It was very hard to see the way opening as I struggled with depression and was told to go to the hospital or I’d be committed by my counselor. So in August 1995 I spent five weeks at the Meadows Treatment Center in Arizona. I was resistant and unfamiliar with such therapy and kept praying that I could go home. As soon as someone arrives there, one receives a complete physical exam, which was beneficial for me. I was severely anemic and kept growing increasingly worse, so I was sent to a physician, with a staff member as if I was “psycho” or so I thought. (I now realize a lot of the surveillance measures were for the majority of the Meadows population who were alcoholics and/or drug addicted.) It turned out that I needed a D&C. Trying to go home; I talked to my Corpus Christi gyn/ob doctor who advised me not to travel home, because if I started to bleed on the airplane, I’d bleed out! Never having had surgery before, I was taken to a large hospital in Phoenix where it was performed. I was scared, but didn't have anyone to talk to about those feelings. Luckily, a female staff person accompanied me, and all I remember is dozing off and on during the ride back to the Meadows. I continued to get increasingly anemic, and so I was sent off to get a blood transfusion. I was left in the small, local hospital for about four hours. While I was receiving the blood, I made all sorts of phone calls, which were not allowed at the Meadows. I talked to many friends lengthily. That was so good for me. (Phone calls were limited at the Meadows, as to time and number.) After that, my hematocrit stopped getting lower, and I seemed to improve physically.
The fourth week was Family Week where CB, 16-year-old DC, and 13-year-old AE came. CB arrived, rigidly resistant to the whole process. (He had almost refused to fly there.) The first day when everyone was asked why his or her “patient” was there, DC said he didn’t know why his mom was there, and that I’d always seemed upbeat. AE said she’d seen me getting depressed and we were a family that never talked to one another! And CB said I was here to be fixed. The next day, CB told me that the Meadows was not a normal place—that the counselors weren’t normal, that the patients weren’t normal, and that anyone who had thought of suicide definitely wasn’t normal. That seemed to mean that he was the only normal one there. AE told me her dad kept telling her how they’d have to watch me all the time when I came home, as I was “different.” He wouldn’t participate in group therapy and was stolidly judging everyone.
Then a miracle occurred on Wednesday morning. CB showed up, looking like the person I’d fallen in love with. He was softer and more vulnerable. He said he’d woken up knowing he could do this. We discovered that we still loved each other. A friend later told me that when CB returned to Corpus Christi, he’d turned into a big teddy bear!
Both CB and I consider that God opened our hearts and minds to each other then. I later learned that my Emmaus Reunion Group, other friends, and people at church were praying for me all the time I was at the Meadows. This was the first time I realized I was part of a community that cared AND that prayer helps somehow! (In the past issue of Weavings, there is an article about making space for God and how prayer does that.)



Imagine a popular program that has existed for 10 years with bipartisan support, providing health insurance to about 6 million low-income children. The State Children’s Health Insurance Program (SCHIP) is up for reauthorization this year and Congress is debating how to extend the hope of coverage to 9 million children who are currently uninsured, while protecting coverage for the 6.6 million children who depend on SCHIP to see a doctor. But SCHIP is caught in the middle of a political battle—between a bipartisan majority in Congress and the nation’s governors on one hand and an isolated, defiant ideological president on the other.
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