Guest guest Posted September 23, 2004 Report Share Posted September 23, 2004 Melody, I have a Kandee dog too. Kandace Shuler is her full name, her mom is Lulu Anne Shuler. Their names are bigger than they are. They weigh 5-61/2 lbs. Aggie Quoting Melody Moris : > MessageI bet your Jordan and my Candy would get along famously - they are > both finicky potty prisses! LOL > > Melody Moris, Leader > TOPS #TX 1454, Pleasanton > http://www.texastops.org > > Re: Hello everyone > > > Well, rocks definitely go along with it!! And fire ants can make it a > lot of fun! And when it's 90 degrees and 90% humidity, that adds to the > fun! And finding a place to go potty is loads of fun! Trying to cook over > a fire or even on a camp stove is just loads of fun! But if anybody has any > ideas for what they think makes it fun, I'll be willing to listen!! > > Clara > > > > EMAIL TEXAS-STYLE!! > > > > > > > EMAIL TEXAS-STYLE!! > > > > > > EMAIL TEXAS-STYLE!! > > > > > > > EMAIL TEXAS-STYLE!! > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 3, 2007 Report Share Posted October 3, 2007 Gail, So good to have you join us, but sorry with all my heart that you are so sick. This group is here to help one another. We are all in the same boat. We are fighting the fight with the monster called PF. I was daignosed 10 years ago with open lung biopsy. There are differing opinions about whether to have biopsy, but for me it literally saved my life. I was sooooo sick and I was not getting a diagnosis that made sense. I was diagnosed with PF secondary to Mixed Connective Tissue Disease, primarily Lupus. So, we have autoimmune disease in common. Diabetes and s are on the list of literally hundreds of autoimmune diseases. So many of them involve the lungs. For me, once diagnosed, my pulmonologist sent me to a different rheumatologist and they have worked together to keep my Lupus, etc. under control as much as is possible. It has been a tough uphill fight, but here I am. Once the biopsy is finished, if you have not done so.....try to find a facility that specializes in Interstitial Lung Disease. Even one visit will help you understand your disease. Read, Read, Read....and learn everything that you can. Keep records. You are welcome here and we will help you in any way that we can....and you can help us. May God be with you...you are soooooo young. Hugs, Joyce D.PULMONARY FIBROSIS/LUPUS 1997 BRONCHIECTASIS 2004 INDIANA 2 COR. 12:10 ....when I am weak, then I am strong.>> Hello everyone.My name is Gail.I'm 37 years old and just found out I > have PF.I don't know very much about it except what i have read > online.I have to go to a surgeon Thursday to find out when they are > going to do a open lung biopsy.I'm a little scared of that.I also have > type 1 diabetes and addison's disease which is autoammune diseases and > that's why they think I now have PF.It has really been neat reading all > your messages.Please fell free to e-mail me at any time.I live in a > very small town in Alabama and there's no support groups here.> > > > Prayers and Wishes to all of you> Gail> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 3, 2007 Report Share Posted October 3, 2007 Gail, So good to have you join us, but sorry with all my heart that you are so sick. This group is here to help one another. We are all in the same boat. We are fighting the fight with the monster called PF. I was daignosed 10 years ago with open lung biopsy. There are differing opinions about whether to have biopsy, but for me it literally saved my life. I was sooooo sick and I was not getting a diagnosis that made sense. I was diagnosed with PF secondary to Mixed Connective Tissue Disease, primarily Lupus. So, we have autoimmune disease in common. Diabetes and s are on the list of literally hundreds of autoimmune diseases. So many of them involve the lungs. For me, once diagnosed, my pulmonologist sent me to a different rheumatologist and they have worked together to keep my Lupus, etc. under control as much as is possible. It has been a tough uphill fight, but here I am. Once the biopsy is finished, if you have not done so.....try to find a facility that specializes in Interstitial Lung Disease. Even one visit will help you understand your disease. Read, Read, Read....and learn everything that you can. Keep records. You are welcome here and we will help you in any way that we can....and you can help us. May God be with you...you are soooooo young. Hugs, Joyce D.PULMONARY FIBROSIS/LUPUS 1997 BRONCHIECTASIS 2004 INDIANA 2 COR. 12:10 ....when I am weak, then I am strong.