Guest guest Posted February 6, 2004 Report Share Posted February 6, 2004 Sara, If I may butt in here......I will give you the advise of a wise friend of mine who's daughter was diagnosed a few years before . When I told her that I was upset about the upcoming first anniversary of 's diagnosis. You may just try looking at that date in a different way. If you had not gotten the info you did, when you did, Zach would be a very sick kid right now. Be thankful for the day that you got a diagnosis, think of it not as a dark day but as a day of rebirth (no, I do not mean that in a religious way! LOL) Be thankful that your son was diagnosed, unlike so many kids who go through their lives sick and get little or no treatment for this illness. Be thankful that you live in a country where you can get the meds that your child needs, not somewhere that doesn't have the resources to give Zach the best medical care possible. Maybe you can use that day just to appreciate what you have as a family and not dwell on the way you felt at diagnosis. Just some advice that I was given. And yes, it did help me, so I hope it helps you a bit. mom of 5 with CF and one on the way Re: jax florida mystery gift/Diagnosis question Sue, I did not send the gift, but read the end of your post and wanted to comment on something else. You said your daughter was diagnosed on christmas eve. How do you handle that? We are quickly approaching the 1st anniversary of Zach's diagnosis. It is a sad day and I was curious how you handle the diagnosis being so close to a holiday. We are trying to plan a day trip to get our minds off of it. Sara > would like to say thank you to the person(s) who sent the tiger puzzle and the cute little white " hug me " musical bear. There is only one problem, there is no name. I don't know if this is on purpose or not and it doesn't matter. We just wanted to say thank you for thinking of . It will be something for us to do (like during the CODE T last night during the tornado warnings when we had to sit out in the hall). It will definately come in handy. > Anyway, thanks to whoever sent it, it really means a lot to us. > > L & H > > Sue Pettit of Tupelo, Mississippi > mom to - 17 wocf, driving and being the most responsible 17 yo I have ever known, pitching her first season as a fast-pitch pitcher for her softball team at school; - 13 wocf, playing school baseball, trumpet in the band, and trying very hard to work through the horrible hormone effects 13 yo have; - 12 yo wcf and cfrd, diagnosed with cf at 8 days old at LeBonheur Children's Medical Center in Memphis, TN on Christmas Eve, 1991, currently playing basketball, softball, the flute in the school band, and enjoying life to the fullest, now seeing Drs. Lyrene, Makris, and Hagood at UAB Children's Hospital in Birmingham, Alabama - all of whom are excellent doctors ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. ------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2004 Report Share Posted February 6, 2004 OMG did I spam you?? I have been having a lot of weird e-mails sent from my address to " bob " at different domain names. I am going to have my husband try to fix it. Sorry if that is what is happening. Sara > > would like to say thank you to the person(s) who sent the > tiger puzzle and the cute little white " hug me " musical bear. There > is only one problem, there is no name. I don't know if this is on > purpose or not and it doesn't matter. We just wanted to say thank > you for thinking of . It will be something for us to do > (like during the CODE T last night during the tornado warnings when > we had to sit out in the hall). It will definately come in handy. > > Anyway, thanks to whoever sent it, it really means a lot to us. > > > > L & H > > > > Sue Pettit of Tupelo, Mississippi > > mom to - 17 wocf, driving and being the most responsible > 17 yo I have ever known, pitching her first season as a fast- pitch > pitcher for her softball team at school; - 13 wocf, playing > school baseball, trumpet in the band, and trying very hard to work > through the horrible hormone effects 13 yo have; - 12 yo > wcf and cfrd, diagnosed with cf at 8 days old at LeBonheur > Children's Medical Center in Memphis, TN on Christmas Eve, 1991, > currently playing basketball, softball, the flute in the school > band, and enjoying life to the fullest, now seeing Drs. Lyrene, > Makris, and Hagood at UAB Children's Hospital in Birmingham, > Alabama - all of whom are excellent doctors > > > > ------------------------------------------- > The opinions and information exchanged on this list should IN NO WAY > be construed as medical advice. > > PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. > > ------------------------------------ > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2004 Report Share Posted February 6, 2004 YOU, Sara did not spam anyone, but you may need to do computer main tenance, update virus definitions, possibly resubscribe to your virus-scan program and be aware that Yahoo reads as spam any posts sent in a series with the same subject line; they are protecting Yahoo and us from Mydoom (Novarg) virus, which is a computer catastrophe for entire networks, which Yahoo is. You can download a fix or patch for the Mydoom virus, and go from there. We are all still speaking here! Love, n--you get the patch from Microsoft.com or call your computer manufacturer; there IS life after spam! Re: gift/Diagnosis question OMG did I spam you?? I have been having a lot of weird e-mails sent from my address to " bob " at different domain names. I am going to have my husband try to fix it. Sorry if that is what is happening. Sara > > would like to