Getting Ready for Mardi Gras

by Greta on January 27, 2012

I can’t believe this is going to be my 6th Mardi Gras season here. We just re-financed out home, and “permanent resident of the greater New Orleans area” has a nice ring to it! Coming out of my fog from my dad passing, I realize I have so much to do to get ready for Mardi Gras and the kids’ Mardi Gras school vacation (yep – they get that week off). My cousin asked me if we decorate for Mardi Gras – yep sure do. I have a few things outside – totally bush league – but am trying. Inside I display all the cool throws and doubloons we have collected so far (still need to do that).

Now for the checklist

* Weight to lose before parades and balls begin – check (phew). I tend to gain more weight than the holidays during these festivities due to good food, adult beverages and my love for King Cake.

* Gowns – check – (got 2 consignment shop steals I adore).I think we are only planning on one ball this year and that works for me.

* Spanx – check

* Ball tickets – check

* Wagon to haul stuff to parades – shoot – ours broke last year and was shot out at the firing range. Gotta get a new one!

* Make plans to hit parades with friends and their families…must get on that.

Yes, folks…my kids will be at all the parades with me – it is very family oriented! Not all the 3 kids love parades equally, but all have a great time once they are there. As for hubby…he would skip parades, except the one he rides in if I let him. Nope -he never gets off the hook and always has a wonderful time!

Laissez les bon temps rouler! (Let the good times roll).

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Caregiver Void

by Greta on January 20, 2012


Caregiver: a person who provides direct care (as for children, elderly people, or the chronically ill)

Void: an empty space; emptiness

My father passed away peacefully in his sleep on January 8th, 2012 as a direct result of Alzheimer’s Disease. For the 6 months leading up to his death, we took him into our home (my hubby, 3 kids, dog and 4 cats) and I became his primary caregiver. We had some help along the way with hired sitters during weekdays and an occasional weekend night, but for the most part it was me. When someone says they are caring for someone 24-7, they often mean it. Dad could not be left alone at all in the house at all or unattended for without checking on for very long. If he was in a room, someone, even one of my kids, was in there with him as much as possible. It was difficult to get him in and out of my car, so running to pick up a kid from an activity or grabbing an ingredient from the grocery store, became a challenge. Thank goodness my fabulous husband, understanding and helpful kids and friends were there to pitch in when a sitter was not available. The household priority became caring for Dad, no regrets, we all changed, became a team and moved into this role with ease.

For those who do not know, Alzheimer’s patients often get all messed up regarding sleep. Sleep pills that would knock an elephant out, did not necessarily make a difference on Dad. Nights became a whole new part of my day. As I adjusted to lack of sleep when the kids were babies, I somehow survived on broken sleep the entire time he was here. My body and brain accommodated and my need to do extra things changed. Things that may have once seemed urgent to do, often dropped low on the priority list. Before he arrived, I worked out 6 days a week, dropped to 4-5 days for 5 months and pretty much stopped exercising the last month. Once someone with a very active social life, my family watched me transform into a homebody, often found on the couch next to dad with a book or watching TV with him. I turned down a gazillion invitations for media events, get-togethers in New Orleans (40 minutes away), parties, lunches etc… but told people to keep inviting me as this was only temporary. From being on the go all the time, I huddled at or close to home with my family and close friends during the past 6 months. I transformed into a different version of me that was created out of the need to take care of others first.

Early in December, Dora, Dad’s full-time weekday sitter passed away unexpectedly. We became extremely close and were happy to see each other each day. If Dad was still asleep, we shared a cup of coffee together and chatted away. After she passed, I caught myself looking for her, preparing extra coffee for her and even called out her name (could have sworn I heard her walk in). Her final gift to me was preparing me for things to come with my father as habits are hard to break and I truly missed her. Since his passing, I have found myself going to check on him often and running errands in a hurry to get back to home-base. Will I go back to my previous lifestyle? Probably not…but a happy medium. Not that I consider that a bad thing at all, we all change throughout our lives, hopefully for the better.

I have done what I hope is most my personal grieving, been to his funeral and have a small ceremony planned with the Hospice Chaplain this weekend for the family. I have shed more tears than I expected to, but am truly at peace that he is at peace. I am back to sleeping at night now (after a few days of Ambien), working out, and have gone out a few times with friends and hubby. Knocking off the to-do list is actually happening, though “important and necessary” has taken on a whole new meaning. Life is a gift, each moment is ours to make the best of it. Time to move forward without Dad here physically and cherish the memories. He would have wanted it that way!

And for the record, writing and sharing this journey through social media has been cathartic. I can’t thank you enough for all the support and kind messages along the way. My goal was to help even just one other person and I think that mission was accomplished. This journey truly helped me to become a better person…THANKS DAD!

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Mensch

January 13, 2012

Not sure how it happened, but somehow my entire life I have been blessed to be in the presence of many men who could unequivocally be called a “Mensch.” So…what is a Mensch you might ask? Jewish Healing pretty much sums it up by saying: A mensch literally means “a person” in Yiddish, but figuratively [...]

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Memories Linger On Forever

January 9, 2012

For the past 6 months, I, along with my loving husband and 3 wonderful children, had the honor of caring for my father, Sherman Marcus on the final leg of his life journey. Alzheimer’s Disease is difficult, but we all made the best of it each and every day, spending quality time with him, smiling [...]

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Hospice, Dying and Smiles

January 5, 2012

We are all going to die – how, where, why and when are the unknown we live with from day to day. Dying naturally does not have to be depressing, sad maybe (if you choose to see it that way)…but not depressing. This is why we are reminded over and over throughout our life to [...]

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Alzheimer’s and Houdini Magic

January 2, 2012

This is Dad’s new addition to his face, compliments of his Houdini abilities! Alzheimer’s Disease is by far the most unpredictable thing I have ever encountered (besides my mood off my hormones LOL). I look at all the stages that have been studied and seem to have created some new classifications via Dad – Zaydeh [...]

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The Zaydeh Zone

December 29, 2011

My Dad, known as Zeydeh to everyone (Jewish Grandfather for you slow kids), has happily entered in his Alzheimer’s Disease, what we now refer to as the “Zaydeh Zone.” In a previous post I wrote about his end of life “working.” The “working” post was referring to him overriding all his sleep medications and staying [...]

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10 Things I Have Learned About Hospice

December 23, 2011

Yep, we are in full-swing with the “H” word and things are running as smoothly as possible. My previous post on hospice (a damn good post if I must say so myself – so go read it!) talked about how I would embrace it and not fear it when it came. Dad turned 83 on [...]

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Singing Ay-oh, Spin the Dreidel

December 20, 2011

From my house to yours – Happy Hannukah! Thanks to Barbara Miller for this one:)

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End of Life Alzheimer’s Work

December 13, 2011

Dad is sinking more and more into his happy world and away from us. I view Alzheimer’s Disease as a process of unlearning and unpredictable firing of the brain. As time goes on, his brain may have unlearned many of the things we take for granted, such as chewing food or putting on glasses, while [...]

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