09-Sept-2021 — Spanish conservative bishop Xavier Novell Goma has resigned from his office because he has fallen in love with the author of satanic-erotic ..
08-Sept-2021 — When Spanish bishop Xavier Novell resigned last month, the Roman Catholic Church cited strictly personal reasons without going into detail.
When
Spanish bishop Xavier Novell resigned last month, the Roman Catholic
Church cited strictly personal reasons without going into detail.
It has now emerged in Spanish media that he fell in love with a woman who writes Satanic-tinged erotic fiction.
In 2010 at the age of 41, he became Spain's youngest bishop, in Solsona in the north-eastern region of Catalonia.
It
came as a shock when Religión Digital reported that he had fallen for
divorcee Silvia Caballol, a psychologist and erotic novelist. The news
site said that the former bishop was now looking for a job in the
Barcelona area as an agronomist.
Caballol's
books include titles such as The Hell of Gabriel's Lust and the trilogy
Amnesia. In the blurb for one of her works, the reader is promised a
journey into sadism, madness and lust and a struggle between good and
evil, God and Satan with a plot to shake one's values and religious
beliefs.
Neither
the ex-bishop, who is now 52, nor the novelist have responded to the
reports although Religión Digital quoted him as saying "I have fallen in
love and want to do things properly". ...........................................................................................................
Love is the greatest because God showed us, through His Son Jesus Christ, how great His love is for us. Therefore, through that expression from God, ...
From
his home in Portola Valley, California, Sanjiv Gambhir logged on to an
important meeting for his startup one afternoon in April 2020. He kept
the video camera off.
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This
was unusual, not least because he cherished face-to-face connections
and was obsessed with visibility. A pioneer of molecular imaging and the
director of Stanford’s Canary Center for Early Cancer Detection,
Gambhir, known as Sam, had spent decades trying to make small, hidden
tumors inside the body easier to see. Nearly 600,000 people in the U.S.
die from cancer every year, mostly because we tend to catch tumors when
they’re too late to effectively treat.
“Cancer doesn’t need to be a
death sentence,” Gambhir would tell the researchers in his lab, as he
reminded them of the actual patients they were trying to save. By the
time he was 50, his breakthroughs in early detection—including
developing the reporter genes used in positron emission tomography, or
PET scans—had led to three startups, millions in seed funding, and 40
patents.
His latest startup, Earli,
was the culmination of a decade’s-worth of research into whether you
could force tumors to show themselves, by having them send out a signal
that could be detected in blood tests or PET scans. If that worked, you
could open up a new frontier in cancer detection. Gambhir had pioneered
the technology, but cofounder Cyriac Roeding, an energetic e-commerce
entrepreneur had convinced him to turn it into a company. By the start
of 2020, they had already raised $19.5 million in venture funding to
fuel the commercialization of their technology.
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But
in 2019, doctors had detected something inside Gambhir. A tumor of
unknown origin was quietly spreading in his bones. The irony of cancer
sneaking up on him was as brutal as the prognosis: After finding such
metastasis, the median survival time is three to four months. But
Gambhir turned his cancer and his experimental treatments—every few
weeks in Munich—into a learning opportunity for himself and his
colleagues. Now, a year after his diagnosis, he was bedridden and weak
from the treatments. But he was determined to be on this call.
For
three hours, Gambhir and the rest of the five-person board—including
Jorge Conde, a biotech veteran and partner at the prominent venture
capital firm Andreessen Horowitz—discussed manufacturing challenges, the
search for more cash, and the results of a recent study the company had
done in mice. “He was sharp as a tack. I mean, for God’s sake, the guy
was still pulling apart the science,” says Earli cofounder and chief
scientific officer David Suhy. “But you could hear in his voice, he was
physically weak.”
Gambhir
was often reminding his cofounders how bedeviling biology could be, how
resistant it was to commercialization. “The world of biology will
always find a way to screw you over,” he’d warned Roeding as they were
founding the company in 2018. After establishing Stanford’s
Multimodality Molecular Imaging Lab in 2003, Gambhir had helped develop
an armory of futuristic advances for spotting tumors, including a smart
bra to continuously monitor for breast cancer and a smart toilet for
detecting colon cancers. But much of the tech was still experimental.
