Tuesday, February 5, 2013
Marci's Update
Here we sisters are at Morgan's wedding in December. If my mom were in this picture, I'd have all my besties in it.
I have noticed in the last year or so that not only am I not hearing things, I'm not understanding them. I went to a movie with my friend Kathy Konold, I kept leaning over and asking what was said. I do it at church too. Unless the person at church is standing at the microphone when giving a prayer, the only way I know it's over is the big amen at the end.
I had my hearing checked in December and sure enough I have been losing more on the "good" ear. She suggested I see Dr. Harris at UCSD. I have seen him before about the tinnitus, but figured it couldn't hurt to see him again. Today was my visit with him. Apparently you can have Meniere's Disease without having the attacks normally associated with it. Usually after an attack, a person with Meniere's can have some hearing loss. I don't have "attack's" like others have described. I do have dizzy spells, pressure, and pain occasionally. I guess this is my version of an attack.
Several things can happen at this point. I can continue to lose my hearing gradually over time. I could possibly wake up and find that my hearing is terrible or gone one day. People who have this type of Meniere's can have fluctuations in hearing from day to day, but it's not a good thing. If that starts happening I need to go in asap and get steroid shots into my ear and possibly take steroids orally from then on out as well.
I have been put back on a low sodium diet, which by the way is really not fun. I have also been started on a diuretic and potassium supplements that I will take from here on out. I am literally a walking pharmacy. I shudder to think what my liver will be like by the time I'm dead. I will be the only Mormon out there with liver failure, haha.
Believe it or not, there is good news. As long as the nerve in my ears stay 'alive', which they both are currently, I am a candidate for cochlear implants. For some reason I had thought all these years that it wasn't an option. So, the good news is I may not ever be totally deaf. Well, if I get the implants I won't be. I am still planning on learning sign language. I cannot express enough how much I enjoy using it over straining to hear what people are saying. I find myself kind of checking out more and more in social situations. It's just easier to read a book, close my eyes, whatever, than it is to try to listen to people talk. The Dr. did say that the cochlear implants can help some people with tinnitus and hyperacusis (sensitivity to sound). That's a quasi silver lining.
I started taking boxing classes a little over a month ago. I love it. I am horrible at it, and it's a lot harder than it looks, but I love it. I was told today, however, that I can't spar with people. All I said was I started boxing and my Dr, said NO before I said anything else. Decided training is alright to do, but not against another person. I was never really planning to get in the ring, but I have been sparring a little. No more of that. Still in school, last class is in June. By July I will have a degree in Health Informatics.
UPDATE
Kate's eye surgery is never happening. Ok, it is, but no idea when. Ethan is convinced they are completely ignoring his calls we have called her eye surgeon so many times. Kate is beyond ready to get it done, as are we. She needs new glasses desperately, but they are $400 and as soon as she has surgery, which should happen any day now (hahaha), she will need a different prescription. Ugh!!
Kate and Huck. He's such a sweet dog, who knew I could learn to love a dog! Kate just loves him. He is quiet and playful. Destroys everything in sight, but I'm told that's a puppy thing.
Huck wiggles his tail so hard when he sees the kids his whole bottom half shakes. So stinking cute. Kate is the queen of taking him for walks. I find myself stepping back sometimes and marveling that this is the same girl who was in that rotten body cast. Who thought standing next to her walker was a huge accomplishment, and it was.
On the bright side, Kate is walking really well and running is becoming very natural looking. Kate is seeing her hip surgeon on March 13th to discuss surgery to take out plates and pins in her hips. She is also seeing her back doc that same visit, I believe. Pray for things to be the same. The hardware will likely come out this summer.
Kate is quite tall. She is 8 years old and wears size 12 jeans and shirts. She even wears a pair of 14's. She wears a women's size 6 shoe. Abby, Kate and I all wear about the same size. Completely share clothes with Abby now, I do. Kate is right behind. Crazy.
Kate and Huck. He's such a sweet dog, who knew I could learn to love a dog! Kate just loves him. He is quiet and playful. Destroys everything in sight, but I'm told that's a puppy thing.
Huck wiggles his tail so hard when he sees the kids his whole bottom half shakes. So stinking cute. Kate is the queen of taking him for walks. I find myself stepping back sometimes and marveling that this is the same girl who was in that rotten body cast. Who thought standing next to her walker was a huge accomplishment, and it was.
Kate is quite tall. She is 8 years old and wears size 12 jeans and shirts. She even wears a pair of 14's. She wears a women's size 6 shoe. Abby, Kate and I all wear about the same size. Completely share clothes with Abby now, I do. Kate is right behind. Crazy.
