <allie08520@yahoo.com> wrote: > > I was wondering does anyone know for sure, > > are aides or monitors > > required on buses for the preschool disabled > > programs? > > We are being told by our district that they do not > > have aides, but it > > sounds absurd to us. Any answers or where I can > turn > > to find this out > > for sure? > > Allison > > > > > > > > > > > > > > --------------------------------- > > Get the free Yahoo! toolbar and rest assured with > > the added security of spyware protection. > > __________________________________________________________ > Moody friends. Drama queens. Your life? Nope! - > their life, your story. Play Sims Stories at Yahoo! > Games. > http://sims.yahoo.com/ > > > > > > > > --------------------------------- > Ready for the edge of your seat? Check out tonight's > top picks on Yahoo! TV.
__________________________________________________________ Bored stiff? Loosen up... Download and play hundreds of games for free on Yahoo! Games. http://games.yahoo.com/games/front
Tina, I have found another local support group for families of those affected by Hydrocephalus. "Hydro" for short, is a condition where there is too much fluid (Cerebro spinal fluid) in the brain, part of my sons medical issues include a form of this, where the fluid is not in the ventricles, but in the external layers of his brain. We were very lucky, he has not needed surgery or shunts put into his brain for this. Could we include a link to this group on the Care to SHare site?? We have a lot in common, these children have developmental delays, and usually need combined types of therapies like you have worked so hard to get for your son. I'm looking forward to seeing you on Thurs nite, my best to your husband too. Diane
This support group will be meeting on the third Saturday of every month.We will be sharing information and support for children (and their parents) diagnosed with hydrocephalus.Children are welcomed. There will be guest speakers and available information for parents.
Parents may enroll in the group by contacting Nancy Vassallo, RN at 732-321-7000 ext 65362, or e-mail us at CNC@.... Our monthly mailing will update the group with scheduled events. Meetings will be hosted by:
The Children’s Neurological Center
A Division of The New Jersey Neuroscience Institute
At JFKMedicalCenter
65 James Street
Edison, NJ08818.
We look forward to meeting parents at our next support group on
July 21, 2007.
10:00am-12:00noon
Please RSVP by June 8th to Nancy at the phone # or email listed above, or to Kim Illions at kai0424@...
Hi everyone,
I had the pleasure of speaking with Tina this afternoon and she
encouraged me to join this support network as a professional. I have
worked with children with Autism for 9 years. 5 of which have been in
Hillsborough's public schools as a teacher. I am looking to start my
own ABA therapy business in September. Please feel free to contact me
if you are interested in therapy for your child:908-334-8279.
Robin Pidany
Enjoy, this is funny!!! We will have to get the research going on that asteroid/ hemorroid problem!!!! HA HA LOL LOL Hey, I just fixed it, If I LMAO, I dont have either one anymore!! Hey, I'm a genius!!