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As
Gambhir pursued this research, his wife, Aruna, battled back breast
cancer—twice. Then, in 2013, biology reared its head in another,
horrible way: Their 15-year-old son, Milan, was diagnosed with a rare
form of the most aggressive kind of brain cancer, the very type of tumor
Gambhir’s lab had been studying. Gambhir’s need to translate his work
from lab to practice had never been more urgent. But Milan’s cancer
proved quicker than the pace of medicine. He died in 2015, at the age of
16.
Five years later, as a tumor spread in his own body, Gambhir
felt a different kind of urgency. “The problem is, he knew too much,
even with Milan,” says Aruna. Now Gambhir’s ideas and multi-disciplinary
insights into molecular imaging—his one-of-a-kind knowledge of the
field—would need to go to the scientists and doctors who could make the
most of it, even in his absence.
When President Nixon launched the
war on cancer 50 years ago, Sidney Farber, the president of the
American Cancer Society, declared that with enough resources, scientists
could conquer cancer in seven years. Instead it has been a protracted
war with a roving target. Despite hundreds of billions of dollars spent
on research, cancer is now vying with heart disease to be the number one
cause of death in the U.S. “Since 1970, there’s maybe 50% improvement
in cancer survivors,” says Leland Hartwell, an advisor to Earli whose
work on cell growth earned him a Nobel Prize in Biology. “Given all the
effort, it’s not great.”
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The
hope now isn’t a cure, but finding the right combination of diagnostics
and treatments to manage it. And after years of relatively miniscule
government funding, detection is getting more attention. The race to
catch cancer earlier has given rise to a $168 billion industry
touting a new class of tests that promise to detect tiny signs of
cancers in your blood or stool. Most are pursuing an approach known as
“liquid biopsy,” using a blood test to look for abnormal pieces of DNA
shed by cancer cells.
Finding bits of cancer cell sheddings,
however, is notoriously hard. Earli’s approach compels tiny tumors to
produce new signals, sending out flares—naturally-occurring
proteins—that can be more easily detected in a blood test or illuminated
for an imaging scan. A reliable diagnostic that could be administered
once a year by a doctor to find and pinpoint very early, aggressive
tumors in apparently healthy people could have a profound impact on
healthcare and its costs.
“Once you find [a tumor] and you can
localize it, you can act on it, and then it becomes protection, not just
detection,” Roeding says. Someday, Earli’s “synthetic biopsy” platform
could even be useful for targeting cancer cells with personalized
medicine, immunotherapies, or mRNA vaccines. Already the company has
shown an ability to detect certain cancers in mice and dogs; in June, it
began dosing its first human patients as part of a clinical trial. But
it still has a long way to go.
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Back
at the board meeting, Roeding reviewed the results of their first trial
in mice. The synthetic biomarker they were using to tag tumor cells had
shown up in PET scans of cancerous mice—a little glowing lighthouse in a
sea of uncertainty. Suhy and Roeding were ecstatic. Gambhir was
circumspect. “He asked us four questions,” Roeding recalls. Did the test
actually detect cancer? Did it have a low false negative rate? Was it
differentiating between malignant and benign? Could it determine the
stage of cancer?
The trial was promising, but Gambhir needed more
than promises. In June 2020, three months after the board meeting—and
the day after receiving Stanford’s Dean’s Medal, its highest honor—he
died at home at the age of 57.
For
the field of early cancer detection, the loss was devastating. Tributes
poured in from researchers around the world, and colleagues held a
string of academic symposia dedicated to his legacy. Last September, the
Journal of Nuclear Medicine bucked a 55-year tradition for the cover, trading its typical medical imagery for a full-page portrait of Gambhir.
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His
company, meanwhile, is forging ahead and confronting another big
question: Can they manifest a technology without the visionary who
dreamt it up? “We are working on a very low probability, but potentially
high impact thing,” says Roeding. “It’s a moonshot. There’s no doubt
about it.”
Light-haired and boyish, Roeding was born in
Germany, and yet is the archetypical energetic Silicon Valley
entrepreneur-investor. A veteran of business consulting, smartphone-era
startups, and venture capital, he can repeat a well-rehearsed pitch
verbatim and never sound scripted—skills that helped him build up the
in-store discount app Shopkick and sell it for $250 million to the
biggest telecom company in South Korea.