Tuesday, September 11, 2012
Eye Surgery Postponed
So here's the deal. It's been recommended, because of Kate's other health issues, that she have her eye surgery done at Rady Children's Hospital. Dr Heichel, her eye surgeon, does not currently have privilege's at Rady's. He is trying to get them, it's a several month process and he is several months into it, so the call may come tomorrow or 2 months from now. I think it's best to not push the surgery date and have it done at Shiley, I feel better about it being at Children's. No reason other than mother's intuition? Hopefully it will be sooner than later.
In the meantime, Kate is doing really well in 3rd grade. She had two friends over the other day and Kate was a good head taller than both of them. She has mentioned that she is the tallest in her class. It will just be this way through elementary I think. In middle and high school she will blend in better, although everyone will think she is older than she is. Can't win everything.
In the meantime, Kate is doing really well in 3rd grade. She had two friends over the other day and Kate was a good head taller than both of them. She has mentioned that she is the tallest in her class. It will just be this way through elementary I think. In middle and high school she will blend in better, although everyone will think she is older than she is. Can't win everything.
Thursday, August 30, 2012
Eye Surgery Update
Hello everyone,
Right in the middle of my timed Medical Terminology final, I got a phone call from Dr. Heichel's assistant at Shiley Eye Center. They spoke to Kate's cardiologist and it was decided that the surgery should take place at Rady Children's Hospital. The surgery date is currently unknown. I will post when I hear something.
I think this is a good thing. I was trying to give her medical history to the RN at Shiley and I just cannot spew out that much information in a coherent way. The Dr.'s should have access to her medical records at Children's which is nice. And just in case, it's a full scale hospital. There won't be a just in case, but still. Just in case.
Off to La Quinta Resort tomorrow to bake and swim. Have a fun Labor Day weekend everyone.
*Aced my final, by the way. Yay for the little stuff.
Right in the middle of my timed Medical Terminology final, I got a phone call from Dr. Heichel's assistant at Shiley Eye Center. They spoke to Kate's cardiologist and it was decided that the surgery should take place at Rady Children's Hospital. The surgery date is currently unknown. I will post when I hear something.
I think this is a good thing. I was trying to give her medical history to the RN at Shiley and I just cannot spew out that much information in a coherent way. The Dr.'s should have access to her medical records at Children's which is nice. And just in case, it's a full scale hospital. There won't be a just in case, but still. Just in case.
Off to La Quinta Resort tomorrow to bake and swim. Have a fun Labor Day weekend everyone.
*Aced my final, by the way. Yay for the little stuff.
Tuesday, August 28, 2012
Eye Surgery Date Change
| Eye Test |
Today Kate and I went to Shiley Eye Center for her pre-op appointment. We got there are 10, and left about 12:30. They actually shuttled us to the first room pretty quickly, but then the inevitable stall out. They took Kate's vital signs and then we spoke with a pre-op nurse who gave Kate her own little bag to bring back to surgery. It was full of prescriptions that I need to go fill a few days before surgery. She has to have antibiotic drops in her eyes every day for a few days before surgery. The nurse also attached a coupon for each prescription. Can't wait to see how much they cost me.
We then took a little tour to the surgery floor and recovery room where Kate immediately decided that surgery had once seemed like a good idea, but was no longer on her to do list. The anesthesiologist came out and talked to us, aka. me, because Kate had clammed up and was being rather serious about this no surgery thing.
| The ever famous snack stand at Shiley |
Right now she is scheduled to have surgery in the Shiley center, but given her distended aorta, the surgery may be moved to a hospital. We will find out a few days before surgery. They are going to be talking to her cardiologist to OK the surgery. Always a chance we will have to see him before surgery as well.
After the tour we were sent back down to get Kate an EKG and have her eyes measured. The EKG was fine, she is a pro, but she hates those sticky pads like no other. It took a lot of alcohol wipes and patience to get them off without her screaming bloody murder.
And then we sat, long enough for me to really start thinking. That is never good. For months I have been saying how I can't wait for this surgery, for Kate's eyesight to be improved. But at that moment, all I could think about was what if it doesn't go well and she ends up blind. I wanted to find her Dr. and ask him about the odds. Then, of course, I had this whole discussion with him in my head. He couldn't possibly say that everything was going to be fine, they never say it in those words, lawsuits I suppose. So, in my head of course, I started yelling, "but are the odds in our favor?" And then I started thinking about Hunger Games and conversation started sounding like a movie. Thank goodness they came to get us for her last eye test. After we got that done, we were out of there. I was feeling rather guilty about the whole sticky pad moment so we hit the snack shack and ditched the rest of the school day. HA! I know you wish I were your mother. :)
This weekend we are heading to the desert, to swim, get hot, swim, get hot, and repeat until Monday.
