There is still much work to be done to prevent changes that could make it more difficult for people with Cystic Fibrosis to receive disability benefits. Now it's time to talk to those senators!
Send a message to your senator by clicking here.
The CF Foundation recently worked with several House Representatives to send letters to the Social Security Administration that explains the concerns about the proposed disability benefit eligibility changes. The last post asking for your help resulted in over 9,000 messages (collectively) from advocates throughout the US. Let's work together and do the same with the Senate!
Well, summer is here! So is coughing. : / Going from hot and humid to A/C isn't always the best for me. So needless to say, our house isn't usually that cool inside. We don't mind though. As long as we have a fan on at night we can usually make it through ok...lol. We haven't had TV channels for over 5 years either! It's amazing what you really can live without. I don't have FaceBook at this time either. Gosh, what do I do with my time? A lot of other things!
My next doctor appointment is coming up June 10th so I'll give another update later. Thank you for all that you do! Together, we will keep adding tomorrows to lives of all people with CF - Including ME!