By Steve Bilski
It’s shocking how one day
everything is going great, life is good, you’re working hard to support your son, and suddenly nefarious people come into your life. They are people you’ve never met, you don’t know, who don’t know you, and they begin saying vile
things about you and sending you mail that’s full of lies and false accusations. It’s shocking and so incredibly hurtful. And there is practically nothing you can do about it.
But this is not the beginning of my story, and I pray it won’t be how it ends.
My story begins with the birth of my son Keith who experienced a devastating beginning to his life. He was born early on the morning of June 17, 1981, and he was healthy--at least for a short while.
A few hours later, though, he developed breathing problems. The doctor thought it was allergies and so he did nothing. But it was not allergies. It was b-strep infection: Spinal Meningitis. At one point Keith even stopped breathing.
He ended up spending almost a month in the hospital. Then, about a year later, he was diagnosed with cerebral palsy and epilepsy. Keith is now also non-verbal, autistic and mentally challenged.
In 1985 and early 1986, with advice from a lawyer, Keith’s mother and I filed a malpractice suit against the doctor and
the hospital. In 1993 Keith was awarded three million dollars.
I separated from my wife in 1986 due to her infidelity, and the divorce was finalized in May of 1987. In November of that year and while involved in a serious relationship with a new boyfriend, she gave birth to a second child. At the time I began
drinking heavily and had trouble handling everything that was happening. Then in 1988 I received a DUI while suffering what was a very low point in my life. However, the power of change is infinite and wisdom does come with time. So I am
now proud to say that I have been sober since January 1992.
the divorce decree, Keith’s mother and I had joint custody of him, which included joint decision making. Plus I had visitation every other weekend and one day during the week.
As it is, since 1992 I have had my son a minimum of three days per week as well as every weekend except one. The stipulation is, as long as I am nice and
cooperate with my son’s mother, I am allowed to see Keith. But I have not been allowed to make important decisions in his life.
I had heard stories about mothers playing games with visitation, and this could not be more true than with my son’s mother who played many of them. I did my best to avoid fighting with her,
to protect my son, and be with him whenever possible. However, one time I suffered for eight weeks without seeing Keith due to an argument with his mother. There were many other instances I was denied visitation as well.
I would show up at her door to pick up my son to take him out for a great time and she would deliberately
start an argument about some irrelevant thing and then end it with: “You’re not taking him!” This happened so many times I lost count. So I decided to pick my son up from school on Friday afternoons and drive and return him to school
on the following Monday just to avoid confrontations with his mother.
can remember almost every time I dropped him off at his mother’s home. By the time I had gotten back into my truck parked on the street in front, Keith was inside and had crawled up to peer out the living room window. He would push the drapes aside
and squeeze his face into the window pane so he could watch as I drove off. Oh my God, the sad, painful expression on his face! It was like, where are you going, Dad? Why are you leaving? He would do this almost every time after I dropped
him off. I can still see him in that window, and would every night after I arrived home and be unable to sleep.
Because of his disability, Keith can’t talk. So he shakes his head to show he means no and nod his head up and down when he expresses yes. Often while I would be driving him back to his mother’s
his little head would be moving from side to side, saying, “No! No! No!”
His physician, Dr. Mary Keen, told me that Keith has what is called separation anxiety. She prescribed medication, and it has helped. Keith also has had behavior and social issues which throughout his life have held him back. I still pray
every day he will get the help he really needs. As it is, he has changed schools on average every two years and most of his numerous teachers simply did not know what to do about his behavior or how to handle him. Numerous professionals told me that
Keith could do better if his parents would agree on putting his needs first—which obviously we hadn’t.
During the 1980’s I paid six thousand dollars per year for two years so Keith could attend a highly recommended special education school. This was a school he would have been able to attend for
most of his life, even through high school and beyond.
The school was located less than thirty minutes from his mother’s house, and his attendance was good and he started making progress. During these two years his behavior was good and not an issue. But after the second year
he was not allowed to return because during that summer while he was at home he began the bad behavior all over again. So the school felt it was wasting its time and didn’t allow Keith to return for a third year.