Tuesday, August 21, 2012
Eye Surgery and Physical Therapy
Kate went back to Shiley Eye Center on August 10th to have her retina's checked by Dr Goldbaum. She needed to to have her retina's given the go ahead before we proceed with surgery on her lenses. People with Marfans Syndrome are at risk for retinal detachment. The hits just keep coming. Actually, I wish the hits would please stop. No more issues.
Miss Kate had to get her eyes dilated again. The only respite was knowing that after you get dilated, you get to go to the snack cart outside. She chose Doritos, as you can see on her lap. She digs the shades when things get too bright.
Kate has her pre-op appointment with Dr Heichel, the surgeon who will perform her lens replacement. That had first told us that she would have her eyes done separately, a couple weeks apart at a time. Now, because she has to go under general anesthesia, the Dr has decided to do both eyes at once. I'm quite happy with that decision. She will wear plastic lenses over her eyes to keep her from touching them for 24 hours then every night for a week or so.
Surgery is scheduled for September 5th.
Kate is doing pretty well, but she still has some muscle weakness. She is going to physical therapy a few more times to try and build up her strength. I know this picture is small, but she is smiling so cute, I couldn't help but put it up.
School starts tomorrow, 3rd grade! Noah is starting middle school, and Abby is starting high school. So wrong.
Monday, July 16, 2012
Update on The Hips
Busy, busy, and really busy. I took Kate to see her hip surgeon about three weeks ago. I know, terrible. Since then we have been to Utah at the cabin, Bear Lake in Idaho, and a couple days at Disneyland, of course, Legoland, and Sea World. I think that's pretty good. I'd like to relax the rest of the summer, reading and doing absolutely nothing. Well, it's good to have a dream, right?
Kate's Dr. said she is healing well and we just need to continue building up her muscle strength. She did pretty good running around everywhere. Some rides at Disneyland and some of the activities at Bear Lake made her hips ache a little, but overall she is doing fantastic. We were told that she should have her hardware out next summer. Major bummer. I thought we would have a couple years off. Should be relatively easy surgery, as surgery's go, but still, no fun.
I went through Kate's closet and took bags, yes multiple, of clothes to her cousins in Utah. She is wearing size 12 everything. She turns 9 in October. That is a little depressing.
I am planning on making an appointment with a retina specialist this week so she can be checked out to see if she is a good candidate for her surgery. People with Marfans are at risk for retinal detachment.
Took all the kids to the dentist today. I don't know why it didn't occur to me, but because Kate had recently had surgery with hardware, they just did an exam, no cleaning. I had thought about the heart and having them treat her prophylactically with antibiotics, but the hips just did not occur to me. Another call to the Dr to see what to do about that the next time we see the dentist.
Kate has started going to Indian Princess camp with her dad. This last weekend they went to the beach. Kate got up on the surfboard and was a real pro. This is a picture of her at the beach. Gotta love the hat.
We are heading back to Utah the first week of August for South Weber Days. Can't wait!
Kate's Dr. said she is healing well and we just need to continue building up her muscle strength. She did pretty good running around everywhere. Some rides at Disneyland and some of the activities at Bear Lake made her hips ache a little, but overall she is doing fantastic. We were told that she should have her hardware out next summer. Major bummer. I thought we would have a couple years off. Should be relatively easy surgery, as surgery's go, but still, no fun.
I went through Kate's closet and took bags, yes multiple, of clothes to her cousins in Utah. She is wearing size 12 everything. She turns 9 in October. That is a little depressing.
I am planning on making an appointment with a retina specialist this week so she can be checked out to see if she is a good candidate for her surgery. People with Marfans are at risk for retinal detachment.
Took all the kids to the dentist today. I don't know why it didn't occur to me, but because Kate had recently had surgery with hardware, they just did an exam, no cleaning. I had thought about the heart and having them treat her prophylactically with antibiotics, but the hips just did not occur to me. Another call to the Dr to see what to do about that the next time we see the dentist.
Kate has started going to Indian Princess camp with her dad. This last weekend they went to the beach. Kate got up on the surfboard and was a real pro. This is a picture of her at the beach. Gotta love the hat.
We are heading back to Utah the first week of August for South Weber Days. Can't wait!
Subscribe to:
Posts (Atom)





