Guest guest Posted July 14, 2004 Report Share Posted July 14, 2004 (((((((((((Sparky)))))))))))))) De Faith is the ability to not panic. -----Original Message-----From: Randy Hines Sent: Tuesday, July 13, 2004 9:37 PMTo: HepatitisCSupportGroupForDummies Subject: Re: Hello? Thank you! I need to be loved right now............That ole depression is creepin' up on me....Damn it! I hate this! Sparky Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 14, 2004 Report Share Posted July 14, 2004 Get a lawyer or try one of those father's rights organizations. Colleen Randy Hines wrote: Her adoptive father cut all ties with me and told her how bad of a person I was. Everything I sent got returned and I was hung up on when I called/ I just don't know what else I can do. I really screwed my life up! RBirth and Death are the two noblest expressions of bravery. - ---Kahlil GibranFor what is it to die, But to stand in the sun and melt into the wind? And when the Earth has claimed our limbs, Then we shall truly dance. --Kahlil Gibran Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 14, 2004 Report Share Posted July 14, 2004 Get a lawyer or try one of those father's rights organizations. Colleen Randy Hines wrote: Her adoptive father cut all ties with me and told her how bad of a person I was. Everything I sent got returned and I was hung up on when I called/ I just don't know what else I can do. I really screwed my life up! RBirth and Death are the two noblest expressions of bravery. - ---Kahlil GibranFor what is it to die, But to stand in the sun and melt into the wind? And when the Earth has claimed our limbs, Then we shall truly dance. --Kahlil Gibran Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 21, 2010 Report Share Posted January 21, 2010 hi whatthe hell is going on here why are u all acting this way?first if u belong to this site your child is sick second nobody with a sick child has the time or deserves to be called names,made to feel bad about there donations etc......donations are a personal thing,unless u people r the hollywood types and give money to have your egos built up,[i do not belive this to be the case]there seems to be people in this group bulling other people....i know it sounds stupid but cant we all get along?we all have a sick kid and that comes with stress,anger and sometimes helplessness......unless u have something nice,useful or charming to say please stop......lets get back to helping eachother get through this dark tunnel of scolilosis.......respect each other and remember this is about children we love that are sick........ Subject: Re: name calling?To: infantile_scoliosis Date: Thursday, January 21, 2010, 12:16 PM If we are going to be bringing up the name calling, then maybe we should look at giving low blows to innocent children who are fighting the same disease as everyone else?>> NO NAME CALLING. I dont mean to threaten here and realize this was all in> the heat of the moment, but if I see anyone name calling, they will be> removed. I believe this is stated clearly in the Netiquette that was> actually made for a reason and am appalled that someone would do this.> UNACCEPTABLE no matter what the reason.> HRH> > > Can we ask for no name calling? ; )> >  Heidi, Bexon's Mama, (2.5 years old, in 5th cast from Salt Lake City> > Shriners, currently down from 61 degrees to 23)> >> >> >> >> > ____________ _________ _________ __> > From: "heather@... " <heather@... >> > To: infantile_scoliosis @yahoogroups. com> > Sent: Thu, January 21, 2010 9:57:22 AM> > Subject: RE: [infantile_scoliosi s] Support group > >> >  > > Isnt that the truth.....It happens at least once once a year. We are all> > here to love and support each other. If members cant be supportive,> > empathic, understanding & rule compliant they should start their own list> > serve. Simple as that....> > HRH> >> >>> >> Beautifully said Tasha.> >>> >>> >>> >> I read through the posts just now and I immediately thought "here we go> >> again." Like Tasha, I have been a member of this group for a few years> >> now and every once in awhile there's a big blowout. People threaten to> >> leave, people fight about who does more, etc. Every time it happens I'm> >> discouraged. ..I'm frustrated.. .I'm upset...and mostly I'm saddened for> >> all> >> of the new members that have joined recently. Because for the MOST part> >> this is a great group of wonderful and supportive members. I think we> >> all> >> need to look outside of our selves and think "is this post helpful?" If> >> it isn't - then maybe it shouldn't be made public.> >>> >>> >>> >> ~> >> Noah 4 1/2 years old> >> 9 months of casting in SLC; Currently on 1 1/2 years of bracing at 6* in> >> brace> >> And Mariella 11 months old - resolved Infantile Scoliosis> >>> >>> >>> >>> >>> >>> >> To: infantile_scoliosis @yahoogroups. com> >> From: ryanswalkyahoo (DOT) com> >> Date: Wed, 20 Jan 2010 06:42:38 -0800> >> Subject: [infantile_scoliosi s] Support group> >>> >>> >>> >>> >>> >>> >>> >> I have held back trying to think about what to say. I went to bed> >> thinking about all the DRAMA that unfolded last night. And I woke up> >> thinking about it. I prayed about this morning....needless to say it has> >> been on my mind. What went on last night got way out of hand.> >> This is not what this group is about. Anyone new reading this PLEASE do> >> not let this cloud your views of this SUPPORT group.> >> We ALL have helped in some way to promote ISOP. And we do not have to> >> prove that anyone. No one is better than the other.> >>> >> There are many ways to help:> >> -answering questions to a new, very frightened parent -selling> >> bracelets for ISOP> >> - telling a stranger about IS> >> -holding a fund raiser> >> - giving money to Shriner's, ish Rite or ISOP(its YOUR> >> money....YOUR> >> choice!)> >> -making videos> >> -sending info to pediatricians> >>> >> -being a part of this SUPPORT group(every view is needed! you may not> >> click with everyone, but you may click with someone)> >>> >> Bottom line is we are going to have different views.> >> ****Attacking one another for what ever that reason might be is wrong> >> and> >> should not be public knowledge!!! ***> >> What kind of message are we sending to new members?! My heart is sad> >> this> >> morning and confused about what this group is all about. And now good> >> parents are leaving the group. This is shameful!> >> We should stand behind each other and be happy for anything that is done> >> to help get the word out about Early Treatment.> >> YES, ISOP is what got casting to the US and I am ever so grateful! BUT> >> that may not be your passion.> >> My son, , did not benefit from Mehta treatment with casting, BUT I> >> vowed to spread the word. That is MY passion. I don't have lots of money> >> to give, but I know what to tell people about Infantile Scoliosis. That> >> is what matters to me.> >> Sure without ISOP I would not know anything about Early Treatment, but> >> without Texas ish Rite Hospital for Children would probably be> >> looking at surgery. I have been on the group now since July 2006. I have> >> got SUPPORT here and have seen the support grow. Lets not go in a> >> direction that changes what this group should be about.> >> I am ready for a new day and to be a support to anyone here on the> >> group.> >> Come on people lets show new members how great this group really is!!!!> >> Love you ALL!!!!> >>> >>> >> Tasha> >> Mommy of 4 year old twin boys- and > >> Fort Worth, Texas> >> Series of 6 casts for 14 months and now in a night brace.> >> is treated at Texas ish Rite Hospital.> >> You can read 's story at....> >> http://www.infantil escoliosis. org/stories. html> >>> >>> >>> >>> >>> >>> >>> >>> >>> >>> >>> >> ____________ _________ _________ _________ _________ _________ _> >> Hotmail: Trusted email with Microsoft’s powerful SPAM protection.> >> http://clk.atdmt. com/GBL/go/ 196390706/ direct/01/> >> >> >> >> >> >> Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.