Im not sure if Im allowed to share this here or not. But it goes along with my post below. My story is included...but essentially, our family is going to have to file for bankruptcy if I have to pay for this in cash. ..I just keep thinking of my sweet daughter and how I have continued to work 50 hours a week through all of this just to keep us going. 50 hours a week through all the pain of RSD, Addisons Disease, chronic fatigue, DDD, a spinal fusion...the list never ends. And when I finally found a treatment that worked, after so many failed...It is killing me that Cigna wont pay for it. That my house, and my cars and everything that Ive worked so damn hard for and went to school for a million years to get degrees and accumulated student loan debt...to reach the top of my career only to have the rug pulled out from under me. Well, were all in the same shitty boat over here I suppose. I just have a desire to hold insurance companies accountable for the awful decisions they are making with peoples lives. Ive had the treatment. It works for me. Now pay for it... Advocacy for this disease and the wrongs of insurance companies is a mountain I am willing to die on. Help Support Tiffanys RSD Treatment Fund giveforward Tiffanys friends and family are uniting to raise money to help with her battle against Type II CRPS- an incurable nervous system disorder. In 2011 after a terrible car accident while 8 months pregnant and a series of failed spine surgeries, Tiffany was diagnosed with Type II CRPS. Complex Regional...
Posted on: Sun, 20 Oct 2013 22:08:52 +0000
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