In 2016, a couple years
after that deal, Roeding was in the Bay Area looking for his next
startup idea. An interest in brain-computer interfaces brought him to
Stanford’s campus, which in turn led him down the rabbit hole of
precision medicine. But the deeper he got, the more confused he became.
Here were all these scientists saying they each had the solution to the
world’s various biggest problems. “I’m not a biologist,” says Roeding.
“I didn’t know who was wrong.”
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By
Thanksgiving, three months into his search, Roeding was feeling
deflated. That morning, his wife handed him a copy of Stanford’s alumni
magazine and suggested he read the cover story, about a prominent
radiologist’s struggle to save his son from metastatic brain cancer. The
piece shook him, and early that afternoon he sent an email to its
subject, Gambhir. “I can only imagine how hard especially holidays like
today’s are for you and your wife,” Roeding wrote. “But perhaps just on a
day like this, it is worth remembering that Milan, your journey to try
to save him, and the powerful ideas that have come from this journey,
have inspired others like me.” Roeding introduced himself, and said he,
too, was interested in health monitoring. “Perhaps there are ways we
could work together.”
Two months later, they met on a sun-drenched
Saturday at a small restaurant in Portola Valley, a town near Palo
Alto. They talked about innovation and science and the yawning chasm
between academia and commercial medicine. After years of navigating the
bureaucracies of biomedical research, Gambhir was drawn to Roeding’s
left-field thinking. The lunch became the first of many Saturday
meetings. Gambhir agreed to teach Roeding biology (“largely in vain,”
says Roeding) and introduced him to even more scientists. But Roeding
was more eager to hear what Gambhir was working on. When Gambhir told
him about his lab’s work around using biomarkers to catch tumors earlier
than other diagnostics, Roeding was hooked.
They used $400,000 of
their own money to get started, incorporating the company in June 2018.
They negotiated a licensing deal with Stanford for Gambhir’s related
patents and tapped Suhy, who previously led gene therapies at Australian
biopharma Benitec, to serve as chief scientific officer. Gambhir would
be a scientific advisor and Roeding became CEO.
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Roeding
was an unusual choice to helm a breakthrough biotech company. He
recalls asking Gambhir: “Should someone with my background bother the
world of biology with my presence?” The field of biology has a surplus
of experts and no generalists, said Gambhir, and few people who knew how
to run a startup. On top of that, he said, biology is fickle:
biological exploration will always take longer and be harder than you
think. He argued that being able to move fast—and, yes, fail fast—could
help the company resist the inertia of experiments, trials, and
regulations.
At the start, Roeding’s aggressive targets raised
eyebrows among investors. “We said, we want to be in humans within three
years, and they kind of chuckled,” says Roeding. Most weren’t
convinced, but the pitch caught the attention of Andreessen Horowitz’s
Conde, who is a biotech industry veteran. Before the year was out,
Gambhir and Roeding had secured just shy of $19.5 million in seed
funding from a group led by Andreessen Horowitz that included Salesforce
founder Marc Benioff, Menlo Ventures, and Chinese venture firm
ZhenFund.
Even with buy-in from the likes of Andreessen and
Benioff, the founders knew their operation faced an uphill battle.
Diagnostics that require injecting patients face a phalanx of clinical
trials, a process that takes years even with the enormous resources of
giant pharmaceutical companies. While Earli had shown some promise in
the lab, there wasn’t a guarantee it would translate to animals. And
scientists had never tested synthetic biomarkers in humans: There were
likely to be unusual regulatory hurdles to getting a clinical trial
approved.
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For
the first year, Suhy and Roeding met with Gambhir every four to six
weeks to talk about the company’s progress. They managed day-to-day
operations, but Gambhir could find the holes in their thinking and minor
successes—an invaluable perspective in setting the direction until
their next meeting. As the hours wore on, their conversations would
inevitably give way to heady discussions on the state of science.
In
late spring of 2019, Roeding got a call from Gambhir. His voice sounded
funny. He told Roeding that he was sitting on the couch with his wife.
They had just found out that he had cancer, and it wasn’t clear where it
had started. By definition, it was metastatic and almost impossible to
treat. If they didn’t know where it originated, they couldn’t know what
they were fighting.