It was after this when Keith began changing schools almost every two years.
He went through numerous teachers, like I said, and he was traveling farther and farther away from home to get to school. The years passed and he became old enough to attend high school. The school he was to attend, however, was one and a half hours travel
time one way. And this was in violation of Illinois special education law. The high school, though, was inappropriate for Keith. Plus his case manager, Laura Pearlman, did nothing for him. She wouldn’t even attend his IEP meetings.
I, for one, did not want Keith traveling that far to and
from school every day, and have to do it for four years. But I was given no say in the matter! Laura Pearlman would not talk to me and I believe she undermined the relationship I had with anyone. She even sent me a letter regarding my back surgery
I had to have and how inconsiderate it was of me to pick the date I did for the surgery. The truth was I had no rights, and Keith was in the wrong place. It all reminded me of a scene from the movie “My Left Foot” with Daniel Day Lewis where
they put him in a class with students who are worse than he is, and he manages to yell “Get me out of here!”
I know that not all options were looked at by Keith’s mother and definitely not by his case manager. My opinion did not count and I was not allowed to make any decisions regarding Keith’s
schooling or welfare.
I visited and interviewed other high schools and
found there were several that would accept him. As it is, the School District requires that students must live in the district at least four nights a week. At the time, however, he was living with me three nights a week and sometimes four. But neither
Keith’s mother nor his case manager Laura Pearlman would agree to Keith changing schools, even if it meant his attending a better school that offered a better education and which was closer to home.
My son’s last day of high school was on a Friday in August of 2002. The following Monday I drove him to start his attendance
at a workshop for special needs children, but officials there would not allow us to enter. He was not allowed to attend because no one had registered him for the workshop. The thing to know is when you have a special needs child it is very important to plan
for him in advance—sometimes even years in advance. It is often very difficult to find a good day program or workshop. There are not many openings because these programs are usually filled with special needs children who stay enrolled with them
for the rest of their lives.
I was seriously taken aback. I did
not understand what the heck was going on for no one had informed me Keith had not been registered. I immediately telephoned his mother, and she acted surprised and said, “I will call Laura Pearlman.”
Keith’s case manager then called me and informed me there were no plans for Keith after high school.
Why she hadn’t informed his mother or me of this, she didn’t say. But I suddenly felt extremely despondent. There would be no more physical therapy, no more speech therapy, no more music therapy, and no more interaction with peers!
I volunteered to become his caregiver during the days and weekends.
settlement had been handed over to a judge named Benjamin Novacelsky, and to the probate court because my son was a minor. Then my son’s settlement was put into a trust held by Northern Trust Bank and Patty McLeroy. And an attorney, Roberta
Evans, was appointed to make sure my son did not get cheated out of his money!
Along with a guardian ad litem named Jean Adams and case manager Laura Pearlman, (Owner of Consultants on Disabilities). A budget was set to pay for these individuals and other services, as well as provide for all of Keith’s cares and needs
only during his time spent at his mother’s home. In addition, his mother was receiving a monthly budget of $4,115.00 plus child support from me, and also was paid twenty hours of in-home attendant care at $16 per hour each week.
I received totally nothing--zero dollars!--during all these years even though Keith lived with me three-plus
days a week. It was a financial struggle, which I somehow managed to survive. And no one cared at all about, to say the least.
Early on, a new specialized 1993 Chevy van was purchased with his money, complete with a wheelchair lift to transport him to school, doctors’ appointments, hospital visits therapy sessions, social
events, etc. My ex-wife, Keith’s mother, would not allow me to use my son’s van to drive him anywhere. Roberta Evans had told the judge that I could not obtain car insurance because of the DUI I received in 1988.
But I emphatically informed the judge this was not true. I had insurance and it covered any vehicle I wished to drive. But to this, the judge said
nothing, and the subject was quickly dropped. Clearly the judge did not want to hear what I had to say.
