Living with ALS: The Douglas Family Story

[@mariannahanley500]

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.

[@DougClough]

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]

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

[@HDWorldclass]

How very sad

[@judyclark5544]

Heart broken 💔

[@countryqueen78]

I pray for a day that they cure this horrible disease

[@renataloren2384]

Rest in Peace Chris!! ❤

[@trishstevenson3022]

condolences to you all. rip chris

[@catman8670]

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

[@caspergreen8931]

Rest In Peace Chris

[@andymcgovern6615]

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]

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.

[@davey989]

RIP, Chris.

[@eleanorward4824]

God bless you all

[@angelesa9302]

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

[@dazeldibujosfeos8435]

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]

Si mi esposó fue diagnosticado en junio del año 2019

[@dazeldibujosfeos8435]

@@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

[@anne-marienordin7636]

🙏🙏🙏❤️

[@HDWorldclass]

Darling man and darling Wife

[@anacarolinagarcia9025]

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.

[@TheIllegalalienfool]

How and why these people always and always have spouses?

[@applejellypucci]

You again. Do you ask this question on every ALS video?

[@janheard3826]

TheIllegalalienfool Strange question. Why should they NOT have spouses? They are always of the age where most people would be married.

[@officetechtyping]

They married before diagnosis.

[@tpfmike1976]

Stupid question..

[@syedaaqsafasu3702]

@@tpfmike1976 y even the have the wrights to have wife and children.

[@ebenburger111]

☺ 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. ☺

[@annetteslife]

Rest in peace Chris