Guest guest Posted October 30, 2002 Report Share Posted October 30, 2002 GREAT. let me know when we can order .I will take at least 4 to start (if they aren't real expensive, I can order more later ) LOVE, GRDMBEV New CF Awareness Pin Hi all, I hope this finds you all well and if not on the mend very soon. Lenora and I have been working on a new CF Awareness pin. We are very excited to bring it to you at this time. The pin reflects the same characteristics as the ribbons we made for the CF Awareness week. Each pin ordered comes with a card explaining why we use the phrase " 65 Roses " as a way of teaching children how to say Cystic Fibrosis. Help us spread the word about CF everywhere you go by getting your pin today at www.milanfoundation.org. Tucker Mom of Milan 4 wcf www.milanfoundation.org P.S. Last night I attended a fundraiser for one of the candidates running for City Council in my area. It was a great time and I think I must have educated nearly 10 new people about CF. It was great making new contacts for the foundation as well. If at all possible, consider getting involved in a campaign or other project, you never know who you might meet. I met several well-to-do attorneys, a congressman, and a couple of the board members of the ACLU. PLEASE do not post religious emails to the list. ------------------------------------------- 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 October 30, 2002 Report Share Posted October 30, 2002 GREAT. let me know when we can order .I will take at least 4 to start (if they aren't real expensive, I can order more later ) LOVE, GRDMBEV New CF Awareness Pin Hi all, I hope this finds you all well and if not on the mend very soon. Lenora and I have been working on a new CF Awareness pin. We are very excited to bring it to you at this time. The pin reflects the same characteristics as the ribbons we made for the CF Awareness week. Each pin ordered comes with a card explaining why we use the phrase " 65 Roses " as a way of teaching children how to say Cystic Fibrosis. Help us spread the word about CF everywhere you go by getting your pin today at www.milanfoundation.org. Tucker Mom of Milan 4 wcf www.milanfoundation.org P.S. Last night I attended a fundraiser for one of the candidates running for City Council in my area. It was a great time and I think I must have educated nearly 10 new people about CF. It was great making new contacts for the foundation as well. If at all possible, consider getting involved in a campaign or other project, you never know who you might meet. I met several well-to-do attorneys, a congressman, and a couple of the board members of the ACLU. PLEASE do not post religious emails to the list. ------------------------------------------- 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 October 30, 2002 Report Share Posted October 30, 2002 GREAT. let me know when we can order .I will take at least 4 to start (if they aren't real expensive, I can order more later ) LOVE, GRDMBEV New CF Awareness Pin Hi all, I hope this finds you all well and if not on the mend very soon. Lenora and I have been working on a new CF Awareness pin. We are very excited to bring it to you at this time. The pin reflects the same characteristics as the ribbons we made for the CF Awareness week. Each pin ordered comes with a card explaining why we use the phrase " 65 Roses " as a way of teaching children how to say Cystic Fibrosis. Help us spread the word about CF everywhere you go by getting your pin today at www.milanfoundation.org. Tucker Mom of Milan 4 wcf www.milanfoundation.org P.S. Last night I attended a fundraiser for one of the candidates running for City Council in my area. It was a great time and I think I must have educated nearly 10 new people about CF. It was great making new contacts for the foundation as well. If at all possible, consider getting involved in a campaign or other project, you never know who you might meet. I met several well-to-do attorneys, a congressman, and a couple of the board members of the ACLU. PLEASE do not post religious emails to the list. ------------------------------------------- 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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