Matt Moscato Charity Golf 2015 Friday July 31, 2015.

Matt Moscato Charity Golf 2015 Friday July 31, 2015.

Friday July 31, 2015 1:00 Shotgun (lunch starts at 10:30) – Sylvan Glen

This years golf will be in support of helping Izzy to be pain free, so please help us fund her surgery.

Izzy’s problem’s all started with a 6-week battle with bronchitis and sinus infections in November of 2012. When Izzy, then 12 years old, finally began to feel better, she was left with a constant headache.  

She has seen multiple specialists, at University of Michigan Hospital, Beaumont Hospital, and Michigan Head and Neurological Institute. She went through endless tests – MRI’s, MRA’s, MRV’s, EEG’s, heart tests, constant blood work, nerve blocks in her temples, forehead, and back of her head, and even tried Botox injections. She has tried spinal taps, which always ended with a painful blood patch to try to help the additional spinal headache that would follow the initial spinal tap. All in hopes that it would break her constant headache. She tried what seemed like hundreds of medications with no results to end the head pain. She was even hospitalized to try more invasive prescription treatments, spending her 15th birthday there, all to leave without any answers. Doctors, who were said to be the “best in the world”, always repeating that Izzy was a complicated case, a mystery.

For these three and a half years Izzy’s parents were paying up to $1400.00 a month for insurance alone. Dr. Amerlak in Texas, after reviewing all of Izzy’s medical history, believed that he could help Izzy. Izzy flew to Texas in February of 2015 and had two appointments with Dr. Amerlak. One performing specialized nerve blocks that left Izzy with no pain in her temples for the first time in three years! (This “pain free” period lasted for three hours; the longest it would be expected to last was four.) Two days later, at the second appointment, he then performed specialized deep Botox injections to her face, neck, and head.

The next step is to have nerve decompression surgery that would hopefully allow Izzy, now 16 years old, to have a headache free day. The surgery is not covered by insurance.

Izzy’s strength and perseverance through this has been remarkable. In spite of the constant head pain she has been able to remain an A/B student and is determined to hopefully attend Michigan State University one day to become a neuropsychologist. She has goals, she has plans, and hopefully this surgery will help her achieve them.

Thomas Richards Charity thanks you for your contiuned support.


You can pay for participation in the Matt Moscato Golf Outing safely and securely using PayPal. You do not have to be a PayPal member to use this feature.

Thomas Richards is a non-profit 501(c) 3 charity all donations are tax deductible to the full extent of the law.

We will contact you after payment to get the names of all of the Golfers and/or Participants in the Dinner. Thank You for your support!!!!

2014 Matt Moscato Charity Golf


This year the event will be the same weekend as the Rochester High School class of 1989 25th reunion. The 2014 recipient will be Lexi Mancini daughter of Allyson Mancini (Blaker) class of 89.Lexi a sweet 14 year old girl who needs your help with the rest of her life…..
Most girls her age have basic teen-age concerns: playing sports, having sleepover parties, and counting the minutes until the next school dance. When Lexi was one year old she was diagnosed with Turner Syndrome, a chromosomal disorder that affects many parts of the body. She produces no hormones of any kind. Lexi has been receiving growth hormone injections since she was two years old, and began taking estrogen last year. She will have to continue to take hormones (estrogen and progesterone) the rest of her life. Future concerns from Turner Syndrome are life-threatening heart issues and kidney problems, along with increased risks for certain cancers. This aliment alone would be enough for anyone to struggle a lifetime with; however,Lexi is also afflicted with Common Variable Immune Deficiency (CVID), a life threatening and incurable disorder. Something as common as the flu or pneumonia can lead patients to hospitalization and in worse cases, death. This creates many problems. First and foremost, the high risk of infection. She has to be wary all the time of what she touches, who she touches. She experiences additional side effects such as joint inflammation, reoccurring gastrointestinal pain, and weight loss. Future concerns from the immune deficiency are enlarged spleen and lymph nodes, lung tissue damage, autoimmune diseases, and an increased risk of cancer, especially cancer of the lymphoid system, skin and gastrointestinal tract. She takes numerous prescription medications on a daily basis along with numerous supplements.
She needs IV infusions of gamma globulin every three weeks for the rest of her life, which takes approximately six hours. Amazingly, Lexi is a 4.2 student. Her treatments, although necessary, are not pain-free, nor risk-free. Side effects range from mild headaches, which she experiences, to severe anaphylactic shock and death, but without them she could die.
She will never be “healed”.The family has changed health insurance four times since 2011. Insurance companies don’t want to cover her because her illness is considered “catastrophic. Every time her family changes insurance, there is a risk of missing a treatment. Insurance is billed on avg. 250,000 + a year the family has paid on avg. $28,000 a year, with no end in sight. With her turning 18 soon we don’t know what will happen to her coverage. With the United States insurance in question we have no idea what the cost will be in the future.any questions contact Tim Ciotti 3107040806 or tciotti@me.comGolf will be at Sylvan Glen Golf Course and lunch at Camp Ticonderoga