>> Hello everyone.My name is Gail.I'm 37 years old and just found out I > have PF.I don't know very much about it except what i have read > online.I have to go to a surgeon Thursday to find out when they are > going to do a open lung biopsy.I'm a little scared of that.I also have > type 1 diabetes and addison's disease which is autoammune diseases and > that's why they think I now have PF.It has really been neat reading all > your messages.Please fell free to e-mail me at any time.I live in a > very small town in Alabama and there's no support groups here.> > > > Prayers and Wishes to all of you> Gail> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 3, 2007 Report Share Posted October 3, 2007 Gail, So good to have you join us, but sorry with all my heart that you are so sick. This group is here to help one another. We are all in the same boat. We are fighting the fight with the monster called PF. I was daignosed 10 years ago with open lung biopsy. There are differing opinions about whether to have biopsy, but for me it literally saved my life. I was sooooo sick and I was not getting a diagnosis that made sense. I was diagnosed with PF secondary to Mixed Connective Tissue Disease, primarily Lupus. So, we have autoimmune disease in common. Diabetes and s are on the list of literally hundreds of autoimmune diseases. So many of them involve the lungs. For me, once diagnosed, my pulmonologist sent me to a different rheumatologist and they have worked together to keep my Lupus, etc. under control as much as is possible. It has been a tough uphill fight, but here I am. Once the biopsy is finished, if you have not done so.....try to find a facility that specializes in Interstitial Lung Disease. Even one visit will help you understand your disease. Read, Read, Read....and learn everything that you can. Keep records. You are welcome here and we will help you in any way that we can....and you can help us. May God be with you...you are soooooo young. Hugs, Joyce D.PULMONARY FIBROSIS/LUPUS 1997 BRONCHIECTASIS 2004 INDIANA 2 COR. 12:10 ....when I am weak, then I am strong.>> Hello everyone.My name is Gail.I'm 37 years old and just found out I > have PF.I don't know very much about it except what i have read > online.I have to go to a surgeon Thursday to find out when they are > going to do a open lung biopsy.I'm a little scared of that.I also have > type 1 diabetes and addison's disease which is autoammune diseases and > that's why they think I now have PF.It has really been neat reading all > your messages.Please fell free to e-mail me at any time.I live in a > very small town in Alabama and there's no support groups here.> > > > Prayers and Wishes to all of you> Gail> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 3, 2007 Report Share Posted October 3, 2007 Gail, Welcome to our group, I am so sorry you have this monster pestering you. Hopefully we can comfort and inform you of a few things we know. Just please remember you are not alone and you DO still have living to do..a LOT of living. do not believe the numbers and all that mess. God knows. We do not have an expiration date. God Bless you. Love and Prayers, Peggy ipf 6/04 Florida " Worry looks around, Sorry looks back, Faith looks up. " Hello everyone.My name is Gail.I'm 37 years old and just found out I have PF.I don't know very much about it except what i have read online.I have to go to a surgeon Thursday to find out when they are going to do a open lung biopsy.I'm a little scared of that.I also have type 1 diabetes and addison's disease which is autoammune diseases and that's why they think I now have PF.It has really been neat reading all your messages.Please fell free to e-mail me at any time.I live in a very small town in Alabama and there's no support groups here. Prayers and Wishes to all of you Gail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 3, 2007 Report Share Posted October 3, 2007 Gail, Welcome to our group, I am so sorry you have this monster pestering you. Hopefully we can comfort and inform you of a few things we know. Just please remember you are not alone and you DO still have living to do..a LOT of living. do not believe the numbers and all that mess. God knows. We do not have an expiration date. God Bless you. Love and Prayers, Peggy ipf 6/04 Florida " Worry looks around, Sorry looks back, Faith looks up. " Hello everyone.My name is Gail.I'm 37 years old and just found out I have PF.I don't know very much about it except what i have read online.I have to go to a surgeon Thursday to find out when they are going to do a open lung biopsy.I'm a little scared of that.I also have type 1 diabetes and addison's disease which