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Life After Brown
Do you know anyone with Multiple Sclerosis?
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<blockquote data-quote="ajblakejr" data-source="post: 763012" data-attributes="member: 18807"><p><span style="font-family: 'Tahoma'">MS and leadership.</span></p><p> </p><p><span style="font-family: 'Tahoma'">What a concept.</span></p><p><span style="font-family: 'Tahoma'">What an unpredictable idea.</span></p><p><span style="font-family: 'Tahoma'">The only sure thing about MS is that it is recognized as unpredictable.</span></p><p> </p><p><span style="font-family: 'Tahoma'">I would like to thank everyone on BC for the unconditional support since I allowed my deep dark secret see the light of a BC day.</span></p><p> </p><p><span style="font-family: 'Tahoma'">My moderation responsibilities moved from being a moderator to a Fantasy Football NFL Commissioners of two leagues on the MS support website. It is exciting to feel the passion brewing for a sport I live for by new friends that never considered cheering for any other team but the stale "home team" of their city.</span></p><p> </p><p><span style="font-family: 'Tahoma'">And I appreciate the friendship of someone here that offered me help with the Fantasy Leagues... </span></p><p> </p><p><span style="font-family: 'Tahoma'">My heartfelt appreciation for all the moderators on BC. </span></p><p><span style="font-family: 'Tahoma'">I have watched and I have listened.</span></p><p><span style="font-family: 'Tahoma'">I have learned by observing…</span></p><p> </p><p><span style="font-family: 'Tahoma'">I have used the phrase </span></p><p><em><span style="font-family: 'Tahoma'">"remember to see your doctor before following any advice posted on this website"</span></em><span style="font-family: 'Tahoma'"> and </span></p><p><em><span style="font-family: 'Tahoma'">"remember that this is just an observation; please refrain from providing unsolicited advice...we all recall that life altering feeling when the doctor told us we had MS..."</span></em><span style="font-family: 'Tahoma'"> and on and on.</span></p><p> </p><p><span style="font-family: 'Tahoma'">And I know that this is "ALL ABOUT ME"...but it really is all about everyone here that made it easy to bring AWARENESS to MULTIPLE SCLEROSIS.</span></p><p> </p><p><span style="font-family: 'Tahoma'">It is all the private messages.</span></p><p><span style="font-family: 'Tahoma'">It is all the stories that pass from my eyes to my heart about family, friends and co-workers with MS.</span></p><p><span style="font-family: 'Tahoma'">It is all about the few others that quietly know the awfulness of the MS life sentence because it is the face they look at every morning.</span></p><p> </p><p><span style="font-family: 'Tahoma'">I am here. </span></p><p><span style="font-family: 'Tahoma'">I listen. </span></p><p><span style="font-family: 'Tahoma'">I know.</span></p><p> </p><p><span style="font-family: 'Tahoma'">I just ask that when I am sent a private message...never apologize for having MS.</span></p><p> </p><p><span style="font-family: 'Tahoma'">Blessings</span></p><p><span style="font-family: 'Tahoma'">aj</span></p></blockquote><p></p>
[QUOTE="ajblakejr, post: 763012, member: 18807"] [FONT=Tahoma]MS and leadership.[/FONT] [FONT=Tahoma] [/FONT] [FONT=Tahoma]What a concept.[/FONT] [FONT=Tahoma]What an unpredictable idea.[/FONT] [FONT=Tahoma]The only sure thing about MS is that it is recognized as unpredictable.[/FONT] [FONT=Tahoma] [/FONT] [FONT=Tahoma]I would like to thank everyone on BC for the unconditional support since I allowed my deep dark secret see the light of a BC day.[/FONT] [FONT=Tahoma] [/FONT] [FONT=Tahoma]My moderation responsibilities moved from being a moderator to a Fantasy Football NFL Commissioners of two leagues on the MS support website. It is exciting to feel the passion brewing for a sport I live for by new friends that never considered cheering for any other team but the stale "home team" of their city.[/FONT] [FONT=Tahoma] [/FONT] [FONT=Tahoma]And I appreciate the friendship of someone here that offered me help with the Fantasy Leagues... [/FONT] [FONT=Tahoma] [/FONT] [FONT=Tahoma]My heartfelt appreciation for all the moderators on BC. [/FONT] [FONT=Tahoma]I have watched and I have listened.[/FONT] [FONT=Tahoma]I have learned by observing…[/FONT] [FONT=Tahoma] [/FONT] [FONT=Tahoma]I have used the phrase [/FONT] [I][FONT=Tahoma]"remember to see your doctor before following any advice posted on this website"[/FONT][/I][FONT=Tahoma] and [/FONT] [I][FONT=Tahoma]"remember that this is just an observation; please refrain from providing unsolicited advice...we all recall that life altering feeling when the doctor told us we had MS..."[/FONT][/I][FONT=Tahoma] and on and on.[/FONT] [FONT=Tahoma] [/FONT] [FONT=Tahoma]And I know that this is "ALL ABOUT ME"...but it really is all about everyone here that made it easy to bring AWARENESS to MULTIPLE SCLEROSIS.[/FONT] [FONT=Tahoma] [/FONT] [FONT=Tahoma]It is all the private messages.[/FONT] [FONT=Tahoma]It is all the stories that pass from my eyes to my heart about family, friends and co-workers with MS.[/FONT] [FONT=Tahoma]It is all about the few others that quietly know the awfulness of the MS life sentence because it is the face they look at every morning.[/FONT] [FONT=Tahoma] [/FONT] [FONT=Tahoma]I am here. [/FONT] [FONT=Tahoma]I listen. [/FONT] [FONT=Tahoma]I know.[/FONT] [FONT=Tahoma] [/FONT] [FONT=Tahoma]I just ask that when I am sent a private message...never apologize for having MS.[/FONT] [FONT=Tahoma] [/FONT] [FONT=Tahoma]Blessings[/FONT] [FONT=Tahoma]aj[/FONT] [/QUOTE]
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Do you know anyone with Multiple Sclerosis?
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