To register – click here




Pinot’s Palette Thursday June 26, 2014

Moonlight Through the Trees
Pinot’s Palette

Thomas Richards Charity Fundraiser, in support of Chris Bagley, is proud to Paint It Forward with Pinot’s Palette. Pinot’s Palette Rochester Hills will donate portions of the class proceeds to Chris Bagley’s kidney journey. For those of you that do not know Chris, he is a 25 year old young man who was diagnosed with Polycystic Kidney Disease (PKD) when he was thirteen years old. While PKD is a genetic disease, which attacks both kidneys, Chris was one of the 10% of patients where it mutated, most likely because it was a recessive gene in both parents. Unfortunately, in late fall of 2013, Chris learned that his kidneys had taken a turn for the worse. In January 2014 Chris’ kidney function was down to 16%, deeming him eligible for and needing a kidney transplant. He has been evaluated by the University of Michigan Transplant Center and was placed on the UNOS transplant list in February. He is currently hoping to find a live donor as the transplant waiting list in Michigan is in excess of five years. Please help us fill up this class for a great cause and Paint It Forward to help us contribute to Chris’s medical expense trust.


per painter
There are only 63 spots available so sign up right away, the class will fill up quickly 
Click the link below to sign up.

Celebrate MI In The Village Sunday May 18, noon-5:00pm

Troy Historic Village (THV) will partner with Thomas Richards Charities on Sunday, May 18, 2014 to host Celebrate Michigan in the Village at the THV. This fun family afternoon will feature great food, beverages, games for the entire family, and live music. Troy Historic Village will have crafts, “Selfie Zones” where visitors will be able to take “Selfies” at designated fun zones in the Village, costumed interpreters in the buildings, and old time games on the green. Food and beverages will be offered from Fieldstone Wineries, Foran’s Grand Trunk Pub, The Big Salad and Billy Sims Barbeque. The live music will feature Tritone Paradox and Sweet Crystal performing with special guest Amy Susan Heard and Gail Engling. Admission is Free with all proceeds from the sale of food and beverages supporting THV and Thomas Richards Charities.

Free Admission

Sunday May 18th, noon-500

Noodles Monday October 21, 2013 11-9 to support Lisa Head


Noodles and company
Monday October 21, 11:00 a.m. till 9:00 p.m.
25% of what you eat and drink will be donated to the charity on.
Noodles 6836 Rochester Road

Lisa Head is a wonderful teacher; she is a friend and colleague to many, and serves as an inspiration to anyone who has the honor of knowing her and of working with her. Lisa has been a teacher for the Avondale School District for seventeen years throughout which she has changed the lives of hundreds of children.
However, on June 15th, 2013…disaster struck. Lisa was involved in a bicycle accident and suffered serious injuries. Thanks to the help of an anonymous Good Samaritan, who happened to be passing by at that very moment, Lisa is alive today. Her family and friends will be forever grateful to this person.
Lisa’s journey over the past few months has not been an easy one. She was in a coma for three weeks and she continues to receive physical and occupational therapy as she recuperates. Through hard work and perseverance, Lisa has made progress and she is determined to return to work at Woodland as soon as she can. Her family has received an outpouring of love and community support throughout this ordeal and Lisa is grateful for the support that this fundraiser will provide as she continues on the road to recovery.

