New Doctor

This morning Cody drove me down to meet with the new doctor that had been recommended by my colleagues at Heritage school, PCP. She did a standard check up and she is also concerned that my blood pressure is elevated. I never had a problem before the surgery, but now it seems the blood pressure is a concern. I also had the headache the other day, so PCP puts me on Zomig (this was the last thing I was on before I stopped having the migraines years ago) for some crazy reason my insurance company only allows 4 per month! She also keeps me on blood pressure medication. I also ask what I can do because I seem to have some irritation in my pelvic area where my skin is peeling, and I think it's "diaper rash" she recommends some Desitin cream on it and to let her know if its not getting better. We drop off the prescriptions and pick them up later. I take a shower, and blow dry my hair, putting on my diaper rash cream so I can put on my Depends. I head back into the bathroom to put up my blow dryer and come back to the bed and I notice some poop on the floor. I tell Cody I think Castro has had an accident, and he tells me he doesn't think it's Castro's. He's right, it's mine. Regardless of the accident, I'm totally excited for tomorrow and promotion for my Kinders at school! First time I've seen them since the end of April, last day of school!!!

Finally!!!!

Cody comes back in the morning after giving Castro his food and insulin. Hopefully today will really be the day that I can be discharged. The neurosurgeon's partner comes to see me this morning and finally gives me the okay to leave. The neurosurgeon's partner and attending physician are both concerned that my blood pressure is still on the high side, but give me a blood pressure medication to help keep that under control until I can see my PCP. The neurosurgeon's partner tells me to schedule a follow with their office because they fill up quickly. I should be up walking around, I have Percocet for the pain, a steroid to help with the swelling, the blood pressure medication, an antibiotic and Valium for nerves. I ask if I can please take a shower before I leave the hospital (because they have a shower chair), and am told that I can, but then it seems like they are trying to rush me out. I insist that I'm not leaving until I take a shower, they ask when I think I'll be ready to leave and I say about an hour. Cody helps me carefully take a shower. I can't stand for long periods of time, so the shower chair really helps. We check out and head home. I'm so happy to see Castro and our house, but I am exhausted from not really having slept the night before. So I end up sleeping for a bit. Cody runs to the store and gets some essentials, my prescriptions filled and a McDonald's Mocha Frappe (if I can't have a Starbucks this will do!) while I nap. I hurt, and my back feels tight, so I take one of the Percocet. I still feel numb down my left leg and in the saddle area. The neurosurgeon's partner had said that this could take months to come back. I had Cody take a picture of the incision because I hadn't seen it yet. We take it easy relaxing in the bed, watching t.v. shows that I missed out on while I was in the hospital, and call it an early night.

Sunday...

Normally, Sundays are one of my favorite days of the week. I get to relax (usually kick back with a Starbucks) and take a look at the Sunday paper. I love to look at the ads and check out the sales. In the hospital though, this is not as fun. Besides, the fact that I'm still sore and the medications are driving my blood pressure and blood sugar all over the place, I just can't relax, I want to go home. Cody makes an effort to get Castro his insulin and food early so that he can be with me when the neurosurgeon comes to check on me. Cody gets there nice and early (since yesterday the neurosurgeon came around 8am) and we end up waiting for a bit. As soon as I step into the bathroom to try and pee, he shows up. He talks to Cody, and me through the bathroom door. He says that he's not really comfortable releasing me with the blood pressure issues, the fact that I'm still working to control my bladder, and I'm still retaining even after peeing. He's not ruling it out, but he'd like to re-evaluate later in the day to see how I'm doing. I ask if I can at least take a shower, and he said that would probably help me feel better, so to do so with the help of Cody or a nurse. When I ask later for showering supplies (towels, soap, etc) they are told that there is no record in my file that I was given the o.k. to shower, so it is put off again! Later in the evening Cody and I relax, (he brought his laptop from home) and we share the little overbed table. Him on one side playing a game on his laptop, me on the other. I do some reading, I put in a Scholastic book order so my kiddos get their books before the last day of school, I play some games on my iPad. The neurosurgeon does not come back to check on me. The attending physician comes through and says that a urologist will be coming to see me at some point today because they are worried that I might have a secondary urinary infection because there had been blood in my urine (because they make you pee into a cup so they can measure your urinary output). I once again state that of course there is blood in my urine, I am MENSTRUATING!! (Really... how many times do you have to state the same thing over and over and over). I pee again, and they scan and it shows I'm only holding 100ccs (just over 1/3 cup), this has been considered acceptable. So a couple hours later a urologist comes through. He had been told I was on a catheter (I'm not), he had been told I was retaining large amounts in my bladder even after peeing, which is also no longer true. I also let him know that they put me on an antiobiotic just in case I had a urinary tract infection. He leaves a card and tells me to follow up later with my PCP or with his office to ensure there really is no urinary infection. By now its getting late into the afternoon, and I'm starting to realize I am not going home today either. The attending physician comes through and says that I will be staying again, until I have more control over the bladder, blood sugar and blood pressure. My blood sugar is apparently too high, so I get another 2 units of Inulin Lente before dinner. Cody leaves to get Castro his insulin and food, as well as some dinner for himself. I take a small nap, and wake up as I realize I have to pee, but just can't make it fast enough. Small accident, but this is what they were talking about with control of bladder. Cody comes back and we relax some more together, but I convince him to go home and try and get a good night's sleep so he'll be better ready to take care of me when I come home tomorrow.... because it has to happen... I have to go home tomorrow or I will go insane. Cody goes home to get some sleep. I try, but after about 30 minutes I can't sleep. I get up and walk around the floor, I watch some Netflix, I watch some t.v., I read, I get up and walk around some more and I pee a lot. It's finally 4am before I fall asleep, then at 4:30 they draw more blood, and take blood pressure and blood sugar. I finally fall back asleep for until around 7am.