I had in fact a pickup truck which I regularly used for my roofing and snow plowing business. Since I could not use his van, I had to physically lift Keith into the front seat and then lift and secure his wheelchair into the bed of
my truck where it had to be tied down and covered up to protect it from the weather. This whole process had to be done in reverse each time I returned him to his mother’s house. Okay, this was not so bad when Keith was really young and small
and weighed little. But as he grew in size and weight, it really exacted a toll upon my back.
I took a chance and hired an attorney. I ended up spending tens of thousands of dollars on many attorneys over time but this one managed to get Keith’s bills finally reimbursed. What’s funny is that I still have to submit
receipts while Keith’s mother never has to account for what she does with his money. It also cost Keith tens of thousands of dollars spent for attorneys hired by his mother to oppose every word I spoke and effort I made to help Keith. The
typical monthly budget for Keith’s mother would include (among other things) $250 for clothes, $350 for diapers, $300 for utilities, $125 for parking and tolls, $200 for gas, $400 for activities, and $1,575.00 for miscellaneous!
All of this was for only three to four days per week when she had custody of Keith. Meanwhile, I was paid nothing for costs and expenses. Plus
I paid her child support, which I daresay I was proud to do on behalf of Keith.
I always made sure my family had insurance. My insurance was based on how many hours I work, and I always made certain to work sufficient hours no matter how many were needed to obtain the best possible health insurance.
What I found telling was how my son’s mother would almost never attend court.
She rarely came and only for the guardianship hearings. As Keith became an adult Judge Miriam Harrison became Keith’s new judge. Around this time I hired another attorney. All I wanted to do was ask Judge Harrison if I could please
have some help for him so I could go to work when I needed to. For Keith’s mother refused to care for him during my allotted time.
But when in court for this action, Judge Harrison looked me straight in the eyes and told me I didn’t have an obligation to pick up my son, so no help needed to be provided and my work was
not an issue. To this, I was shocked! And I thought: Oh, but I’m obligated to pay child support, huh? But I don’t have an obligation or right to father my own son? It seemed apparent to me when my son suddenly got this huge
financial settlement that I was no longer needed. What judge would dare ever think that children don’t need their fathers?
In 1996 I sold my pickup truck and quit my snow plowing business. I did this because I could no longer take Keith with me while I plowed. For it wasn’t fair to Keith. I ended
up using the equity in my house and bought a used 1988 Ford van with a wheelchair lift. I now drive a 2004 van also purchased with my equity.
Eventually my back gave out from all the years of lifting Keith and his wheelchair. This led to my having to choose surgery so I would be able to return to my job as soon as possible.
Laura Pearlman had repeatedly reported to the court that I was not working, when in fact I was. Actually I had worked off and on for two years while going through all kinds of medical tests and procedures. I also received therapy for my back in hopes
of returning full time to my job to keep my benefits. So I had my first back surgery in 1998 which made things only worse.
picked up part-time work delivering magazines to make ends meet. I currently have no insurance for myself. Keith also had surgery in 1998 (to which I did not agree with the hospital or the doctor chosen). Still, a petition was filed by his lawyers to
proceed with his operation without my consent. Again they wanted to modify the divorce decree! And again I had to pay a lawyer to withstand their legal onslaught.
Still, Keith never received the therapy he needed and stopped walking after high school and getting exercise.
Then a brand new 2000 van was purchased (for my son’s mother to mainly use) to replace the 1993 Chevy van. Some years
later they purchased yet another handicapped van, and Keith had never been in either of the last these two vans purchased. I drove him to all his doctors’ visits. I used the equity from my home to purchase two special vans of my own to use when
with Keith. In effect, I ended up practically spending my life savings to help Keith and be with him and to pay for lawyers to facilitate this. All this I did only to get stomped on by his mother, the attorneys she hired using Keith’s trust
fund, as well as by a bias court system only too ready to always rule in her favor. For I came to learn exceedingly well how unfair the court system is to fathers and their children.