STOP the Los Angeles Unified School District from Closing Special Education Schools

The LAUSD is Violating Federal Law,
Lying About Its Actions
Harming Disabled Students

What Are Special Education Schools?

Special education schools are dedicated exclusively to serve a small percentage of disabled students who have highly intensive needs. These students have severe difficulties with learning,sensory, orthopedic, medical needs, behavior issues, safety awareness and more.Special schools provide for their needs in a comprehensive, safe setting with trained staff. Children attend special schools because IEP teams, consisting of knowledgeable school staff and parents, have determined that the nature or severity of their disabilities does not allow them to be educated satisfactorily in regular schools. In a safe setting with dedicated, trained staff, they thrive! They can learn what they need to learn! They can be cheerleaders, attend school proms and social events, be on sports teams, and participate in activities appropriate to their abilities, needs and interests.

Don’t Believe the LAUSD’s Lies!

LIE #1: LAUSD falsely claims it is not closing special education schools.

FACTS: In the past few years, LAUSD has closed four special education schools and converted four others to Career Training Centers. This represents a closure of half of the special schools.

Pacific Blvd. School was closed in 2005, immediately following the installation of an adapted playground for its orthopedically handicapped students.

Sellery and West Valley Schools for severely disabled students were closed in 2009.

Frances Blend School for blind students was removed in July 2013 from the LAUSD Guide to Schools and Offices, with no public hearing and no notification to parents, staff and community. Decisions were made in secret and still have not been made public.

Widney, Miller, Willenberg, and Perez Schools, formerly comprehensive special schools
serving severely disabled students through high school, have been converted to Career Training Centers for mildly disabled students ages 18-22, thus closing enrollment to middle school and senior high aged students with severe disabilities.

Banneker, McBride, Salvin, Lowman, Lull, Leichman, Lanterman, Lokrantz, and Marlton
Schools have all had their enrollments slashed by the LAUSD and critical resources removed. Lanterman, McBride and Lull have had whole classrooms moved to general education schools, often without parents knowledge. The LAUSD is aggressively working to close these schools.

LIE #2: The Districtfalsely claims it is transferring students out of special schools to comply witha federal law to educate disabled students with non-disabled students.

FACTS: Federal law requires special schools for students who need them. All school districts are required to maintain a Continuum of Alternative Placements for disabled students. This includes special schools.

Federal law requires disabled students to be educated with non-disabled students to the
maximum extent appropriate.What is “appropriate” must be determined individually through
assessment and by an IEP Team(Individualized Education Planning Team) consisting of parents, teachers and other relevant specialists as equal participants.

Federal law provides for special classes as well as special schools if the nature or severity of the disability is such that education in the regular classes with the use of supplementary aids and services cannot be achieved satisfactorily. Only 2.6% of students with disabilities currently attend special schools.

The State of California has132 public special schools. Only those in the LAUSD are closing.

LIE #3: The District also claims it is doing this to comply with a court order called the
Modified Consent Decree.

FACTS: The Modified Consent Decree states “The parties agree that special education centers are part of the continuum of program options for a full continuum of special education and related services in the least restrictive environment.”

LIE #4: The District is falsely attributing the closure of some schools to “low enrollment.”

FACTS: Low enrollment has been artificially created by the District. The LAUSD:
‣ No longer allows pre-school classes in special schools.
‣ Refuses to inform parents of the option of special schools.
‣ Refuses to allow any new students to enroll at special schools.
‣ Is arbitrarily removing targeted groups of students, such as pre-schoolers, elementary or
middle school students.
‣ Has closed all classes of non-disabled students who previously attended special schools for
integration purposes.

