I was just wondering if anyone might have a suggestion on what to do. I'm 35 I have been a single divorced mother for 5 years. I have a 10 year old son who has special needs I have worked in the medical area of the animal/pet care field for 14 years. Last year my sons mental issues got to the point where child care for him is no longer an option. He attends a special school during normal school hours but my job field requires longer hours. I had to leave my job. We have been living off of my boyfriend for the last year. He also has two young boys who both have special needs. He has a good job but his ex wife gets so much child support that we can hardly pay our bills, even though we have his kids at our house all the time. We have asked the courts to ease up the child support and let us have his kids more in exchange but the judge wouldn't even listen to him. He has to work so much to try and support us. I want to go back to work, I love my job and hate being at home but my son has to been the only child in order to be in any kind of childcare as other kids spark his issues. I have no family that is able to help and the few people I have found willing to watch him charge so much I would be spending most or all of my paycheck for the care. Does anyone know anything I can do or have any suggestions? I'm getting really depressed sitting here at home because I need to be able to support myself and my son.
I am a single mom I have two sons ,one typical developing an the other a special needs teenage son. We have been poor an struggling for years..but it seems to be getting tighter an tighter an harder on us. I use to think we were poor ..but everything is tighter now then ever has been. we dont have tv turned on..(no cable or direct tv no tv shows at all. We never have had cell phones ..count ever afford to have those. now adays i see poeple saying their poor but yet the whip out a cell phone an text or talk..My mouth drops open an say wow if their poor then what as i ? now adays little kids have phones an tv an so much ..parent have gas to take them to an from places. my boys we try to plan things out before leaving the house to go anywhere so to try to save our gas. or i see if they can grab a ride with someone going our direction. I have good boys..i just wish they could have one nice pressent under the tree for each of them . i hate to event put up the tree this year knwoing i cant afford to get them anything this year. usualy i get them each one thing..but this year.. i jsut dont see how i will be able to . I been helping people clean their homes ect.. but thats going towards rent an utuilites..an gas for vehical. I hear things will get worst before better with econimy ..oh dear.. lets hold on to our seats i think its going to be a rough ride ,.,.eekkk.
Barack Obama, US President; Beverly Perdue, Governor of North Carolina; US Senators from North Carolina: Kay R. Hagan, Richard Burr; US Representatives from North Carolina: Brad Miller, David E. Price, G. K. Butterfield, Heath Shuler, Howard Coble, Larry Kissell, Melvin L. Watt, Mike McIntyre, Patrick T. McHenry, Renee L. Ellmers, Sue Wilkins Myrick, Virginia Foxx, Walter B. Jones; ------------------------------------
I am desperate and have no where else to turn. I will present a synopsis of my situation, I am not offering a justification for my circumstances, merely an explanation and a plea for rectification of this matter.
I am a single mother. I work hard and receive no public assistance. I have an 18 year old son, of whom I am legal guardian and sole provider. He has been diagnosed ADHD, Bi-Polar, OCD, Autisim, Personality Disorder and MR. These diagnosis has affected Zach, and myself, negatively in so many ways. All of the information I am provding may be confirmed if need be or you could refer to SSI application which has lengthy documentation.
I applied on July 21, 2011 for disabilty benefits for Zach. I provided every documentation requested and also other information I felt may be beneficial for his case. On September 8, 2011, I called the office of Social Security to inquire as to what the status was regarding his claim. At that time, I was informed that medical records from Dr. Susan Ferrell's office had not been received, I contacted Dr. Ferrell's office and had them refax the medical records. I called on September 23, 2011 and was told he may need IQ testing, she thought not but she would notify me via mail within one to two weeks if he did require IQ testing. Testing was obtained within last year (sent to SS) and his score was 58. Zach was diagnosed with the variety of special needs since he was apx. 3 years old, requiring numerous meds and testing every aspect of his lack of capabilities. At that point, I had not had any communication with the SS office advising needed addtional testing since September 23rd when I last called. October 5, 2011, I called SS office and I am informed that all medical records had been received but they had not been written up nor submitted to doctor. Also, called Disability Examiner on October 5th, I left a message informing the examiner of the dire financial need that Zach was experiencing and the monies that had to be paid by myself for insurance, medications and visits to his team of doctors. I inquired in my message was there anything that I personally do to speed up this process and ask that she please return my call, she did not return call nor have any sort of communication to me. October 14, 2011 at 8 AM and was told couldn't tell what claim status was and that the disabilty examiner would be calling me promptly regarding Zach's claim, again, no phone call or communication on her part (Disability Examiner-Chiqueta Wilson, phone 800-887-0821,ext. 6226).