When Keith turned eighteen in 1999 I filed for guardianship.
At this time Keith’s lawyers petitioned for his mother to be Keith’s sole guardian. Then I received a notice to appear for a deposition. Everyone
involved with Keith’s case was there including the two divorce attorneys and Roberta Evans who had been hired to oversee Keith’s money. What ensued was a proverbial case of them against me.
Divorce Attorney Frances Krasnow asked me if I wanted a lawyer and I said yes. They then phoned Judge Harrison and she
ordered I proceed without one. So I answered their questions to the best of my ability--and oh boy, did they drill me. They tried to paint me as a bad father. But all I wanted in my life was to provide for Keith’s welfare and his needs
to be looked after.
For years I had been taking Keith to the dentist for
regular checkups. The dentist chair was a bench seat with a high back and it wasn’t comfortable for Keith because he could not extend his legs due to his Cerebral Palsy. Each appointment I would talk him through it and assure him everything
would be okay, and he usually did well at appointments. Then in February of 1995 Keith’s school notified his mother with a note that his teeth were bothering him. X-rays showed that his teeth were impacted and overcrowded. The dentist
said something had to be done soon or Keith’s teeth would start coming out from the top of his mouth. And sure enough, that’s what happened!
His mother said she would take care of this. Keith was in pain and I wanted to help him. I needed to help him. But by October still nothing was being done to fix
his teeth. So I made an appointment with an oral surgeon. He immediately told me that a simple solution was to pull out a certain tooth. I had grown frustrated waiting for his mother, so I took Keith to have this tooth extracted, and then drove
him home to his mother’s house.
She kicked up a storm and asked me
why he had not been in school that day. I told her that I could not sit back and do nothing to help Keith’s situation and that he badly needed this tooth taken out and she had done nothing about it. So I took it upon myself to follow through
with the dentist’s recommendation to help our son.
called the attorneys for the estate and they sent me a letter stating I had no right to take him to the dentist without his mother’s knowledge and consent. But according to our divorce decree, it states that in the case of an emergency I have every
right to take such action.
Soon thereafter I received a letter from Roberta
Evans and Jean Adams stating I had put Keith at risk because I failed to supply the oral surgeon with Keith’s prescription list. This was totally false, for I acquired a copy of the medical form which I had filled out prior to the tooth extraction,
and it clearly states all his medications.
Keith does not see a dentist on a regular basis as recommended by his Doctor.
In another incident, I received a letter in the mail from Jean Adams claiming I had failed at various times
to provide Keith his medicine. And this was patently false. Soon, I reached the stage where I was in constant fear of opening my mail! Strange how these lawyers could fabricate all these false accusations when all they had to do was make
a few phones calls to verify actual facts. But I know they wouldn’t do this and don’t do this because their purpose was to try and destroy me!
Keith began seeing a psychiatrist who wanted arm restraints put on Keith’s wheelchair. He claimed this was necessary so Keith would not hurt anyone. So
they put arm restraints on his wheelchair. But they just made him angry and more aggressive so I removed the straps, for they also left bruises on his arms. In no time I received a copy of a letter from Jean Adams telling the court I had sliced the straps
off. But in fact I only unscrewed them. Meanwhile, another conscientious doctor wanted to give Keith electric shock treatments. I was about ready to lose it. Oh, my God, I thought! Who are these people?
At a hearing in court Jean Adams stood next to me and told the judge that I had not been giving Keith his
medication. I looked at her in shock. This is not true, I exclaimed! How malicious and dishonest could this “official of the court” be, I wondered.
Then attorney Adams petitioned the probate court to take $2,000.00 from Keith’s trust fund to use to have our divorce decree modified giving
Keith’s mother sole custody. In addition to this, Keith’s mother hired a divorce attorney named Ms. Petrucci who needed to be paid a retainer of $2,000 for her services. Immediately Jean Adams petitioned the court to authorize money
taken from Keith’s estate to pay for this.
