Herald on Sunday

How a COLD left a 12- year-old girl paralysed

Gabby, 12, lost the use of her legs to a rare complicati­on from a common cold. Now she is fighting back.

- By Susan Strongman

Acommon cold has left an active, healthy 12-year-old Auckland girl paralysed from the waist down. In June this year, Gabby Wright went from playing representa­tive netball one day, to being unable to use her legs the next.

After a weekend of sport, she complained for two days of a sore back to her mum Vanessa, who told her to have a bath. It worked the first day but on the second day her legs began to feel painful.

“I went to the toilet but then I couldn’t get off, I just collapsed on the ground.”

Gabby was rushed to Middlemore Hospital then transferre­d to Starship, where she was diagnosed with Transverse Myelitis — an inflammati­on of the spinal cord causing paralysis.

A cold two or three weeks earlier had probably caused a viral infection that led to the inflammati­on.

“We thought nothing of it at the time,” Gabby’s mum said.

“It was just a normal cold — she didn’t even have a day off school.”

Gabby spent the following five weeks in hospital, enduring needles, catheters, central lines, nasogastri­c tubes, suppositor­ies, plasma transfusio­ns, blood tests, poking, prodding, physio and lots of frustratio­n, fears and tears, her mum said.

She was then transferre­d to Wilson Trust Child Rehabilita­tion Centre, where she had nine weeks of intensive physical therapy.

Things are improving slowly, and Gabby can now feel deep pressure in her legs. But she still can’t move, or feel hot and cold. This week she has a small muscle spasm, which the family are taking as a positive sign.

For Gabby to recover, her nerves need to regenerate.

“That’s our goal, and that’s our hope. But sometimes it just doesn’t happen. The stats are 30 per cent chance of a full recovery, 30 per cent partial recovery.” The remainder is no recovery. But now that Gabby’s been home in Ardmore for a week, things are starting to get back to normal. She’s arguing with her little sister, and her friends from school visit each weekend.

She’s even playing wheelchair basketball, and looking up wheelchair stunts on YouTube.

“She’s not letting anything hold her back — she’s accepted that this is her life at the moment,” Vanessa said.

“She said to me: ‘It’s just like what Dory [from Disney movie Finding

Nemo] says: When life gets you down, you know what you got to do? Just keep swimming’.”

Vanessa hopes to buy a special motorised exercycle bike for Gabby, to help improve her chances of recovery.

The $17,000 to $20,000 functional electrical stimulatio­n bike uses pulses of electrical current to stimulate the nerves that make her muscles contract. The Wilson centre does not have one, and they’re not available to rent in New Zealand, Vanessa said.

She has set up a Givealittl­e page to help buy the bike.

After Gabby’s recovered, they will donate it to Wilson Trust Child Rehabilita­tion Centre or Starship Hospital.

Since the page was set up last week, Vanessa has been blown away by the response. They’ve even had young Silver Fern Maia Wilson get in touch — calling Gabby and promising to visit when she’s next in Auckland.

Neurologic­al Foundation medical director Dr Jon Simcock said Transverse Myelitis is an uncommon condition. It can result from many bugs, including the common cold, although in many case the cause isn’t found.

“Generally if the person is still able to move their legs, they make a pretty good recovery.”

 ?? Doug Sherring ?? Gabby Wright, with her parents Vanessa and Clinton, and sister, Felicity, is tackling the challenge of being paralysed.
Doug Sherring Gabby Wright, with her parents Vanessa and Clinton, and sister, Felicity, is tackling the challenge of being paralysed.

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