Jessica Rockey <rebelangel1980@...> wrote:
Date: Sat, 23 Jun 2007 19:43:54 -0700 (PDT) From: Jessica Rockey <rebelangel1980@...> Subject: Fw: Fwd: Very thought provoking and funny To: lissa stine <badassrebelgirl81@...>, diane lang-lamorticella <dianelanglamorticella@...>, laura loner-rutkowski <atrophoenix@...>, adam rockey <adarock@...>, ali hall <shubiehall830@...>, marilyn allen <mallen426@...>, bruce kirkland <Ubstoney@...>, Eden michael Gibbs
<drgnprnc13@...>, Missy Robinson <jailnurse3643@...>, jennifer <wildcatfan@...>
----- Forwarded Message ---- From: "marilpau@..." <marilpau@...> To: rebelangel1980@... Sent: Saturday, June 23, 2007 8:05:54 PM Subject: Fwd: Very thought provoking and funny
-----Original Message----- From: cfischer1 To: Marilyn Pautz ; Janet Nelson ; Sandy Neidig ; Chris J Neidig ; kim wykoff ; Patti Gardner ; Ellen ; Barb ; richard ball Sent: Sat, 23 Jun 2007 3:20 pm Subject: Fw: Very thought provoking and funny
Hi Everyone, I have heard that the EI kids can get an Audiology eval once a year from Summit Speech School. Does anyone know if this sounds correct? Of course, I did NOT find this out from my "service coordinator" my son has had problems on his audiology exams, and we have a good ENT for him, but I have heard that the audiologist at Summit Speech School is very thorough, and does a really good eval. I will be calling my "service coordinator" on Monday, and let her know that my son needs this, I guess she didnt hear me tell her that he has already been diagnosed with some mild hearing loss!! Gee, I only told her in December, and I told the two women who did his EI Eval on March 1, I have also given them copies of his previous audiology evals. DING, ring the bell, the next boxing match will begin!!! thank God I have the strength and a big mouth to use for my son!!! LOL I hope everyone has a great
weekend! Diane
Allison DiGiovanni <allie08520@...> wrote:
Diane We had our IEP meeting and they do provide transportation, just not an aid unless you have a medical need. Just becuase my son can not speak according to the district it does not qualify for an aid. My husband and I are going to pursue this. We will see where it gets us. Thanks Allison --- Diane Lang-LaMorticella <dianelanglamorticella@yahoo.com> wrote:
> Allison, You should DEMAND a IEP meeting to get > this worked out. They want you to take over the > transportation to save them the money!!! You > should also keep track of the mileage, I have heard > that if the township makes you drive, that they have > to reimburse you for the mileage. Use a reason, not > a want, to communicate the need for a bus aide, ie > if you child has speech problems and cant > communicate with the bus driver, then a bus aide is > needed!!! In Montgomery, they just voted on a $57 > million dollar budget for the next school year, so > it's not that they dont have the money, that is > BOLONEY!!! They are also required to provide > transportation, It needs to be stated clearly and in > detail in your child's IEP. I hope it works out > well for you
and your family! Diane > > Allison DiGiovanni <allie08520@yahoo.com> wrote: > Kim > Thanks for responding that is what I am being told. > We have no medical reason, so I guess I will be > driving my son, as I do not think a bus driver can > do > both jobs. > Allison > --- Kim Szeremeta <three2many2000@yahoo.com> wrote: > > > Allison, > > The only way the district will put an aide on the > > bus is through your IEP. You have to have it > written > > in your IEP an it will have to be a good reason, > not > > just because your child is young and you would > feel > > more comfortable knowing someone is taking care of > > them on the bus ride to school. Most school > > districts won't buy that, I believe
every school > bus > > should have an aide on the bus, it should be the > > law, but it is not. It is absurd to think the bus > > driver can do both jobs. Good luck. > > Kim > > allie08520 <allie08520@yahoo.com> wrote: > > I was wondering does anyone know for sure, > > are aides or monitors > > required on buses for the preschool disabled > > programs? > > We are being told by our district that they do not > > have aides, but it > > sounds absurd to us. Any answers or where I can > turn > > to find this out > > for sure? > > Allison > > > > > > > > > > > > > > --------------------------------- > > Get the free Yahoo! toolbar and rest assured with > > the added security
of spyware protection. > > __________________________________________________________ > Moody friends. Drama queens. Your life? Nope! - > their life, your story. Play Sims Stories at Yahoo! > Games. > http://sims.yahoo.com/ > > > > > > > > --------------------------------- > Ready for the edge of your seat? Check out tonight's > top picks on Yahoo! TV.
__________________________________________________________ Bored stiff? Loosen up... Download and play hundreds of games for free on Yahoo! Games. http://games.yahoo.com/games/front
Diane
We had our IEP meeting and they do provide
transportation, just not an aid unless you have a
medical need. Just becuase my son can not speak
according to the district it does not qualify for an
aid. My husband and I are going to pursue this. We
will see where it gets us.
