Living with ALS: The Douglas Family Story

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Chris and Peggy Douglas are raising awareness and advocating for change to help families facing ALS. The ALS Association is a leader in supporting global, milestone-based research. Visit alsmn.org for more information and to find resources near you.

Опубликовано:

29 сен 2024

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Комментарии : 46

@mariannahanley500 5 лет назад

Hello Chris, this is just a little note from Canada. What a special person you are talking care of a family of 6. Working full time, I’m so impressed. I wish you many more years with you family. Thank you for sharing your story.

@davey989 2 года назад

RIP, Chris.

@anne-marienordin7636 4 года назад

🙏🙏🙏❤️

@catman8670 3 года назад

I’m glad ALS associations are going th Congress for funding!

@DougClough 6 лет назад

We had our 20th last year also. What a great couple. I sort of dragged my wife along to the Hill and many other places as well. Like you guys, we have been so incredibly blessed during our ALS journey. Keep on keeping on.

@donnahague8983 2 года назад

Rest In Peace Chris… past away September 18, 2020. 🕊🤍

@HDWorldclass 2 года назад

How very sad

@judyclark5544 2 года назад

Heart broken 💔

@countryqueen78 2 года назад

I pray for a day that they cure this horrible disease

@renataloren2384 Год назад

Rest in Peace Chris!! ❤

@trishstevenson3022 Год назад

condolences to you all. rip chris

@andymcgovern6615 3 года назад

Hello Chris. I wish you well. Very sad story and such a lovely family. But then every story of ALS/MND is sad. Myself, I have survived 43 years with the ugly thing. MND. The world is waiting for a breakthrough or something to arrest this galloping disease. Research are making very poor progress. Nevertheless, we will try to hang on?. Andy in Ireland.

@misskay8131 Год назад

Hi Andy, I hope you’re well. I have been researching this ugly disease and you are the first person I’ve come across who has lived so long with this disease. 43 years?? You are a warrior. Sending you love and light and hope you’re still going strong.

@caspergreen8931 2 года назад

Rest In Peace Chris

@HDWorldclass 2 года назад

Darling man and darling Wife

@anacarolinagarcia9025 Год назад

Dios nos de la fuerza que necesitamos para sobrellevar esta enfermedad, pero especialmente tener la FE de saber que en la voluntad de Dios, El permite que vivamos esta enfermedad para algo, un propósito de salvación de nuestras almas y de otras más que estan cerca de nosotros.

@annetteslife Год назад

Rest in peace Chris

@angelesa9302 4 года назад

😭 😭 😭 😭 me identifico estamos en el mismo barco 🚢 Dios nos ampare y nos de toda la fuerza 💪 que necesitamos Bendiciones .

@dazeldibujosfeos8435 4 года назад

También tienes un familiar con ELA? o eres paciente, mi papá acaba de ser diagnosticado a los 59 en marzo de este año, y le damos vitaminas y celulas madre en México, dicen que pronto llegará un tratamiento llamado Nurown que puede incluso detener por completo y revertir la ELA, no desesperes y ten esperanza.

@angelesa9302 4 года назад

Si mi esposó fue diagnosticado en junio del año 2019

@dazeldibujosfeos8435 4 года назад

@@angelesa9302 Busca "Nurown" en twitter o internet, busca los casos de Mark Bedwell o Matt Bellina, Thurmand Maynard, el caso más excepcional es el de Mark Bedwell, que con ese tratamiento en fase experimental pudo volver a correr y a hablar, la verdad no es una cura pero es un tratamiento esperanzador, Ánimo y fe en esta lucha

@eleanorward4824 5 лет назад

God bless you all

@ebenburger111 5 лет назад

☺ Infected water/food - Cyanobacteria - Cytotoxins & Mycotoxins - Release toxic heavy metals - Affect organs and Nervous System - Als, Parkinsons/Alsheimers........ Treatment: Probiotics ☺ . Share if you care. ☺ Happy to forward the research docs I found. ☺