Diana Montenegro's Fundraiser
Finding a cure for cavernous malformation
Join me and help make a difference!
We are no longer accepting donations on this campaign, but there are other ways for you to support us today!
Lisa Natale
"you are incredible Diana!!"
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Niamh Higgins
"Sending you so much love Diana xoxo"
$30
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Bhadra Vora
I donated in support of this campaign.
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Aileen Martino
"Praying for you and your family, Diana🙏"
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Lissette Perera
"Fuerza y apoyo Diana para seguir adelante y en nombre de Dios."
A supporter of Diana Montenegro
I donated in support of this campaign.
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Gloria Lara
"Dianita, suerte con esta causa. Ojala encuentren una cura. Abrazos"
$100
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Christine Ayarza
"Muy bien hecho amiga!"
$100
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Amarilis Sanchez
I donated in support of this campaign.
$100
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Yelitza Ortega
"Todo estara bien el manos de Dios. Un abrazoYelitza"
A supporter of Diana Montenegro
"Blessings to you and your family Diana. … Ask and it will be given to you; seek and you will find; knock and the door will be opened to you :-)"
A supporter of Diana Montenegro
I donated in support of this campaign.
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Sarah Karlo
I donated in support of this campaign.
$30
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Sara McIntire
I donated in support of this campaign.
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Emily Borreca
"We're rooting for you always!"
$50
A supporter of Diana Montenegro
"Such a great idea. Sending you prayers for continued positive outcomes!"
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Fernando Montenegro Ramos
I donated in support of this campaign.
$40
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Jennifer Aders
"Thanks for sharing. We support you!"
$50
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Alexandra MONTENEGRO
I donated in support of this campaign.
$50
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Natalia Buffa
"In Honor of our friend Diana, may a cure be found."
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Susan Sessums
"Thank you for sharing & warm wishes for continued good health managing CCM-we walk with you in spirit & hope for a cure. Here for you & your family."
$250
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Christine Rhyne
"Diana, you are very courageous! Prayers for you and your family and I hope your condition will improve."
$50
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Hadley Rivers
"Wishing you all the bestHadley Rivera"
$20
A supporter of Diana Montenegro
I donated in support of this campaign.
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Claudia Garcia
"Un abrazo grande desde Boston! Los extrañamos mucho."
$100
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Mansi Goel
I donated in support of this campaign.
$50
A supporter of Diana Montenegro
I donated in support of this campaign.
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Frani Bliss
I donated in support of this campaign.
$25
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Adriana Estevez
"Unidos en oración por encontrar un tratamiento alterno no invadió para curar CCM. Los Delgado"
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Lena Visconti
I donated in support of this campaign.
$50
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Paula Castano
"We love you and your entire family. We hope more research is done!"
$100
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Sara Brown
"Proud of you! Keep up the walking. 🚶♀️"
$100
—> Thank you so much for your support! Any further contributions will be greatly appreciated to help the Alliance Foundation reach their $30k goal!
(En español más abajo)
Dear Friends and Family,
Help me fund the research for treatments and a cure for cavernous malformation, a rare condition that affects many lives, including mine. Join me as I walk at least 1 mile every day, enjoying this beautiful sunrise, for 30 days!
Cerebral Cavernous Malformation (CCM) is a rare disease characterized by the formation of leaky blood vessels in the brain or spinal cord, leading to bleeding and debilitating symptoms. Children and adults affected by this condition can experience migraines, seizures, and strokes. Currently, the only treatment available is brain or spine surgery, which can result in additional deficits.
I experienced my first brain bleeding in May 2023, followed by a second one days later. I am immensely thankful to God for His miraculous healing power, as my condition is currently stable. While I must continue to undergo yearly exams, I pray daily for complete healing to avoid surgery. God is giving me peace, and I know He is always protecting me. I am also grateful for the grace I have received to transform my journey into a positive impact for others through Chain of Joy. @chainofjoy.gifts
My heart goes out to all the children and adults in pain and suffering, struggling with frustration in their recovery after surgery. Due to the unpredictable nature of cavernomas, many of us have experienced anxieties, panic attacks, and fear.
On May 15th, Cavernous Malformation Awareness Month begins, along with the Strides to Cure CCM Challenge! I am thrilled to participate and raise funds in support of The Alliance to Cure Cavernous Malformation, an organization that is close to my heart and has provided tremendous help. The Alliance is dedicated to advancing scientific understanding, promoting collaboration, and driving innovation in the fight against CCM.
Any contribution, no matter how small, will make a meaningful impact and is greatly appreciated. Thank you!
GOD BLESS YOU!
Diana
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Queridos amigos y familia,
Les pido su apoyo para ayudarme a recaudar fondos para la investigación de tratamientos y una cura para las malformaciones cavernosas, una afección rara que afecta a muchas vidas, incluida la mía. Los invito a donar mientras yo camino al menos 1 milla todos los días, durante 30 días!
La malformación cavernosa cerebral (MCC) es una enfermedad rara caracterizada por la malformación de vasos sanguíneos en el cerebro o la médula espinal, lo que provoca sangrado. Los niños y adultos afectados por esta afección pueden experimentar migrañas, convulsiones y accidentes cerebrovasculares. Actualmente, el único tratamiento disponible es la cirugía cerebral o de columna, que puede provocar déficits adicionales.
Tuve mi primera hemorragia cerebral en mayo de 2023, seguida de una segunda días después. Estoy inmensamente agradecida con Dios por su milagroso poder curativo, ya que mi condición actualmente es estable. Si bien debo seguir sometiéndome a exámenes anuales, oro diariamente por una curación completa para evitar la cirugía. Dios me está dando paz y sé que siempre me está protegiendo. También estoy agradecida por la gracia que me ha dado de transformar este proceso en un impacto positivo para los demás a través de Chain of Joy. @chainofjoy.gifts
Mi corazón está con todos los niños y adultos que tienen dolor y sufrimiento, que luchan contra la frustración en su recuperación después de la cirugía. Debido a la naturaleza impredecible de los cavernomas, muchos de nosotros hemos experimentado ansiedad, ataques de pánico y miedo.
¡El 15 de mayo comenzó el Mes de Concientización sobre las Malformaciones Cavernosas, junto con el desafio “Camina para una cura de CCM”! Estoy feliz de participar y recaudar fondos en apoyo a La Fundación Alianza para Curar la Malformación Cavernosa, una organización que tengo muy cerca del corazón y que me ha brindado una gran ayuda. La Alianza se dedica a promover la comprensión científica, promover la colaboración e impulsar la innovación en la lucha contra CCM.
Cualquier contribución, por pequeña que sea, tendrá un impacto significativo y será muy apreciada. ¡Gracias!
¡DIOS LOS BENDIGA!
Diana