Thanks
Allison
--- Diane Lang-LaMorticella
<dianelanglamorticella@...> wrote:
> Allison, You should DEMAND a IEP meeting to get
> this worked out. They want you to take over the
> transportation to save them the money!!! You
> should also keep track of the mileage, I have heard
> that if the township makes you drive, that they have
> to reimburse you for the mileage. Use a reason, not
> a want, to communicate the need for a bus aide, ie
> if you child has speech problems and cant
> communicate with the bus driver, then a bus aide is
> needed!!! In Montgomery, they just voted on a $57
> million dollar budget for the next school year, so
> it's not that they dont have the money, that is
> BOLONEY!!! They are also required to provide
> transportation, It needs to be stated clearly and in
> detail in your child's IEP. I hope it works out
> well for you and your family! Diane
>
> Allison DiGiovanni <allie08520@...> wrote:
> Kim
> Thanks for responding that is what I am being told.
> We have no medical reason, so I guess I will be
> driving my son, as I do not think a bus driver can
> do
> both jobs.
> Allison
> --- Kim Szeremeta <three2many2000@...> wrote:
>
> > Allison,
> > The only way the district will put an aide on the
> > bus is through your IEP. You have to have it
> written
> > in your IEP an it will have to be a good reason,
> not
> > just because your child is young and you would
> feel
> > more comfortable knowing someone is taking care of
> > them on the bus ride to school. Most school
> > districts won't buy that, I believe every school
> bus
> > should have an aide on the bus, it should be the
> > law, but it is not. It is absurd to think the bus
> > driver can do both jobs. Good luck.
> > Kim
> > allie08520 <allie08520@...> wrote:
> > I was wondering does anyone know for sure,
> > are aides or monitors
> > required on buses for the preschool disabled
> > programs?
> > We are being told by our district that they do not
> > have aides, but it
> > sounds absurd to us. Any answers or where I can
> turn
> > to find this out
> > for sure?
> > Allison
> >
> >
> >
> >
> >
> >
> > ---------------------------------
> > Get the free Yahoo! toolbar and rest assured with
> > the added security of spyware protection.
>
>
__________________________________________________________
> Moody friends. Drama queens. Your life? Nope! -
> their life, your story. Play Sims Stories at Yahoo!
> Games.
> http://sims.yahoo.com/
>
>
>
>
>
>
>
> ---------------------------------
> Ready for the edge of your seat? Check out tonight's
> top picks on Yahoo! TV.
________________________________________________________________________________\
____
Bored stiff? Loosen up...
Download and play hundreds of games for free on Yahoo! Games.
http://games.yahoo.com/games/front
Allison, You should DEMAND a IEP meeting to get this worked out. They want you to take over the transportation to save them the money!!! You should also keep track of the mileage, I have heard that if the township makes you drive, that they have to reimburse you for the mileage. Use a reason, not a want, to communicate the need for a bus aide, ie if you child has speech problems and cant communicate with the bus driver, then a bus aide is needed!!! In Montgomery, they just voted on a $57 million dollar budget for the next school year, so it's not that they dont have the money, that is BOLONEY!!! They are also required to provide transportation, It needs to be stated clearly and in detail in your child's IEP. I hope it works out well for you and your family! Diane
Allison DiGiovanni <allie08520@...> wrote:
Kim Thanks for responding that is what I am being told. We have no medical reason, so I guess I will be driving my son, as I do not think a bus driver can do both jobs. Allison --- Kim Szeremeta <three2many2000@yahoo.com> wrote:
> Allison, > The only way the district will put an aide on the > bus is through your IEP. You have to have it written > in your IEP an it will have to be a good reason, not > just because your child is young and you would feel > more comfortable knowing someone
is taking care of > them on the bus ride to school. Most school > districts won't buy that, I believe every school bus > should have an aide on the bus, it should be the > law, but it is not. It is absurd to think the bus > driver can do both jobs. Good luck. > Kim > allie08520 <allie08520@yahoo.com> wrote: > I was wondering does anyone know for sure, > are aides or monitors > required on buses for the preschool disabled > programs? > We are being told by our district that they do not > have aides, but it > sounds absurd to us. Any answers or where I can turn > to find this out > for sure? > Allison > > > > > > > --------------------------------- > Get the free Yahoo! toolbar and rest assured with > the added security of spyware protection.