The Day After Surgery

Cody stayed the night with me, but he needed to leave to get Castro his morning food and insulin. I'm still very sore from the surgery and my saddle area is numb. I fight with the nurses to remove the catheter and to be able to wear underwear and sanitary napkins. Donna arrives and is with me when neurosurgeon comes to visit this morning. He is upset that I didn't get up and do any walking around the night before. This is just as the nurses are changing shifts (7:30am) and I get the same AM nurse as I had the day before. She said she knew that I was clear to walk without a brace. I explain that the night nurse did not know this, and there was nothing in the notes to indicate, and normally they don't allow patients to walk after back surgery without a brace. He says that we can remove the catheter and see how I do on my own for peeing. He says if I can manage my bladder and get walking there is a chance that I can go home today. I ask if I can please wear underwear and a sanitary napkin now, and he says yes. Luckily, Cody not only brought me my favorite Starbucks breakfast (Venti White Mocha Non Fat No Whip with 2 pumps Raspberry and a Perfect Oatmeal yummmm), but also some undies and napkins so I put some on. Now I've just gotta get walking around. Cody is disappointed that he didn't get a chance to see the neurosurgeon, who'd have thought that the doctor would be in at 7:30 on a Saturday! Donna leaves because she has to do Karaoke that night (and she's barely seen Gordon or Tiffany since this all started) and Cody takes me for a lap around the floor. When we get back, Cody leaves to go check on Castro, he's been home alone a lot! While Cody is gone checking on Castro, I convince the nurses to remove the I.V. and Jason and Carrie come to see me. I'm looking totally awesome since I haven't had a shower since uhm Wednesday (4 days) and am not feeling too confident in hospital gown. At least am sitting in the little recliner that they have, and Jason and Carrie take the other chairs. They are so sweet and bring me some pretty purple flowers and gift cards to Mimi's Cafe and Rock Bottom Brewery so that Cody doesn't always have to cook when I finally get to break out of this place! The attending physician comes in to see us. He is concerned because I haven't peed since they removed the catheter and its been about 4 hours (hello, teacher's bladder). I pee a little, but they can feel my bladder and tell it wasn't nearly enough. They tell me everytime I pee, I will have to have a bladder scan (ultrasound) They come do the ultrasound and I'm holding about 300ccs still, which is like 1 and 1/4 cups. So they reinsert a catheter to drain it. The nurse tells me that the catheterising should hurt, but I don't feel anything, still numb in the saddle area, then they remove the catheter. They are also concerned about my blood sugar (which was up around 300) and my blood pressure (162/109). They say that these can be related to the steroid, dexamethasone, that I am on to help with the iflammation from surgery. Before dinner they give me 8 units of Inulin Lente and my blood sugar drops to just over 100, and that is after eating dinner.  I get up and do more walking. The attending physician comes back and says that because I'm retaining too much urine and my blood pressure is high (due to being in a hospital AND the steroid they have me on for the inflammation in my back) I'm not going home today. I am devastated. Cody stays the night again tonight after going back to check on Castro, but I know that sleeping in the chair can not be comfortable for him. The night nurse comes and checks my blood sugar again, and its high (about 150) but she decides not to give me any insulin, because she wants to check it again later to make sure its not related to the dexamethasone. She checks later and it is closer to normal, so no more insulin tonight.

Carrie says that this should be our Christmas Card for this year!