Sunday, December 24, 2017
Thursday, October 19, 2017
Thursday, October 12, 2017
Monday, October 9, 2017
About Me
- c jagadish chandran
- Thiruvananthapuram, Kerala, India
- Working for the benefits of future generation in the universe. Victim of the Pesticide ENDOSULPHAN, used by the Plantation Corporation of Kerala in the Kasargod District of Mulleria Government High School - worked as Mathematics High School Teacher in my life as a first Government Employee in the High School Section wef 20.01.1989. (Along with my newly wedded life partner G.C Kumari Meena 01/05/1965 - 04/04/2006) Before that worked as Primary Department Teacher wef 31st August, 1987 in the Upper Primary School, Cheecode, Malappuram District till 19th Janauary 1989. Relieved from there to join as High School Assistant in the Govt HS Mulleria, Kasargod Dist wef 20th January 1988 FN. Due to the areal spraying of the harmful pesticide ENDOSULPHAN in the Plantation Corporation of Kerala made my betterhalf to die due to the Metastatic Adeno Carcinoma in the Gall Bladder. ( DOD 04/04/2006). Also already HYDROCEPHALUS shattered the life of my own girl child MEENU, K 19 yrs is a bed patient with 8 or 9 life problems of medical disabilities.
The space between heartache and happiness: Two sons with adrenoleukodystrophy: From the Thriving blog
The space between heartache and happiness: Two sons with adrenoleukodystrophy: From the Thriving blog |  |
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Posted: 04 Oct 2017 12:01 PM PDT
Learn more about the results of the clinical trial, recently published in the New England Journal of Medicine, that halted the progression of Brian’s ALD.
ALD is short for adrenoleukodystrophy, a debilitating brain disease that simply goes by its initials.“Life before ALD was pure happiness without worries,” Paul says. “It was anything a parent could wish for — two boys with no medical issues, active, athletic, the healthiest boys ever.” The two were inseparable. They played sports together in their hometown of Dover Plains, New York; idolized superheroes; danced like crazy; and dreamed of someday inventing video games. Brian was Brandon’s shadow.  The first signs of ALDIt all began with a phone call from Brandon’s school in May of 2014.“They asked, ‘Is everything OK at home?’” explains Paul. Brandon, then a 6-year-old first-grader who excelled at reading and math, was showing signs of fatigue and an inability to focus. “Nothing is going on, everything is good. I am good,” Brandon told his mom and dad. “Like any parent, you let things play out,” Paul says. “Little did we know.” A month later, the Rojases received another call: “He’s having difficulty with basic math and reading comprehension.” “They were concerned,” recalls Paul. “And so were we.” At that point, Brandon was displaying only one neurological symptom — slight drooling. “We assumed it was because he had lost his two front teeth,” Liliana explains. The doctor came in and said, ‘Mr. and Mrs. Rojas, we need to speak to you.’ When they say something like that, when they walk you out of that room, you know something is wrong. However, the moment Brandon walked into the pediatrician’s office, the doctor noticed him leaning to the left side. “She wasn’t too concerned,” says Paul. “But to cover all the bases, we were referred to a pediatric neurologist.” The neurologist noted the same left-side weakness. Brain scans were ordered: an MRI and an electroencephalogram (EEG). Weeks later, Paul and Liliana waited patiently for results in Brandon’s hospital room at the Montefiore Medical Center in Bronx, New York. They already knew the EEG was abnormal, a slow frequency for a child his age, but the MRI would reveal whether there was damage to the brain tissue. “The doctor came in and said, ‘Mr. and Mrs. Rojas, we need to speak to you,’” recalls Paul. “When they say something like that, when they walk you out of that room, you know something is wrong.” Paul and Liliana sat side by side in a conference room flanked by four doctors who shared Brandon’s presumed diagnosis — adrenoleukodystrophy. “What is that?” Liliana asked. “How do you even say that word?” The doctors explained how adrenoleukodystrophy is a genetic mutation on the X chromosome, passed from mother to son; how it causes a buildup of very long chain fatty acids that destroy the protective sheath around nerve cells, responsible for thought and muscle control; how it primarily affects young boys between the ages of 4 and 10, leading to permanent disability or death within four to eight years. Then, they asked, “Do you have any other children?” “It was a nightmare,” Paul says. “In one sit-down, they give us a diagnosis on Brandon, and then we learn it’s possible Brian has the same thing.” The following day, the Rojases took the train to Mount Sinai Hospital in New York City, where Brandon’s blood was drawn and scrutinized to check for high levels of very long chain fatty acids and for genetic testing to confirm the diagnosis. Paul and Liliana knew Brian also had to be tested, but it was too much too soon. “We wanted to confirm with Brandon first,” Liliana explains. Three weeks later, they learned the worst. Brandon had ALD. “We talked to him about what was going on with his body, about the disease,” Paul says. “We told him, ‘Mom, Dad and the doctors are all working together to fight it, not to worry, we will always be by your side.’”  