__________________________________________________________ Moody friends. Drama queens. Your life? Nope! - their life, your story. Play Sims Stories at Yahoo! Games. http://sims.yahoo.com/
HI Melissa, I also live in Montgomery Twp. I guess our outrageous taxes are good for something after all, LOL!!! I live near Carrier, off 601. Are you going to the meeting/social on June 28?? Maybe we could carpool? I have a minivan (of course, the typical Mom-mobile!! LOL), I will drive if you like. I wish you all the best with your child, I keep hearing via the "grapevine" that our township is pretty co-operative with IEP stuff, but, of course, we parents hardly ever get to take off our boxing gloves when it comes to our kids!! Lord, give us strength!!! Diane
Melissa Cunningham <mcunningham@...> wrote:
Our district – MontgomeryTownship automatically provides aides on all the PreK Disabled Buses. It is heaven sent b/c some kids get up out of their seats and poses danger to the driver.
Kindest Regards,
Melissa Cunningham
732-407-8238
From: Care-to-ShareSupportNetwork@yahoogroups.com [mailto:Care-to-ShareSupportNetwork@yahoogroups.com] On Behalf Of allie08520 Sent: Monday, June 11, 2007 4:20 PM To: Care-to-ShareSupportNetwork@yahoogroups.com Subject: [SPAM] [Care-to-ShareSupportNetwork] Aides on Preschool Disabled buses for Public School
I was wondering does anyone know for sure, are aides or monitors required on buses for the
preschool disabled programs? We are being told by our district that they do not have aides, but it sounds absurd to us. Any answers or where I can turn to find this out for sure? Allison
Sick sense of humor? Visit Yahoo! TV's Comedy with an Edge to see what's on, when.
Welcome to the group! We are neighbors, I am in Hillsborough and I think you will find allot of local families in the network.
Your children are older than allot of our members and I know that a few of our families who have young teens could benefit from your experience and wisdom.
We look forward to offering you the support you need and hope that you will attend some of our workshops and support meetings.
Sincerely,
Tina Rear
From: Care-to-ShareSupportNetwork@yahoogroups.com [mailto:Care-to-ShareSupportNetwork@yahoogroups.com] On Behalf Of cindy57cathy Sent: Sunday, June 17, 2007 7:45 AM To: Care-to-ShareSupportNetwork@yahoogroups.com Subject: [Care-to-ShareSupportNetwork] New Member
Hello all :) . My name is Cindy Zalenski and I live in Raritan, NJ. I have 3 daughters, aged 20, 18, and 17. My oldest is Asperger's autistic, and my youngest is "classic" autistic. I just joined your group and am looking forward to being a new member of your support group.
Tina, Thank You so much for that info!! I feel encouraged and empowered by you and the other members of Care to Share. I will try to deal with EI again through the Somerset county person, but, if I dont like the answer and if I call Shakira, I will take your advice and not tell her what you or anyone from Care to Share said. I have a friend who is a physical therapist herself, and has MS, and is a mom of four kids, and she told me that EI is so great just because they come to your home. I tried to explain to her that it is not anyone's wish to have their child need EI in the first place. It is amazing how we can take so much for granted. I hope you and your family had a terrific Father's Day! See you on the 28th! Thanks Again for your reinforcement! Sincerely, Diane LaMorticella
Tina Rear <tina@...> wrote:
Diane
One has nothing to do with the other. Since he qualified for EI in the first place means that he was delayed in two areas. Identify what they were and target those areas for therapy. They can call the
therapies anything they want. Based on what you told us about your son I cannot even phantom how they can try to justify 1 - 2 hrs a week of any therapy.
Shakira Linzey - Regional Family Support Manager - Central NJ Maternal & Child Health Consortium Mid-Jersey CARES Early Intervention Collaborative
I would not recommend that you tell her that one of us told you to call her.
Good luck.
