A family is saddened as their three-year-old son is diagnosed with dementia and loses his ability to walk.

After being diagnosed with a rare form of dementia when she was born, a youngster has lost her abilities to walk and speak.

Florence Swaffield was born with the ability to walk.

In September 2021, she even ran down the aisle carrying the rings as the flower girl during her parents’ wedding.

But, within months, her condition had deteriorated to the point that she was falling over 100 times per day and had lost part of her speech skills.

Family devastated after their baby diagnosed with dementia at the age of three loses ability to walk

Her parents claim she can now just speak “uh oh.”

CLN2 Batten’s illness, for which there is presently no cure, has been diagnosed in her. Florence is unlikely to grow without medical advancements because those who have it have a life expectancy of six to twelve years.

According to the physicians, as the sickness progresses, she will lose her capacity to communicate, walk, and eat or drink independently, causing her to regress to a baby-like state.

Florence’s mother, holding on to a sliver of hope, describes her daughter as a cheeky, charming character who is ‘full of life’ and has ‘the most infectious belly laugh,’ and she vows to do ‘whatever it takes’ to give her ‘the finest life imaginable.’

‘The footage of Florence sprinting down the aisle and delivering the rings to Joe is just priceless to us,’ Pheobe, a government worker for the Department for Transport from Coventry, West Midlands, said.

‘In some ways, we’re glad we were unaware of Florence’s condition because it allowed us to create such amazing memories with her that we’ll remember for the rest of our lives.’

A series of testing indicated that she had CLN2 Batten disease and had unwittingly passed it on to Florence.

Her illness is so uncommon that just about 50 people in the United Kingdom are affected.

Florence, on the other hand, has another unusual genetic complication: Ververi-Brady Syndrome, a disorder characterized by minor developmental and speech delays. This was determined to be a natural occurrence.

Her parents claim she is the only person on the planet who has both mutations at the same time.

‘We were trying to persuade the physicians that Florence was not like other children her age,’ Phoebe explained, ‘but I just felt really unheard and out of control.’

‘I had no idea life could be so cruel, and I had no idea it could happen to our family,’ Phoebe, her mother, added.

Florence receives an enzyme injection every two weeks at Great Ormond Street Hospital in London as part of her treatment, which she will have to endure for the rest of her life.

There is a glimmer of hope that gene therapy may become available and aid her treatment, but in the United States, clinical trials have yet to be approved by the Food and Drug Administration, so the treatment is still in the research stages (FDA).

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