LIE #5: The District falsely claims these placement decisions are being made by IEP Teams, in accordance with federal law.

FACTS: The LAUSD is violating parents’ rights by making arbitrary placement decisions:
‣ Parents are not being included in these decisions.
‣ Placement decisions are being made by the Division of Special Education prior to IEP
meetings, an unlawful practice.
‣ IEP amendments to change placement have been held by telephone with parents not
understanding their rights.
‣ To achieve this massive transfer of students, IEP amendments are being rushed through
with parents not being allowed to disagree. This runs completely contrary to federal laws
relative to the IEP process.

LIE #6: The District falsely claims that special schools are “segregated.”

FACTS: Specialization for a beneficial purpose is not segregation.

Parents choose to have their children in special schools. There are many kinds of special schools in LAUSD,each of which represents a choice for students who may need these schools.

LAUSD operates seven types of options schools, each serving a different type of student. These are campuses with low student/teacher ratios offering instruction to students who are deemed at risk of not completing their education.

Included are continuation schools, schools for pregnant minors, opportunity schools, alternative schools and community day schools. In addition there are magnet schools for gifted students, skill centers, and a variety of other schools which represent options for students and their parents.


Lie #7: LAUSD claims it is “integrating” special education students.

FACTS: The opposite is true. These students are becoming much more isolated. The four schools that have been converted to Career Training Centers for mildly disabled students (ages 18-22) have no interaction with the non-disabled students.

While closing special schools, the LAUSD has dramatically increased the percentage of special needs students in non-public schools. These are privately owned schools, funded by taxpayers. Students are sent there when the district does not have an appropriate placement. Non public schools have no interaction with non-disabled students.

Non public school placement(at taxpayer expense) has increased by 50% in the past few years while public special school placement has been reduced to less than half.

Classes of students who have been moved from special schools to general education sites are totally isolated with little or no interaction with non-disabled students and are unable to participate in academic, elective or extra-curricular activities.

LIE #8: LAUSD falsely states that “Research supports that both individuals with disabilities and their non-disabled peers achieve improved outcomes when they are educated together.”

FACTS: LAUSD has failed to provide any such research.

“Educational benefit”has been ruled to be a necessity by the courts.

Innumerable studies have shown a lack of improvement of educational outcomes when severely disabled students are educated with non-disabled students. Improvement has been shown in the area of acceptance but not educational outcomes..

Blind and deaf students are very successful in general education classes after they acquire specialized and access skills. These skills have been carefully taught in a comprehensive setting such as Frances Blend School for the Blind and Marlton School for the Deaf.

Severely handicapped students, when in a “fully included” classroom, do not receive instruction at their level or to meet their assessed needs.

LIE #9: LAUSD falsely claims that all services provided in a special school will be
provided on a general education campus.

FACTS: This is impossible from both a safety and educational viewpoint.

Providing a 1:1 aide who does not know braille for a blind student is vastly inferior to a
classroom with a teacher skilled in braille and in techniques to teach the blind.

Itinerant specialist teachers,who travel from school to school, have an average caseload of over 20 students.They cannot possibly provide enough time to meet IEP goals and assessed needs.As itinerant teachers have retired, their positions have not been filled.

Severely handicapped students are not allowed to “shine” or be celebrated on general education campuses,the way they are at the special schools, where they can participate in intramural sports, perform at school assemblies designed for their needs and interests, or participate in a host of other school activities tailored for their needs. In a special school, classrooms have kitchen areas and adjoining bathrooms for students who need to learn health and personal care skills.

Safety for medically fragile students and students with limited safety awareness is a very serious issue for students on a general education campus.

For disabled students who can thrive and be successful in a traditional school setting, a general education campus is appropriate and desirable. For students with intensive needs that a regular campus cannot meet, our dedicated special schools are best, and should be celebrated as a beneficial option.



For further information, please contact us or attend a meeting!

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