Guest guest Posted September 25, 2009 Report Share Posted September 25, 2009 Beth Thank you. I will pass the info on to him. I feel bad for him and almost guilty sometimes about being sick if that makes any sense. YET another side benefit of this monster. Walt (52) on Whidbey IPF,Nsip.Uip. 06 Courage doesn't always roar. Sometimes courage is the quiet voice at the end of the day saying, "I will try again tomorrow.†Subject: New Online Support Group has been createdTo: "Breathe Support Caregivers" <Breathe-SupportCare givers@yahoogrou ps.com>, "Breathe-Support Grief" <Breathe-SupportGrie f (AT) yahoogroups (DOT) com>, "Support" <breathe-support@ yahoogroups. com>Date: Thursday, September 24, 2009, 10:52 AM Hello all, Just wanted to let you know that a new Online support group has been created. This group is for children and young adults whose life has been affected by pulmonary fibroisis. We are asking to keep the age limit of the group to 25 and under. (my daughter) wanted to start this group because she felt she had no place to go to talk about what was going on inside her when I was diagnosed back in 2003. who is 22 will be the moderator. Here's the link: http://health. groups.yahoo. com/group/ Breathe-SupportF amily/ If you know of any children or young adults who you feel will benefit from this type of support group, please pass along the link. Thank you. Leanne Storch Executive Director Pulmonary Fibrosis Foundation 1332 N. Halsted, Suite 201 Chicago, IL 60642-2642 www.pulmonaryfibros is.org P F A cure is just a breath away Quote Link to comment Share on other sites More sharing options...
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