The house is empty again. After I left for orchestra rehearsal last night, William and Kimberly began their long ride back to Seattle. The house felt cold and empty when I woke up this morning.
I am exhausted not just from their visit but from the continuous stream of energy zapping things without much downtime. A real killer for me. Today, I am going to rehab, swing by the store for the makings of caramel corn (Winnie is coming for lunch on Friday) then the plan is to sit in the back yard. Quietly. Maybe a nap.
Tomorrow, we are going to the cocktail party for the beginning of my 40th high school reunion. Saturday will find me working in the gardens then nothing, sweet nothing, on Sunday.
I received the below in an e-mail from the good people at CPF. This might be very helpful especially for readers of this blog who are in countries around the world where the latest information regarding Pulmonary Fibrosis is so limited. Follow the directions and you can join this Webinar.
"The Coalition for Pulmonary Fibrosis (CPF) is pleased to invite you to a free webinar on September 14th entitled "New Directions for IPF Treatments: Understanding the Basis for Current Clinical Trials". Reserve your Webinar seat now at:
https://www1.gotomeeting.com/register/992892200 (note: do not reply to this email to register - click on the link provided).
It is part of PF Week at the ATS (Sept. 11-18) - and also in tandem with National PF Awareness Week (Sept. 18-23). This patient-education web event is presented by the American Thoracic Society (ATS) in partnership with the CPF and is hosted by Andrew Tager, MD. You'll want to invite your family, friends and caregiver(s) to join this free event, too!
What? Join us for a Webinar on September 14 -
New Directions for IPF Treatments: Understanding the Basis for Current Clinical Trials
When?
Date:
Wednesday, September 14, 2011
Time:
2:00 PM - 3:00 PM EDT
Space is limited.
Reserve your Webinar seat now at:
https://www1.gotomeeting.com/register/992892200
After registering you will receive a confirmation email containing information about joining the Webinar.
System Requirements
PC-based attendees
Required: Windows® 7, Vista, XP or 2003 Server
Macintosh®-based attendees
Required: Mac OS® X 10.5 or newer"
6 comments:
Wow ! what an interesting blog .Thanks for
sharing this information.Your information is really informative for us.
Nice blog on Pulmonary Fibrosis.
Keep sharing more & more..
Thanks for your comments, Daniel. I am so lucky to be connected with one of the top university hospitals in the US who is leading the research on PF. Everything I learn, I try to pass along. This information is just not out in the general pubic, yet. So happy it is helpful!
This is such an informative post. Reading this article adds more knowledge about that kind of illness.
Great post. This helps the people to understand this kind of illness. Thanks for sharing this to us.
Thank for finding me and so glad it has helped!
We all know that pulmonary fibrosis has no treatment. Reading this post helps us to add more knowledge about this illness and also on how to avoid this.
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