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Bejeweled Patient & Box O’ Love

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Yesterday Quinn got a big box from Dawn shipped from Ohio. A while ago Dawn spread the word on her blog and twitter that Quinn was about to get her ears pierced and she wrote this great post about my girl and her little self and then she asked people to send Miss Quinn earrings and you know what? People did.

The “Internets People” (Quinn’s term) sent (so many!) earrings and necklaces and treats and stickers and goodies and pens and note pads boxes and jewelry holders and books and more…you would not believe her eyes and her excitement! Hence the reason some of the boxes of jewels and goodies got separated from their notes and so, I have no idea who gave what…but I will tell you this, you Internets People!

You are amazingly generous and I’m humbled by your willingness to give a little sunshine to a sweet little girl. My girl.

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My girl inspected everything, attempted to read every note and said shrieking “OOOOOOooooo, look at these, Mommy! And these! They are beautiful! I love them!” And my personal favorite, “Hey, wait! We have matching earrings! Can I go show Daddy?” She asked AGAIN in how many days can she change them and we looked at them all a few times over and talked about them and she said things like, “I have never seen any earrings like this! There are Qs and Monkeys and Flowers and Sparkles and Danglies and Stars and Pink and Purple and Green and…” I could seriously go on. But I will spare you.

So, thank you Dawn, Brett, Erica, Margie, Becky, Roni, Jess, Sarah, Rose, Dee, Jen, Heather, Jessica, Allie. If you are not on this list and you sent something, please let me know! Thanks too for those of you that remembered Gage. That was way sweet for a brother that Quinn loves but who is annoyed by her persistence to be near him! Also, I’d like to link your blog (or your shops!) in this post, so email me or leave a comment and I will.

Thank you for the time you all took out of your day to send something for my girl. Quinn really needed a distraction and this was just what the doctor didn’t order.

So much love from the Internets People!

Complicated

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My Gage; he is complicated.

No surprise to anyone out there with a routine-craving child that we’ve had some difficulty with re-entry into the real world since returning from the fabulous NYC trip.

Gage has had a considerable amount of trouble getting into the swing of things relating to school and home. Other than that! He’s a been a jewel!

I think Gage is challenged by the following…re-entry, being off routine, seasonal depression, regular depression, social awkwardness, lack of appetite (from new med), lack of ability to sleep, sensory issues, and a defiance/impulsive disorder. He seems very angry and sad right now. I guess it’s the one step forward, two steps back.

We’re tightening up the reins on the behavior mod program and encouraging strongly in different ways to get it under control. The psychiatrist said it’s not out of the realm of possibility for the need to increase Gage’s anti-depressant. We’ll be checking back in 2 weeks from now. She also recommended we get him up an hour early to have enough time and energy to eat a hearty breakfast. We started that last Thursday. And by “we” I mean Julian, because I do not work well with 6am. We still don’t get a along. Waking up early helped Gage eat better, but we didn’t see much improvement in his behavior/focus on those two days.

I can go on about the challenge of parenting Gage, but let’s face it; it’s Sunday night and I don’t have the energy. So let’s just take eating as an example. Gage doesn’t eat meat (with the exception of an occasional hot dog, do we count that as meat?). And his okay-to-eat food list is small, at best. I’ve had to get a little creative lately because on Concerta he’s lost 5 pounds of the very precious ones he put on since his transplant.

Gage will eat…bananas with peanut butter, peanut butter straight, milk, cheese, apples, broccoli, watermelon, PB&J, peanut bars (see a theme?), peanut butter crackers, yogurt, sunflower seeds, almonds, pecans, a few select cereals, occasionally hummus, cheetos/cheese crackers, pancakes/waffles, poptarts (strawberry and brown sugar) and let’s see. That’s about it. Oh, and pumpkin pie. Let’s all agree that we won’t tell Gage it’s Sweet Potato Pie. Somehow that sounds healthier to me. Because that’s been his entree for about 10 days straight. Photographic evidence…(click to enlarge, because it really is that strange)december-044

Just to recap…

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Dawn sent me an email earlier to ask where in the process we were with the evaluation for Gage. I’m not suprised she is confused, because, frankly, I am confused. I’ve been going so much on Momma-Just-Get-It-Done- Instinct that I am not sure I’ve recorded it entirely here, and I want to have it recorded!

Ah, behold the insanity with me!

