Kepral's Syndrome and Cystic Fibrosis: A Request from a BioWare Writer
Débuté par
Patrick Weekes
, juin 15 2011 08:00
#26
Posté 15 juin 2011 - 08:52
@ 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
Posté 15 juin 2011 - 08:54
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
Posté 15 juin 2011 - 08:54
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.
I'll do my bit to help our CF association down here in New Zealand.
#29
Posté 15 juin 2011 - 08:56
Thank you for the infomation. My prayers go out to your friend....
As for Thane........You better make cry.
As for Thane........You better make cry.
#30
Posté 15 juin 2011 - 08:57
Modifié par PsychoWARD23, 15 juin 2011 - 08:57 .
#31
Posté 15 juin 2011 - 09:01
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
Posté 15 juin 2011 - 09:13
This was very enlightening. Thank you for posting it. Retweeted.
#33
Posté 15 juin 2011 - 09:53
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
Posté 15 juin 2011 - 09:58
Retweeted, donation incoming this payday. Thanks for making this thread.
#35
Posté 15 juin 2011 - 10:03
Sad thing is, CF is genetic.
Kepral's is at least acquired.
#36
Posté 15 juin 2011 - 10:06
Great post! tbh I have known about CF only by name.
#37
Posté 15 juin 2011 - 10:12
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.
I'll do what I can, will repost on FB and make a donation when I can.
#38
Guest_The Big Bad Wolf_*
Posté 15 juin 2011 - 10:16
Guest_The Big Bad Wolf_*
I'll do what I can Patrick. One of my cousins has CF.
#39
Posté 15 juin 2011 - 10:34
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.
Time to think less about ourselves and more about what's going on around us, I guess.
Thank you for posting this.
#40
Posté 15 juin 2011 - 10:40
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.
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
Posté 15 juin 2011 - 11:26
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
Posté 15 juin 2011 - 11:28
Thanks for posting this, Patrick. I've made a donation, and I hope they find a cure in the near future.
#43
Posté 15 juin 2011 - 11:40
I'll see what I can do. Thanks for letting us know, Patrick.
#44
Posté 16 juin 2011 - 12:09
My closest cousin has struggled with Cystic Fibrosis for her entire life. You're doing a great thing here; thank you
#45
Posté 16 juin 2011 - 12:21
More people need to read this.
My heart goes to all who witnessed a loved one suffering from illness.
My heart goes to all who witnessed a loved one suffering from illness.
#46
Posté 16 juin 2011 - 12:37
My cousin's daughter has CF. She was also told she wouldn't live past 5 and she's almost a teenager now.
#47
Posté 16 juin 2011 - 01:17
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
Posté 16 juin 2011 - 01:17
This is a wonderful post. Thank you and I will be sure to donate.
#49
Posté 16 juin 2011 - 01:28
Cure Thane Krios people afflicted with cycstic fibrosis for ME3! real life.
Thanks for the awareness ^^ ill see what i can do.
Thanks for the awareness ^^ ill see what i can do.
#50
Posté 16 juin 2011 - 02:07
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.





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