Niama, 2 years old, is a beautiful little girl from and living in Salé, Morocco.



She was born with a congenital giant nevus, which corresponds to a skin malformation visible from birth in the form of moles or even patches covering the child's body.



They come in all shapes and sizes; their dark brown color clearly distinguishes them from other birthmarks. Most of the time a nevus does not exceed 1 cm², but in rare cases—about one birth in 50,000—it covers a very large area, ranging from 10% up to 90% of the infant's body!



Congenital naevi are “production errors” that occur during a child’s intrauterine life. Their causes are not entirely known, but they are probably due to a single acquired mutation in a cell occurring from the end of the first month of pregnancy or later.

One hypothesis suggests that the earlier the mutation occurs, the larger the extent of the nevus will be and the more numerous the other small naevi scattered around, which are often observed with congenital giant naevi.



This is a congenital condition (present from birth) but not hereditary, and it must be treated from birth because of its potential to develop into skin cancer. Treated in time, surgical treatment gives spectacular results.



The mother expresses her suffering at the fear shown by other children when they cross paths with her daughter.






No child wants to play with Niama, isolating her more and more from her classmates every day.



The mother feels pity for her child and has therefore appealed to our association, supported by her relatives.



As we have already explained, these lesions can evolve into skin cancer, hence the urgency of rapid care for little Niama, who has already gone far too long without treatment.




Here is the estimate provided by the Acibadem facility located in Turkey:



We need your support to allow Niama to receive dignified care.

Thank you to all the hearts who will respond to this call for help.



The fundraiser covers PayPal fees, air transport and accommodation.

Niama thanks you.



We inform you that in the event of death the funds will be transferred to another child.

You can also send your donation by bank transfer, indicating the child’s name in the payment reference:



If you cannot contribute financially, share this fundraiser as widely as possible. Because sharing is also helping, you can support the campaign by recommending this donation page via social networks.

You can contact the association via our Facebook page: https://www.facebook.com/lilotcalinsdessoeursetfreresdecoeur/ or directly by email: [email protected]

THANK YOU!






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Israe, 5 years old, lives in Morocco and suffers from various health problems, mainly affecting her esophagus.

The poor little girl ingested acid, causing her terrible pain and esophageal damage due to an unfortunate combination of circumstances.



Israe lives confined at home, unable to move like other children.

Medical care is part of her daily life and the little girl is exhausted.



Comfort care follows one after another without resolving the root of the problem.

Israe requires a complex operation that is not performed in Morocco.

The various treatments and interventions therefore need to be carried out abroad.



An esophageal dilation is thus recommended to resolve the dramatic consequences of this accident, which prevents the girl from feeding properly and makes life impossible for her.



Israe is not enrolled in school and suffers greatly from her isolation.



Tears give way to laughter. Her mother cannot bear the costs of these interventions alone. That is why we call on your generosity and charity. We thank in advance the hearts who will respond to this call for help.

ISRAE needs all your support.



Israe suffers physically and psychologically. Her esophagus is adhered and requires an operation which we hope will restore her full ability to eat and swallow properly.

Please be numerous in responding to her call for help.

We hope for a speedy recovery for this little girl who has been suffering for too long.



Israe has great difficulty feeding and doctors often have to use a feeding tube to re-nourish the child.



Here is the estimate issued by the Acibadem facility:



The fundraiser covers PayPal fees and travel-related expenses.



We inform you that in the event of death the funds will be transferred to another child.

You can also send your donation by bank transfer, indicating the child’s name in the payment reference:



If you cannot contribute financially, share this fundraiser as widely as possible. Because sharing is also helping, you can support the campaign by recommending this donation page via social networks.

You can contact the association via our Facebook page: https://www.facebook.com/lilotcalinsdessoeursetfreresdecoeur/ or directly by email: [email protected]

THANK YOU!