Thursday, June 25, 2009

A Rehab? Really?

I haven't been to the hospital yet today, but I have talked with Claudia a few times. This morning the pain specialists came and removed her femoral blocks. Woo-Hoo total feeling is just around the corner! The nurse took out both of her IV's yesterday, leaving her with just the catheter to lug around when she goes out for her twice daily walks (which, by the way, she is getting much better at). Yesterday, she was able to make it all the way around the nurses station with braces on both of her legs. Today, she did it again, minus the cumbersome braces. That is the first time she has been able to stand without the braces since the surgery Monday. Way to go Claud!!! She is going to kill me for mentioning this, but since it has been a fact of life lately, I'm going to throw it out there anyway... (spoiler: the following will contain discussion of a disgusting adult nature) Apparently, there has been some concern about whether or not her bowels are working properly, and some talk about nurses "helping her along". I am very happy to report that will no longer be necessary. While that is admittedly gross, it is a FANTASTIC sign, that means she is more ready to leave the hospital than she may realize. In fact, the hospital's official statement was something along these lines: If you are going home to your daughter's, we will wait and discharge you tomorrow. If you choose to go to a rehab facility, we can discharge you today. Based on the title of this post, what do you think she chose? That's right, people. She is headed to some rehab facility in Orem later today. Since she won't be reading this any time soon, I can tell you what I really think. I feel bad. I realize that she has to do what she thinks is best for her, but it makes me feel badly that she thinks this is better for her than letting me help her. I cannot imagine that a bunch of strangers can do a better job of taking care of my mother than I can. Part of my problem is that I am trying so hard to be so many things to so many people right now, that this is making me feel like a failure. I can't seem to balance my life right now, and I was hoping that getting her home would help that. (If it seems like I am speaking in tongues, let me try to explain.) I am trying to be a good mom to my kids and falling short- Brock told my mother in law that I don't love him anymore because he has to go to her house and I don't want him at the hospital. I'm not with them, because I am with my mom. I am trying to be a good wife, but honestly, right now, Scott is at the bottom of my list, because he is the most self-sufficient. He is picking up my slack at home as best he can. I am trying to be a good daughter by spending time with my mom and trying to help her with this, but because I am it, as far as our family goes, I feel like I also have to step up and try to fill my dad's shoes. That means, where the daughter in me would maybe hang out with her an hour or two, I feel pressure to stay longer- to not leave her alone too much. I am only one person. I CAN"T be in all those places at once. I was just hoping that I could get her home to my house, where all of the different roles I am playing right now can work together instead of clashing. I'm sure this rehab thing will turn out fine, and this is only a tiny speed bump in the road. I am over-reacting and wallowing in a little self-pity. I need to put on my happy face and go help her get transferred. She is happy about this change, and I will buck up and be happy for her (and cross my fingers that it is short lived).

Wednesday, June 24, 2009

One Step Forward... Two Steps Back...


I just got off the phone with my mom. She is having a harder time today, feeling a little depressed, and struggling with the pain. Apparently, when she decided that her spinal had worn off yesterday (because she wasn't itchy anymore) she was wrong. It really wore off last night. She could tell because of the horrible pain she suddenly found herself in. It would seem the femoral blocks by themselves don't actually block that much pain, or perhaps without them she would REALLY be a mess. She was beating herself up because she has regressed. She has reduced her bending to 60 degrees- 10 degrees less than she was doing yesterday, and she was only able to walk out to the nurses station- which a few posts ago I mentioned was just a stone's throw away. She is also having dizzy spells when she gets up. Mark, the PT says she is right on schedule for one knee, and is still doing phenomenally well for having both of them done, but she is still disappointed in herself. So, ladies and gentlemen, here is my thought: give her a call. Tell her she is doing GREAT! Let her know that you are thinking of her and pulling for her. Lift her spirits a little, and take her mind off of her problems for a few minutes. I'm sure that hearing from those she loves will buoy her up and help her get through this!

Tuesday, June 23, 2009

No Plopping!

Corbin and I went to the hospital and spent about four hours with Claudia. She is doing remarkably well. Her doctor has even told her that he will probably be sending her home Thursday or Friday, instead of Saturday like he had originally thought. She was also scheduled to phase off of her femoral blocks onto a morphine pump tomorrow, but they are going to forgo the pump and go straight to pain meds. That is GREAT news!! When we got there, she was eating and bending (gotta love the CPM- it's her new best friend). I have a sneaky feeling that will be what her life looks like for a while to come. She was ready and eager to go for her second walk of the day, but the PT kept putting her off because every time he came to her room, he would find someone else from the hospital staff had beat him to it. Quite frankly, I don't think there are too many employees left at Utah Valley Hospital that she hasn't met. She had the Occupational Therapist, the Physical Therapist, the Pain Specialists, the Discharge Nurse, the Hospital Bishopric members, her own doctor, her nurses (numbering 3), and the cute little girl who delivered her meals all visiting her at one time or another. Finally, things calmed down enough that her physical therapist, Mark, and his assistant of the day, felt they could come and take her for a walk. Before she could walk, she had to be prepared to walk, so they stretched and pulled and pushed her legs until she was ready. They tied her into a brace per leg to keep her legs from buckling underneath her and then spun her legs off of the bed. She put her feet down and the show began. She stood and began walking, or rather shuffling, but moving in a forward direction none the less. She cruised right out of her room and made it all the way down the hall before her leg buckled. Mark demanded she turn around immediately and return to her room, since she had already exceeded his expectations. When she got back to her bed, it became evident that the real issue was how she was going to bend her knees enough to sit back down. After thinking it over, she announced she was going to just plop backwards and let her legs pop up instead of trying to bend. Mark, his assistant, and I jumped in and screamed no right before she was able to put her ridiculous plan into action- thank heavens. We were able to brace her and steady her enough that she could sit, not quite like a normal person, but at least she didn't just plop. Since she is worried about losing her femoral blocks tomorrow, she is trying to push herself hard today while it isn't as painful. She had Mark put the CPM back on (he thought she should rest first) and upped the degree to 70. Needless to say, by the time we left, she was hating life. I switched the machine to her other leg (which the nurse did not really appreciate) and headed out the door. Hopefully, she took Mark's advice and rested after that last set. It should be interesting to see what tomorrow brings, with the feeling returning to her legs.