If Zach is not promptly approved for SSI and the Medicaid that comes with it, I will be forced to terminate his school enrollment so that he would be eligible for Medicaid. Zach's medications are numerous and there is no way I can pay for these out of pocket. His medications, mental health appointments and monitoring drugs now taken due to the quanity and adverse affects are vital for Zach to maintain any sense of normalancy in his life, without them, he is uncontrollable and dangerously impulsive, becoming a danger to himself and others.
I am pleading with you, please don't ignore my cries for help enabling Zach to become just another statisic.
Receiveing calls on my job jepordizes my position and maintaining consistent employment is mandatory since there are no other forms of financial support in my home. Due to this factor, I authorize my sister, Deborah Collins Booe (336-331-3985) to discuss this matter with you as well as relay information to you. I am so desperate for Zach at this point it is disheartening, I have been his only advocate since we began this journey and now that he is reaching another milestone in his life (becoming 18) we still continue to struggle in obtaining reasonable expectations from the government.
I look forward to hearing from you soon. I appreciate the opportunity to address my concerns with you and for the prompt, positive input that I trust will be forthcoming.
in response to smeenatchu...whoever you are, you keep changing your name as mine stays the same at every site. Yes, I have now gotten my third grandson who many people online do know about. Mind your own business and sounds like you need alife of your own. Why does your name change at each site?
Why do you follow me from site to site are you jealous or just that bored with your own life. My life is nothing to be jealous of believe me. lol Yes, I admit I do beg, I do it out of love. Please get a life dear.
What if your child is in college or 12th grade and drives themselves from home to school should the public school and the college reimburse me for the money I have to pay for gas and travel? Also, Do you know where I can get an advocate for myl chlid in SanBernardino and Riverside County? Also, how can I find out what resources I can get for my children through an IEP? Tx BPP
Hello everyone I am new here I need advice and information oh how to get health insurance I find out on yesterday that due to my daughter being 18 I am no longer eligible for Medicad right now I have the pink eye and cannot get my prescription refiled no insurance I did get my over the counter drops.
I was not informed I was losing my Medicad and to me my worker she was being smart aint funny lady so please all the information on how to get some insurnace free clinics etc I live in Roanoke,VA
in response to bluemom...You are welcome . I am on the net a lot with my emails, friends, looking for part time work, and was just going to take a break. I leave computer on while I take a nap. Getting older, I am wishing for the energy I had in my younger days. I am Just a person who helps out with information when I can.
Take care
Starshine
Hello and you are welcome. No I haven't found anyone getting grant money for special education. You can try this and see if it will help but I never used it.
in response to Starshine...Thanks for all the info, Starshine. I'll be busy looking at all of these sites. Have you ever known of anyone to be successful in getting grant money for special education? I did hundreds of hours of research several years ago and there was just nothing out there to help with my daughter's school. All the best to you.
I just discovered this website today. I'm a single mom of 2 girls. One daughter has special needs and is in her 4th year of a special school. I've been looking for work since last summer. It's almost like there's an invisible black ball against me. I work very part-time and have even looked online for opportunities or work from home. I have sold all of my silver and gold to pay bills. I've also listed dozens of items on craigslist for sale in order to pay bills. I have no family for 1500 miles. In order to pay for my daughter's school, I have spent almost all of my retirement money. I need help with either finding some work, work from home and paying my bills, which are coming up next week - rent, etc. I worked for over 25 years in my field and have always supported myself. Now I'm faced with this situation where I just want to get my daughter through her last 2 months of school this year and I owe money for her tuition. I've thought of every possible way to gain funds to stay afloat. I had emergency eye surgery in November and need to figure out how to pay the multiple bills for that.
Hello I am tested 2 just joined on my daughters 18th birthday she is a special needs teenager I have been going through a lot last 2 weeks she was born with Trismony Downe's Syndrome at birth as of last week she now has grand mal seizures she has had 2 in school one the lifesaving had to be called her one on one aide rode with her Monday.