A race against adrenoleukodystrophyIt had been a month since the Rojases first heard the word “adrenoleukodystrophy.” They began to notice subtle changes in their 7-year-old son. “His smile was crooked,” remembers Paul. By October, he was in a wheelchair and no longer able to speak.The Rojases tirelessly researched ALD, connected with doctors and families, collecting any information they could get their hands on. They sought a second opinion in Baltimore, Maryland, at the Kennedy Krieger Institute’s Moser Center for Leukodystrophies, namesake of ALD pioneer Hugo Moser, portrayed in the 1992 film “Lorenzo’s Oil.” Dr. Seyed Ali Fatemi, director of the Moser Center, examined Brandon. “Dr. Fatemi explained there was no treatment for Brandon — he was far too advanced,” says Paul. “But he taught us how to give Brandon the best quality of life, and told us, ‘Please, let me know when you find out about Brian.’” That November, on a spur-of-the-moment Disney World vacation, Brandon’s Make-a-Wish trip, the Rojases learned the terrible news. Four-year-old Brian also had ALD.  Liliana remembers how difficult it was to hold herself together. “We were devastated, but we didn’t want to ruin the trip for the boys. Brandon was still able to see and feel things, so we had to manage to enjoy that moment.” Their first phone call was to Fatemi. He told them about an ALD gene-therapy study at Dana-Farber/Boston Children’s Cancer and Blood Disorders Center, an experimental treatment for asymptomatic boys, in which their own blood cells are removed, treated with a virus carrying the gene for the ALD protein and then reinfused. The added gene would enable Brian to make the protein needed to process certain fats. Without it, the fat gradually builds up, destroying the myelin sheath, which protects nerve cells in the brain. The Rojases would have to move quickly. Although Brian was not exhibiting any symptoms, adrenoleukodystrophy progresses rapidly.  Surviving adrenoleukodystrophyThe Rojases made their first trip to Boston in January of 2015. They stayed in the city for one month, while Brian underwent prescreening tests.In the meantime, they took a leave from their jobs — Paul, who works for the Port Chester School District in New York, and Liliana, who works at a Whole Foods Market in Connecticut. “Our employers were so understanding and so supportive,” Paul says. “We are both grateful for that every single day, and for the love and support of our local communities, family and friends.” Much to their relief, Brian was accepted into the trial and expected back in Boston by the third week of February. By then, Brandon had a feeding tube and his motor skills were diminishing, but Paul and Liliana took turns caring for him and spending time with Brian in the hospital. “The doctors said, ‘The younger the child, the easier it will be for them to recuperate,’” Liliana says. But still, it was difficult to watch 4-year-old Brian undergo infusions and chemotherapy to prepare him to accept the newly gene-corrected blood stem cells. Finally, Brian received the gene therapy treatment: a single infusion that everyone hoped would prevent this disease from affecting his brain. Back home in August, Brian prepared to start kindergarten. Remarkably, there was no sign of disease activity. And there hasn’t been since.  Coping with uncertainty, living with hopeThe joy the Rojases feel for Brian is tempered by the sorrow they feel for Brandon.Through Facebook, Liliana has connected with several moms who have children with adrenoleukodystrophy. “When I find out that another ALD warrior has lost his battle, it frightens me.” So, she hugs Brandon again — and again. She tells him how much she loves him, sings and reads to him. “I feel bad because I do a lot more for Brandon than Brian, but I don’t know how much time we have left with him. I think Brian understands.” Sometimes, Brian watches old videos of him and Brandon playing and goofing around. He says to his mom, “Oh, that was so much fun.” And he asks, “Brandon is going to get better, right Mommy? At a recent visit to Boston Children’s, the Rojas family met Dr. David Williams — chief scientific officer of Boston Children’s Hospital and president of Dana-Farber/Boston Children’s Cancer and Blood Disorders Center — who along with other researchers, helped mastermind Brian’s treatment.  Meeting him was a moment of sheer happiness. There were smiles, laughter, and there was hope, maybe not for Brandon, but for other boys. “Our mission is to move forward to the day when ALD is no longer here,” Paul says. Part of that mission is a push to add ALD to routine newborn screenings nationwide, spreading the word on a public Facebook page, Battling with Brandon. An estimated 1 in 21,000 male newborns will test positive for ALD every year, yet only a handful of states test them at birth — a cost of only $2.50 per baby. Newborn screening, together with FDA approval of ALD gene therapy, could, finally, mean hope for families who had no hope before. “Because we didn’t know, we didn’t have an opportunity to save Brandon,” says Paul. “This could be life changing.” In private, Liliana admits she cries. “I cry when I see pictures of when Brandon was healthy. I ask myself, why can’t I have him back like that? Then, he gives us that smile, and I know. He is still with us.” 
