Actor Isabelle Tate dies from rare Charcot-Marie-tooth disease
Share and Follow

A tragic loss has struck the entertainment world as the family of 23-year-old actress Isabelle Tate, known for her role in “9-1-1 Nashville,” has announced her death. Tate was battling a neurological disorder that impacts approximately 3 million individuals globally.

The devastating news of Isabelle Tate’s passing was made public on Thursday, following her death on the preceding Sunday. Her family disclosed that she was afflicted with Charcot-Marie-Tooth disease (CMT), a genetic disorder that progressively damages peripheral nerves, particularly those in the hands and legs.

According to medical experts, patients with CMT initially experience muscle weakness in their legs and arms. As the condition advances, it can lead to difficulties in movement and a loss of sensation in affected areas.

While CMT is typically not life-threatening for the majority of those affected, there are rare instances where it can severely impact muscles required for breathing, leading to a depletion of oxygen. Isabelle Tate’s family revealed that she endured a particularly severe form of the disease.

In rare cases, however, it can affect muscles needed for breathing, gradually starving someone of oxygen. Tate’s family said their daughter had a severe form of the disease.

In an Instagram post in 2022, Tate opened up about her disease and revealed how her condition had ‘really progressed’. 

She said: ‘When I was 13, I got diagnosed with a progressive neuromuscular disease that weakens leg muscles over time.

‘Over the years, I was going on with my life and would notice little things get more difficult for me, but not so much where it stood out to me.’

An obituary for Isabelle Tate describes her as someone who 'wanted to change the world' and 'full of fire'

An obituary for Isabelle Tate describes her as someone who ‘wanted to change the world’ and ‘full of fire’

She continued: ‘Recently, it’s really progressed, and I’ve come to terms that if I want to live my life to the fullest, I need to use a wheelchair at times.

‘This has been a difficult journey for me because having to accept help and surrender to the progression of this condition has been hard.’

CMT is considered to be a rare disease, but is one of the most common inherited nerve disorders, estimated to affect one in 2,500 people in the US and 3million worldwide.

It is named after the three doctors who described the disease in 1886, Jean-Martin Charcot, Pierre Marie and Howard Henry Tooth.

There are more than 160 subtypes that have been identified to date, the Charcot-Marie-Tooth Association says, all caused by genetic mutations that cause essential proteins for nerves not to function properly.

Among the most common are CMT1, where fatty sheets coating nerves degrade, causing damage to the cells, and CMT2, which affects the nerve fibers that transmit impulses from nerve cell bodies to muscles and sensory organs.

Among the deadliest form is CMT Type 4J, which is caused by mutations in the FIG4 gene, important for controlling the transfer of nutrients in nerve cells. 

This type of the disease can progress rapidly and cause respiratory complications, with many sufferers dying in childhood.

It was not clear which type Tate was suffering from.

Isabelle Tate received a Bachelor's Degree in business from Middle Tennessee State University

Isabelle Tate received a Bachelor’s Degree in business from Middle Tennessee State University

Isabelle Tate played Julie in the pilot episode of the Leann Rimes-led show 9-1-1 Nashville; Seen in a still above

Isabelle Tate played Julie in the pilot episode of the Leann Rimes-led show 9-1-1 Nashville; Seen in a still above

Patients suffering from the condition normally have the disease diagnosed between the ages of five and 15 years, when symptoms first start to appear.

Early warning signs can include appearing unusually clumsy or accident-prone, difficulty walking and toes dropping forward as someone lifts their feet.

In later stages, patients suffer from weakened muscles and a lack of sensation in the arms and feet. 

They may also have cold hands and feet caused by poor circulation, and feel tired regularly as a result of the extra effort it takes to move around.

Doctors diagnose the disease using a physical examination for muscle weakness, a nerve conduction test and a genetic test.

There is no cure for the disease, but therapies are available to help reduce the symptoms of the condition. 

Many patients will be offered physical therapy to strengthen muscles and reduce the risk of unwanted contractions. Patients may also receive walking aides, such as insoles in their shoes, and therapy to help them identify areas in life where they are struggling.

Country singer Alan Jackson also revealed he was diagnosed with the disease.

Jackson was not diagnosed until he was 52 years old and is still alive today, having turned 67 years old this month.

Share and Follow
You May Also Like

FBI’s Kash Patel Heads to China to Tackle Fentanyl Crisis

Next month, FBI Director Kash Patel is scheduled to travel to China…

Fox News True Crime Update: Unraveling Alex Murdaugh’s Legacy, BTK’s Family Challenges, and Bryan Kohberger’s Financial Struggles

‘HE KNEW HOW TO SWIM:’ The family of a man found dead…

Trump Rallies Virtually to Energize GOP Momentum in New Jersey Governor’s Race

Late Friday, former President Donald Trump made a strong appeal to New…

Uncanny Resemblance: Aunt Claims Photos of Melodee Buzzard Mirror Her Image Perfectly

A relative of missing 9-year-old Melodee Buzzard has expressed hope that recently…

Watch: NYPD Officers Heroically Save Missing Dog Moose from Manhattan Subway Tracks

After a thrilling rescue operation by New York Police Department officers, a…

St. Louis Woman Sentenced for Diverting $11M in Children’s Food Funds

ST. LOUIS (KTVI) – In a significant legal verdict, a former leader…

Historic Day at Dodger Stadium: 2,100 Immigrants Embrace American Citizenship

EL PASO, Texas (Border Report) — Fernando Valenzuela, a name synonymous with…

MAD DADS Organizes Justice Walk and Community Search for Clues in Young Jacksonville Father’s Tragic Death

MAD DADS Jacksonville, alongside the family of Baron Greenwade III, plans to…