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Showing posts with label HealthCares. Show all posts
Showing posts with label HealthCares. Show all posts

Wednesday, 14 May 2014

'Born Schizophrenic': 2 Mentally Ill Children Threaten to Tear Family Apart

Susan and Michael Schofield have no letup in their grueling day –- 11-year-old Jani is one of the youngest children ever to be treated for schizophrenia, and now her 6-year-old brother Bodhi, though not officially diagnosed with the same disorder, has violent outbursts and self-harming behavior that suggest he might also have the disease.

“I had thought I had seen it all,” Michael Schofield, a 38-year-old part-time college professor, told ABC News. “What could possibly be worse than a young daughter in a psychiatric hospital?”

Their son has been diagnosed with severe autism and intermittent explosive disorder and has had five hospitalizations at a UCLA psychiatric facility this year, his parents said.

“The first challenge is you’re not sure your children are going to make it,” said Schofield. “Right now, we are afraid Bodhi will crack his skull open or at least severely injure himself. With Jani, there was the fear of suicide after she made a couple of attempts. It’s a threat to the basic survival of your children.”

The Los Angeles couple, who have been married since 1994, went public with their story to highlight the struggle of parents raising children with mental illness. They have devoted their entire lives to keeping their family together and not sending their children to a psychiatric institution. But the strain is taking a toll.

“There is a significant divorce rate in at least 75 percent of couples in these situations,” said Susan Schofield, 44, an Internet radio show host. “With hardly any respite care, there have been problems in our marriage. We haven’t been out on a date in 15 weeks. There just isn’t enough support out there.”

The Schofields’ difficult journey with Jani has been highlighted by Discovery Fit & Health television in several episodes since 2010. On May 26 during the network’s “Psych Week,” a sequel, “Born Schizophrenic: Jani and Bodhi’s Journey,” will air.

When Jani was younger she had visual and auditory hallucinations –- rats that she named “Wednesday” and cats named “midnight” and little girls named “24 hours.”

Jani is now on medication and making great progress, but Bodhi is not, the Schofields said. Mental illness runs in both sides of the family.

"Black Swan" analyzes ballerina's descent into schizophrenia.
Dr. Mark DeAntonio, who is treating Bodhi, said the boy has “something different” than his sister.
“What led us to Bodhi’s diagnosis was she was having auditory and visual hallucinations that were bizarre and morbid,” he said in the documentary. “It was a fantasy world animals lived in.’

“Bodhi’s behaviors and psychiatric issues are consistent with someone who has autism,” said DeAntonio. “He has episodes of severe agitation and self-harm and there is no clear reason why he is falling down and hurting himself, biting himself. It’s most distressing.”

His mother is convinced Bodhi will eventually get a similar diagnosis as Jani. “I believe it will come out later as basically schizophrenia with a lot of autistic traits.”

Childhood schizophrenia is rare, according to psychiatrist Dr. Igor Galynker, director of the Family Center for Bipolar at Mount Sinai Beth Israel in New York City. Fewer than 1 percent of all cases start in childhood.

“Having two children with COS is probably even more rare by an order of magnitude,” said Galynker, who did not treat Jani.

Schizophrenia onset before age 13 is characterized by behavioral and cognitive symptoms that overlap with features of autism spectrum and disruptive behavior disorders, according to a 2007 article in Psychiatric Times. Early diagnosis is important to maximize treatment.

Today, Jani is about to finish sixth grade and is now calm enough to leave a program for emotionally disturbed children and go into a contained classroom in a junior high school. “I never expected that to happen,” said her mother.

“The boys her age are older and bigger and some of them, because of their illnesses, have the potential for violence and aggression,” said her father. “For her own safety, that is best. It’s a huge step for her.”
She may go to college eventually, but the focus now is on adaptive life skills and hygiene, which is typically problematic for those with schizophrenia.

“It’s critical to her survival because loss of hygiene is the first step on the road to homelessness,” said Michael Schofield. “There is a disconnect between the mind and the body and they don’t feel what we would.”

Bodhi is on an array of anti-psychotic medications, as is his sister -- lithium and the antipsychotic Zyprexia. But Bodhi is not as verbal, so he cannot tell his parents what he is seeing or feeling. And events as simple as having to go to the bathroom can trigger an explosive fit.

Several times a year, when his parents cannot control his violent outbursts, the Schofields take him to the hospital where he is sedated and restrained in a “modern day straight jacket” to prevent him from hurting himself, said Susan Schofield. “The hospital says it was the worst case they had ever seen.”

The family has health insurance, but Michael Schofield has been forced to limit his teaching to online classes. They have difficulty paying the bills because for them, Jani and Bodhi are a full-time job. The couple also runs a nonprofit for autistic children, Jani’s Foundation.

“We have begged the regional center for respite care to give us some time off,” said Susan Schofield. “For just two to three hours, we could go out on our own.”

But often help doesn’t show up and there is no back-up.

The couple has had marital problems as a result. Michael Schofield had an affair, for which he “takes full responsibility.” His wife said she also blames herself for being “so tired” at the end of the day.

“Our second fear is that our children will never be entirely independent,” he said. “What are they going to do when we are dead and gone? Who will provide the support?”

Neither have extended family who could help out with the children. Michael Schofield was born in Australia and hasn’t seen his mother since he was 15. Susan Schofield’s parents are “too old to physically handle the situation,” she said.

Still, both parents feel hope about their children’s future.

“Jani has come so far,” said Michael Schofield.

“She is an inspiration,” echoed his wife, who said she is “working through” her husband’s infidelity. “We have to keep the family intact.”
Benjamin Ekpenyong

Baby Born With Rare 'Butterfly' Skin Condition

Baby Born With Rare 'Butterfly' Skin Condi …

 

 

 

 

 

 

Mom Seeks Diagnosis for Baby Covered in Blisters

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Brittany Weingart knew something was wrong with her son about a week after he was born when she found tiny blisters on his chin and mouth and couldn’t explain them.

Baby Lane is now 6 months old, and doctors are almost certain he has a rare condition in which his body cannot properly make the protein that anchors skin in place, resulting in painful blisters on his skin.

“Up until about a week ago, I would have told you that he is the happiest baby,” Weingart, 24, of Edinburgh, Indiana, told ABC News. “He still smiles and he’s still happy most of the time, but now he fusses and whines. When you touch him, he flinches.”

As Lane gets older and becomes more mobile, he gets more blisters, which Weingart has learned she must pop and bandage before they can grow and spread, she said.

The condition is called epidermolysis bullosa, and it affects about 1 in 50,000 live births, though it can vary in severity, according to the National Epidermolysis Bullosa Registry. Nicknamed the "butterfly" skin condition because it makes the skin so fragile, epidermolysis bullosa has no known cure.
  Lane’s case is so mild that only a genetic test will tell whether he has the condition for sure, but Medicaid has refused to pay for it, Weingart said.

At a loss, Weingart created a Facebook page to raise awareness about the condition, and share Lane’s story. Through the page and other fundraising efforts, she said she’s been able to afford the $3,000 test out-of-pocket.

The genetic test can take up to 12 weeks to process, but her family should have answers this summer.
“The diagnosis is important to us because it's scary knowing he has something but not know for sure what it is,” Weingart said. “No, there is no cure or treatment, but a confirmation will give us peace of mind just knowing what exactly it is.”

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