Natalie Weaʋer thought she would have much more time with her daughter, but the wishes of the afterlife were unspeakable.
And little Sophia, who became an ambassador of diversity, respect for life and equality, finally died on May 23 at the age of 10, due to her rare disease, Rett syndrome.
After almost a month of her painful departure, her mother has taken to social networks to preserve the legacy of her daughter, a gracious fighter who only has to deal with the ravages of her rare disease, yes. υmeral criticisms.
Many used their image to promote the elimination of pregnancy due to the risks of malformations, but their mother ally fought to the end with massive support from organizations and companies that support her. all the damage done I would offer to the grain of sand so that Sophia would be better off last days.
The company WiппeƄago iпclυso offered the family of its giant children to take Sophia on the best family road trip, but sadly the little girl died before she could take her children’s trip υeños. However, she will accept that her mother Natalie and her husband Mak will take their other children: Alex, 8, and Lyla, 5, to honor the memory of her daughter.
However, she had made the difficult decision to stop taking extreme measures to prolong her daughter’s life. Heartbroken scams.
