MICOL is A CHILD WITH A SMILE IN THE EYES (as her website www.ilsorrisonegliocchidimicol.it says, which I invite you to visit to shop, and which works as a support and subsidy for her home care and for all the alternative therapies that mother Beatrice insists on doing with all their lioness strength) suffering from a rare genetic disease called wwox gene malformation.

The disease manifested itself from the first days of life. The disease causes drug resistant seizures and many respiratory blocks supported by a non-invasive mechanical respirator because his lungs are a bit sluggish and not expanding properly, but with a lot of exercise they are improving, he has a very severe delay in psychomotor development and Anita helps Mom Bea to warn her in moments of Micol's crisis.

Noemi is a lively, cheerful girl and leads a practically normal life thanks also to her mother and her family but her genetic mutation brings her hyperinsulinemic crises and many other problems (anaphylactic shocks, epileptic seizures, rheumatic pains ...) onset and discovery of the disease occurred at two years. Cuma and Noemi have been inseparable for 4 years now and the good Golden Retriever reports her hypoglycemic crises so that the child corrects herself in time without losing consciousness. As we have seen above, the problem of epileptic seizures has been added and Cuma would like to prepare her for this too. Naomi often comes to the IAA center with the other animals we have ... she likes all animals but alpacas in particular