She has missed days of school last 2 weeks trying to get various things straighten out she just started her seizure medicine Wednesday went to school today and yesterday did good now I watch her more then ever then on top of this Sunday I had to ask my boyfriend to move out he was demanding I wanted to contiune to go with him but he said once a woman says that that is it but he calls i do talk to him he has said he wonts to move back in asked could he spend the weekend that is another story well if any of you have any information I wont to see if she can someone told me SSD please send me all the information and how to go about that that as soon as possible
Hello and I read your post. Like many here but some worse than others you have been through so much. I hope the test come back saying you don't have lymphoma that would be a great Christmas gift. For you son for Christmas you can try this and see if you can get help there for Christmas for him.
Hello, Happy holidays to everybody that is kind and loving enough to read this,also to the others that somehow found themselves on the other end of the Holiday giving tradition. For years I found myself giving during the holidays(only usually) except for St. Jude,But it has recently dawned on me that I really should have given year round,even though it may not have been much,It would've for sure helped somebody. My son is 8 yrs. old now and has special needs,For years the Doc. and the school system have changed his diagnosies at least 5 times,very fustrating,Iv'e come to the conclusion that my son has mild Asburger's syndrom,He has a diagnosies of Cognitive Impairement, I really don't care about what it's called anymore, I focus on getting him the education and compassion he deserves,My little angel is in a Life Skills class and he is finally making the friends he so lovingly deserves. I'm not really sure if the stress of my husband being unemployed for 10 yrs. and loving and caring for a special needs child but the past 2 yrs. Iv'e had several surgerys,7 days in the hospital when I contracted a staff infection from my job, hours of surgery later I went home only to be out of work for another 2 weeks, then tumors on my uterus,In Feb. of this year I had a hysterectomy, I'm 37 now but it still was a low blow,Please understand I'm not complaining entirely because I know others aren't lucky enough to recover like I had,BUT.. Recently there were 2 lumps in my throat and after a CAT Scan they aren't sure what to make of it, I need another Cat Scan, after 8 weeks of antibiotics the lumps grew, they think lymphomia??? I pray to God if it is I'm early enough! My little boy needs me,that's what I WANT 4 CHRISTMAS..But because of my constant time off work and being basically black balled from one of my jobs for needing time off and apparently the other employee's didn't think it was fair,I have failed to keep up on some,well on all of my bills. I AM PRAYING that there maybe could be some help for Christmas for just a gift or 2 for my son,my son deserves it,really he does,he is the most compassionate person I know,I would never change him even if I had a free wish. My son loves the simple things,Lego's, board games,sorry sliders,perfection,roller blades,He wouldn't care,and neither would I. If someone actually get's through this book,God bless you. Thankyou from our hearts to your's. ALWAYS THANKFUL!
in response to marie t...This sounds very similar to what we are going through right now. My son was suspended for 10 days in Fauquier County and has been referred to the Southeastern School in the county. I would like to talk with you in more detail. My son also hit a girl on the bottom and it was documented as sexual harassment. We've decided we are going to fight this one. The school has drawn a line for our son that is not reasonable for any child.
in response to marie t...http://www.doe.virginia.gov/special_ed/regulations/state/procedural_safeguards/english_procedural_safeguards.pdf
DO NOT do an IEP by phone. DO NOT sign anything that you don't agree with. If you sign an IEP and don't agree you have the right (and should) to write out why you disagree and what you want changed or added. MAKE sure they include a behavior plan for him. TRY to get an advocate to help. Search for one online. There should be a advocacy group that may at least point you in the right direction.
This site is great so check the whole thing out... you may even find your answer if you search their site... it's where I started. This link goes to your state but check their home page too:
http://www.wrightslaw.com/virginia/regs.index.htm
http://www.yellowpagesforkids.com/help/va.htm
A whole list of advocates in your state. They may be able to help you for free and if not maybe tell you who can.