Get more information about how to enroll in the ALD gene therapy clinical trial.
The post The space between heartache and happiness: Two sons with adrenoleukodystrophy appeared first on Thriving Blog. |
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Meenu, K Do Jagadish Jagadishchandran Passed x from the G H S S, Medical College, Tvpm 695 011 in the Academic year 1916-I7.
Jagadish Jagadishchandran Meenu, K Do Jagadish Jagadishchandran Passed x from the G H S S,
Medical College, Tvpm 695 011 in
the Academic year 1916-I7.
Medical College, Tvpm 695 011 in
the Academic year 1916-I7.
Wednesday, September 20, 2017
MEENU K D/O JAGADISH JAGADISHCHANDRAN. CURRENT AFFAIRS.
K. MEENU, D/O OF JAGADISHCHANDRAN DOB 27/12/1995
IS A STUDENT OF PLUS ONE AT MEDICAL COLLEGE HIGHER SECONDARY SCHOOL,
THIRUVANANTHAPURAM 695011
Yes Nick Vujicic with the grace of God, please cross the boundaries, to build the bridges that bring people to the love and hope found in Jesus Christ...Inspire and spark the flame of hope in people's lives. Months back I came to view the video of you and downloaded in the computer and repeated viewed for the self satisfaction. Video shows when you fell down how you stand up without anybody's help except Jesus. Fantastic demo of your life in front of a group of school girls. Now I came to s
Great Encouragement for my life like millions in the world. I am having a child 16yrs old done a Brain Surgery for the sickness HYDROCEPHALUS at the age 1. V.P. Shunt done at the right side of Brain. Congenital hydrocephalus. By God's grace she can move with support and do all kinds of talk. Non schooling child is named by Meenu. Her mother passed away 5 years back due to cancer in Gall Bladder. The First child is studying in a Polytechnic College for the technical course. Pray for us and
JAGADIENDRAN J
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UNIVERSITY OF KERALA
Thiruvananthapuram
Date : 20/09/2017
Name of Programme : BTech Computer Science & Engineering ( 415 )
Semester : 8
ExamCode : 41513801
Month & Year of Exam : Apr 2017
Candidate Code : 13402064
Name of Student : JAGADIENDRAN J
Statement of Marks
Subject Code Subjects Credits SM UM Total Letter Grade
13.801 Cryptography and Network Security 4 28 8 36 F 13.802
Computer System Architecture 4 29 41 70 F 13.803
Distributed Systems 4 24 24 F 13.804
Elective III 4 23 30 53 F 13.805
Elective IV 4 27 32 59 F 13.806
Algorithm Design and Graphics Lab 4 37 49 86 F 13.807
Project Work and Viva Voce 5 126 71 197 B+
Semester : Failed Sem
Total : G.P.A : for Controller of Examinations
Thiruvananthapuram
Date : 20/09/2017
Name of Programme : BTech Computer Science & Engineering ( 415 )
Semester : 8
ExamCode : 41513801
Month & Year of Exam : Apr 2017
Candidate Code : 13402064
Name of Student : JAGADIENDRAN J
Statement of Marks
Subject Code Subjects Credits SM UM Total Letter Grade
13.801 Cryptography and Network Security 4 28 8 36 F 13.802
Computer System Architecture 4 29 41 70 F 13.803
Distributed Systems 4 24 24 F 13.804
Elective III 4 23 30 53 F 13.805
Elective IV 4 27 32 59 F 13.806
Algorithm Design and Graphics Lab 4 37 49 86 F 13.807
Project Work and Viva Voce 5 126 71 197 B+
Semester : Failed Sem
Total : G.P.A : for Controller of Examinations
FINAL YEAR RESULT OF THE JAGADIENDRAN J
UNIVERSITY OF KERALA
Thiruvananthapuram
Date : 20/09/2017
Name of Programme : BTech
Computer Science & Engineering ( 415 )
Semester : 8 ExamCode : 41513801
Month & Year of Exam : Apr 2017 Candidate Code : 13402064
Name of Student : JAGADIENDRAN J
Statement of Marks
Subject Code Subjects Credits SM UM Total Letter Grade
13.801 Cryptography and Network Security 4 28 8 36 F
13.802 Computer System Architecture 4 29 41 70 F
13.803 Distributed Systems 4 24 24 F
13.804 Elective III 4 23 30 53 F
13.805 Elective IV 4 27 32 59 F
13.806 Algorithm Design and Graphics Lab 4 37 49 86 F
13.807 Project Work and Viva Voce 5 126 71 197 B+
Semester : Failed Sem Total : G.P.A :
for Controller of Examinations
JAGADIENDRAN J 13402064 BTech Computer Science & Engineering ( 415 ) College S.C.T College of Engineering,Thiruvananthapuram (402 )
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Thursday, August 31, 2017
Kerala man kills parents, sister to ‘separate souls from bodies’
DECCAN CHRONICLE
PublishedApr 11, 2017, 4:58 pm IST
UpdatedApr 11, 2017, 5:17 pm IST
The suspect was fascinated by the concept after coming back from Australia where he had studied engineering.