Again there is Keith’s
case manager Laura Pearlman, another individual appointed by the court. She has attacked my character repeatedly over the years without ever providing evidence or facts to support such attacks. She claims to be a mediator, but instead, she’s
anything but. One of her many harmful acts was when she modified a school letter so it would appear that Keith’s behavior worsened whenever he is in my care.
Ms. Pearlman would pick up Keith’s mother and provide transportation for her at various times. This was because Keith’s mother could not
drive by herself, for she had been diagnosed with agoraphobia. Ms. Pearlman would charge Keith’s estate ninety dollars per hour to drive his mother around. Naturally with all occurred without my knowledge or consent. Ms. Pearlman also
facilitated the actions of Keith’s doctor. The doctor would prescribe medication for my son without consulting or informing me.
I found out, he informed me that he had been led to believe Keith’s mother possessed sole authority to make medical decisions for Keith. However, Keith’s mother and my divorce decree clearly states we are to make medical decisions jointly!
Everyone involved with Keith knew and knows this, including Laura Pearlman.
the time Keith was on my roofer’s insurance he was eligible for a new wheelchair every four years, which worked out very well, I believe.
my insurance ceased when I could no longer do my job after my back surgery in 1998. So he has not had a new wheelchair since then. According to his doctor, he had outgrown this wheelchair. Despite this, we applied for a new one and
he was fitted for it back in August 2011. We are still waiting for it to be funded by the state. But I cannot understand why we have to wait so long and wait to get one from the state when there is more than enough money in Keith’s trust
account to purchase one immediately, especially since he needs a new one right away.
As of the writing of this letter, I have learned
that Keith has to return to Easter Seals to be remeasured for a new wheel chair because his previous measurements have been lost.
I came to hire a new attorney named Theresa Varnet from the law firm of Spain, Spain & Varnet who was herself the mother of a handicapped girl. I thought she would never let anything like this
to happen to her Daughter so she would have some compassion for Keith and see how he was being mistreated and neglected. What Ms. Varnet immediately did was put a young attorney from her firm on my case. Her name was Jamie Levin Murial.
Ms. Murial told me that Jean Adams had contacted her stating she was going to petition
for $2,000 from Keith’s estate to hire a mediator the help Keith’s mother and me settle matters between us.
But instead of doing this, Jean Adams filed a petition to used Keith’s money to modify the divorce decree to give Keith’s mother sole custody and be able to make all decisions regarding Keith’s life. Looking
back, I didn’t know who was lying (or perhaps lying the most!): Ms. Adams or Ms. Murial. But I immediately stopped the services of Spain, Spain & Varnet. I still owe them some money. No matter. Roberta Evans then hired Ms. Murial
to file an Obra 93 trust. I became curious to know if Ms. Murial was paid what I owed her firm from Keith’s trust. I thought to myself: Hmm!
A few weeks later I had a private pre-hearing meeting with Jean Adams and an unknown judge. This judge recommended that I should drop my guardianship petition because no judge would
grant me guardianship after they opened and read my son’s case file. Because in his file is a litany of documents chronicling all the irresponsible, destructive behavior I had supposedly carried out which put my son in danger. I was stunned!
I said to this judge that all of it was lies.
Well, a few weeks later
it was time to go to trial, and once again we met first in a private room. Present were Jean Adams, Roberta Evans, Laura Pearlman, divorce attorneys Frances Krasnow and David Eide, Keith’s mother, my friend Angie, and myself.
At this meeting the lawyers tried to persuade me to drop my guardianship petition, and they were all very intimidating. I knew with all the letters and threats they had made
that things would only get worse. However, I love my son very much. Though my heart was racing and my body was shaking, I stood up to them. Then it was time to go and the meeting was concluded. Before departing, Frances Krasnow approached
me and said that if I did not drop my petition for guardianship, visitation to see my son would be taken away.