May – I worry Gage doesn’t have a remorseful bone in his body because, ON MOTHER’S DAY he draws a picture out of anger, of me tied down on a train track, and him on train, with the words “Do it!” in talking bubbles. It was, by far one of my low lights in being a mother.

June – Same ole, same ole. He’s defiant and largely uninterested in extra activities like soccer and piano. We’re loose on the behavior mod, and Quinn pays for it because he is mean to her. Why she idolizes him, I’ll never know. We do keep up on time-outs, but they are starting to be ineffective as a deterrent to meanness.

July – A few days before vacation Gage drop kicks Quinn in the gut while Julian is out of town. And during a time on the phone when I need Julian to agree that Gage is out of control, he says the one thing that most hurts me. I spend a few weeks not getting over it. Then one day, I just forgive him. This evening I sent an email to our behaviorist, but to no avail. I believe he must be off for the summer or on sabbatical. This does not please me, because I know that I will have to find someone else to help us, and pronto.

During vacation I mention something that included the words “remember when you were on dialysis?” when I was referring to a time period and Gage replied “When I almost died?” It was a pivotal moment for me because while I knew something was amiss (he’d just started the “I want to die” statements) during the previous weeks and we need to address it, it sure solidified my desire to do it quickly.

July 22-26 – I called a friend who gave me name of a therapist who a friend of hers recommended because her son also had talked about wanting to die.

That therapist wasn’t taking new clients and referred me to another therapist.

That therapist said she could see Gage but she thought another therapist would be better because she’d dealt with kids who’d had medical interventions/trauma.

That therapist called me back and agreed to meet us a week later.

Gage’s talk about wanting to die intensifies, as does my desire to ease his pain.

July 31 -We have a bad experience during a lab draw that pisses me off.

August – A week before the first day of school we met her and began a weekly play therapy session for Gage. Two weeks into this process he is diagnosed with clinical depression and we start to seek meds to help him.

I call the transplant team to see if he can even have meds for depression and he can, in fact, many kids that have had transplants are on them.

I call the pediatrician for meds. Five days later she says no go.

I call our local nephrologist to see if she has experience prescribing anti-depressants and she doesn’t call me back. When I do talk to her a week later she apologizes and we hardly talk about Gage, because she is alarmed about Quinn and now she wants to talk to the transplant team about Quinn’s unusual situation with her creatintine numbers being pesky.

I declare to Julian that our life is insane, and he agrees.

I call the transplant team and tell them about the trouble getting Gage prescribed an anti-depressant and the coordinator (love her) said she’ll ask the transplant team psychologist for a recommendation/referral of a psychiatrist. They call me back 5 days (includes a weekend) and the coordinator told me the psychologist said for me to call our behaviorist. Um, yeah, already thought about and tried that.

I reach out to our out-of-town nephrologist, Dr. Wonderful, who has her own little freak out session about the situation and asks my permission to contact their head of pediatric psychiatry. The chief says I can come there or he will contact the hospital here, which incidentally is across the street from our own Children’s Hospital, to see if he can help. He says he knows the head at Emory. And he refers him to the head of a new clinic for kids and he provides me the number and contact names of two psychiatrists – who have a 4-6 week wait to get in.

I take the new doctor in the group because I can get an appointment the next day. I call to get a referral from my ped. I call again the next morning because I have to take it with me to the appointment. They fax it to me within a couple of hours.

That was three weeks ago. The doc says she needs to do an evaluation. I give her permission to talk about Gage to these people.

Special Ed Teacher, Transplant Team, Liver Doc, School Counselor, Therapist and Pharmacy at Children’s. This takes three weeks.

So here we are. I have Zoloft in hand. We’re to start a very low dose and if the first two weeks on it go well, then we will up it.

I’m keeping expectations low. Because, well, I’m trained that way, you know.

Waiting sucks.

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This much I know.

The reason I know this is because I do it a lot in the care of my kids and they do it a lot. We wait for results of tests, we wait in waiting rooms, we wait for doctors and nurses to get back with us. We wait for kidneys to fail. We wait. We wait. It completely sucks. And this time is no different.

We saw the psychiatrist today and gave her the back story. She only met Gage briefly because, well, he has a very long back story. She only met Julian briefly because is wasn’t necessarily one of the days where Gage is compliant. He wasn’t mean while being non-compliant, but he was all over the place. And one of the things you can’t do with Gage on one of these days, is leave him to his own devices.