HELLO MY NAME IS TINA AND MY CHILD HAS ADHD HE ALSO HAS AN IEP I'M LOOKING FOR AN ADVOCATE FOR HIM. I LEAVE IN VIRGINIA FAUQUIER COUNTY. MY SO TRANFERD FROM ANOTHER SCHOOL AND HADE HIS IEP FROM THAT SCHOOL. THE NEW SCHOOL THATS HE IS AT HAS NO IEP IN PLACE. MY SON WAS SUSPENDED FOR HITTING A GIRL ON THE BOTTOM AND PUSHING ANOTHER CHILD PLAYING. HE IS OUT FOR 10 DAYS WITH LONG TERM WE APPEALED THEY CALLED USE BACK TODAY AND GAVE HIME UNTIL THE END OF THE SEMESTER AND THEY WANT HIM TO ATTEND AN ALTERNATIVE SCHOOL WHICH IS REAL BAD FOR A CHILD WITH ADHD. BUT NOW THERE CALLING TRYING TO GET US TO DO AN IEP FOR HIM BECAUSE THEY SAID THAT BECAUSE OF LEGAL REASON THEY HAVE TO HAVE AN IEP IN PLACE. BUT THEY PUT HIM OUT OF SCHOOL!!!! HE ALSO HAS A BEHAVIOR PROBLEM WHICH THEY KNEW ABOUT FOR HIS IEP FROM IS OTHER SCHOOL BUT THEY DIDN'T IMPLIMENT HIS IEP I REALLY DONT KNOW WHAT TO DO TRYING TO CALL SCHOOL BOARD OF EDUCATION MY SON NEEDS WERE NOT BEING MEET BUT THEY USED HIS PAST BEHAVIOR PROBLEM TO PUT HIM OUT OF SCHOOL AND CALLING LIKE CRAZY FOR US TO DO AN IEP OVER THE PHONE.PLEASE LET ME KNOW WHAT I CAN DO OR SOMEBODY THAT I CAN CONTACT.
I've already done that. There is nothing infectiious on my pc. I have no spyware, no malware, nothing. I have no viruses. (I have Kaspersky which does a really good job and this is the first time in all my years online I've had this issue). When I was having issues posting on the old browswer it was suggested I use a new browser. I downloaded Firefox and the first few days were great, but now I'm back to having issues. I've clearned caches, I've done everything humanly possible on this end and it's not my pc. I have no idea what it is to be honest. So yes, I guess I was "complaining", but not without trying to be proactive and find a solution. What else should I try?
Anora Eldorath, I'm sure people from AidPage Team are actually trying to help you. Perhaps it is matter of misunderstanding, but 'It is only you' doesn't mean 'you are not welcome here', rather more obvious conclusion - perhaps there is a malicious software running on your PC and it is creating these problems for you.
Looking at you recent posts it is obvious that there is additional text in the end, that appears as a piece of code and I'm rather sure you are not typing it by hand. This is just the visible side effect. Most likely there also hidden control characters that affect your pages.
AidPage system is constantly automatically checking for such anomalies and errors and if spotted and cannot be fixed it will be deleted. That keeps the system healthier and better working for all of us.
In any case this is not a thing to complain about, but a situation where you or some helper should check your PC for viruses and malware.
I forget to breathe too and shallow breathing doesn't help. I know all about Mercury as it is the ruler of my rising sign, and in my midheaven and when mercury goes retrograde all things mechancal go and communications go astray..I wouldn't sign the papers on the only new car I bought till mercury was out of retrograde!!! I use to be really into astrology as I have tapes, books and two charts done somewhere here..As the old saying goes take it easy ....
Thanks hun. I'm trying to remember to breathe. I'm just a tad stressed over it. I think it's the weather though to be honest. It's dark and gloomy and I've been a bit more sensitive then most times. I think Mercury is still active so that may very well have something to do with it.
in response to Anora Eldorath...If they didn't say that then just forget the coding stuff and move on and do what you do here. One lady here had an add on here sight for a company she googled to helps someone out..I think like a past post office friend told me don't take things to personal..Come on try again Anora. Things are just real stressful for you, me and many others here. take it easy ok???
