Re: New Online Support Group has been created

[Guest guest]

Leanne

with a mom like you i am confident that your daughter will be a great moderator

Pink Joyce R (IPF 3/06) IFA 5/09 Pennsylvania

Donate Life Listed 1/09 Inactive 4/09

www.transplantfund.org---

Subject: New Online Support Group has been createdTo: "Breathe Support Caregivers" <Breathe-SupportCaregivers >, "Breathe-Support Grief" <Breathe-SupportGrief >, "Support" <breathe-support >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

[Guest guest]

Awesome! I'll pass this along to my two adult children. C_53_Familial IPF_5/09WashingtonTo: Breathe Support Caregivers <Breathe-SupportCaregivers >; Breathe-Support Grief <Breathe-SupportGrief >; Support <breathe-support >Sent: Thursday, September 24, 2009 7:52:41 AMSubject: New Online Support Group has been created

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