Oh, my God! After all the lies and false accusations and fabrications they had set against me and put in my son’s file and all the pain they caused me and how they defamed my character in front of the judges
and had harassed me, I suddenly panicked, I could not go on, and said okay, you win. I could not stand there in front of the judge and get bombarded with more of their lies and vile, dishonest stories. I literally could not get to my feet and stand up,
and dropped to the floor!
Weeks later, after it was all done, one day I
opened my mail and there was a statement from the Northern Trust Bank. The statement showed that fees were paid to Frances Krasnow and David Eide for over $19,000! I couldn’t believe that Judge Harrison had approved payment—and such a payment--to
two divorce attorneys.
Over $19,000.00 of Keith’s money was appropriated
to pay off these divorce attorneys from the law firm of Neal, Gerber and Eisenberg. Why the divorce lawyers were brought in for this to begin with, I never understood. They had threatened me to drop my petition or I would never see my son again.
So, because I was devastated at the thought of not seeing Keith again I dropped my petition. As it was, I could not afford to pay for another attorney.
My savings were gone! My equity was gone! All the money I had spent on lawyers I could have spent on Keith—if only to buy him a new wheelchair which these supposed protectors of his welfare would not purchase with his own money
Ms. Roberta Evans, attorney for Keith’s estate, reminded
me that Keith could not have two guardians. She seemed very pleased with the decision I made.
Around this time I tried to get more speech therapy for Keith. The court approved the purchase of a computerized talker for about $8,000.00. But Keith was only given thirty minutes of training per week with this machine. Keith’s
therapist soon told me that he could be doing much better if more time and training were provided to him. She even gladly wrote a two-page letter for me to give to Judge Harrison recommending more speech therapy and how Keith would benefit from it. But
naturally Judge Harrison denied any funding.
I wondered how anyone in
Keith’s condition could benefit from this tiny amount of thirty minutes of therapy per week, which lasted for five months during the year of 2000. Eventually, Keith began receiving no therapy because of the therapist’s unavailability. Again,
I was horrified by the fact that Keith’s mother and case manager Laura Pearlman never attended a single IEP meeting in the four years it was given to assess Keith’s progress or development. Why pay someone to do a job that they’re not doing.
Keith’s physical therapist (PT) quit in 2003 and was never replaced. He would
only come once a week anyway. That is not enough therapy for Keith. He has had Multiple Surgery’s and without the proper therapy, Keith would not benefit from the surgeries. Laura Pearlman once again fails and Keith pays the price.
I take Keith to the pool to swim and play, and to ride his bike which he loves to do. And I taught Keith to walk 1000 feet which he would always do when he was with me. Now
he doesn’t walk at all. All this has been very hard to accept. Still, Keith has worked very hard and has made great progress despite all these obstacles and setbacks over the years.
Keith participates in the Special Olympics! He bowls, swims, plays baseball and basketball. Plus Keith has won 39 gold medals, 9 silver,
and a few bronze metals, too!
We travel to Florida and to other states.
We go to concerts (Keith loves Bruce Springsteen) we have seen him perform over 50 times, Willie Nelson (we have a picture taken with him) Huey Lewis and The News, Vince Gill and many more and to lots of parades! Keith’s mother has never been to
any of Keith’s practices or tournaments. She takes him nowhere because of her anxieties.
I know if something happens to me, that all of this will stop. There is no one in Keith’s life other than me to continue caring about his well-being and happiness. There is No Plan. I wish I could do something about this, and do so
much more for Keith. But I am not allowed to.
Because of the neglect of Keith’s health, he had two severely decayed teeth removed
in the spring of 2012. This was preventable and Keith should have never had to go through such suffering and pain. It was all totally unnecessary.
