NOTE: This blog is now available as a book with added comments and thoughts. It is a fundraiser for MSA research. Please consider purchasing either a kindle version from the Kindle store @$3.99, the Paperback version at Amazon @$19.99 and letting all your friends and family know. We can help find treatments and a possible cure for MSA and other alphabet diseases! It can be purchased here.
Also visit my original, "all-purpose" blog http://www.justsomeposts.blogspot.com/

Sunday, June 12, 2011

Thanks

I wanted to take a moment to thank all the people from around the world that offered their condolences. I greatly appreciate your thoughts and prayers. The pain has been made easier to bear by the kind words.

I am not sure yet what I am going to do with this blog. I will see. If anyone has any questions or thoughts they would like to share or ask, please do so.

My best to any and all afflicted with or affected by this horrible disease (or any of the alphabet diseases).

Again, thanks,

Scott

Sunday, June 5, 2011

Laugh, Live, and LOVE

This past week has been a surreal experience. I have had the unfortunate experience to lose many family members over the years including my father, but nothing has been close to this. I have had many, many thoughts - as I have stated here before, I am more "creative" when emotional (as you can see in the previous posts from the past seven days).

Here are some thoughts on life:

Probably the biggest advice/most important thing I can pass along is amost a tired cliche - live every day as it is your (or your loved one's) last day. Although my wife had a terminal illness, I thought we had time to do and say what we wanted. If you have something you have always wanted to do, if there is any way you can do it (or a close substitute) financially - I recommend you DO IT! If there is something you want to say - same advice - SAY IT! Besides the loss of my lifetime companion, things left undone or unsaid are the hardest for me. This is especially true if these things are simple things. You may want to go for ice cream. If you are a caregiver for someone that cannot move well, that can be hard. It is easier to say to yourself (or your loved one) - "We will do that tomorrow". I used to tell my kids (in fact we had a little chant that I bet they remember) - tomorrow never comes. By definition that is true - yesterday's tomorrow is today. So, waiting for tomorrow is fruitless in many ways.

Try to find something to laugh at. This one was probably one of the things that my wife and I did the best. She had a great sense of humor and I and am a reknown idiot. I do remember we laughed at many things last Saturday (her last day conscious). I am very glad for that. Oh, there were days we wept togther as well. I feel that is important too, but laughter is great for everyone involved. Try to find something that can make you laugh, as often as you can.

Involve family and friends. I feel my wife and I left this one a bit short. It was so easy for us to withdraw and just have each other. That is great, but it means two people are trying to "recharge" each other. When you get run down and depressed, that can be impossible. I believe the most important thing you get by contact with people that love you, and you love, is strength. We all need to be recharged with love, faith, and friendship to make it. Our internal "batteries" can only go so long without a charge. Like I said, if both of you are low on "juice" that will not happen. You are running on empty. The first two points above can help recharge to a point, but ultimately you need other people to pull the "power" from. Our kids and family were close, but see point one - everyone thinks there is going to be a tomorrow to visit. If you are the caregiver, remember YOU need recharging. This is probably the area that I was most remiss in. I felt like I needed to be with my wife every moment I could. Don't get me wrong, I am greatful for every minute. But, going back to point one, I wonder if I had stepped away occasionally if I would have had the strength (or drive, or gumption, or whatever) to take my wife out more, even if it was just to ride around. Caregivers, take care of yourself. I know I am not the first to say that by any means, but it is important enough to repeat often.

Tell those you love that you love them - do it often. Then repeat. 'Nuff said.

As a follow up (and maybe conclusion) to the above points I will get personal again. We have had family and friends around all week. We have had food enough to feed small countries. We have cried together and we have laughed together. All of that has been wonderful In fact, I do not know how I would have made it through the week without it. However, my wife (and I) would have LOVED to have the people, the food, and the fellowship when she was alive. If you know someone that is suffering with an illness, especially if they are limited in movement - go see them! If they are family, you are REQUIRED to! Any of the gatherings we have had this week, had they happened last anytime in the previous weeks, would have thrilled my wife (and me) to no end. If you know a family that is going through something like mine just did, take them a meal or a dessert. Drop them a call. Send them a card. Offer to go shopping for them. I am lucky in that I have six children that all live fairly close by and they helped me with this, but we still did not get everyone together and commune like we have this past week. Like I said, my wife would have loved it, as I am sure most people in her condition would have. Make a point to contact them.

Enough for now. I realize I got a bit "preachy". Sorry. I do feel strongly about this for obvious reasons. I hope I can live up to my own words as I go forward.

Saturday, June 4, 2011

TEARS

As I wipe my eyes again
I know,
I'll never be the same.
I think I'm done, 
but they can well back up
whenever I hear your name.
Sure
I laugh at things.
But it's more for them than me.
I wonder if life will ever seem
the way it used to be.

Thursday, June 2, 2011

Obituary

Carol's obituary -

Carol Poole

Carol J. Condon Poole of Winston-Salem, 56 left her wheelchair behind forever Monday May 30th after more than five years battling MSA (multiple system atrophy). She departed after a final selfless act of organ donation with her loving family by her side.

Carol was born in Pennsylvania to Marlen Condon but grew up a true Florida girl in Plantation, Florida. After graduating from Plantation High School Carol attended Western Carolina University where she met her husband-to-be. After becoming a certified operating room technician at Presbyterian Hospital in Charlotte, N.C., she went on to become a R.N. Carol was retired on disability from Forsyth Medical Center where she worked in the operating room for over ten years. Carol was known at work for her compassion, professionalism, and sense of humor.

After WCU, Scott Poole and Carol were married. On May 16th they celebrated 38 years together as husband and wife. Carol was a loving mother of six children – Christi Waiters, Kimberly Bowers, David Poole, Stephani Poole, Patrick Poole, and Bailey Poole; and a grandmother to Hannah Byerly, Landon Byerly, and Alyson Bowers, all of the greater Winston-Salem area. She was a doting Mom and Nana to all. Her love as a wife, mother and grandmother was endless.

Carol is survived by her above mentioned family as well as her mother Marlen Condon of The Villages, Florida, and her twin sister Karen Parsons and her family of Summerville, S.C

Carol's life will be celebrated on Thursday June 2nd at the Regency Ballroom of the Quality Inn & Suites 2008 S. Hawthorne Road. W-S N.C. from 6:30 – 8:30 pm. All that knew her are asked to come and share your memories and listen to others share theirs. Food and beverages will be provided. Dress as you wish.

In lieu of flowers, please send donations to:

Team Carol

c/o Trinity Center

640 Holly Avenue

Winston-Salem, N.C. 27101