Tina
From: Care-to-ShareSupportNetwork@yahoogroups.com [mailto:Care-to-ShareSupportNetwork@yahoogroups.com] On Behalf Of Diane Lang-LaMorticella Sent: Saturday, June 16, 2007 1:54 PM To: Care-to-ShareSupportNetwork@yahoogroups.com Subject: Re: [Care-to-ShareSupportNetwork] Misc.
information............
Hi Tina, Could you please send me Shakira Linzey's contact info? I briefly met her at a meeting, the topic was transitioning from EI to local school services, at the Bridgewater library. What is her title? Does she work for EI/ somerset county? We are getting a physical therapy consult for my son to determine his need. I was told that if we bring in a physical therapist specifically, that we would have to decrease his overall "intervention" time from 2 weekly to once a week? Apparently EI wants to provide "intervention" and keep it as broad as possible, but my sons worst delays are gross motor, he is functioning at half his calendar age in the gross motor area, the good thing is that we do see progress, but, so far EI is providing people who are not physical therapists. I like the
fact that they are doing this consultation with a physical therapist, but I dont like the idea of cutting back on his twice a week IFSP to bring in another hour of specific physical therapy. He has delays are varied, and I think the physical therapy should be done in combination with what we already have. Thanks, Diane LaMorticella na Rear <tina@caretosharenj.com> wrote:
Autism Society of Ohio's Parent Guide to Autism Spectrum Disorders
This manual
provides an overview of the world of autism spectrum disorders (ASD). It was developed by Ohio parents of individuals with ASD who have a broad range of experience with interventions, resources and services. Members from ASO, ASA Central Ohio, ASA Cleveland, ASA Northwest Ohio and Akron ASA, among others, helped to write the manual. The group's work began with the question: What do you wish you had known the first year your child was diagnosed? The manual covers a wide range of topics of interest to families, and each chapter contains rich reference materials, including books, websites and names of organizations where additional information on each topic may be obtained. It was made possible by OCALI - the Ohio Center for Autism and Low Incidence. The manual is downloadable (in full or by chapter) from the following website: http://www.ocali.org/family/fs_res_guide.php For more information, please contact Barbara C. Yavorcik, President, Autism Society of Ohio, at askASO@autismohio.org.
Welcome to the Family Center on Technology and Disability. The Department of
Education’s Office of Special Education Programs (OSEP) created the Family Center on Technology and Disability (FCTD) to provide current and accurate information about assistive technologies (AT) to organizations that work with the families of children with disabilities. The Center is administered by a partnership comprised of the Academy for Educational Development (AED), the Alliance for Technology Access (ATA), and the Parent Advocacy Coalition for Educational Rights (PACER Center), the Center for Assistive Technology and Environmental Access (CATEA) and InfoUse, Inc.
There are currently more than 2100 organizations in the FCTD Knowledge Network. Recently we learned of your organization and we are pleased to offer you membership in the Network.
A knowledge network is one in which participating organizations not only share information for mutual benefit, but which, together, create new information resources. Participation in the Family Center’s
network requires no financial contribution of any kind. The Center is supported entirely by OSEP.
As a member of the Network, you will receive monthly newsletters, information about our online discussions, and other resources as they are produced. We invite you to visit our site (
www.fctd.info) for more information about the Family Center and to access our searchable AT databases, transcripts of online discussions led by national AT experts, inspiring AT success stories, our newsletter archive, illustrated AT glossary, and more.
We look forward to providing you with useful material concerning assistive technology. If for any reason you would prefer not to receive information from us, please let us know by sending a message to fctd@... with the word UNSUBSCRIBE in the subject line.
Eyewitness News has learned that RC2 Corp. recalls
various Thomas & Friends wooden railway toys due to lead poisoning hazard.
More on 7online.com http://abclocal.go.com/wabc/story?section=alerts_recalls&id=5393261s wooden railway toys due to lead poisoning hazard. More on 7online.com ------------------------------------------------------------------------------------------------------------------------- From former DLC PROP pres Cathy Douma.