One day I received a letter dated march 24, 2011 from Jean Adams. Apparently about some confusion over medication that was prescribed by Dr Keen. Keith’s Mother had asked that
we not advise the court. Again Jean Adams threatened me, if I ever undertook to make any medical decisions in the future for Keith without first notifying Cindy that they would be compelled to bring the matter before the court. And my failure to cooperate
could result in my visitation with Keith being terminated.
mother and I had been with Doctor Keen when the doctor prescribed Risperdal for Keith in 2006. However, if Ms. Adams would have contacted Dr. Keen she would have gotten the facts. Instead, like always, she and Keith’s mother overreacted. They continually
threaten to take my father’s rights away, use Keith’s funds in nefarious ways, and apparently have nothing better to do than send me threatening letters every chance they get.
I have contacted many probate lawyers in Cook County and most of them will not help because they know Jean Adams. She is well-respected
and not to be trifled with. My son’s mother is an ex-employee for her village in the local police department and she campaigns for the mayor, state representatives and senators and even The President.
I have filed a complaint with the states attorney’s office and they simply told me they are understaffed. I have also contacted Equip for Equality on three different
issues, and they told me their funds are limited and plus they have ties with Judge Harrison.
What is clear is this: Keith’s mother, all her attorneys, Keith’s case manager, and the court are unified and set against me. They continue to spend ample time and more and more of Keith’s money with the aim of defaming
me, harassing me, degrading me, while ignoring Keith’s needs. Throughout this time and during all the years this same probate court should have been helping and doing what is best for Keith. The money in his trust account is for this purpose
and for serving and helping him. How can the court expect to help Keith if they know nothing about him and make no effort to know him and have no interest in knowing what his needs are or what his Skills are?
I had no idea what to expect when I became the father of a handicapped child. I had to find out the hard way on my own.
I dedicated my life to this task and to becoming the very best father possible for Keith. However, no one else is dedicated to this. And instead of helping their clients and the parents of children, especially handicapped children, the probate
court and its court-appointed attorneys use people--as they have used Keith--for their own personal agenda and financial gain.
All I have ever wanted for Keith was to see him happy and be well taken care of. I want him to have everything he needs and be able to reach his potential. I want him to have friends, do the things he enjoys,
to live comfortably, and be healthy and safe. He needs to be around people who will assist with personal growth, help boost socialization, and who are devoted to his achieving and maintaining fitness goals.
However, since my son received a three-million-dollar malpractice settlement early in his life and his money was put into a
trust, Keith’s life has suffered immensely. I’ve witnessed a slew of people over years dedicated to nothing more than to get at his money and line their own pockets with it. I’ve had to suffer, too, being prevented from helping
Keith and doing for him all I wanted and could have done for him. In fact, it has been hell to me having to witness my son’s needs being neglected and mismanaged, as well as watch him regress due to lack of education, therapy, and care, and from
the blatant bias of the courts and family legal system.
As I have enumerated
herewith, Keith’s health has been sorely neglected. He still does not get regular and much-needed dental exams or physicals, and his trust funds are not being spent properly but rather being pilfered away from a host of greedy, uncaring individuals.
I also have been humiliated, defamed, and threatened by lawyers supposedly hired to
protect my son and look out for his best interests. That I have been the only person who has protected him in every way possible and who has had Keith’s best interests at heart, but been threatened and sometimes prevented by these individuals from
doing so, is a travesty of the most heinous and unjust kind.
I love my
son more and more every day. I want people to know what's going on. But I fear I might incur the wrath off my ex-wife--Keith’s mother--and her powerful lawyers and political friends, and the wrath and tyranny of the court itself. And
risk losing everything--including most of all--not being able to see the son I love more than anything in life.
TO FOLLOW STEVE BILSKI
AND HIS SON KEITH'S CONTINUING SAGA, VISIT THEM ONLINE AT: https://www.facebook.com/steve.bilski?ref=ts&fref=ts.
DON'T HESITATE TO NETWORK WITH STEVE THERE. AND PLEASE DROP HIM A NOTE AND LEND YOUR SUPPORT. HOPEFULLY, SOON, JUSTICE CAN BE SECURED FOR STEVE BILSKI AND HIS LOVING SON KEITH!