She Walks!

I was exhausted last night, so I didn't get around to updating again. By the end of the day yesterday, Claudia was doing better than anyone expected. She was lifting her legs up and twirling her toes around. The nurses were amazed. The physical therapist came in and put her on the continuous passive motion machine, one leg at a time. She tried to convince them to do both at the same time and to up her degree of bending beyond what her doctor recommended. They said no way! Not being able to feel your legs, tends to make you think you can do more than you really can. She was eating mushy foods and keeping everything down. In fact, she didn't throw up once- HURRAY!!! When I left her last night, she said she was going to crash and try to sleep off the anesthesia. I spoke with her this morning around 8:30. She was a million times more coherent than yesterday and doing great still. She was bursting with pride that she had just gotten up and been able to walk to the hallway (with only two people assisting her). She said that trying to stand created the weirdest sensation in her toes. It felt like the she was pushing the floor out from under her. She tried over and over to put her heels on the ground, but couldn't quite manage it. It seems to be a common problem, because the PT got her some braces designed to help with that and they were off. She told me it was a little frustrating to have your feet not keep up with the rest of you, but she was so happy to be able to start healing and improving. Her attitude is unbelievable! I wonder if it will still be that good when she can actually feel her legs... (all of the nerve blocks are still in place and working beautifully) She is hoping to be able to skip the morphine pump and go straight to pain meds for the pain she will soon be feeling. Her blood is done recycling, so they have disconnected her from the machine. That's awesome since it eliminates 3 of her tubes that keep tangling up. Also, they were able to quit monitoring her pulse ox levels, so she's actually down 4 tubes. That's making her life a little easier for now. The physical therapist is coming back between 12-3 for a second walk, and I intend to be there for the show. I'm off for now, so I don't miss it.

Monday, June 22, 2009

The Patient Has Arrived

Claudia is in her room now. They tried to settle her in as best they could, but she just wants them to leave her alone. We have decided that it is completely retarded that they wake you up to tell you to go back to sleep, only to wake you up again. She is having a hard time keeping her pulse ox level above 90 right now, so the machine keeps beeping at her waking her up. To add to that, she seems to be having a reaction to the spinal block they've given her, and she can't stop itching- especially her nose. The itching is made worse by the oxygen they have up her nose. It is a vicious circle: itch, yank out the oxygen to scratch, fall asleep, oxygen drops, machine beeps, wakes her up, puts the oxygen back in, itch, and around we go again. I had a similar reaction to the spinal block they gave me when I had Corbin. I keep telling her she needs to give in and get benadryl, but it is awfully difficult to reason with someone who is so drugged. She has all sorts of contraptions and tubes attached to her. There are the basic ones, like the IV, the catheter and the pressure cuff, and the more specific ones like the pumps on her feet, the ice machine circulating cool air on her legs, the wires feeding into her groin that are blocking her nerves, and the machine that is circulating her own blood out of her knees and back into her arm (that is kind of neat). True to form, as soon as she was awake enough to check, she pulled the covers back to check out the damage. She was disappointed to find her knees were too bandaged to see anything. She spoke to my kids for about 20 seconds- just long enough for them to know that she is okay then closed her eyes and drifted off. She can point and flex her feet, which I thought was almost as exciting as seeing a pig fly. Her toes keep changing colors- purple to pink. I guess she was right about not painting them before surgery. You know what they say... Mother knows best. For now I am going to let her rest and sneak off to the cafeteria. It has been a long time since 4:30 this morning.

We Have a Room!

Okay, so I still haven't seen her yet. In fact, I am not sure when she will be joining me in her teeny tiny closet, er, I mean hospital room. She is in room 480 East. The direct phone is 1 801 357 5480. The phone number to the hospital is 801 357 7850. I doubt if she will be up to taking your phone calls until a little later tonight though. She is almost right next to the nurses station. She's close enough that if she loses her nurse button she could just yell. She just arrived. I will post more later.

Off to Recovery-

Dr. Jackson just came out to speak with me. He says she is now "bionic"! He finished the operation successfully and they are finishing up getting the bandages on her right now. He says she will be off to recovery in a matter of minutes. They will keep her there for one to two hours and then find her a room. The knee replacement is so traumatic that they keep those patients in the recovery longer than they would for other procedures. That's okay with me, because it gives her more time to puke on them instead of me. The first 24-36 hours following this surgery, they do a nerve block to help manage the acute pain. Dr. Jackson said she should be pretty happy as far as pain managment goes, until that wears off. She will be in the hospital until Friday or Saturday and then it's home to Rita's Rehab Facility. Maybe I'll even let her borrow my mantra for a while- she can do this....she can do this....she can do this.....she can do this....she can do this...