Roeding tried to stay optimistic. “It’s battle
time,” he told his cofounder. Gambhir said there were possible
treatments, but he was also clear-eyed. They agreed that they needed to
prepare the company for a world without Gambhir.
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“We
have to make sure that our science is advanced enough so that we can
move forward without having to rely on his input at a deep level
continuously,” Roeding recalls realizing. “For us, really the main
question became, does Earli have enough escape velocity so that we can
become what [Gambhir] wants us to be?”
The biggest victories
in the war on cancer have been scored via anti-smoking campaigns and
cigarette taxation. They’re largely responsible for the 27% drop in
deaths from cancer in the U.S. between 2009 and 2019, according to the
Center for Disease Control and Prevention (in lung cancer, advances in
targeted therapies also played a role). Still, little has progressed in
screening, which scientists see as the best opportunity to find cancer
before it gets out of control.
Chances are, you’ve been through
multiple cancer screenings: mammograms, pap smears, colonoscopies, when a
doctor takes a look at the weird mole on your back. Long-time smokers
over 50 years old might get a CT scan. For certain cancer types, these
screens, which mostly rely on seeing physical changes, can save lives.
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But
there are lots of forms of cancers that can’t be screened for: ones
that are too small to see or that haven’t necessarily caused any bodily
changes. Tumors mutate and evolve in unique ways, so each person’s
cancer is a little different. A tumor that’s benign in one body could be
deadly in another. “What we’re faced with is just enormous diversity,”
says Earli advisor Hartwell.
As a result, cancer treatment has
become more personalized, with scientists tailoring dosage and type of
therapeutic to the genetic makeup of a cancer’s cells. But some
scientists, including Hartwell, think that developing better earlier
detection methods will offer a far less invasive—and far more
affordable—path to lowering cancer deaths. So far, however, early
detection has proceeded in fits and starts. “The cost per advance is not
impressive,” he says.
The
latest and greatest tools in cancer diagnostics are genetic testing and
liquid biopsy tests. Genetic testing alerts doctors to potential genes
that are associated with an increased risk of cancer, like BRCA-1 and
BRCA-2 for breast cancer. Liquid biopsies capitalize on advances in
machine learning to analyze blood samples for the tiniest clues of
cancer, by detecting and analyzing fleeting fragments of cells that
tumors shed. These can include DNA, RNA, proteins, and other pieces of
cancer cells that circulate in the body and sometimes contain clues
about their location.
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Menlo
Park-based Grail—one of dozens of companies that Gambhir advised—now
sells a liquid biopsy test called Galleri, which purports to find 50
types of cancers in apparently healthy people. The test, at $950, is not
covered by insurance, but that could change after full FDA approval,
which Grail intends to seek in 2023. Another California company,
Redwood-based Guardant Health, is currently running trials of its
early-stage colorectal cancer test, eyeing a market for early detection
that’s expected to reach $280 billion by 2027.
Not everyone is so
bullish on liquid biopsies, however. “I should be careful what I say. I
could make myself persona non grata,” says Judy Garber, Director of the
Center for Cancer Genetics and Prevention at Dana-Farber Cancer
Institute and board member to Earli. Several liquid biopsy companies,
she says, “want to find all cancer at once, which I agree would be
great. But I think that hasn’t been what the data supports, and yet they
seem to be in this huge rush to sell their test.”
The most compelling recent data
showed that Grail’s test could positively identify stage I to III
cancer more than 67% of the time in a set of twelve cancers including
head and neck, liver, and pancreatic cases. Overall, the test had a
false positive rate of 0.5%, and was able to identify the tumors’ organ
sites 88.7% of the time. But its ability to detect other cancers was
lower: It identified less than 20% of thyroid, kidney, and prostate
cancer cases, for instance.
One
major challenge with looking for natural biomarkers, like cell
sheddings, is that young tumors produce far fewer of these fragments.
Even when these cancer bits do make it into the bloodstream, they spend
less time in circulation, making it exceedingly difficult to pull them
out in a sample.
Earli’s diagnostic takes a more proactive
approach to the search for tumors. The platform consists of an
injectible compound that carries a reporter gene, engineered to activate
at the faintest hints of tumor cells, wherever they are. Once it’s
tapped into the cellular pathways driving the tumor’s uncontrolled
growth, the gene is designed to express a synthetic biomarker,
effectively “boosting” the cancer’s signal. For its biomarker, Earli
chose an enzyme that typically only appears during embryonic
development. (A Cambridge-based startup called Glympse is developing
synthetic biomarkers to identify liver disease, though cancer detection
is also on its roadmap.)
