‘A ray of hope’ for family of boys with deadly condition



Leslie and Lynda Martin with sons Ciaran and Cathal, who have metachromatic leukodystrophy
Leslie and Lynda Martin with sons Ciaran and Cathal, who have metachromatic leukodystrophy

The parents of two little boys diagnosed with a rare genetic disorder have appealed for help in raising €250,000.

Leslie and Lynda Martin, from Rathnew, Co Wicklow, were told by doctors in December that Cathal, who is nearly three, has metachromatic leukodystrophy (MLD).

The condition, which affects the nervous system, is terminal for Cathal.

Trial

Then they learned last month that one-year-old Ciaran also has the condition.

However, as Ciaran was diagnosed at an earlier stage, he can take part in a trial in Italy which has been shown to delay the onset of further symptoms.

The treatment has had a positive outcome for six of the nine children who have taken part in past trials.

While partially funded, the treatment will take six months and require round-the-clock nursing care.

The family are planning to do two 12-hour shifts each…



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