As a sibling of a Cystic Fibrosis patient, I know first hand what my sibling does on a daily basis to maintain her quality of life. Her SSI disability is a huge part of helping her stay alive. Her treatments take hours each day to complete and working is not feasible in order for her to maintain her health. Just because someone isn't in the hospital on a regular basis, doesn't mean that they are able to work full time and support themselves financially. Working will cause my sister to become sick and her health will deteriorate as a result. Not having SSI will force her to work to pay for all of the treatments that she needs. Please reconsider these changes. It not only affects my sister but also thousands of those with Cystic Fibrosis.
Comment from Herms, Maggie, Relative of CF Patient
This is comment on Proposed Rule
Revised Medical Criteria for Evaluating Resiratory System Disorders
View Comment
Related Comments
View AllPublic Submission Posted: 04/03/2013 ID: SSA-2006-0149-0035
Apr 05,2013 11:59 PM ET
Public Submission Posted: 04/05/2013 ID: SSA-2006-0149-0106
Apr 05,2013 11:59 PM ET
Public Submission Posted: 04/03/2013 ID: SSA-2006-0149-0027
Apr 05,2013 11:59 PM ET
Public Submission Posted: 04/05/2013 ID: SSA-2006-0149-0088
Apr 05,2013 11:59 PM ET
Public Submission Posted: 04/05/2013 ID: SSA-2006-0149-0063
Apr 05,2013 11:59 PM ET