The approach has several apparent
advantages over current liquid biopsy technologies. Because it uses a
synthetic biomarker, Earli can more easily control the amplitude of the
signal. Where liquid biopsy companies use the genetic code of cancer
fragments to try to determine a tumor’s location in the body, Earli
pinpoints the tumor itself. This could also help physicians better track
the success of ongoing therapies, and lead to novel therapies: With an
additional molecule designed to trigger an immune response in cancer cells, Earli’s surveillance platform could eventually be harnessed to kill elusive tumors too.
Hartwell
remembers hearing Earli’s concept for the first time, and being struck
by it as “incredibly brilliant.” “You sort of wonder why it took us so
long to think of it,” he says. “But that’s not what makes a successful
company.” If Earli is going to be “a company rather than just a research
project,” he stresses, it needs to quickly identify—and market—an
application of its technology. “That’s a race that you can’t predict.”
When
Gambhir died, the company was still in semi-stealth. Earli barely had a
web presence, save for a recruiting website, and had interesting, but
nascent progress in mice. It needed more cash, to hire more scientists,
double down on pre-clinical research, and start building out a new lab.
Before
Gambhir’s last board meeting, the company began getting feedback from
his longtime colleagues and friends, a Who’s Who of cancer pioneers:
Hartwell and Garber, but also Nobel Prize-winning cancer researcher Jim
Allison, Moderna founder Bob Langer, Charlie Rudin, who heads up
thoracic oncology at Memorial Sloan Kettering, and Aruna, who now runs
another company related to her husband’s research called CellSight,
which is working on technology that recognizes if cancer treatment is
working.
In fall 2019, Langer dashed off an email to investor
Vinod Khosla, founder of Khosla Ventures, introducing him to Earli and
laying out how it differed from liquid biopsy firms. Khosla had for
years passed on high-flying biotech investments, but says he was drawn
to Earli’s “orthogonal approach” to early detection, versus the
“incremental” efforts of other ventures. Khosla likens Earli to
Cambridge-based Commonwealth Fusion Systems, one of his biggest
investments, which is aiming for the moonshot of nuclear fusion. “In our
fund, we sort of say, ‘large impact, large technology breakthroughs
that cause a large impact’—if you do that, the money will follow.”
In
January 2020, Khosla Ventures led Earli’s $40 million series A,
alongside Andreessen Horowitz. The board now includes Conde, Justin Kao,
who led Khosla’s investment, and Marc Andreessen, who serves as a board
observer.
“It’ll never be quite as good as if Sam was working
on it himself,” Khosla admits, “but they’re at a proof point that is
substantially lower risk today than it was two years ago.” He pointed to
“a cadre of world-class scientists” that Earli has recruited as
advisers. “If it can be done, I think this team can do it.”
With
the funds, Earli went on a hiring spree: 29 researchers now work at its
headquarters in South San Francisco. And Roeding and Suhy decided to
pursue a proof of concept in dogs. The company worked with the
Comparative Cancer Center at the University of California Davis School
of Veterinary Medicine, which connects sick dogs with clinical trials.
Together they studied the biomarker at four different doses in a total
of 23 dogs to see if it would show up in blood work.
Michael
Kent, director of the center, says that Earli’s compound was well
tolerated, with only a few dogs developing a brief and low-grade fever.
Full trial results of the trial will be published later this year, but
the results were favorable. “This isn’t going to be in your doctor’s
office next year, but this could be game-changing,” Kent says. Unlike
the liquid biopsy tech Kent has tested, Earli doesn’t depend upon
serendipity to spot cancer. “You have something making a clear signal
and saying, ‘Hey, I’m here!” That’s unique.” Earli is now funding
subsequent trials with dozens of dogs.
Demonstrating that the
test was nontoxic for dogs was crucial in getting the Australian
government to agree to let Earli begin its first human trials in the
country, which began this past September. So far, two people have been
dosed, and another is on track. The aim is to detect advanced-stage lung
cancer in already diagnosed patients—and to amass the data Earli will
need to convince the U.S. Food and Drug Administration to let it proceed
with a U.S. trial of its novel technology.
