aviolentworld

just got Windhand S/T in the mail from Midheaven.  can't wait to put the kids to bed to listen to this.
 
also i'm pretty sure it was a 1st press black.  only thing i could see on discogs, unless they did more than 6 pressings.  either way i'm pretty stoked.

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

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

Good luck man. Current charity $ is tied up in AHA, but hopefully I can throw you a little $ next go round.
 
Also, your daughters are adorable!

cheers man

as always my man, my best to you and your family!

Do it, this guy is great

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

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

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

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

Get your foot in the door over at Suburban Home Records..

Get your foot in the door over at Suburban Home Records..

Get your foot in the door over at Suburban Home Records..

since we are taking a break from all that is doom and getting to know each other here is probably the best family photo we have ever taken.  girls b-day again.

here is a pic from my girls 4th birthday

Best wishes for the new kid!

Good luck duder!

My younger brother and his wife went through a situation similar to yours. Everything eventually worked out for them so I'm sure the same will happen to you. Good luck!!!

Definitely sending good vibes 'tords you and the wifey for the awaited addition to your lineage !

alright my doom brothers.  i'm bringing this here because it's not vinyl related and the fact that this is pretty much the only thread i frequent now a days. 
 
anyhow my wife and i have been trying to have our 3rd kid for about 17 months now.  we had a miscarriage early on and came up empty handed until this month.  she is getting her HCG levels tested until the doc thinks we are in the clear.   We are at almost 900 and need to be around 2000 for her to say we are golden.  with the miscarry we only made it to 80 so we are looking real good. 
 
we aren't telling family quite yet and i needed to get this off my chest.  just keep us in your prayers if you do that kinda thing.  if not at least blast some FUCKING DOOM for vs. 3 my brothers.  thanks for taking time to read this.

Good luck buddy! I took us 5 months and even that took a bit of a toll on me. I can't imagine adding a whole year to the process. 
 
Hope it comes up + real soon. 

Positive doomy thoughts coming your way bro!

Hope it all works out, dude! Best of luck on spawning a human.

Deflategate.