The receptionist had mentioned there were “toys” in the waiting room when I set up the appointment. Now you know where I am going with this, right? Because a few stuff animals on a sad, worn out shelf, in a large, open waiting room does not equal “toys.” So Gage was unimpressed with the “toys” but he did love the hallways that led to nowhere and he loved the scary basement, and he loved all the nooks and crannies in the place. In fairness to them, they said it is a new* office.

Gage will have to wait for medication for his clinical depression – if that is what she thinks he has when she is done with her evaluation. Who knows how long. When I spoke to Dr. Kind last night I told her this would happen. I told her I didn’t think I would walk out today with a prescription for my boy. “A month, at the very least!” I said. She was shocked. I said you know, I am sure it will be at least a couple of weeks for his evaluation and then reporting, then the back and forth. “Really?” she says. This much I know.

Gage has to wait. For almost every little bit or big bit of treatment. While I know in my reasonable type of person brain that this doctor is doing her job it’s still frustrating for my non reasonable type of person brain. I explained my frustration about this because I sincerely just want my son to be able to cope a little bit better. Oh, and I did mention I’d like to take the edge off of his death wish.

When I told the good doc how “I knew it! I knew it would take so long! It’s just never easy!” I can’t be sure, but I think she kinda gave me a verbal slap…asking/telling me that she was sure I didn’t want her to “do harm” because as a doctor, safety is her priority. She also said that it only took a day to get in for an appointment. While that is true, the wait was 4-6 weeks for the two doctors that were referred to me for this appointment. And well, the only reason we got in the next day was because she was NEW and doesn’t have any patients yet. So I don’t think that counts. I did tell her that it took me a week to find her and I had to go through a doctor in another state for a name. Blah, Blah, Blah.

I said, “I deserve the right to be frustrated, don’t I?” She had to agree. I have to say I did think it was funny that she told me I could have gone through the Children’s Hospital (transplant team) psychologist and that might have helped us get there quicker. HAHAHAHAHA! I know the two entities are closely tied in function and proximity, but that person just referred me to my own behaviorist! She didn’t even know about the Child Mood and Disorder Center.

She was nice enough, however slow this process will take. Gage talked with her; well he answered her anyway.

So, the plan, before she will consider medication is…

  • Appointment with Julian for his take
  • 2 Appointments with Gage
  • Talk with Dr. Kind
  • Talk with Special Ed teacher
  • Talk with Play Therapist
  • Talk with Transplant Team

Now, you know this is going to be some back and forth between this crowd of people. This is not a process that will happen quickly. I am saying that I think we have a 5-8 week for meds, and that’s IF she thinks he needs them.

So, we’ll just wait. And even though I just wrote all of this to get it out of my system…guess what?! It still sucks! That much I still know!

* “New” wouldn’t necessarily be the word I would use to describe this office. It’s in an old mental hospital. And it looks every bit like an old mental hospital. Like horror-movie, strapped-a-person-down-in-the beds, mental hospital.

Using the Cute Faces

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Ever since I was invovled with the PKD Foundation when Quinn was 4 months old I’ve let them use our family story for awareness. At first, I didn’t think much about it. Since then I’ve had to weigh the pros and cons and for us, the pros outweigh the cons.

I know at some point the kids won’t want me to share so much. And I will have to let them direct that when they get to the age that they care what their peers think. But for now, I’m comfortable with using their images to further awareness. And raise funds.

This is an HTML image from an email that went out last week to 13,000+ people who have participated in the Walk for PKD before but hadn’t yet signed up this year. (don’t click on the links, they won’t work on this screen shot). But if you want to donate to research in honor of Gage and Quinn, let me know in comments or an email and I will send you a link, of course! And there are tons of Walk for PKD events across the world, so check out www.pkdcure.org and look for your city. Then sign up and go!

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Hey, you! Yeah, you.

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You know who I am talking about . All of you staff people at the PKD Foundation…I would be talking to you. And about you.

I realize I am only 2 days post Convention, but I had to say THANKS for putting on such an informative event. After 7 times attending, I’m still learning. That could mean that you really chose your speakers carefully taking into consideration the many topics that have been presented in the past or it could mean I’m a litle dense.

I try to tell you in person what it means to be to be able to go to an event like this, but that is not always possible.