Suhy says he’s
encouraged by the speed with which the FDA approved mRNA vaccines during
the pandemic. That suggests regulators are amenable to novel medical
technology like Earli’s diagnostic. Still, he notes, those approvals
were based on years of data. And even if Earli achieves FDA approval, it
will need to convince doctors to add a novel diagnostic to their
workflow.
Nora Pashayan, a professor of Applied Cancer Research at
University College London who is not affiliated with Earli, calls its
concept “amazing.” But says “it could take a long time” for Earli to
come to market. And its approach faces several pressing questions, she
says, related to the design of the biomarker, how often it’s deployed,
and in whom.
These elements—how and who—matter, because contrary
to conventional medical wisdom, early detection doesn’t always save
lives. The problem is that doctors can’t always tell the difference
between a benign or malignant tumor and therefore may treat a tumor out
of an abundance of caution. “Other than the psychological burden [of
diagnosis], there are side effects of treatment—going into chemotherapy,
endotherapy, or surgery,” says Pashayan. “So the harms are much more
than the benefits, [if] this cancer was not going to do anything.”
A failed public health effort in South Korea serves as a cautionary tale.
Between 2000 and 2011, thanks to a government recommendation, doctors
in the country started screening everyone for thyroid cancer.
Unsurprisingly there was a surge in thyroid cancer diagnoses and surgery
to remove these tumors. However, after ten years, deaths from thyroid
cancer remained stable. The screening campaign wasn’t preventing death.
If anything, it was creating problems for people who were experiencing
complications from unnecessary surgery. For companies like Earli, the
protocols around a diagnostic matter as much as whether it works.
The
greater scientific research community still believes that early
detection tools, like Earli’s, are critical. Cancer drugs treat, but do
not cure—and are immensely expensive. The hope is that finding cancer
early, identifying the tumor profile, and stopping it before it spreads
could one day make getting cancer a relatively anxiety-free experience.
“What we need to show are the success cases of what it means to find it,
get rid of it, and live on,” says Roeding. “And in order to do that, we
need to find more early stage cancers.”
More than 1,600
people logged into Gambhir’s memorial service, which was held at the
height of the pandemic, in July 2020. Colleagues described his
generosity and far-sightedness. “It would not be entirely accurate to
say that Sam presented a ‘vision’ for the field of molecular imaging,
because that sounds a little like the elements of the vision were out
there and others were also aware of it,” said Norbert Pelc, Stanford
University professor emeritus of radiology. “Sam created the vision and
then articulated it. He was able to do that: See a path ahead many years
ahead of his time and explain it to an audience at a wide range of
levels.”
“He gave you confidence in that future,” says Christina
Zavaleta, an assistant professor of biomedical engineering at USC and
one of Gambhir’s hundreds of former students. Sam may not get to see
where all of his ideas will travel, but “he was already there in his
mind,” she says. “We’re the ones that have to catch up.”
[Photo: courtesy of Earli]
Gambhir’s
technology is bound to introduce new conundrums, about if and how to
treat previously hidden tumors. Even if Roeding and Suhy can
successfully render Gambhir’s novel early detection technology into a
marketable diagnostic, it won’t end our battle with cancer. Still, if
they can pull it off, it could give patients and doctors the luxury of
choice, something that Sam and Milan Gambhir didn’t have.
“It’s
a cruel irony that Sam’s own cancer was only detected after it had
spread to his bones,” Aruna, Sam’s wife, said at his memorial, her voice
breaking. “Perhaps if some of the tools in precision health were in
place, he would have had a chance to live and contribute even more. He
told me towards the end days that he felt he had another decade of
productive work left in him. Imagine what that could have meant for
humanity.”
'If there is effective prosecution, only then we will get justice, but first let them (NIA) run the case honestly in court.'
IMAGE: Residents and police officers clear
debris at a blast site in Malegaon, about 260 km northeast of Mumbai,
September 30, 2008. Photograph: Reuters
Photographs and videos of Bharatiya Janata Party member
of Parliament Sadhvi Pragya Singh Thakur have emerged on social media
showing her buying shoes from a store in New Delhi's Connaught Place and
playing sports with youngsters.
