Coleen Rooney likes fan’s tweet slamming Rebekah Vardy’s vile plot to use her disabled late sister Rosie to further story leaking deception

By William On Oct 19, 2023

Colin Rooney has liked a fan’s tweet which alludes to Rebecca Vardy’s plans to use her late disabled sister Rosie to boost her leak story.

On Wednesday, the 37-year-old Wagga made headlines following the release of her Disney+ documentary Colin Rooney: The True Wagga Story, a limited series chronicling her legal battle with the footballer’s wife, 41.

In 2019, Coleen publicly accused Rebecca of publishing stories from her personal Instagram account in The Sun newspaper, leading to a High Court battle, in which private WhatsApps revealed Rebecca’s references to Coleen’s sister.

Amidst Coleen’s three-year quest to uncover a ‘snitch’ on her private account, she unfollowed Rebecca – who was revealed to have texted her agent Caroline Watt to say she should ‘say something about Rose’ in order to get back into Colin.

Colleen’s parents Colette and Tony McLaughlin took Rosie in as a foster child when she was two before later adopting her. She passed away at the age of 14 in 2013 after a lifelong battle with Rett syndrome, a rare disorder that causes severe disabilities.

Harmful: Colin Rooney liked a fan’s tweet referencing Rebecca Vardy’s plans to use her late disabled sister Rosie to boost her leaked storyline

Tragic loss: Rosie passed away aged 14 in 2013 after a lifelong battle with Rett syndrome, a rare brain disorder that causes severe disability (pictured in 2006)

Heartbreaking: On Wednesday, Wagatha, 37, hit the headlines following the release of her Disney+ documentary Coleen Rooney: The Real Wagatha Story, a limited series chronicling her legal battle with her footballer husband, 41.

Outrageous: Amidst Coleen’s three-year attempt to uncover a ‘snitch’ on her private account, she unfollowed Rebecca – who was revealed to have texted her agent Caroline Watt to say she should ‘say something about Rose’ in order to returned to Colin’s fold

The Wagatha Christie story has dominated headlines for years, and Colleen finally told her side of the story in a Disney+ documentary.

After explaining how she realized Rebecca was to blame for the leak, she revealed her first instinct was to simply unfollow the star – thus removing Rebecca as one of the followers on Cole’s account.

Soon after, Coleen revealed she was approached by Rebecca, who texted her saying: ‘Hi my love… hope you’re ok?… I saw you unfollowed me…

“And I unfollowed you on Instagram… I just wanted to ask… Did I do anything or offend you in any way?”, after which Coleen stated: “I just thought… you” so duplicitous’, into the camera.

Coleen then read a message from Rebecca Caroline, saying: “I never usually text her and say hello. Maybe I should say something about Rosie.

Disgusted, Colleen said of the dastardly plan: “Planning to make a story that will make me respond is one thing, but using my sister who has passed away is just…wrong.”

Earlier in the documentary, Coleen broke down in tears while discussing Rosie.

While explaining why VAG struggles to open up about her concerns, Colette revealed that it stemmed from growing up caring about Rosie.

Unheard of: The Wagatha Christie story has dominated the headlines for years, and Coleen finally told her side of the story in a Disney+ documentary, after revealing that Rebecca had started leaking stories about her since 2017.

Touching@ The McLaughlins took Rosie in as foster children when she was two and while they previously only provided respite care, Coleen noticed that “Rosie was different”

Collette shared: “Colin keeps things to himself. She doesn’t want to be a burden on me and I can relate that to Rosie. She was so special.’

The McLaughlins took Rosie in as foster children when she was two and while they had previously only provided care, Colleen noticed that “Rosie was different”.

She explained: “When Rosie came she was a big part of our lives. She was the sister I never thought I’d have.’

Speaking to her mother and father Tony, she continued: “I used to do her hair and I loved picking out clothes with my mum for her. She brought that little extra to the house. We fell in love with her.’

However, the family soon realized that Rosie was struggling with her development, and after a series of hospital tests, she was diagnosed with Rett syndrome.

Colin explained: ‘Rosie, she fought. She couldn’t walk or talk and would be in pain and sick, but she still put a smile on her face.

“Sometimes she had a habit of forcing herself to smile.” I think it was just to make mom and dad happy. Gradually, her brain stopped working and she could no longer eat, talk, move.’

Rosie needed 24-hour care and after suffering “a lot of complications” and being admitted to intensive care, Colette revealed the family decided to bring her home to spend her final days surrounded by her loved ones.

“We had a sleepover, a last sleepover, all together,” she explained. ‘And then we had a big party to celebrate her life.’

Family: Colin was reunited with his father Tony and mother Colette as they discussed Rosie’s final days in emotional scenes on the Disney+ show

A tearful Coleen said: ‘Losing a child is the worst thing that can happen to anyone, but when you look back, she gave us so many good years of happiness and love.’

Revealing the impact Rosie’s death had on her 10 years later, Colleen explained: ‘Because of the things that have happened in my life, I try to be strong for others.

“I don’t want people to worry about me when they have other things going on in their lives, but sometimes I can snap.”

Collette went on to suggest that her daughter didn’t fully process the pain she went through until she was in America when Wayne moved to DC United.

She explained: “It’s been 10 years and Coleen has never really talked about it. She had a lot of time in America, so she had to think a lot then.

“But she hides a lot, so it’s hard to tell what’s going on in her head.”

Getting Up: Colleen won the fight with Rebecca

WHAT IS RATT SYNDROME? A NEUROLOGICAL DISORDER THAT LEAVES CHILDREN UNABLE TO SPEAK, EAT, WALK, TALK AND BREATHE

One child in 12,000 is born with Rett syndrome, but few people have heard of it.

The genetic disorder affects almost exclusively women, causing them to regress neurologically and physically.

The progression of the disease can be roughly divided into four stages.

During the first stage, from about six to 18 months, the baby slows down in development, loses interest in play, stops making eye contact, begins to walk clumsily and makes repetitive hand movements.

The second phase, known as ‘rapid destruction’, begins between the first and fourth years.

The child finds it increasingly difficult to communicate and learn, and other brain functions often deteriorate.

Symptoms include inability to control the hands, sudden stress combined with screaming, unsteadiness, breathing problems, difficulty sleeping, slow head growth and digestive problems.

The third stage, the ‘plateau’, begins between the ages of three and ten.

Limbs become thin, epilepsy may develop, and weight loss and teeth grinding may occur.

However, many parents report that children are less anxious and show more interest in their surroundings.

The final stage can last for decades. A severe bending of the spine – scoliosis, as well as loss of the ability to walk – usually develops.

Almost all cases are caused by a mutation in the MECP2 gene that prevents nerve cells in the brain from working properly.

Currently, there is no cure and only the symptoms are treated.

According to the data, about three quarters of the sufferers will live into their 50s Rett UK. National Institute of Health says that it is not possible to make reliable estimates of life expectancy after 40 years.

According to Rettsindrome.orgdata from the Natural History Study found that a girl with Rett had a 100 percent chance of reaching age 10, a greater than 75 percent chance of reaching age 30, and a greater than 50 percent chance of reaching age 50.

But because of Rett’s rarity, very little has been published about life expectancy.