Told my little boy wouldn't ever walk but he's standing and toddling along
- 10 months ago
A little boy with a rare condition which caused his feet to permanently fill up with fluid is standing and toddling along - despite being told he'd never be able to walk.
Brodie Arbon-Davis, one, was born with the PIK3CA mutation - leaving him with birth defects including a blood vessel malformation on the bottom half of his body, as well as cysts on his kidneys and thickened bone marrow.
This has caused his legs to permanently swell - and scans show he technically only has two toes on each foot.
Doctors warned his mum, Holly-Louise Mackie, 26, that the tot would never walk unaided or wear shoes.
But despite the odds, Brodie has been able to pull himself up and toddle along while holding on to a walker and furniture.
Holly-Louise says her son is “smiley and thriving” - and loves to make people laugh.
Holly-Louise, a full-time mum, from Dover, Kent, said: “Brodie was born this way - and it’s a blessing in disguise.
"He can’t do the stuff other kids are doing - but he’s thriving anyway.
“He’s a strong little fighter.
"He seems to be a pusher, he’s ridiculously happy - in fact, the only time I don’t see him smiling is when he’s in pain.”
Brodie was born nine weeks prematurely, weighing 5lbs 4oz, on November 26, 2021, after Holly-Louise says she “coughed one day” and her “waters just broke”.
Nothing concerning had flagged during scans while she was pregnant and Holly-Louise and and her partner, Liam Arbon-Davis, 27, a builder, believed Brodie's premature birth would just make him “short”.
But as soon as Brodie was delivered, his parents could see there was something wrong.
She said: “I could see his legs were ridiculously swollen and purple when he was born - at first, I thought it was a port wine stain.
“He had to go through so many tests within the first month - no-one knew what was wrong with him.
“He had bloods, and they did ultrasounds on his kidneys and a skin biopsy. That was when they found the mutation
“The PIK3CA mutation is basically a malformation in the blood vessels - affecting the lower half of his body.
“It wasn’t hereditary - neither myself or my partner carried it. It’s what they call a mosaic anomaly - just a freak accident, basically.
“It was heart-wrenching - but I loved him to pieces as soon as I first saw him.
“He spent a month in the NICU - and doctors found he had deformities on each foot, a build-up of fluid in both legs, cysts on his kidneys and a bone marrow thickening from the waist down.
“His legs are in the 0.4th percentile - which means his bone quality is very low. He’ll never be able to walk unaided.”
Brodie was allowed home from the NICU on December 23, 2021.
But he has regular blood tests in case more of his organs are affected by the mutation - and he has constant access to a ward in case he’s ever ill or in pain.
Brodie Arbon-Davis, one, was born with the PIK3CA mutation - leaving him with birth defects including a blood vessel malformation on the bottom half of his body, as well as cysts on his kidneys and thickened bone marrow.
This has caused his legs to permanently swell - and scans show he technically only has two toes on each foot.
Doctors warned his mum, Holly-Louise Mackie, 26, that the tot would never walk unaided or wear shoes.
But despite the odds, Brodie has been able to pull himself up and toddle along while holding on to a walker and furniture.
Holly-Louise says her son is “smiley and thriving” - and loves to make people laugh.
Holly-Louise, a full-time mum, from Dover, Kent, said: “Brodie was born this way - and it’s a blessing in disguise.
"He can’t do the stuff other kids are doing - but he’s thriving anyway.
“He’s a strong little fighter.
"He seems to be a pusher, he’s ridiculously happy - in fact, the only time I don’t see him smiling is when he’s in pain.”
Brodie was born nine weeks prematurely, weighing 5lbs 4oz, on November 26, 2021, after Holly-Louise says she “coughed one day” and her “waters just broke”.
Nothing concerning had flagged during scans while she was pregnant and Holly-Louise and and her partner, Liam Arbon-Davis, 27, a builder, believed Brodie's premature birth would just make him “short”.
But as soon as Brodie was delivered, his parents could see there was something wrong.
She said: “I could see his legs were ridiculously swollen and purple when he was born - at first, I thought it was a port wine stain.
“He had to go through so many tests within the first month - no-one knew what was wrong with him.
“He had bloods, and they did ultrasounds on his kidneys and a skin biopsy. That was when they found the mutation
“The PIK3CA mutation is basically a malformation in the blood vessels - affecting the lower half of his body.
“It wasn’t hereditary - neither myself or my partner carried it. It’s what they call a mosaic anomaly - just a freak accident, basically.
“It was heart-wrenching - but I loved him to pieces as soon as I first saw him.
“He spent a month in the NICU - and doctors found he had deformities on each foot, a build-up of fluid in both legs, cysts on his kidneys and a bone marrow thickening from the waist down.
“His legs are in the 0.4th percentile - which means his bone quality is very low. He’ll never be able to walk unaided.”
Brodie was allowed home from the NICU on December 23, 2021.
But he has regular blood tests in case more of his organs are affected by the mutation - and he has constant access to a ward in case he’s ever ill or in pain.