Misty’s Surgery - More details

17 12 2005

Staples removedI have attached 2 pictures; one with my 29 staples being removed on my mid left backside, other picture is what my spine was taken right after surgery was done. It will be there permanently.

Back X-ray - amazing!The procedure is called a left thoracotomy for L1 corpectomy and fusion with instrumentation. The L1 which was fractured and compressed spine was removed and inserted a rod with fusion, He inserted titanium bridge on T12 and L2 to keep L1 rod in place permanently.

For more detailed information on my procedure, click that website

I hope you found it very interesting!  Happy Holidays!!!!

Misty Laird

Grant W Laird Jr.
http://blog.grantlairdjr.com

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Misty’s Surgery

12 12 2005

Hospital #2My wife Misty had her back surgery on November 30th at Presbyterian Hospital in Dallas. She was supposed to have surgery one month earlier but decided to postpone due to death in family.

It turned into a nightmare than I expected – maybe I was expecting a lot less than I thought.

Her neurosurgeon doctor originally said it would take five to seven days before she can go home. The surgery itself took five hours long and it went very well. For some reason, the doctor was concerned about her because of lack of blood volume her body had, she was sent to ICU room for pain management and blood transfusion just for one night with her mother.

Hospital #1On Thursday, we finally moved upstairs on 8th floor next day. I agreed to stay overnight to keep her company and help whenever she need like drink or talk to nurse since she have hard time reading paper while she was on morphine. (Pain killer, antibiotics, etc.)

My sister in law agreed to stay overnight on Friday evening. I did stayed few hours during the day but spent all night with her rest of the week except last two days. My mother in law stayed during the day time so she can help communicate with nurses, doctors and another staffs.

It has become a concern because we didn’t want to leave our teenager girls and dogs alone at home too long. Misty understood and she had to deal herself alone overnight on her last day.

On 9th day, we were eagerly waiting for doctor’s decision to send her home or not. Due to difficult time with her bowel movements and left shoulder pain, she stayed longer than we expected. Social worker, therapist and doctor suggested her to move to next building for additional five days for more therapy – however after we had lengthily discussion with them, they agreed to sent her home. They will send someone to come over my house and help her with physical therapy and other things.

Hospital #4At this point, I am sick of the hospital already and excited that Misty was coming home finally after 9 days. This is longest week I ever had – I even called in time off from my work.

Other things… we did have interpreter from DAC of Dallas on 1st day but unfortunately, she wasn’t with us during pre-surgery preparation because she was in the wrong floor and one of the staff told her to wait / cannot see us because we were already inside pre-surgery room. It was rather a very disappointment.

After the surgery finished, our interpreter was able to stay and do her thing with Misty before she left at 4:00 PM. Lucky, a social worker who handle interpreter requests has an email address, I was able to get in touch with her and ask for interpreter again next day. Since it was a last minute, all they can get us is 3:00 to 5:00 PM. I am glad we get something out of it anyway. Social worker also brought us TTY in box – we laughed but said nothing. Of course, we did not use it at all. They don’t have any public Internet access anywhere – lucky I have my PDA with Bluetooth. I was able to get online with my laptop from time to time.

Hospital #3Also, I saw TTY phone in surgery waiting room and it wasn’t working at all!! I also saw couple more TTY phone at main lobby and elsewhere. It looked nice but pretty much useless.

All those 9 days that I observed a lot of things going on in Misty’s room. As you realized that my father in law were staying at same hospital about one month ago before he died at home. My family is pretty familiar with that same hospital. I hate to say that but I’ve noticed many nurses are either lazy or not following doctor instruction in all shifts. Of course, most of the times, they did OK.

For example, our doctor instructed that Misty need to change her position every 2 hours to avoid bedsore and as well as leg massage pump – nurses or other assistance did not do it at all. Next day, doctor visited us again and he found out that nurses did not do it; he wasn’t too happy and instructed them again what need to be taken care of.

Hospital has a weird policy – Misty has few prescriptions that she has to take daily. Since she’s staying at hospital, she’s not allowed to take it. They will special order it for her everyday. Can you image how much it would cost our insurance for all small stuff including medicine?

With our insurance, they gave us portable potty chair, walker, shower chair and rental wheelchair. Apparently, our hospital has a contract with Walgreen and they delivered the goodies to us at Misty’s room before we went home. It’s very nice.

When we were leaving, they gave us few different prescription lists for home. We went straight to CVS store near my house to get those filled ASAP. Unfortunately, they can only fill out 4 out of 5 – one of them is for pain killer. They are out and it was really irritating me.

My mother in law quickly called another CVS store and found another store do have it in stock. At this point, I told 2nd CVS store that I had to come because another store ran out of this medicine and I already had to wait one and half hour for it. They said too bad, come back in an hour because they have too many people in line. Sigh… I did check Wal-mart pharmacy too see if they have it since nobody is in the line but they doesn’t have it in stock.

As of today, she’s managing okay – I know she’s very happy to be home again.

Grant W Laird, Jr.
http://blog.grantlairdjr.com

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Dad-in-law

20 10 2005

Misty wrote short letter about her father:

Due to my Dad’s situation, he will be going home today with only one hour nursing and hospice care. Mom needs my help next couple of weeks. I have decided to cancel my surgery on 26th. I plan to reschedule for end of November. I will let you know as time approaches.

Christy (my sister), Carla (my mom), and I had a very LONG weekend with my Dad. He was taking chemo and after 7 days out of 10 days of treatment, his white blood cells count was dropping a lot and that was the sign it was not working for the tumor. Last Friday, we had a talk with his Dr and asked Dad if he wanted to continue the chemo. Dad said he wanted to stop it which we honored. We decided to wait until Monday this week to have another MRI. Unfortunately the tumor has grown by the stem, the Dr saw another new spot but is uncertain if it is a tumor. Without any treatment the tumor will continue to grow.

Where the tumor is located is causing him to be so sleepy, difficulty in swallowing anything, speech problems, weakness, clumsiness, confusion, etc. It is not operable or accessible where the tumor is located. He also has developed a blood clot in his leg which is being treated with a certain blood thinner.

Dad has not been eating since September 20 except for few ice chips. He has been on TPN (nutrition IV which we call milk shake because it is creamy white stuff) daily. Mom, Christy and I have to decide whether to keep him on TPN to keep him around for a while or take him off the TPN and he will eventually go sooner. It has been extremely difficult for us but we are trying to manage and make the best decision for him. I wanted you aware what was going on.

Thank you so much for your continued support and your thoughts and prayers.  –Misty Laird

Hopefully, everything will be okay. Only time will tell us…sigh.

Grant W Laird, Jr.

http://blog.grantlairdjr.com