Ayuda para el pequeño Eliab
Help for little Eliab
¡Hola a todos!
Hello everybody!
I'm Eliab Boadas, I'm 4 years old, I'm a very happy, curious and talkative child. I love pizza and chicken. I'm always laughing and for some reason other people laugh a lot with me when we talk, I'm just very funny.
When I was forming in my mom's tummy I could feel my family's excitement to know that I existed, dad always talked to me from the outside and told me that he was very anxious to meet me. But I kept a secret.
While my little hands and feet were growing, a strange lump was also growing on my back. As soon as I was born everyone was happy, but I couldn't explain to them that I was in a lot of pain and my head was getting bigger than my body. The doctors said it was because I had a condition called myelomeningocele or better known as spina bifida.
fuente/source
The lump I had on my back, through a wound drained hydrocephalic fluid (water from inside my head), and also had the connections that should be attached to my spine, and for this reason I could not feel my legs. The pain I felt in my sword was due to this disease, because of it, since days after I was born I had to be operated on multiple occasions, one of them was to place a valve to drain the fluid that accumulated in my head and made it bigger. For months I was imprisoned in the hospital, my mother did not rest but at every opportunity she had to see me she gave me all her love, she helped me to calm down because I spent all day and night crying because of the pain. Dad did everything he could to make sure I lacked nothing, he even had to buy the gloves for my operations, besides, his love has never been lacking, he is a very good daddy. Daddy, mommy, aunts, uncles, grandmothers, grandfathers, friends and acquaintances fought alongside me in my battle to get out of the hospital, even though I had complications in my recovery, I can now say that I am healthy. It has been a long road but I like each day to be better than the last. At that time mom and dad brought another little sister, she is already walking around the house, but I will never be able to do it. Because I have spina bifida I will never be able to walk, that makes me very sad because I really like to explore, go to the yard or out front and go for walks, I don't get in my car like I used to. Everyone says I need a special wheelchair for my condition, but dad and mom even though they try so hard, they can't afford it. However, I will continue to give them my big smile and happiness, because I love them very much and they make me happy. At this moment the whole family, friends, acquaintances and strangers are doing our bit to help in the fundraising for the purchase of an ergonomic wheelchair and thus improve the quality of life of little Eliab, in addition to perform some medical tests and therapies. This brave little boy has suffered more in his first 2 years of life than I have at 22 years of age, I admire my little nephew so much because I have seen the courage and unwavering strength he has shown, he is my little hero. If any monetary help or resource you wish to contribute is born from his heart, it will be gladly received, and all proceeds from this post will go directly to Eliab's relief fund. Las imágenes presentes son propiedad de los padres del niño y solo se puede hacer uso de ellas bajo su consentimiento. The images herein are the property of the child's parents and may only be used with their consent.
¿Cómo ayudar al pequeño Eliab a mejorar su calidad de vida?
How to help little Eliab improve his quality of life?
Muchas gracias por leer y si deseas saber más sobre el pequeño Eliab y cómo va este proceso, déjamelo saber mediante un comentario y con mucho gusto le responderé.
Thank you very much for reading and if you want to know more about little Eliab and how this process is going, let me know in a comment and I will be glad to answer you.
Este niño es un guerrero. Apoyemos todos al pequeño Eliab. Te felicito, tu post es muy emotivo.
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