Hello,
My husband and I have been encouraged strongly by numerous doctors to have our 13 year old son genetic tested for CF. He has had two negative sweat tests in the last 4 years the first was a 38 and the other was 17. He has had GI issues his whole life, 2 sinus surgeries, lots of allergies that we treat with shots and meds, lots of throat and lung infections when he was younger. Very thin almost 5'10 and 120. Which is a gain since he started new GI meds. He is a very strong athlete and has played competitive sports since he was very young. It is so hard for us to believe he could have CF. However many of the doctors have mentioned that CF can present differently in people.
Anyway.... we are very leery of doing the gentic testing for fear of discrimination on medical insurance in the future. We currently have BCBS PPO and have had it for many years through my husbands job. Have any of you had your insurance dropped or riders put on since being diagnosed?
We are scheduled in April to meet with the genetics doc, We think we might just wait and not get tested. Thoughts?
My husband and I have been encouraged strongly by numerous doctors to have our 13 year old son genetic tested for CF. He has had two negative sweat tests in the last 4 years the first was a 38 and the other was 17. He has had GI issues his whole life, 2 sinus surgeries, lots of allergies that we treat with shots and meds, lots of throat and lung infections when he was younger. Very thin almost 5'10 and 120. Which is a gain since he started new GI meds. He is a very strong athlete and has played competitive sports since he was very young. It is so hard for us to believe he could have CF. However many of the doctors have mentioned that CF can present differently in people.
Anyway.... we are very leery of doing the gentic testing for fear of discrimination on medical insurance in the future. We currently have BCBS PPO and have had it for many years through my husbands job. Have any of you had your insurance dropped or riders put on since being diagnosed?
We are scheduled in April to meet with the genetics doc, We think we might just wait and not get tested. Thoughts?