aviolentworld

Family dinners are Crazy man.

yeah i would offer Maclin first for sure.  the hardest part is that people always go by the numbers and don't look at everything first before deciding in this league.  they always say the point difference is in my favor but they fail to see the minus 10 they have because of someone on a bye that week.   

newest addition to the doom family.  everyone meet Owen Arthur.
 

hey guys - amnstypls here. some good things coming soon.

Congrats my man.

not sure how many of you dudes like Kowloon Walled City, but there is a picture from Gilead Media of the new test presses for their new record.  thing looks sweet as fuck.

not sure how many of you dudes like Kowloon Walled City, but there is a picture from Gilead Media of the new test presses for their new record.  thing looks sweet as fuck.

not sure how many of you dudes like Kowloon Walled City, but there is a picture from Gilead Media of the new test presses for their new record.  thing looks sweet as fuck.

That time again.  Just got my CF walk information for the Cleveland Zoo on 5/16 and figured it would be a great time to make another thread.  Below is a photo from last years walk and a couple others




 
 
hey guys,
my girls have a genetic abnormality called CFTR related
metabolic syndrome. They don't have cystic fibrosis, but could have
problems and develop a milder form of it it in the future. I'm raising
money to help find a cure for Cystic Fibrosis

I'm a CF carrier
and gave the gene to my girls. My wife has a tiny typo on her gene that
when paired with mine can POSSIBLY cause atypical CF (much milder
symptoms of CF or symptoms at an older age) - lung problems/infections,
sinus problems, and pancreas problems and trouble gaining weight due to
stickier than normal mucus in their bodies. They have borderline
elevated higher levels of salt in their sweat, but not high enough to be
considered cystic fibrosis. The girls are monitored by a CF specialist
every 3 months, but so far are doing fantastic. They are happy, healthy,
growing, and thriving.
 
Click the link if you would like to know more about CFTR related metabolic syndrome.
http://www.cff.org/AboutCF/Testing/Genetics/CRMS/
 
any donation is greatly appreciated. even if its a couple bucks!!! thanks dudes and dudettes.
http://fightcf.cff.org/site/TR/GreatStrides/104_Northern_Ohio_Cleveland?px=1774452&pg=personal&fr_id=3482

Threw in a little more so you'd hit your goal.

Threw you a few dollars, every bit helps right?
I work on a hospital ward here in the UK for children with Cf, in the last 20yrs there have been such innovations in care, treatment & research, have to believe we're closer to a cure.
Walk well my friend

couldnt throw in much, but you got the rest of my paypal balance. good luck!

how much did you throw in? Even though I already donated, I will match yours. In a decent good mood tonight and willing to give
 
PM me the info if you want

I'm in

This is either the second or third year I've donated something. Always a worthwhile cause. Those girls are precious!

You're halfway there.

Your girls are the cutest!! Happy to help out!

Just tossed you a couple bucks. Good luck hitting your goal!

That time again.  Just got my CF walk information for the Cleveland Zoo on 5/16 and figured it would be a great time to make another thread.  Below is a photo from last years walk and a couple others




 
 
hey guys,
my girls have a genetic abnormality called CFTR related
metabolic syndrome. They don't have cystic fibrosis, but could have
problems and develop a milder form of it it in the future. I'm raising
money to help find a cure for Cystic Fibrosis

I'm a CF carrier
and gave the gene to my girls. My wife has a tiny typo on her gene that
when paired with mine can POSSIBLY cause atypical CF (much milder
symptoms of CF or symptoms at an older age) - lung problems/infections,
sinus problems, and pancreas problems and trouble gaining weight due to
stickier than normal mucus in their bodies. They have borderline
elevated higher levels of salt in their sweat, but not high enough to be
considered cystic fibrosis. The girls are monitored by a CF specialist
every 3 months, but so far are doing fantastic. They are happy, healthy,
growing, and thriving.
 
Click the link if you would like to know more about CFTR related metabolic syndrome.
http://www.cff.org/AboutCF/Testing/Genetics/CRMS/
 
any donation is greatly appreciated. even if its a couple bucks!!! thanks dudes and dudettes.
http://fightcf.cff.org/site/TR/GreatStrides/104_Northern_Ohio_Cleveland?px=1774452&pg=personal&fr_id=3482

Let me ask my buddies. Not sure who has tickets

What I really want is the store's video footage of me going to the deodorant aisle afterward and spraying my ass with Axe.

Sept 22nd. Looks like there are a bunch of us expecting around September and October. Dads of VC unite.

Fucking A...... just won the Helmet lady records test press giveaway on instagram.  Hawkeyes - Poison slows you down.  Pretty fucking stoked about that.

Fucking A...... just won the Helmet lady records test press giveaway on instagram.  Hawkeyes - Poison slows you down.  Pretty fucking stoked about that.

Fucking A...... just won the Helmet lady records test press giveaway on instagram.  Hawkeyes - Poison slows you down.  Pretty fucking stoked about that.