As a mother to sick kids, I spend a lot of time trying to find information about (current) treatments, research and what the future holds (treatments and research) and I am never disappointed at what I find at the Convention. In fact, sometimes there are things I haven’t even thought about yet, but there you go pushing them at me anyway.

I’m grateful that I have the information before I actually need it. I told someone there that while Gage’s dialysis and impending transplant was a wildly scary time for our family, I felt like at least I knew the basics of the phases we were entering. It didn’t occur to me that there are people who don’t even want to know about dialysis and transplant for their (kidney challenged) kids. But having that knowledge prior to Gage actually receiving both of those was exceptionally helpful.

This Convention has put my mind in the future again, with all the research on immunosuppressant drugs, the reproductive choices (or lack there of) for the kids, and about them moving forward in life as transplant recipients. I appreciate all that you do for this group of people; my people. I appreciate that you all are committed to raise awareness, and money and that you educate us. I appreciate, that while you are not affected personally with the disease (with the exception of DK), you are committed with a passion I’ve never seen in a group of staff anywhere. And I thank you.

Thank you for connecting me with other families that we look like (kind of). They’re mutants too and we love them and they are there for us in a way that isn’t really possible for anyone not living with crappy kidneys. These are the people that go with us on this scary path and without them I am not sure I could find my way each and every day of this journey. Thank you for bringing me to the people that will always share a history with me and my family.

There is no way to explain to you what it means to me to know that I have the most current information there is to draw from in health care advocacy for my kids. It means a great deal to me because my kids, wild Gage and sassy Quinn, only have us parents to depend on.

And well, they have you.

I can’t say I know all the risks and challenges my kids have in the future as a result of being PKD patients and kidney recipients, but I do know this: without the PKD Foundation behind me, I wouldn’t feel as nearly as prepared for them, whatever they shall be.

Many thanks and much gratitude. Now get some rest! Because it’s almost Walk for PKD time.

Gage and Quinn’s grateful mom,

Julia

Repro.

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For the first time in a long time I have been thinking of the ramifications of transplant on Gage and Quinn’s reproductive systems and choices because of a session called “Reproductive Issues.” There are immunosupressant and BP drugs that have been shown to cause fetal abnormalities. There are serious considerations for a transplant recipient regarding carrying a pregnancy. And well, there are a million questions I have about their growth and their entrance into puberty with all the drugs that they (will) require and the ramifications on their perfect little bodies.

Last year when we were in the mode of saving Gage’s life, I didn’t once think about these things.

But I sure thought about them today. That’s the thing about coming to the Convention each year. It forces one to look at things in the future. I didn’t have to go to that session. There was a perfectly good, well-crafted session on dialysis (um…right) and the reproductive session looked interesting.

It can be messy. This kidney thing.

I’m off.

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I’m taking a few days off to go the PKD Convention in Dallas. Somehow, someway a few of my favorite moms are all attending the conference without kids…just like me! Sadly, we’ve had to pawn the kids off on about 4 people for three days because Julian is at a big conference in San Fran for a big client. Seriously, the preparedness we’ve had to do is insane between lunches, meds, coverage schedules for picking up and sleeping with and making sure kids are ready for tutoring and lessons.

I have visions of us moping around all weekend, wondering how the families are managing. I am sure we’ll dash our way to the hallways in haste in between sessions to phone home to see how things are on the home front.

I see myself sleeping in a bed alone, only myself to take care of. You know you need to get away when the promise of sitting in conference rooms learning about your kids’ disease and research looks like way too much fun.

Off to Dallas! Will try to blog and maybe make my friends each do a guest post! Cause they’re fun like that.

Taking Mother’s Day to New Level

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I taught Sunday school today and Gage made a comment:

“I will kill Quinn.”

To which my reaction was calm but serious, about how we don’t talk like that and I put him in time out outside the classroom door where I could see him. I was thinking this was his way to avoid the Sunday school lesson so I decided to make him do the lesson in timeout.

It was a simple assignment. Draw a picture of you and your mom. A few minutes later I checked to see what he was working on and it was a picture of a train track. I recognized the picture because on many occasions in the past he has drawn the two of us playing trains together.

But this one was different. He had drawn me on the track and him on the train. Across the bottom of the page there were several word bubbles with “Do it” inside of them. He explained (calmly) the picture to me. The train was going to hit me and there were people telling him to do it. I said it hurt my feelings and made me sad.