is autoammune diseases and that's why they think I now have PF.It has really been neat reading all your messages.Please fell free to e-mail me at any time.I live in a very small town in Alabama and there's no support groups here. Prayers and Wishes to all of you Gail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 3, 2007 Report Share Posted October 3, 2007 Gail, Welcome to our group, I am so sorry you have this monster pestering you. Hopefully we can comfort and inform you of a few things we know. Just please remember you are not alone and you DO still have living to do..a LOT of living. do not believe the numbers and all that mess. God knows. We do not have an expiration date. God Bless you. Love and Prayers, Peggy ipf 6/04 Florida " Worry looks around, Sorry looks back, Faith looks up. " Hello everyone.My name is Gail.I'm 37 years old and just found out I have PF.I don't know very much about it except what i have read online.I have to go to a surgeon Thursday to find out when they are going to do a open lung biopsy.I'm a little scared of that.I also have type 1 diabetes and addison's disease which is autoammune diseases and that's why they think I now have PF.It has really been neat reading all your messages.Please fell free to e-mail me at any time.I live in a very small town in Alabama and there's no support groups here. Prayers and Wishes to all of you Gail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 3, 2007 Report Share Posted October 3, 2007 Welcome Gail, I only have a few minutes, but wanted to say a quick welcome (and will follow up later.) My name is . I'm 34 and was diagnosed with PF last year. It was at a very early stage though. They caught it very early because I have a genetic disorder that causes PF, so they were watching for it. This is a great group. Welcome! www.heatherkirkwood.blogspot.com Hermansky-Pudlak Syndrome albinism/PF 06 > >> > Hello everyone.My name is Gail.I'm 37 years old and just found out I> > have PF.I don't know very much about it except what i have read> > online.I have to go to a surgeon Thursday to find out when they are> > going to do a open lung biopsy.I'm a little scared of that.I also have> > type 1 diabetes and addison's disease which is autoammune diseases and> > that's why they think I now have PF.It has really been neat reading> all> > your messages.Please fell free to e-mail me at any time.I live in a> > very small town in Alabama and there's no support groups here.> >> >> >> > Prayers and Wishes to all of you> > Gail> >> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 3, 2007 Report Share Posted October 3, 2007 Welcome Gail, I only have a few minutes, but wanted to say a quick welcome (and will follow up later.) My name is . I'm 34 and was diagnosed with PF last year. It was at a very early stage though. They caught it very early because I have a genetic disorder that causes PF, so they were watching for it. This is a great group. Welcome! www.heatherkirkwood.blogspot.com Hermansky-Pudlak Syndrome albinism/PF 06 > >> > Hello everyone.My name is Gail.I'm 37 years old and just found out I> > have PF.I don't know very much about it except what i have read> > online.I have to go to a surgeon Thursday to find out when they are> > going to do a open lung biopsy.I'm a little scared of that.I also have> > type 1 diabetes and addison's disease which is autoammune diseases and> > that's why they think I now have PF.It has really been neat reading> all> > your messages.Please fell free to e-mail me at any time.I live in a> > very small town in Alabama and there's no support groups here.> >> >> >> > Prayers and Wishes to all of you> > Gail> >> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2007 Report Share Posted October 18, 2007 HI Teri! Glad to hear the good news about Jon. Maybe you should make Jon the eggnog recipe that I gave you, along with Peggy's sourcream pound cake! That should do it! (LOL). Teri, take care of yourself, too. I am glad you are better and I miss both of you terribly. Today, I drove to Chattanooga to a job interview at Chattanooga Shooting Supplies for an entry level graphic designer. (What she is looking for) and I looked over at the Courtyard where we all stayed and had such a wonderful time. > > Jon wanted me to post for him,he says i tpye faster..lol anyway he > wanted me to share that he went in for his 36 week checkup for the drug > trial, and AMEN good news.... his numbers went up again, not by much > but are still going up!!!! he has lost 5 lbs which isnt good, so i > gotta try and fatten him up. doc said you eat everything we cant! lol > anyway his 6mw