Nothing wrong with it, except that she refused to attend the National
Investigation Agency court hearings in Mumbai citing ill-health.
Sadhvi Pragya is one of the accused in the 2008 Malegaon blast case
in which seven people were killed and 80 injured. She spent almost eight
years in jail in the terror case before getting bail in 2017.
On Wednesday, December 1, Advocate Shahid Nadeem
filed a petition in the NIA court in Mumbai requesting that the NIA
obtain the assistance of Maharashtra's anti-terrorism squad in court
during the trial.
Nadeem represents Nisar Ahmed Sayeed Bilal whose 20-year-old son was among those killed in the Malegaon blast.
Nadeem also sent a letter to the NIA superintendent in Mumbai with
the same plea, and marked a copy of the letter to the Chief Justice of
India as well of the Bombay high court.
In his letter, Nadeem argued that after eight witnesses turned
hostile in the Malegaon blast case, the Maharashtra AT's intervention
was necessary to prevent more witnesses from turning hostile in court.
"I have apprehension that this case will end up in acquittal like
those of the Mecca Masjid blast, Samjhauta Express blast or Ajmer blast
where witnesses turned hostile," Nadeem tells Syed Firdaus Ashraf/Rediff.com.
Two years ago you filed a plea in the NIA court
requesting the Maharashtra ATS to assist the NIA in the Malegaon blast
case. Why are you filing this petition again?
There is a difference now.
Two years ago, the trial was just beginning in the Malegaon blast
case and that time we told the court that the ATS must come and take
part in the court proceedings because it is their investigation. But
then the court told us that they cannot tell the ATS to attend court
proceedings because it is up to the ATS whether they want to come for
court proceedings or not.
The court further told us that it has no power to call them.
Now, after two years, the situation is different. The court has
examined 208 witnesses out of whom eight have turned hostile and the
hearing is happening on a day-to-day basis.
So, we wrote a letter to the NIA superintendent in Mumbai stating
that he must intervene and take help from the ATS, otherwise the
Malegaon blast case outcome will be the same as in the Samjhauta
Express, Ajmer blast and Mecca Masjid blast (cases) in which witnesses turned hostile and all the accused were let off.
But why are you writing this letter in anticipation that witnesses will turn hostile in future?
I told you eight witnesses have turned hostile in the last three
months. I am attending court daily and I know what is happening. And
therefore, I have apprehension that this case will end up in acquittal
like those of the Mecca Masjid blast, Samjhauta Express blast or Ajmer
blast where witnesses turned hostile. And the court let off all the
accused in those cases.
How many witnesses are yet to be examined and how many have not turned hostile?
That way there are 500 witnesses, but then it all depends on whom
they bring in as witness and whom they do not bring. I can't tell who
they want to examine and who they do not want to examine in court.
Moreover, whatever the witnesses have said earlier, they must stick to
their stance in court.
Why you think the ATS's intervention will help in this case?
All the witnesses in the Malegaon blast case are ATS witnesses. They
recorded the statement of witnesses and not the NIA. NIA officers have
no idea in what situation these witnesses's statements were recorded and
what the consequences were there that time. The loopholes in this case
can be pointed out by the ATS only and not the NIA.
This case was investigated by then Maharashtra ATS chief Hemant Karkare who was martyred in the 26/11 terror attack.
(Interrupts) The chargesheet which he filed, the court has
accepted it. The court has not discarded his chargesheet. Now the
present ATS chief can send his officers to court to assist the NIA.
But this case was handed to NIA in 2011 and
since then the Maharashtra ATS has been out of it. Ten years is a long
time. So why do you need the ATS?
NIA has not done the initial investigation. They have only filed a
supplementary chargesheet in court. Today, there are two chargesheets in
court (one by the ATS and one by the NIA) and the court has taken cognisance of both chargesheets.
NIA did a little investigation and after that they gave a clean chit
to Sadhvi Pragya Singh Thakur. Rest all chargesheet of the ATS has been
accepted by the NIA and therefore the case is going on against Colonel
Shrikant Purohit, Sameer Kulkarni and Ajay Raikar. These all are the
people apprehended by the Maharashtra ATS.
Justice Ranjit More said in his bail order that prima facie there is no case made out against Sadhvi Pragya Singh Thakur, isn't it?
