Guest guest Posted August 5, 2005 Report Share Posted August 5, 2005 Jan, I understand that you have to do what it takes to get yourself better, but you will be so terribly missed by all your RA family. You have been such a positive force with your humor, your caring heart, and upbeat personality. May God bless you in all that you do. Hugs from Dallas Jane > To my RA family and yes, that is the way i think of you especially after all the years i have been associated with the group. > Due to some concerns in my life and the trying to cope with the FMS, i find i am having to rearrange some priorities which has led me to have to withdraw from several groups i belong to because of the time i am able to devote to them. > For some time now, i have been unable to keep up completely with the group as a whole especially with the ever-changing day to day things. > I will miss all the old time people i have gotten to know and love as my family. Especially missed will be a and as not only do i revere them highly, they have always been my first source of information for anything concerning the FMS and the keeping up with the medical world with the autoimmune disease world. I regret not being able to stay in the group longer to learn about my latest diagnosis which is bronchiotactasis (misspelled...of course...but i know they recognize the word and could tell me more about it in an instant). I, now not only cope with the c-pap machine but a contraption called the vest that i need to use several times a day to break up the congestion in my bronchial tubes. The contraption was first designed for CF (cystic fibrosis) patients. > If there is anyone who would like to correspond with me on the one to one basis, i can be reached at azmomacat2@y... or momacatof2 for the IM. > Thank you all for being here for me where you knew it or not. Many a night, deep into the morning has been spent reading over the daily digests and getting to know so many. > Take care and please continue to smile....throughout everything because a smile is the first line of defense against what the world hands you (besides i am told....it hides wrinkles...and i am for that 100%!) > Love and gentle hugs to you all. > Jan in AZ =^..^= > > > > ~ " If I could reach up and hold a star for every time you've made me smile, the entire evening sky would be in the palm of my hand. " ~ > > > > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 5, 2005 Report Share Posted August 5, 2005 Jan, I understand that you have to do what it takes to get yourself better, but you will be so terribly missed by all your RA family. You have been such a positive force with your humor, your caring heart, and upbeat personality. May God bless you in all that you do. Hugs from Dallas Jane > To my RA family and yes, that is the way i think of you especially after all the years i have been associated with the group. > Due to some concerns in my life and the trying to cope with the FMS, i find i am having to rearrange some priorities which has led me to have to withdraw from several groups i belong to because of the time i am able to devote to them. > For some time now, i have been unable to keep up completely with the group as a whole especially with the ever-changing day to day things. > I will miss all the old time people i have gotten to know and love as my family. Especially missed will be a and as not only do i revere them highly, they have always been my first source of information for anything concerning the FMS and the keeping up with the medical world with the autoimmune disease world. I regret not being able to stay in the group longer to learn about my latest diagnosis which is bronchiotactasis (misspelled...of course...but i know they recognize the word and could tell me more about it in an instant). I, now not only cope with the c-pap machine but a contraption called the vest that i need to use several times a day to break up the congestion in my bronchial tubes. The contraption was first designed for CF (cystic fibrosis) patients. > If there is anyone who would like to correspond with me on the one to one basis, i can be reached at azmomacat2@y... or momacatof2 for the IM. > Thank you all for being here for me where you knew it or not. Many a night, deep into the morning has been spent reading over the daily digests and getting to know so many. > Take care and please continue to smile....throughout everything because a smile is the first line of defense against what the world hands you (besides i am told....it hides wrinkles...and i am for that 100%!) > Love and gentle hugs to you all. > Jan in AZ =^..^= > > > > ~ " If I could reach up and hold a star for every time you've made me smile, the entire evening sky would be in the palm of my hand. " ~ > > > > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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