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Re: How can I join this group glr_christian@... I receive many messages but I can't reply

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Welcome to the newcomers... .., you caught my attention. I'm also one of the babies here, age wise. I recently turned 35, but was diagnosed with PF at 33. Welcome to the group! KirkwoodHermansky-Pudlak Syndrome albinism02/pf 06www.heatherkirkwood .blogspot. com>> hiya brandy!> monique here from australia!> I am new here too and am 33 years old and have just been diagnosed with > pf! a very real and scary situation. pretty much an emotional > rollercoaster for the last 2 weeks.> > just wanted

to welcome you and say how welcomed i have felt by other > members on this site, it is amazing how caring and friendly and helpful > everyone here is.......so welcome from me too!> > i have many questions and will surely be asking lots and lots,always > ask,,, thats what i have learnt through my journey so far with > polymyositis and now this!> > kindest regards> monique>

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Hi Gloria, It looks like you are already a member. Your post came through our board so. try to e-mail me back and well see.  Just go to the top of this e-mail and hit reply.We'll go from there. Love & Prayers, PeggyFlorida,  IPF/UIP 2004"I believe that friends are quiet angels who lift us to our feet, when our wings have trouble remembering how to fly."  Welcome to the newcomers... .., you caught my attention. I'm also one of the babies here, age wise. I recently turned 35, but was diagnosed with PF at 33. Welcome to the group!  KirkwoodHermansky-Pudlak Syndrome albinism02/pf 06www.heatherkirkwood .blogspot. com>> hiya brandy!> monique here from australia!> I am new here too and am 33 years old and have just been diagnosed with > pf! a very real and scary situation. pretty much an emotional > rollercoaster for the last 2 weeks.> > just wanted to welcome you and say how welcomed i have felt by other > members on this site, it is amazing how caring and friendly and helpful > everyone here is.......so welcome from me too!> > i have many questions and will surely be asking lots and lots,always > ask,,, thats what i have learnt through my journey so far with > polymyositis and now this!> > kindest regards> monique>

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