I immediately got tears in my eyes but maintained my composure. But I am extremely sad and scared. Julian arrived not long after and took Gage away and talked to him. When they returned to the room Gage would not apologize to me.

After church I enjoyed a lovely brunch with my mom. Then I stopped by church on the way home to retrieve my Mommy and Me picture because I need proof when I speak with the behaviorist.

Julian just took the kids out and instead of me hitting a movie I’m going to curl up in bed for a few hours and watch a movie and nap. And I’m sure I will cry some more.

All of a sudden I am really sad that maybe Gage has no compassion, or empathy, or remorse. I am thinking the worst for his future of course.

As you can see, it’s been a real special mother’s day so far.

Political much?

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Change is the BIG BUZZ word in this presidential campaign. Here is a way you can really help change something. This is near and dear to my heart and can impact our little mutant family. I need your help, by calling your senators TODAY about supporting this bill that will be voted on THIS WEEK.

The Genetic Alliance organization had used our family to show an example of a family whose genetic make up can adversely affect their lives — in more ways than the obvious. Gage and Quinn are especially vulnerable to discrimination from future employers because of their disease. Besides my wish for them to live an average life, I wish for them to be judged on their work ethic and character instead of the genes that we parents unknowingly passed on to them.

Please help make that a law. Do it for Gage and Quinn…right now! What are you waiting for?

What is the Genetic Information Nondiscrimination Act?

The Genetic Information Nondiscrimination Act [H.R. 493, S. 358] is a bill that will prohibit discrimination on the basis of genetic information with respect to health insurance and employment. It was introduced to establish basic legal protections that will enable and encourage individuals to take advantage of genetic screening, counseling, testing, and new therapies that will result from the scientific advances in the field of genetics. It would also prevent health insurers from denying coverage or adjusting premiums based on an individual’s predisposition to a genetic condition, and prohibit employers from discriminating on the basis of predictive genetic information. Additionally, such legislation would stop both employers and insurers from requiring applicants to submit to genetic tests, maintain strict use and disclosure requirements of genetic test information, and impose penalties against employers and insurers who violate these provisions.

From the PKD Foundation today,
Urgent Action Alert: The Senate Will Debate the Genetic Information Non-Discrimination Act
This Week!

The time has come… After much delay, the Genetic Information Non-Discrimination Act (S. 358) could go to the U.S. Senate floor for debate and a vote as early as Tuesday, April 15. A nationwide grassroots effort has begun to convince every Senator to vote for the bill.

Congress has tried and failed to pass this vital legislation for 12 years. The U.S. House already passed this legislation in early 2007. However, if the effort to bring GINA to the Senate floor fails now, there will not be another attempt this year. We need a massive response rate from you and other advocates from all the organizations fighting for this bill to make this effort a success.

Thank you for your efforts on behalf of everyone affected by genetic diseases to support this legislation to help end genetic discrimination.

Here’s What To Do:

This is a two-step Action Alert:

Call Senate Majority Leader Harry Reid’s (D-NV) office and thank him for his efforts to schedule a debate and vote on the Senate floor for GINA. As Majority Leader, Reid controls what bills get a vote in the Senate.

Reid’s office: 202-224-3542. (If it’s busy, keeping trying!)

Sample script
My name is (YOUR NAME), and I am calling to thank Senator Reid for his leadership on the Genetic Information Nondiscrimination Act, or GINA (S. 358). I would like to encourage him to bring GINA to the Senate floor as early as possible. Thank you!

Call your state’s two Senators and ask them to support GINA. You can find their names and contact information listed below. I could only make it so easy for you!

Sample script for you to use:
My name is (YOUR NAME), and I am a constituent living in (YOUR CITY, STATE). I am calling to ask for (NAME OF SENATOR)’s support for the Genetic Information Nondiscrimination Act, or GINA (S. 358), and all the procedural motions needed to support this legislation. This legislation provides fundamental protections against the misuse of genetic information in health insurance and employment decisions. It is vital for all Americans to have these basic protections. Thank you!