test was 17 meters longer then the last one and he is > waiting for a call to see what his dlco was,, it was at 41 i think he > said maybe a little more, my mind isnt young anymore..hehee... but i > will let yall know when he hears. for those that know about > my ''vertigo'' issue, i have had a bad week, was down for 4 days with a > mindblowing headache,, and he was so wonderful to me. i do love that > man dearly!!! anyway wanted to let ya'll know, > peggy,joyce,leanne,jane, marybeth, and jaime and all your families, we > miss ya'll so much!!! i just cant believe what a great weekend that > was. we cant wait for the next meeting! ((((((((hugs)))))))) to > all teri jon ipf 5-06 > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2007 Report Share Posted October 18, 2007 HI Teri! Glad to hear the good news about Jon. Maybe you should make Jon the eggnog recipe that I gave you, along with Peggy's sourcream pound cake! That should do it! (LOL). Teri, take care of yourself, too. I am glad you are better and I miss both of you terribly. Today, I drove to Chattanooga to a job interview at Chattanooga Shooting Supplies for an entry level graphic designer. (What she is looking for) and I looked over at the Courtyard where we all stayed and had such a wonderful time. > > Jon wanted me to post for him,he says i tpye faster..lol anyway he > wanted me to share that he went in for his 36 week checkup for the drug > trial, and AMEN good news.... his numbers went up again, not by much > but are still going up!!!! he has lost 5 lbs which isnt good, so i > gotta try and fatten him up. doc said you eat everything we cant! lol > anyway his 6mw test was 17 meters longer then the last one and he is > waiting for a call to see what his dlco was,, it was at 41 i think he > said maybe a little more, my mind isnt young anymore..hehee... but i > will let yall know when he hears. for those that know about > my ''vertigo'' issue, i have had a bad week, was down for 4 days with a > mindblowing headache,, and he was so wonderful to me. i do love that > man dearly!!! anyway wanted to let ya'll know, > peggy,joyce,leanne,jane, marybeth, and jaime and all your families, we > miss ya'll so much!!! i just cant believe what a great weekend that > was. we cant wait for the next meeting! ((((((((hugs)))))))) to > all teri jon ipf 5-06 > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2007 Report Share Posted October 18, 2007 HI Teri! Glad to hear the good news about Jon. Maybe you should make Jon the eggnog recipe that I gave you, along with Peggy's sourcream pound cake! That should do it! (LOL). Teri, take care of yourself, too. I am glad you are better and I miss both of you terribly. Today, I drove to Chattanooga to a job interview at Chattanooga Shooting Supplies for an entry level graphic designer. (What she is looking for) and I looked over at the Courtyard where we all stayed and had such a wonderful time. > > Jon wanted me to post for him,he says i tpye faster..lol anyway he > wanted me to share that he went in for his 36 week checkup for the drug > trial, and AMEN good news.... his numbers went up again, not by much > but are still going up!!!! he has lost 5 lbs which isnt good, so i > gotta try and fatten him up. doc said you eat everything we cant! lol > anyway his 6mw test was 17 meters longer then the last one and he is > waiting for a call to see what his dlco was,, it was at 41 i think he > said maybe a little more, my mind isnt young anymore..hehee... but i > will let yall know when he hears. for those that know about > my ''vertigo'' issue, i have had a bad week, was down for 4 days with a > mindblowing headache,, and he was so wonderful to me. i do love that > man dearly!!! anyway wanted to let ya'll know, > peggy,joyce,leanne,jane, marybeth, and jaime and all your families, we > miss ya'll so much!!! i just cant believe what a great weekend that > was. we cant wait for the next meeting! ((((((((hugs)))))))) to > all teri jon ipf 5-06 > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2007 Report Share Posted October 18, 2007 Teri and Jon, I'm so thrilled with Jon's numbers!!! That's so exciting and even if it's just a little bit, it's still changing in the right direction!!!! Teri, I'm so sorry that you've been feeling so awful....is the headache completely gone or just somewhat better? You are both in my thoughts and prayers all the time. I miss you and everyone else and can't wait to see you again! Hugs, Beth in NY Fibrotic NSIP 06/06 "At the evening of life we shall be judged on our love." St of the Cross hello everyone Jon wanted me to post for him,he says