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Valerie and Maite Zeledon are two young girls facing an incredibly difficult situation. Their mother was recently deported after missing an immigration court date, leaving them separated from their family and in urgent need of support. As a family friend, I am doing everything I can to help them navigate this challenging time and find a way to reunite with their loved ones. 
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 The funds raised will be used to cover travel expenses, transportation, required documentation, and other essential costs related to their journey home. This includes purchasing passports, clothes, and plane tickets so Valerie and Maite can return to their home country and be with their family. Any remaining funds will help provide basic necessities and support during this transition, ensuring they have what they need to feel safe and cared for. 
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 Please help Valerie and Maite get back to their home country and reunite with their parents. If Honduran cancellation happens, they may have to go to a detention hall, but with your support, we can help them avoid this and bring them home in less than a month. Your generosity will make a life-changing difference for these girls, and we are deeply grateful for any help you can provide.

Help Valerie & Maite Reunite With Family

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<div>Dear friends, family, and supporters:
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<div>Rogelio Perez, a father of 4, was diagnosed with ALS (Amyotrophic Lateral Sclerosis, aka Lou Gehrig’s Disease) on February of 2023. ALS is a progressive neurodegenerative disease causing muscle weakness, paralysis, and eventual respiratory system failure. In the past year Rogelios life has changed drastically, he has become completely dependent on his wife, Diana and at times his own children. Although there is medication to help slow down his symptoms, there is no cure. <strong>Our goal is to give Rogelio the best quality of life possible and the necessary equipment for Diana to be able to take care of him.</strong>
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<div>To many ALS is an unknown disease. According to the ALS Association: “When the motor neurons die, the ability of the brain to initiate and control muscle movements is lost. When voluntary muscle action is progressively affected, people may loose ability to speak, eat, move and breath.” The simple everyday tasks like getting out of bed, brushing your teeth, drinking water, walking, sitting, hugging your children etc… becomes impossible.
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<div>To this date we are very grateful for the love and support of many of our friends and loved ones. Unfortunately the cost of care is extremely expensive, ranging from $100,000 - $200,000 USD every year. They are grateful for the limited health insurance benefits they count with but there are still many costs to be covered. Rogelio, his wife, and his 4 children will need support for costs of in-home medical and personal care, equipment and accessibility renovations to their home, and medical expenses and alternative therapies not covered by insurance.
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<div>Rogelio has always been the provider in his family. Before his diagnosis, he worked hard to provide for his loved ones. Due to his wife being his sole caregiver, they are asking for support in this fight. On behalf of Diana and the rest of the family, they would like to say they will always be grateful for your support. Rogelio has fought ALS with the help of family and friends, but specially with the help of Diana, his loving wife of 18 years. We are asking your support by donating to help Rogelio and his family defray the financial burdens of fighting ALS. Soon ALS, along with all other diseases, will be a thing of the past and “death will be no more, neither will mourning nor outcry nor pain be anymore.” (Revelation 21:4). We love you all! Follow my journey on TikTok: @rogeperezals
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<div>Espanol:
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<div>Rogelio Pérez, padre de 4 hijos, fue diagnosticado con ELA (Esclerosis Lateral Amiotrófica, también conocida como Enfermedad de Lou Gehrig) en febrero de 2023 a la edad de 36 años. La ELA es una enfermedad neurodegenerativa progresiva que causa debilidad muscular, parálisis y eventual insuficiencia del sistema respiratorio. En el último año, la vida de Rogelio ha cambiado drásticamente, se ha vuelto completamente dependiente de su esposa, Diana y de sus propios hijos menores. Aunque hay medicamentos para ayudar a reducir sus síntomas, no hay cura. Nuestro objetivo es darle a Rogelio la mejor calidad de vida posible bajo las circunstancias y el equipo necesario para que Diana pueda cuidar de él.
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<div>Para muchos, ELA es una enfermedad desconocida. Según als.org "Cuando las neuronas motoras mueren, se pierde la capacidad del cerebro para iniciar y controlar los movimientos musculares. Cuando la acción muscular voluntaria se ve afectada progresivamente, las personas pueden perder la capacidad de hablar, comer, moverse y respirar". Las simples tareas cotidianas como levantarse de la cama, cepillarse los dientes, beber agua, caminar, sentarse, abrazar a sus hijos, etc... se vuelven imposibles.
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<div>Hasta la fecha estamos muy agradecidos por el amor y el apoyo de muchos de nuestros amigos y seres queridos. Desafortunadamente, el costo de atención es extremadamente caro, entre 100.000 y 200.000 dólares cada año. Ellos están agradecidos por los limitados beneficios del seguro de salud, pero todavía hay muchos costos que cubrir. Rogelio, su esposa y sus 4 hijos necesitarán apoyo para los costos de atención médica y personal en el hogar, renovaciones de equipos y accesibilidad de su hogar, y gastos médicos y terapias alternativas no cubiertos por el seguro.
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<div>Rogelio siempre ha sido el proveedor de su familia. Antes de su diagnóstico, trabajó duro para mantener a sus seres queridos. Ahora, debido que su esposa es su única cuidadora, están pidiendo apoyo en esta pelea. En nombre de Diana y el resto de la familia, les gustaría decir que siempre estarán agradecidos por su apoyo. Rogelio ha luchado contra la ELA con la ayuda de familiares y amigos, pero especialmente con la ayuda de Diana, su amorosa esposa de 18 años. Estamos pidiendo su apoyo donando para ayudar a Rogelio y su familia a sufragar las cargas financieras de luchar contra la ELA. Pronto la ELA, junto con todas las demás enfermedades, será cosa del pasado y "la muerte ya no lo será, ni el duelo, ni el clamor, ni el dolor". (Revelación 21:4). ¡Los queremos mucho! Sigue mi historia en TikTok: @rogeperezals
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Help Rogelio Perez and Family Battle ALS

Tita Kelly Matamoros

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Tita Kelly Matamoros

Tita Kelly Matamoros

Featured causes

Help Valerie & Maite Reunite With Family

Help Rogelio Perez and Family Battle ALS

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