Support Victoria with cerebral palsy and HSC

Hello everyone,

I present to you my daughter VICTORIA, her name is that because at her young age she has managed to overcome many difficulties, she is currently 2 years 5 months

Victoria is a premature baby, born at 7 months due to complications, days later she was diagnosed with CAH (congenital adrenal hyperplasia: it is a malformation of the adrenal glands. This disease has no cure so it depends on treatment for life, which is why she attends periodic medical appointments with endocrinology to control sodium and potassium, over time she developed a strabismus in her right eye that she is managing to overcome, so she continues with treatment and glasses, despite being with stimulation since she was born, she shows delays in development. She does not feel alone, she does not walk. and his language is scarce, we think it is due to prematurity and a hip dysplasia that was detected very late at 1 year and 7 months due to the negligence of a doctor. We managed to overcome this situation with treatment, but he continued to show signs in his development, so he The neuropediatrician recommended an MRI, an examination that was recently performed at the age of 2 years and 5 months in which the results were not positive, since they found that my baby has cerebral palsy (Tetraparesis paralysis that affects his extremities) which is why he cannot walk. However, this situation once again disturbed our peace of mind because there is no treatment.

The doctors indicate that we can only give him long-term therapies to improve his quality of life (stimulation, physiotherapy, speech therapy among others). .

I am Gabriela, mother of Victoria, because of my daughter's situation and because I am her only caregiver, I have not been able to get a stable job and everything that is achieved is destined for her treatment, now with a new diagnosis where many things are required for it to improve, the situation becomes more complicated.

It is difficult to accept that I need help, I have always thought that I can do it alone, but seeing my daughter who needs so much and I cannot provide her hurts. 😔.💔 So we appeal to your good heart.

Everything we manage to raise will be used for your therapies, food, purchase implements for different therapies such as (postural suit which is not here and must be requested to another country), purchase of medicines and supplements that must be brought by order and more.

Thank you for taking your time and reading this far ☺️

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