No, they didn't tell me that. They said I was the only one experiecing any sort of technical issues here on Mylot. I'm taking that very personally today. I'm very frustrated that my work since 8am this morning is now being called into question, that there is some sort of coding that I dont even know what it is. Their note to me was accusatory but then again I suppose they don't know when people are legit. I took their note to me very personally because I work very hard to provide links to help people find the aid they need. I put in eight hours every day to try to help people via the pc.
in response to Anora Eldorath...What!! You mean they told you, you aren't wanted here?? I don't understand...I don't think they would tell you that and why would they??
in response to Starshine...I think I get it. I'm not wanted on Mylot! The answer for the last week from the Aidpage Team has been "It's only you", so I get it-I am not wanted. Hopefully they will give me time to copy all of my writings so I don't lose them! I'll just have to move everything to my personal blog and give up trying to use this with my adsense! (Which by the way is supposed to be completely legal according to Aidpage who sents up payment through google adsense!)
You know, I've been noticing that as of late and I have no idea what it is to be honest. Maybe aidpage will figure it out. All I've done is use the link insert button.
HEllo I have a 17 year old teenage daughter born with Downe's Syndrome at birth she will be a senior this school year I am in need of jeans a size 18 maybe 19 in Juniors I need some long sleeve tops for cool mornings or tee shirts that come down to her elbow I would appreciate also any information on what websites I can go to also.Thanks to everyone and God bless
Hi I am shyshy 471 on here I am a single mother of a 17 year old downes syndrome teenager Brittany and I have had a long hard journey together she is also adhd which she takes medicine for that Brittany has been in the Easter Seals Program the Chip Program she graduated from the Easter Seals Program she started preschool through Roanoke City Pulic Schools when she was 3 years old in the Reach Program attending Grandin Court Elementary School then being moved to Roanoke Academy School which was closer to her home she graduated from the Reach Program.
Brittany and I have worked and still do a lot of agencies she participates now in the Community
Services Program through Blue Ridge Behavorial services goes out on Thursdays due to funding issues that will end July 30.2010 She graduated from elementary school in June 2004 has attended Addison Middle High School Currently attending my alma mater Patrick Henry High School Brittany will be a Senior in the Fall of this year wheter I let her graduate this year or go for a couple more when that day comes I will sure be one proud mom I have had help from family also this is not easy never will be but when I wont to give up I look around at all her certificates all the programs she has been in and say look how far you have brought her.
Brittany likes to swim listen to music watch tv play basketball which she played for a while on her classmates mother's team in 2005 I just wanted to let my aidpage members know what is like to be a single parent raising a special needs daughter God Bless You All shyshy 471
The school district is dying and things like this will not help it. If my kids can't get the correct special ed services then they don't need to be in this district. There isn't busing for schools out of neighborhood, there are teachers at John Lodge that still use corporal punishment at the Kindergarten level, the special class like art are non existent and the teachers don't have what they need to teach as they should. Yet people wonder why kids leave the system, drop out, or are graduating unable to read. Something has to be done to save our community, our schools, our children and our future.
I read this in a public letter that was sent out as well as posted online and I felt compelled to do some research, as a response letter was not yet posted. (I'm guessing not enough time has passed, nor do I know if the parent actually sent the letter or just posted it online).The parent was concerned because their child was denied ESY, which means Extended School Year. They basically stated in their letter that it was because the district claimed to be out of money and were told not to provide the service. The problem is, districts generally don't make their decisions like that based upon money it is based upon the ability of the child. If the child does not need the extra help (and there are criteria for this) then it makes no sense to have a child come for extended school year help. However, most know me and I had to dig up records.
The above link is for the report which states that the funding for the current school year would stay the same. Meaning, there should be funds available. (Their own documents).
The above link is a memo put out at the end of last school year, which means it would be effective for this school year as to how ESY is chosen in the state of Michigan.
Now, in terms of the allegations of corporal punishment at John Lodge, I cannot find any school in the Michigan system with the name of John Lodge. I've found a street name located in Detroit, but no actual school district, or name. As a teacher reading this particular letter (I didn't cite the entire letter as this was the portion that stood out, I feel that perhaps the school was not listed to protect the child involved, but it's a pretty serious allegation especially when I cannot find anything that states schools in Michigan still use corporal punishment. I know that perhaps there are individual schools that perhaps have it written into their code of conduct, but in the states I've resided and taught typically a parent must give written permission for the school to use corporal punishment. If they parent does not allow it, the school will not use it.
So, if you reside in Michigan and are having issues with special education services, use the following links as evidence of the monies available in your district. You do have a right to appeal any decision made during an IEP meeting, and you do have a right to request further services for your child. If you are having issues with a district, the best thing to do is get an advocate.
