I want to say first THANK YOU, for allowing time out of your day to read our story. My son Cristian suffered a severe hemorrhage stroke at 11 days old on January 14, 2024. We spent 50 days in the hospital to make sure he was hospitalized to be able to take home which was nearly an impossible outlook the first 7 days. After, a long stay in the hospital we finally went home on March 4, 2024. Although, we are greatly grateful and happy the lord allowed us to go home he did suffer a lot of brain danger. With that being said he was left with cerebral palsy, epilepsy, chronic respiratory failure, and developmental delays. Even though it’s been a long journey in only 1 year and 1 month of his life my son is still here trying everyday to do his best. We were left with no future with Cristian if he was to survive this stroke as doctors say but god is always there to show otherwise. We attend therapy 3 days out of the week for my son 2 hours a day. We have lots of hospital appointments with neurology, physical medicine and rehabilitation, pulmonary, ENT (ears,nose& throat) and of course his primary doctor to make sure he is still developing stability. I attend every appointment and therapy god is able to to grant me with health to take him, but it’s not always easy as when he does get sick is mandatory to stay hospitalized. My son has been hospitalized 7-8 times in the icu last year due to him having more seizure activity or having sick symptoms where his respiratory gets hard for him to breath with him having a weak immune system.

Even though we have no been able to take trips, go to a pool or even spend some family time away from any medical concern it’s always been a beautiful experience journey with him at the hospital too. Being in a hospital celebrating his months anniversary and even his 1st CHRISTMAS in the hospital isn’t everyone’s idea of celebrating but it is to myself and our family because his time expectancy was 6 months to 1 year. As that being said with him having many much more appointments, therapy, and being hospitalized on unexpected times or days has not let me provide or have a full time job as he has no nurse. Unfortunately, nursing is hard because neither they quit after some time or quit to never showing up.

To that being said one day I watched a movie called “Lucas World” my uncle sent over on a message saying to watch it. The movie explains the battles and trails as a medical mom goes through and will be willing to do for there kids. The movie was a great experience eye opening for me as it was the same diagnosis as my son. Being based as true story I started digging, emailing and calling the clinics shown in the movie that helped there kid with cerebral palsy. One clinic being in India I have emailed that stated free trials, but got a reply station that there clinical trials are full and have finally been accepted.

The second clinic being in Monterrey, MX. I emailed there clinic with the reply that we be willing to see and treat my son. The treatment is 30 days with an amount of $35,000 US DOLLARS.

The treatment is a machine called “NEUROCYTONIX” which does the following

For more information or to know more about what this will help my son this is the link

1.https://acrobat.adobe.com/id/urn:aaid:sc:VA6C2:99e1ac68-fc52-492d-ab05-e771ccbdb52c

2. http://www.neurocytonix.com/

My son has a sad amount of brain damage that affected his ability to do many things.. as for now he still does not crawl, or walk.. not a lot of head movement or can sit still without support or help.

PLEASE, I am asking to donate anything that you are able to, to take my son to Mexico. It can be $1, but as long as you care share my post everywhere it’ll help so much. Sharing my son’s post $35,000 times can help us have each person donate $1.00 and can amount to his treatment!

I want him to experience and do everything I know he could have done before this stroke took a toll on him. I will try everything in my power to give him the best quality of life! It’s hard mentally for me to know I can’t heal and give my son my body’, strength or brain for him to live a healthy regular life.

Even after all the trials and tribulations my son is here everyday trying with every therapy session and doctor appointment.

God has his purpose and reasons for life experiences as we have encountered, but my love and faith remains the same!

THANK YOU FOR YOUR TIME & God Bless YOU ALL!

Primero quiero agradecerles por tomar el tiempo para leer la historia de Cristian.

Mi hijo sufrió un derrame cerebral severo en Enero 14,2024 a los 11 dias de nacer. Estuvimos en el hospital por 50 días exactos. Salimos Marzo 4, 2024 con la gracia de Dios.

Aunque estemos tan agradecidos con Dios que nos dio otra oportunidad para vivir con mi hijo no a sido tan difícil.

Lamentablemente con el derrame que le sucedió a mi hijo dañó muchas parte de su cerebro que a causado desarrollos atrasados como caminar, correr, y tener fuerza para que el solo mantenga su cabezita y cuerpo solo. También a causado sufrir de convulsiones y problemas respiratorios.

Llevo a mi hijo con a sus terapias 3 días a la semana por 2 horas para que el empiece de nuevo para empezar un día primero Dios a caminar lo decir “mom”. Tiene muchas citas con neurólogo, neumólogo, medicina fisica y rehabilitacion, y otorrinolaringólogo.

Aunque tenga la voluntad de Dios de poder llevarlo también emos estado en el hospital 7-8 veces el año pasado cuando el está enfermo o le da convulsiones. Y aunque no hemos tenido tantas vacaciones, día en el parque o albercas. Si hemos pasado sus días festivos y su primero Navidad en hospital con el. Aunque no es la idea de muchos nomas de tenerlo aquí con nosotros celebrando es lo máximo.

Hago este GO FUND ME por razones de un tratamiento que ai en Monterrey MÉXICO.

Este tipo de tratamiento es una máquina que proporciona estimulación dirigida con precisión para promover el crecimiento de nuevas vías neuronales. El derrame que le dio a mi hijo si le cause mucho daño en partes de su cerebro que nosotros usamos para hablar, respirar para afuera, escribir. Y este tratamiento hará que abrir crecimientos de esas parte que se dañaron.

Dejare 2 links para que vean más lo que le ayudará a mi niño y historia de otros niños que van y ayudan a muchos niños progresar en muchas parte de su cerebro.

1. www.neurocytonix.com

El costo del tratamiento es $35,000 dólares US.

Por falta de enfermera para mi niño no e podido trabajar para poder trabajar hasta de mas para juntarlo para llevarlo. Por eso con corazón pido hasta que $1.00 puede ayudar!!! COMPARTIENDO mi historia puede llegar a 35,000 personas y hacemos los $35,000.

Mientras dios me de licencia voy hacer todo lo que puedo para darle la mejor calidad de vida a mi niño. Porque yo tengo fe que un día hará todo a su tiempo y miraremos atrás de todo lo que él a luchado también.

La última palabra siempre la tiene Dios.

DIOS LOS BENDIGA HOY Y SIMPRE!