To Do What I Do -Alan Jackson, 2004
Good luck~
Lori
"Our greatest glory is not in never falling, but in rising every time we fall." -Confucius
Ellen
nickjoe@yahoo.com
-§»§«:*´`³¤³´`*:» Vicky «:*´`³¤³´`*:»§«§-
Steph, were you having any symptoms (cysts, bleeding, thickening of the endometrium etc)? That would satisfy medical necessity along with bc diagnosis. You can check MSKCC.org and look up my doc, Noah Kauff. On his bio page are links to artlicles he had published regarding brca 1&2 and oopherectomies. Hope this helps! The appeal process can be very frustrating; they hope you will give up, but you can prevail! Good luck!
Frayda
thanks so much for the info, i will look it up... i was not having any symptoms to justify a hysterectomy, so if they want to deny that i really don't mind, it's the OVARIES i want out, i have been having non-descript nausea, lower back pain, irregular periods, really bad pain on the left side (my cancer side) during ovulation time, and after all my reading it seems my cancer does have characteristics for brca1 (although i have not been tested) which would increase ones risk of ov ca dramatically, and i just want the darn things out. !!
thanks for the ammo, i will spend some time reading....
hugs, and wish me luck!
stef
To Do What I Do -Alan Jackson, 2004
I can't remember, have you considered the genetic testing? If you have not been tested, you might consider that to help plead your case. If you tested positive, I think that would seal the deal for insurance company. Before you agree to any testing, you would meet with a counselor and learn all of the pros and cons, especially how the laws protect you and your family on this issue.
Hang in there!
Lori
thanks for the suggestion, and am TRULY not a paranoid person, but somehow i think having this genetic testing done will somehow impact the availabilty of insurance (or medical care) for my daughter in the future. i think that there is a real risk to have that information in a report somewhere that insurance companies can get ahold of... it's the 'holy grail' for them in terms of assessing risk for future diseases, and i don't want that used against my daughter, or any other female relatives (sister, neices, etc.). I think the ethics and ramifications of using that information improperly, outweigh the benefits of me knowing if i am brca1 positive... so thats why in my letter i was careful to say that mine had 'characteristics consistent with brca1'.
make any sense? ;-)
we don't agree on much, do we?? (just kdding!!)
BIG HUG
stef
To Do What I Do -Alan Jackson, 2004
I totally understand your fear....when I did the testing, I met with the genetic counselor first. She answered all my questions related to the same issues. Rememeber, the counseling is just information and discussion, no test. The counselor could provide you the information that might change your mind and decide to do testing, or it might firm up your decision to not do it.
Frayda is right, with HIPAA out there now, it is hard to even get your own records! I paid out of pocket for my tests so that the results would not get to insurance at all...and when I tested negative, I submitted the claims and got it covered. But that could be another option...pay out of pocket to keep it private.
My genetic counseling was done at U of M, through the Cancer Center, but the genetic folks keep a totally separate record. Even my oncologist could not get to see my records, although it was in the same facility.
And even if, big IF, you tested positive, there is no guarantee your kids would inherit the gene. So your test results should have no impact on them. I would encourage you to meet with a counselor in the genetic risk area, and let her/him answer your questions. The worst that could happen is nothing...you can decide not to do the testing after meeting with the counselor. I waited 6 months to get tested after I did the counseling...
And it is OK if we disagree! I still like ya!
L&H,
Lori
thanks i will check that out... i am waiting for the results of this appeal with baited breath!
stef
To Do What I Do -Alan Jackson, 2004
i am waiting for a confirmation letter in the mail.
sorry i haven;t been on the board...family still here from the holidays! i am so truly sorry to hear about Mel... she was so friendly when i met her in myrtle beach... that seems like only yesterday....so so sad... may she rest in peace.
hugs to all,
stefanie
To Do What I Do -Alan Jackson, 2004
Stephanie,
Don't give up the fight with the insurance company yet.....push them on giving you the hyster paid, too. If your company is anything like mine, they are rat bast@#$# to deal with but keep sending paper back at them.
You know, there are so many books out there on how to cope with bc or whatnot but there needs to be one on how to get your way with insurance companies and doctors. (My DH just opened my eyes to something I never even thought of...bargaining with doctors and hospitals. Maybe you all knew this, but it never occured to me to say to them, "Well, I don't care if the bill is $500 all I am only going to pay $150 and no more and you can take me to small claims court to try to recover your costs but I don't think it will look real good before a judge that you're trying to bankrupt a woman with breast cancer..." He went on in that fashion and they said, "OK, we'll take the $150 and write the rest off." I was stunned!)
Don't let them get you down! And as for "medically necessary" just what do they think, that women wake up one day and decide on a whim to have major surgery?! Maybe they need more WOMEN on your review board.....Harumpf!
Love,
Erin