The following links are advocacy groups in Michigan that can help you get the aid you need for your special needs child: http://www.causeonline.org/
A friend sent this out and gave me permission to post it here. Thank you Dee.
In response to so many messages and comments about schools, I wanted to address some of them in a blog so everyone benefits from it as well. I know I post this kind of thing a couple times a year at the least, but it's an ongoing battle and something we as parents need to be aware of.
First of all, if you do not have an advocate for your child who is on and IEP, please get one ASAP! As I have stated so many times before, you would be blown away by what the schools CAN actually do and how much IEP funding they are receiving PER CHILD. I know because I have been there! I have been to meetings and we sit and pull straws as to what to do until the very obvious feeling that the school is giving up on your child overwhelms you.
If I only knew then what I know now, my son would not have fell behind! When the district acts as if they have the child's best interest at heart, yet are doing nothing to accommodate to their Individualized Education Plan, what is that saying about the district? It's all about money, this is true.... But these schools are funded through the government based on the disability, severity of the child. The school administration does not want parents to know this either! Trust me on this.
It's not the teachers, it's the administrative, the "business" end of the school. Your teachers are in a catch 22 so to speak.. They know what's best, yet they cannot put their jobs on the line. The information that I have been told by not one but several teachers and school staff over the years, all in "secret" would blow your mind away. Finding my own advocate was the best thing I ever did. I have actually had a principal try to silence me for giving this information to another parent in the school only weeks ago. As I touched base with my own advocate, I was informed that I was very correct and she was 1. mislead or 2. shutting me down. If you wish to know the exact amount a school district is receiving for your child and a generalized view of where it's being spent on your child, YOU HAVE THE RIGHT TO KNOW THIS! You can get it through the department of education! It's your right to know and no school will tell you this.
My advice? Stay focused, keep mental and written notes of everything, never let the school put anything back on you! It's THEIR responsibility to educate your child!! That is your child's legal and entitled right, to receive a proper education! Do work with them, but use common sense within reason. Know your rights and the rights of your child. If you feel the walls closing in, call a meeting. Bring your advocate to the meeting, not an advocate appointed through the school district either.. They work for the schools best interest, not your child's. So make sure your advocate is a good one and from an outside source.
I can help you find an advocate in your area or you can contact www.autism-society.org to get in contact with the Autism society in your area, who will assign an advocate to you.
Sometimes we as parents need a backup of force to make things happen for our kids. You are your child's biggest advocate! No one will fight for your child harder than his or her own parents! I have read some true horror stories from some of you about some schools. First, get an advocate then in the most extreme rare cases, if need be get an attorney who specializes in special education and IEP laws. I have quite a bit of information on the ugly side of this as well considering my own sister about sued her sons district and was informed by her advocate she had a sound case on that specific issue. Needless to say, the principal of that district lost their job and the school was fined heavily through the department of education. Things have since worked out for her. Some will fight you harder, but most fall into line rather quickly when you bring an advocate to the table. Don't wait until you start having trouble, bring them in when all things are "good". You deserve that back up.
One other thing, if your child is on and IEP and you transport your child to school, something many parents do not know is the school district must pay you for your travel to and from school for every day your child attends.
Anything your school puts on YOU that pertains to the child's education and is based in the IEP, they MUST reimburse you so keep your receipts. And do know that by law, you do not have to cater to the school when they are requiring something of cost. When something is worked into a child's IEP plan, it's the schools responsibility to pay for it. Of course they would like to push it off on you.... But they owe you if they do.
When the school becomes to desperate it shows. Because they become overly dependent on the parent to change any problems with that child. However, it's their responsibility to FIND SOMETHING that works, if that means restructuring the entire program designed for that child, then by law they have to. They have to find something that works or they must hand over funds to other sources of education that can help. If you don't have an advocate, they will convince you otherwise. The goal is not to trash schools, some of these districts are Excellent districts for the typical child, so it's not about degrading schools. It's about making them do what they are required to do by law and the facts are schools are ran like a business, if money is involved they will become greedy. Your child on an IEP is bringing a nice chuck of cash to that district, so they need to use it for YOUR child.