i tpye faster..lol anyway he wanted me to share that he went in for his 36 week checkup for the drug trial, and AMEN good news.... his numbers went up again, not by much but are still going up!!!! he has lost 5 lbs which isnt good, so i gotta try and fatten him up. doc said you eat everything we cant! lol anyway his 6mw test was 17 meters longer then the last one and he is waiting for a call to see what his dlco was,, it was at 41 i think he said maybe a little more, my mind isnt young anymore..hehee. .. but i will let yall know when he hears. for those that know about my ''vertigo'' issue, i have had a bad week, was down for 4 days with a mindblowing headache,, and he was so wonderful to me. i do love that man dearly!!! anyway wanted to let ya'll know, peggy,joyce, leanne,jane, marybeth, and jaime and all your families, we miss ya'll so much!!! i just cant believe what a great weekend that was. we cant wait for the next meeting! ((((((((hugs) ))))))) to all teri jon ipf 5-06 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2007 Report Share Posted October 18, 2007 Teri and Jon, I'm so thrilled with Jon's numbers!!! That's so exciting and even if it's just a little bit, it's still changing in the right direction!!!! Teri, I'm so sorry that you've been feeling so awful....is the headache completely gone or just somewhat better? You are both in my thoughts and prayers all the time. I miss you and everyone else and can't wait to see you again! Hugs, Beth in NY Fibrotic NSIP 06/06 "At the evening of life we shall be judged on our love." St of the Cross hello everyone Jon wanted me to post for him,he says i tpye faster..lol anyway he wanted me to share that he went in for his 36 week checkup for the drug trial, and AMEN good news.... his numbers went up again, not by much but are still going up!!!! he has lost 5 lbs which isnt good, so i gotta try and fatten him up. doc said you eat everything we cant! lol anyway his 6mw test was 17 meters longer then the last one and he is waiting for a call to see what his dlco was,, it was at 41 i think he said maybe a little more, my mind isnt young anymore..hehee. .. but i will let yall know when he hears. for those that know about my ''vertigo'' issue, i have had a bad week, was down for 4 days with a mindblowing headache,, and he was so wonderful to me. i do love that man dearly!!! anyway wanted to let ya'll know, peggy,joyce, leanne,jane, marybeth, and jaime and all your families, we miss ya'll so much!!! i just cant believe what a great weekend that was. we cant wait for the next meeting! ((((((((hugs) ))))))) to all teri jon ipf 5-06 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2008 Report Share Posted January 24, 2008 Greetings, I recently had the opportunity to join your group and I thank for the opportunity. Also, I must thank Costa for making me aware of this group. I am Ahearn and I am an attorney in Wilton Manors, Broward County. For many years I have served as Court Appointed Counsel for individuals in Guardianship proceedings. Of those that I have represented, I have had the privilege of meeting and representing wonderful Special Needs children who were involved in actions where their parent(s) sought to be Guardian Advocates. At the same time I have had the privilege as well of meeting the parents of these children. One common theme that disturbed me when I encountered these parents was the outrageous legal fees these parents paid to bring forward an action to be the Guardian Advocate. In the last few years I have started to represent parents in legal proceedings to be their child’s Guardian Advocate at a fair and reasonable flat rate fee. Please know I always provide potential clients a free 30 minute telephone consultation. Please feel free to call me if you have questions regarding the process to become a Guardian Advocate. I also prepare Special Needs Trusts. While many of you probably don’t know me, Costa has been kind enough to allow me to use her as a reference. and I have worked on many of cases over the years, she is a great attorney and an even greater advocate for Special Needs Children. As well I have worked in the past with Dr. Bonne L. Finfer and McGahee at Cypress Bay High School. Sincerely Mike G. Ahearn, P.A. 2850 North s Avenue Wilton Manors, FL 33311 Telephone: (954) 563-1716 Fax: (954) 568-2152 Email: mgaesq@... The hiring of a lawyer is an important decision that should not be based solely upon advertisements. Before you decide, ask us to send you free written information about our qualifications and experience. 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.