State Member Phone

AK Lisa Murkowski (202) 224-6665
AK Ted Stevens (202) 224-3004
AL Jeff Sessions (202) 224-4124
AL Richard Shelby (202) 224-5744
AR Blanche Lincoln (202) 224-4843
AR Mark Pryor (202) 224-2353
AZ Jon Kyl (202) 224-4521
AZ John McCain (202) 224-2235
CA Barbara Boxer (202) 224-3553
CA Dianne Feinstein (202) 224-3841
CO Wayne Allard (202) 224-5941
CO Ken Salazar (202) 224-5852
CT Chris Dodd (202) 224-2823
CT Joseph Lieberman (202) 224-4041
DE Joseph Biden (202) 224-5042
DE Tom Carper (202) 224-2441
FL Mel Martinez (202) 224-3041
FL Bill Nelson (202) 224-5274
GA Saxby Chambliss (202) 224-3521
GA Johnny Isakson (202) 224-3643
HI Daniel Akaka (202) 224-6361
HI Daniel Inouye (202) 224-3934
IA Chuck Grassley (202) 224-3744
IA Tom Harkin (202) 224-3254
ID Larry Craig (202) 224-2752
ID Mike Crapo (202) 224-6142
IL Richard Durbin (202) 224-2152
IL Barack Obama (202) 224-2854
IN Evan Bayh (202) 224-5623
IN Richard Lugar (202) 224-4814
KS Sam Brownback (202) 224-6521
KS Pat Roberts (202) 224-4774
KY Jim Bunning (202) 224-4343
KY Mitch McConnell (202) 224-2541
LA Mary Landrieu (202) 224-5824
LA David Vitter (202) 224-4623
MA Edward Kennedy (202) 224-4543
MA John Kerry (202) 224-2742
MD Benjamin Cardin (202) 224-4524
MD Barbara Mikulski (202) 224-4654
ME Susan Collins (202) 224-2523
ME Olympia Snowe (202) 224-5344
MI Carl Levin (202) 224-6221
MI Debbie Stabenow (202) 224-4822
MN Norm Coleman (202) 224-5641
MN Amy Klobuchar (202) 224-3244
MO Kit Bond (202) 224-5721
MO Claire McCaskill (202) 224-6154
MS Thad Cochran (202) 224-5054
MS Trent Lott (202) 224-6253
MT Max Baucus (202) 224-2651
MT Jon Tester (202) 224-2644
NC Richard Burr (202) 224-3154
NC Elizabeth Dole (202) 224-6342
ND Kent Conrad (202) 224-2043
ND Byron Dorgan (202) 224-2551
NE Chuck Hagel (202) 224-4224
NE Ben Nelson (202) 224-6551
NH John Sununu (202) 224-2841
NH Judd Gregg (202) 224-3324
NJ Frank Lautenberg (202) 224-3224
NJ Robert Menendez (202) 224-4744
NM Jeff Bingaman (202) 224-5521
NM Pete Domenici (202) 224-6621
NV John Ensign (202) 224-6244
NV Harry Reid (202) 224-3542
NY Hillary Clinton (202) 224-4451
NY Chuck Schumer (202) 224-6542
OH Sherrod Brown (202) 224-2315
OH George Voinovich (202) 224-3353
OK Tom Coburn (202) 224-5754
OK James Inhofe (202) 224-4721
OR Gordon Smith (202) 224-3753
OR Ron Wyden (202) 224-5244
PA Robert Casey (202) 224-6324
PA Arlen Specter (202) 224-4254
RI Jack Reed (202) 224-4642
RI Sheldon Whitehouse (202) 224-2921
SC Jim DeMint (202) 224-6121
SC Lindsay Graham (202) 224-5972
SD Tim Johnson (202) 224-5842
SD John Thune (202) 224-2321
TN Lamar Alexander (202) 224-4944
TN Bob Corker (202) 224-3344
TX John Cornyn (202) 224-2934
TX Kay Bailey Hutchison (202) 224-5922
UT Robert Bennett (202) 224-5444
UT Orrin Hatch (202) 224-5251
VA John Warner (202) 224-2023
VA James Webb (202) 224-4024
VT Patrick Leahy (202) 224-4242
VT Bernard Sanders (202) 224-5141
WA Maria Cantwell (202) 224-3441
WA Patty Murray (202) 224-2621
WI Russ Feingold (202) 224-5323
WI Herb Kohl (202) 224-5653
WV Robert Byrd (202) 224-3954
WV John Rockefeller (202) 224-6472
WY Michael Enzi (202) 224-3424
WY John Barrasso (202) 224-6441

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