The suspect Cadell Jeansen Raja (Photo: File)
Thiruvananthapuram: A man who was arrested for killing four people, told police that he allegedly committed the crime as part of an experiment to ‘detach souls from human bodies’.
According to a Hindustan Times report, psychiatrists were called in after to interrogate the suspect, who also suffered from bipolar disorder. The suspect had claimed that the murders were part of an experiment in the field of astral projection.
Astral projection involves separating one’s soul from its physical body to create an out-of-body experience.
The suspect was fascinated by the concept after coming back from Australia where he studied.
Many pieces of circumstantial evidence had pointed to the culpability of Cadell Jeansen Raja, who was arrested on Monday and was being interrogated in connection with the murder of four including his parents and sister.
The police, during the first day of probe on Sunday, identified the fuel pump at Pattom from where he purchased litres of petrol to burn the bodies. Until minutes before the house was set ablaze, he deliberately tried to hide his presence in the house.
Furthermore, he is suspected to have laced the food eaten by his parents professor Raja Thankam, 60, Dr Jean Padma, 58, and sister Carol, 25, before allegedly murdering them.
Phenol was purchased to camouflage the smell of putrefying bodies and police has identified the source. He stayed with the three dead bodies for over a day planning various ways to dispose them. Finally, he hacked his blind relative Anitha Jane, 70, into pieces on Friday.
In order to avoid the maid, he asked her to cook food and keep it at his relative’s house but did not show up there.
The police were verifying whether a gaming addiction has served as a catalyst to his allegedly murdering his family. Cadell was sent to Philippines to study MBBS but discontinued his studies claiming computer engineering was his forte. Later he studied engineering in Australia but returned home after flunking. He has reportedly co-developed a gaming search engine which he sold to a multinational company earning big bucks that helped him thrive.
Kerala man kills parents, sister to ‘separate souls from bodies’
DECCAN CHRONICLE
PublishedApr 11, 2017, 4:58 pm IST
UpdatedApr 11, 2017, 5:17 pm IST
The suspect was fascinated by the concept after coming back from Australia where he had studied engineering.
The suspect Cadell Jeansen Raja (Photo: File)
Thiruvananthapuram: A man who was arrested for killing four people, told police that he allegedly committed the crime as part of an experiment to ‘detach souls from human bodies’.
According to a Hindustan Times report, psychiatrists were called in after to interrogate the suspect, who also suffered from bipolar disorder. The suspect had claimed that the murders were part of an experiment in the field of astral projection.
Astral projection involves separating one’s soul from its physical body to create an out-of-body experience.
The suspect was fascinated by the concept after coming back from Australia where he studied.
Many pieces of circumstantial evidence had pointed to the culpability of Cadell Jeansen Raja, who was arrested on Monday and was being interrogated in connection with the murder of four including his parents and sister.
The police, during the first day of probe on Sunday, identified the fuel pump at Pattom from where he purchased litres of petrol to burn the bodies. Until minutes before the house was set ablaze, he deliberately tried to hide his presence in the house.
Furthermore, he is suspected to have laced the food eaten by his parents professor Raja Thankam, 60, Dr Jean Padma, 58, and sister Carol, 25, before allegedly murdering them.
Phenol was purchased to camouflage the smell of putrefying bodies and police has identified the source. He stayed with the three dead bodies for over a day planning various ways to dispose them. Finally, he hacked his blind relative Anitha Jane, 70, into pieces on Friday.
In order to avoid the maid, he asked her to cook food and keep it at his relative’s house but did not show up there.
The police were verifying whether a gaming addiction has served as a catalyst to his allegedly murdering his family. Cadell was sent to Philippines to study MBBS but discontinued his studies claiming computer engineering was his forte. Later he studied engineering in Australia but returned home after flunking. He has reportedly co-developed a gaming search engine which he sold to a multinational company earning big bucks that helped him thrive.
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