Joe Blackburn: Did Prader-Willi cause his death? Death & Documentary in Bradford

A character from the documentary The House That Can’t Stop Eating is Joe Blackburn. Many individuals ask if Prader Willi caused his death. Investigate it below.

The 2006 film Can’t Stop Eating chronicles the lives of various Prader-Willi Syndrome patients (PWS).

It takes place at Gretton House, a nearby Kettering care facility in England backed by the government and designed expressly to assist patients with PWS.

Joe Blackburn

Joe Blackburn

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Did Prader-Willi cause Joe Blackburn’s death?

Nearly a day has gone by without someone applying a narrative about Joe Blackburn as a result of the innumerable false rumours and stories that have been floating about recently on social networking platforms.

But in almost every case, these pieces of knowledge result in “Joe Blackburn,” the founder and president of Crypto Coin, passing away too soon.

Nobody had ever considered that things might get worse in a day, but as soon as the news began to circulate on social networking sites, countless comments started making headlines.

However, since just the anonymous studies are making the claims and no genuine research has been made public, a sigh can be heard among these.

The dead had long-standing, serious health issues, according to the original studies or sources. He was therefore being treated by the medical team in order to give him more breath and good health.

Sadly, the treatment that had harmed his internal organs had rendered his health useless. The medical team did everything they could to keep him alive despite all of these factors.

They were unable to influence God’s decision, which made him have to depart from this planet. Studies back up this claim because it isn’t supported by his family’s version of events.

One of the most well-known people on the earth is without a doubt Joe Blackburn, the founder and CEO of “Crypto Coin Trader.”

Joe Blackburn

Joe Blackburn

In addition to these, he is the host of the Bitcoin Radio podcast, which is accessible on Spotify, Apple, and Google Play.

Spreading false information would also not be suitable because he did not share even a single piece of personal information about himself on social media.

As a result, we are unable to make any claims unless something specific is made known.

Only a small number of anonymous studies are claiming the information, as we have already stated, so we are not embracing even one erroneous narrative while assuming that they are the correct one.

Given such, it might not be appropriate to pronounce him dead in the absence of reliable factual facts.

We caution you against believing any of the rumours that are swiftly circulating on social networking platforms.

Details about Joe Blackburn’s family

There isn’t much information available on Joe Blackburn’s family members. He had kept it a secret until just now.

His parents’ names, as well as the nature of their jobs, are kept a secret.

As soon as we obtain a formal statement on the matter, we will update the information. Follow us for further updates by doing so.

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What Is Prader–Willi Syndrome?

Prader–Willi syndrome, also known as PWS, is a hereditary condition that is brought on by the inactivation of several genes located on chromosome 15. The symptoms include a lack of muscle strength, difficulty eating, and sluggish development in neonates. Those who are affected begin to feel hungry all the time as early as childhood, which frequently results in obesity and type 2 diabetes later in life. The disease is also characterised by intellectual impairment ranging from mild to moderate levels and by behavioural issues. Individuals who are afflicted with this condition frequently have a narrow forehead, small hands and feet, short height, and light complexion and hair. The vast majority of them are unable to bear children.

The deletion of a portion of the father’s chromosome 15 accounts for around 74% of all cases. Another 25% of cases involve the affected individual having two copies of the maternal chromosome 15 from the mother but being missing the paternal copy. They end up with no functional copies of particular genes because imprinting causes sections of the chromosome inherited from the mother to become inactive and turn off. PWS is not usually passed down from one generation to the next; rather, the genetic abnormalities that cause it occur either during the production of the egg or the sperm, or during the early stages of development. There are no recognised risk factors associated with the illness. People who have already had one child diagnosed with PWS have a risk of having another child with the condition that is less than 1%. A similar mechanism is at play with Angelman syndrome, with the exception that the faulty copy of chromosome 15 comes from either the mother or the father in two separate copies.

There is currently no treatment for Prader–Willi syndrome. It is possible that treatment will enhance the outcomes, particularly if it is started early. When it comes to babies, feeding tubes can be used to help support them through difficult feedings. In most cases, beginning around the age of three, in addition to participating in an activity programme, stringent supervision about the consumption of food is essential. The use of growth hormone therapy also leads to improved results. Counseling and medicine both have the potential to help with a variety of behavioural issues. Adults frequently have a requirement for living in group homes.

Worldwide, people with PWS make up between 1 in 10,000 and 1 in 30,000 of the population. The illness was first described in great detail in 1956 by Swiss physicians Andrea Prader and Heinrich Willi, who, along with Alexis Labhart, are responsible for giving it its name. John Langdon Down, a British physician, provided an earlier description of the condition in the year 1887.

Joe Blackburn

Joe Blackburn

Signs and symptoms

The symptoms of PWS can vary widely, from low muscle tone in infancy to behavioural issues in early childhood and everywhere in between. In addition to having low muscle tone, one of the most common symptoms seen in infants is a lack of eye coordination. Some infants are also born with eyes that are shaped like almonds, and because of their low muscle tone, some may not have a strong sucking reflex. Their cries are feeble, and they have trouble rousing themselves from sleep. A thin upper lip is another symptom that this disease is present.

Hypotonia and aberrant neurologic function, hypogonadism, developmental and cognitive delays, hyperphagia and obesity, short height, and behavioural and psychiatric abnormalities are some of the other features that are seen in a clinical overview.

Holm et al. (1993) describe the following features and signs as indicators of PWS, although not all will be present:

In-Utero and birth

  • Reduced fetal movement
  • Frequent abnormal fetal position
  • Occasional polyhydramnios (excessive amniotic fluid)
  • Often breech or caesarean births
  • Lethargy
  • Hypotonia
  • Feeding difficulties (due to poor muscle tone affecting sucking reflex)
  • Difficulties establishing respiration
  • Hypogonadism


  • Delayed milestones/intellectual delay
  • Excessive sleeping
  • Strabismus (crossed eyes)
  • Scoliosis (often not detected at birth)
  • Cryptorchidism
  • Speech delay
  • Poor physical coordination
  • Hyperphagia (excessive hunger) begins between the ages of 2 and 8, and continues on throughout adulthood.
  • Excessive weight gain
  • Sleep disorders
  • Delayed puberty
  • Short stature
  • Obesity
  • Extreme flexibility


  • Infertility (males and females)
  • Hypogonadism
  • Sparse pubic hair
  • Obesity
  • Hypotonia (low muscle tone)
  • Learning disabilities/borderline intellectual functioning (but some cases of average intelligence)
  • Prone to diabetes mellitus
  • Extreme flexibility

Physical appearance

  • Prominent nasal bridge
  • Small hands and feet with tapering of fingers
  • Soft skin, which is easily bruised
  • Excess fat, especially in the central portion of the body
  • High, narrow forehead
  • Thin top lip
  • Downturned mouth
  • Almond-shaped eyes
  • Light skin and hair relative to other family members
  • Lack of complete sexual development
  • Frequent skin picking
  • Stretch marks
  • Delayed motor development

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