say thank you to the person(s) who sent the > tiger puzzle and the cute little white " hug me " musical bear. There > is only one problem, there is no name. I don't know if this is on > purpose or not and it doesn't matter. We just wanted to say thank > you for thinking of . It will be something for us to do > (like during the CODE T last night during the tornado warnings when > we had to sit out in the hall). It will definately come in handy. > > Anyway, thanks to whoever sent it, it really means a lot to us. > > > > L & H > > > > Sue Pettit of Tupelo, Mississippi > > mom to - 17 wocf, driving and being the most responsible > 17 yo I have ever known, pitching her first season as a fast- pitch > pitcher for her softball team at school; - 13 wocf, playing > school baseball, trumpet in the band, and trying very hard to work > through the horrible hormone effects 13 yo have; - 12 yo > wcf and cfrd, diagnosed with cf at 8 days old at LeBonheur > Children's Medical Center in Memphis, TN on Christmas Eve, 1991, > currently playing basketball, softball, the flute in the school > band, and enjoying life to the fullest, now seeing Drs. Lyrene, > Makris, and Hagood at UAB Children's Hospital in Birmingham, > Alabama - all of whom are excellent doctors > > > > ------------------------------------------- > The opinions and information exchanged on this list should IN NO WAY > be construed as medical advice. > > PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. > > ------------------------------------ > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 7, 2004 Report Share Posted February 7, 2004 No, my reply cam back as spam. I don't know if I like this new thing from yahoo. Re: gift/Diagnosis question OMG did I spam you?? I have been having a lot of weird e-mails sent from my address to " bob " at different domain names. I am going to have my husband try to fix it. Sorry if that is what is happening. Sara > > would like to say thank you to the person(s) who sent the > tiger puzzle and the cute little white " hug me " musical bear. There > is only one problem, there is no name. I don't know if this is on > purpose or not and it doesn't matter. We just wanted to say thank > you for thinking of . It will be something for us to do > (like during the CODE T last night during the tornado warnings when > we had to sit out in the hall). It will definately come in handy. > > Anyway, thanks to whoever sent it, it really means a lot to us. > > > > L & H > > > > Sue Pettit of Tupelo, Mississippi > > mom to - 17 wocf, driving and being the most responsible > 17 yo I have ever known, pitching her first season as a fast- pitch > pitcher for her softball team at school; - 13 wocf, playing > school baseball, trumpet in the band, and trying very hard to work > through the horrible hormone effects 13 yo have; - 12 yo > wcf and cfrd, diagnosed with cf at 8 days old at LeBonheur > Children's Medical Center in Memphis, TN on Christmas Eve, 1991, > currently playing basketball, softball, the flute in the school > band, and enjoying life to the fullest, now seeing Drs. Lyrene, > Makris, and Hagood at UAB Children's Hospital in Birmingham, > Alabama - all of whom are excellent doctors > > > > ------------------------------------------- > The opinions and information exchanged on this list should IN NO WAY > be construed as medical advice. > > PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. > > ------------------------------------ > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 7, 2004 Report Share Posted February 7, 2004 The funny thing about this coming back as spam to me is that I changed the subject line a bit so it wouldn't spam anyone! Oh, well! that's what I get for trying! anyway, read what I said about dx anniversaries, Sara! Re: gift/Diagnosis question OMG did I spam you?? I have been having a lot of weird e-mails sent from my address to " bob " at different domain names. I am going to have my husband try to fix it. Sorry if that is what is happening. Sara > > would like to say thank you to the person(s) who sent the > tiger puzzle and the cute little white " hug me " musical bear. There > is only one problem, there is no name. I don't know if this is on > purpose or not and it doesn't matter. We just wanted to say thank > you for thinking of . It will be something for us to do > (like during the CODE T last night during the tornado warnings when > we had to sit out in the hall). It will definately come in handy. > > Anyway, thanks to whoever sent it, it really means a lot to us. > > > > L & H > > > > Sue Pettit of Tupelo, Mississippi > > mom to - 17 wocf, driving and being the most responsible > 17 yo I have ever known, pitching her first season as a fast- pitch > pitcher for her softball team at school; - 13 wocf, playing > school baseball, trumpet in the band, and trying very hard to work > through the horrible hormone effects 13 yo have; - 12 yo > wcf and cfrd, diagnosed with cf at 8 days old at LeBonheur > Children's Medical Center in Memphis, TN on Christmas Eve, 1991, > currently playing basketball, softball, the flute in the school > band, and enjoying life to the fullest, now seeing Drs. Lyrene, > Makris, and Hagood at UAB Children's Hospital in Birmingham, > Alabama - all of whom are excellent doctors > > > > ------------------------------------------- > The opinions and information exchanged on this list should IN NO WAY > be construed as medical advice. > > PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. > > ------------------------------------ > > > > Quote Link to comment Share on other sites More sharing options...
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