If you need help or more information, I will do my best to help you out. But I advise you, get an advocate!!! Save yourself the headaches... You will be so grateful you did! :)
Special Education Resources on the Internet is a wonderful tool for parents of a special education child. It can be overwhelming and this website seems to have a great deal of sources at your finger tips.
Education World is a website I've been using for years. This is the link for the special education community that has a variety of resources for parents and educators.
Pacer is a Minnesota based organization for parents and students with special needs. I've had the chance to meet with them before and they offer some wonderful help and resources locally.
I thought I'd tell you a bit about why I'm here. I would like to offer whatever kind of help I can. Since money is tight here and my biggest resource is the time I spend on computer this blog will be my biggest donation.
I will be posting resources on everything I can... information, jobs sites I know to be real jobs, free stuff you can use, educational stuff, parenting, what ever I can find. And not just for the local area (Michigan) but anywhere I can gather reliable information from.
I welcome any post that you can add. If you know of a good resource or a tip on how to.... then please feel free to either share it here or direct people to it.
I will also be blogging about the trials we are facing, the tricks I've come to learn, and what ever else I can think of.
So come around often and share awhile. And welcome to the village. Remember that it takes a village to raise a child, care for a parent, and to help you through. And the village is world wide.
"This registration Web site allows residents with special needs and their families, friends and associates an opportunity to provide information to emergency response agencies, so emergency responders can better plan to serve them in a disaster or other emergency"
Please take a minute to learn how we have come to a time of need and how you can help us overcome this hurdle to move on with our mission....making as many open doors and opportunities for our very special and beautiful daughter, Denae. Thanks. God Bless.
By kragoots - on Aug 15, 2007... modified on Aug 15, 2007
Posted in kragoots
My son has Asperger's Syndrome. He has been accepted to attend a very special school for kids with NLD and AS (a form of austism). It costs $65,800 a year to attend. He has struggled for 14 years in the public school system, and it has been a horrible experience. He is a very creative, intelligent person who has a bright future if he can complete his high school years at this school, Franklin Academy in East Haddam, CT. He needs to go for two years. After that it is his goal to go to college and contribute to society in a positive way. We have put our house on the market and are going to sell it to pay for the first year at F.A. We need help with the second year. Please help and thank you so much!
We are parents of a small child that needs extra help with his education. My husband was fired from his job. Then the IRS announced that our refund would not be forthcoming. We need $15,000 to pay our taxes and insurance and to get a tutor for our child. We are taking care of our mentally challenged older son who is unable to get disability payments right now. Our son has tremendous needs that must be met. We need help fast as our taxes are due. Please help any donations are welcomed.
Here since: Jun 22, 2009
Female, 53
Jen of all trades
Springfield, MO, US
Languages: English
Hi all. I'm fifty years old. I've been divorced about 10 years. I'm a single parent of 2 daughters. The eldest is 21 and about to start college. The youngest is 11, and she has asperger's syndrome, wh... see full post
I am married with a working husband. We have four children; two of them are young adults and are trying their best to go to school and fun themselves. The younger two are 12 and 13. The 12 year old... see full post
Here since: Oct 9, 2006
Female, 38
Home School educator/ Writer
Aspergers Puzzles Peel -Autism Solutions
Brampton/Mississauga, Ontario, Canada
Languages: English
October 10
2006
Asperger’s (HFA) Mom
After fighting with the school board for years and home schooling my son for
grade 3, I have now decided to open a small home based school for High... see full post
My son has Asperger's Syndrome. He has been accepted to attend a very special school for kids with NLD and AS (a form of austism). It costs $65,800 a year to attend. He has struggled for 14 years ...
I'm looking for help to pay bills. I've been seeking employment. I need a way to get some money until I get a job. I do have a car, but it's not completely paid. My main concern is making my car p... see full post
I need help with immediate expenses. Three hundred fifty dollars is the amount of money I would use to make my car payment, insurance, and gasoline. I have no safety net of ... see full post
Here since: Nov 19, 2006
Female, 2012
massage therapist
brookline, NH, US
Languages: english
Hi:
I have a special needs son who is attending a school for severe learning disabled children. My son is profoundly dyslexic, verbally dyspraxic, OCD, Asperger's Syndrome and profoundly gifted. ... see full post
