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Kepral's Syndrome and Cystic Fibrosis: A Request from a BioWare Writer


111 réponses à ce sujet

#26
Karin Weekes

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@ Jebel Krong: Thanks kindly for your support. If it helps, the URL for the Cystic Fibrosis Trust in the UK is: http://www.cftrust.org.uk/. Thanks. :)

#27
felipejiraya

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Phaedon wrote...

It's a shame that this thread is not as popular as it deserves to be.


I suggest one of the mods to fix this thread.

Modifié par felipejiraya, 15 juin 2011 - 08:55 .


#28
Shockwave81

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Thanks for sharing such a personal story with us Patrick. I can't imagine what it would be like for your friend, or anyone else suffering from CF. We all just take breathing for granted.

I'll do my bit to help our CF association down here in New Zealand.

#29
dreman9999

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Thank you for the infomation. My prayers go out to your friend....

As for Thane........You better make cry.

#30
PsychoWARD23

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:crying:

Modifié par PsychoWARD23, 15 juin 2011 - 08:57 .


#31
Noir_Skye

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This is a great post and a great cause. I just checked out the first website. It is very easy to donate and the money can stay within your community if you choose.

#32
CrimsonNephilim

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This was very enlightening. Thank you for posting it. Retweeted.

#33
Leonia

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Fight for the cure just got a whole new meaning, thanks Mr. Weekes for bringing this to our attention. I'll join in with passing on those links. Sending good vibes out to your friend as well.

#34
Raiil

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Retweeted, donation incoming this payday. Thanks for making this thread.

#35
Reapinger

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Sad thing is, CF is genetic. :( Kepral's is at least acquired.

#36
Pepper4

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Great post! tbh I have known about CF only by name.

#37
kaimanaMM

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That's a great post, Patrick.  I don't know anyone who has CF.  My heart goes out to your friend.  

I'll do what I can, will repost on FB and make a donation when I can.

#38
Guest_The Big Bad Wolf_*

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I'll do what I can Patrick. One of my cousins has CF.

#39
Epantiras

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I admit I didn't expect to see this on a forum about videogames.
Time to think less about ourselves and more about what's going on around us, I guess.
Thank you for posting this.

#40
hanar05

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What kind of person would I be if I supported a cure for Kepral's but didn't support curing CF!
Thank you for the link, Patrick. Always happy to donate to a worthy cause!
Best of luck to your friend, she is a truly remarkable person for being that strong.

#41
xIxDarkWolfxIx

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I will try to donate soon, CF is a disease that hopefully thanks to Stem Cell Research and maybe Genetic Modification can be a thing of the past.

#42
Verit

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Thanks for posting this, Patrick. I've made a donation, and I hope they find a cure in the near future.

#43
Someone With Mass

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I'll see what I can do. Thanks for letting us know, Patrick.

#44
AlphaDormante

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My closest cousin has struggled with Cystic Fibrosis for her entire life. You're doing a great thing here; thank you :)

#45
Lady Olivia

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More people need to read this.

My heart goes to all who witnessed a loved one suffering from illness.

#46
Verly

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My cousin's daughter has CF. She was also told she wouldn't live past 5 and she's almost a teenager now.

#47
AerisBru

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Lady Olivia wrote...
My heart goes to all who witnessed a loved one suffering from illness.


And I know this very well.

To be healthy is a privilege and also a responsibility to help other people who, unfortunately, weren't so lucky. I'll surely donate to some institution around here. 

Good thread.

#48
Cyansomnia

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This is a wonderful post. Thank you and I will be sure to donate.

#49
Niniva

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Cure Thane Krios people afflicted with cycstic fibrosis for ME3! real life.

Thanks for the awareness ^^ ill see what i can do.

#50
suprhomre

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I have heard of the this before but never really paid any attention to it. Being a Thane fan I now see it in a different way, thank you.