Her family from Woodford Green, North East London, settled on the sensational choice to move more than 5,000 miles over the Atlantic for elective treatment in January after specialists in England let them know there was nothing more they could do.
So far they have raised £220,000 and say they have seen signs treatment at Hospitales Angeles in Monterrey could give them the glad closure they couldn’t have longed for a year ago.
He revealed to Mail Online: “When we initially went I was extremely wary. However, as a father I needed to go out on a limb and keep that expectation.
“It was around seven days after the primary treatment when the power in her left hand was returning and her strolling was improving. At that point it was the jumping and the playground equipment – genuinely a wonder.
“But since Kaleigh is on the bleeding edge, this is an obscure area for the specialists.
“You continue thinking ahead and asking yourself, ‘will regardless she be here?'”
“The Laus’ choice to take Kaleigh to Mexico for trial treatment is an intense indication of the absence of clinically demonstrated, successful treatment choices for youthful patients determined to have DIPG and the requirement for more research into the infection.
“Youngsters with DIPG get by for not as much as a year, by and large, and just around one out of ten makes due for longer than two years.
“We are charmed that Kaleigh gives off an impression of being reacting emphatically to her treatment in Mexico and we would welcome the chance to gain more from the center’s restorative group about the treatment administrations and advance of the greater part of the youngsters who are being dealt with there for DIPG.”
Mr Lau has propelled a Parliamentary request, which he expectations will see all the more subsidizing directed into mind tumor inquire about.