The case against the rest of the accused was made out. Moreover,
Sadhvi Pragya was only given bail and not discharged. She is facing
trial even today.
The conflict in this case has been there from
day one because the ATS investigated this case from one viewpoint and
angle which was not taken into account by the NIA when it started
investigating, isn't it?
Whatever their viewpoint or angle the fact is the court has accepted
the Maharashtra ATS's investigation into the Malegaon blast case. The
trial is going on according to the chargesheet of the ATS.
The court has recorded only 10 witnesses of the NIA against Sadhvi
whereas other 500 witnesses against Sadhvi was recorded by the ATS. NIA
did further investigation in the Malegaon blast case and filed 50-60
pages of a supplementary chargesheet. There are thousands of pages of
chargesheet filed by the ATS on which the Malegaon blast trial is going
on.
What is going on in court right now in the Malegaon blast case?
Daily
hearing is going on. Some 208 witnesses have been examined out of which
eight have turned hostile. Now, we have apprehension that more
witnesses coming in this case will turn hostile in future.
What about the other 200 witnesses? Didn't they turn hostile?
Most of them were policemen and injured people. How can injured
people turn hostile? Obviously, they will not turn hostile. In the same
way policemen too will not turn hostile.
The people who are turning hostile are the ones who are known to the
accused, their friends and neighbours. They had given statements against
the accused to the ATS, but now they are turning hostile one by one in
court.
These witnesses feel that the ATS is not coming to court and they are
not being watched so they can say what they want as nothing will happen
to them. And this will surely impact the trial in Malegaon blast.
Public Prosecutor Rohini Salian in an interview
to a newspaper in 2015 said that NIA officers told her to go soft on
accused Sadhvi Pragya. Can you comment on it?
I am only saying that if the ATS investigation was false the court
would not have taken that into cognisance. In 2016 all the Muslim
accused in the 2006 Malegaon blast case were discharged by the court
saying that the ATS investigation was wrong. And in the 2008 Malegaon
blast case, the court accepted that the ATS investigation was right.
Now when the trial goes further the court will decide whose investigation is right (NIA's or ATS's).
What about images of Sadhvi Pragya on social media after she told the court she was unwell to attend the hearings?
That is not my concern. Let her do what she wants. My only concern is
that the trial should go in the right direction in court. And, I have
made my statement in the court.
I am a victim and I want a fair trial. And a fair trial will take place only when the ATS comes to court and helps the NIA.
Having said that, it is possible that the NIA does not want to take help from the ATS.
They are two different investigating agencies.
Different investigating agencies, but the chargesheet of both the agencies have been accepted by court.
How will taking help from the ATS help the NIA? What will change?
ATS did the initial investigation and all the panchnamas are written in Marathi. The NIA is a central agency and we don't know whether their investigating officer knows Marathi.
If there are mistakes or loopholes happening from the prosecution
side in the case, then it is only the ATS that can help the NIA
prosecutor.
We want an effective trial. We don't want a time-pass trial of the Malegaon blast.
We don't want this trial to end like that of the Mecca Masjid, Ajmer
Dargah blast and Samjhauta Express trial. All the accused in those cases
too were from the same radical Hindu ideology and they were let off.
How many witnesses turned hostile in those cases?
In the Ajmer Dargah and Mecca Masjid blast (case) 55 witnesses turned hostile. In the Samjhauta Express blast case, if I am not mistaken, 25 witnesses turned hostile.
The trial court said in its observation that because of the inability of NIA we are acquitting the accused.
Therefore, we have apprehensions that the same thing must not repeat in the Malegaon blast case.
In those cases, victims were not keeping a proper watch on the case,
but here in this case we are keeping day to day watch. Therefore, we
have requested the superintendent of NIA to take the help of the ATS
because they are relying on their chargesheet in the court.
There can be only one prosecutor in the court and we are not even
demanding another prosecutor. We are just saying that those
investigators from the ATS who cracked the case, please take their help
in court. They can ask those ATS investigators why witnesses are turning
hostile in the case, NIA can find out.
If there is effective prosecution, only then we will get justice, but first let them (NIA) run the case honestly in court.
Do you mean the NIA is not running this case honestly in court?
Yes, therefore eight witnesses have turned hostile in the Malegaon
blast case. And if the case continues in the same manner, more witnesses
will turn hostile