Tuesday, September 29, 2009

Fashionista has left the house

For years I've enjoyed the ins and outs of fashion. I appreciate the "Project Runway" motto, "One day you're in, the next day you're out". My only purpose in watching the Emmy's Grammy's or Golden Globe, was to see who was wearing what and did they look good in it. Did they make a good fashion choice, or would they go down in fashion history as the woman wearing the swan dress for the rest of her life. Even God cares about clothing. In Exodus God told Moses what the priests should wear in His tabernacle, and how the clothing should be decorated as well. So why not have a healthy appreciation for design and fabric. I have always enjoyed shopping for trendy clothing that fits in my budget. If I couldn't afford the designer version, I would find a well made copy, and feel good about the money I saved.


So you may be wondering at this point what any of this has to do with Dysautonomia. Well..... before I was diagnosed with dysautonomia I enjoyed going on long shopping trips at the mall and keeping up with the latest trends and dressing up. Things have changed quite a bit since my diagnosis.


This Summer shopping is no longer something I can physically do without major planning. Since I'm heat intolerant and cannot be in temperatures over 75 degrees for more than a few minutes. All shopping trips have to be made in early morning or late evening. Since I am usually exhaused after 6:00pm evening shopping is out, and the malls usually are not open till 10:00 am so often a shopping trip in the morning is out as well because of the heat. Long distances are out because I get tired just walking across the parking lot. Forget about comparison shopping, I only have energy for one store, if they don't have what I want too bad for me.


This Summer I received a catalogue from one of my favorite stores. They were having their anniversary sale, and were opening at 8:00 am Woohoo my first outing in weeks. But before I could take this glorious trip to my favorite store I would have to make a plan of action. So here it is;


* Look through the catalogue for all items I want.

* Make a map of where items are in the store and the shortest distance from point A to point B.

* No deviating from the map! If I do;

a) I may not have the energy to complete the list.

b) I may not be able to get back to my car with the ability to drive home.

c) The store may have to call a wambulance because I've passed out from too much shopping.

* Plan where I'm going to park,

a) It must be shaded because I may pass out in the car if it's too warm inside.


b) Park close to the entrance, I may never make it inside if I pass out from exhausion before I
even get in.

* Hit the shoe department first it's right next to the entrance.

* Show the salesman the catelogue with the shoe, I'll be wasting energy looking for the shoe
myself.

* Try on the shoe, don't stand up I may get dizzy and be mistaken for being under the influence
and be escorted out of the store.

* Give the salesman my credit card, and ask for the transaction to be made on the salesfloor, too
tired to stand in line.

* Going up the escalator, hold on the vertical movement throws my heart into tachycardia!

* Quickly move aside for those aggressive anniversary shoppers and hold onto a railing till my
heart slows down to normal.

* I'm pooped, find a saleswoman to find one of the items in the catalogue.

* Found someone woohoo, and she happens to be a personal shopper.

* At this point I'm out of breath, and bless her heart she takes over.

* Personal shopper takes my catalogue and gets my sizes and walks me to a dressing room to
wait for her.

Normally at this point I would be taking great pleasure in choosing my garments, but now I'm just thankful that I might be able to complete all my shopping without an EMT being involved.

* I try on all items brought to me by my new best friend (personal shopper) with spuratic naps
on the most comfortable dressing bench I have ever layed my head on (which was none until
now).

* My new best friend (personal shopper) rings up my items while I'm napping on the dressing
room bench.

* Give new best friend (personal shopper) hug, and head downstairs.

* Relive previous trip on the escalator.

* Cover my face as I pass perfume counter, my new sensitivity to scents may cause breathing
issues, which would most likely be followed by all other dysautonomia symptoms. Avoid
EMT at all cost!

* Head for the car.

* Head for home.

* Bribe my children to bring in shopping bags.

* Take a nap.

* My body will probably pay for this trip for days.

I've come to realize that shopping is just too much work, and catalogue shopping can be almost as satisfying, but I will miss my new best friend (personal shopper). I wonder how she's doing.

Dysautonomia has also pushed my fashion savvy a bit. I've gone from donning my favorite designer, to donning an ice vest, compression stockings and a big black umbrella. I'm sure I'm quite the fashion statement during patriotic observance at my school. I can just hear the teachers in the staff lounge "Wow, did you see Michele in that fashion forward icevest, I wonder who designed it and if they have it in my size", NOT!

The icevest does have it's payoffs though. the other day one of my students gave me a big hug, and wouldn't let go. I tried to get her to let go and head into class, she said "ohhhhh do I have to Mrs. McGough, you're so cool!" Next thing I know half my class is trying to cool off by giving me a hug. Who says teaching doesn't pay!





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2 comments:

  1. Ah Michele...I had to have a little giggle at this one..My Hubby is my bench, i can't believe you wrote about this :0)We have what you call the Royal Melbourne Show, i am still a big kid at heart, so my hubby & son took me, it's like a festival, show bags, animal's & much more & a very large area..I did have fun, but in saying that, i sat walked, sat walked and sat an walked, my hubby was propping me up as we had a long walk back to the car and all i can say is yet again i have spent three whole day's on the couch paying for my few hour's of fun.The only word's i can say are exhaustion, beyond imagination & saw body joint's, that are just unexplainable & terrible brain fog...
    So you hit the nail right on the head yet again,all the thing's that i loved & so simple are now sooo hard & everything has to be planned ahead of time..
    These blog's are such a blessing in disguise, to let other's with this illness, know that they are not on there own, with the way we have to change our live's to live with Dysautonomia....
    Thanks' Again Michele Awesome... :) :)
    Trace!!!

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  2. Hello Michelle,

    I just found your blog. Boy, this post is incredibly comforting to me. I am simultaeously relieved AND sorry that what you are going through is so relatable to me--meaning, I wish you weren't going through it. But, thank you so much for sharing your experience with me. I just got diagnosed in April and have yet to be able to see a dysautonomia specialist. I've lost many friends who thought I was "faking" or just think I'm depressed. Reading your post makes me realize that someone really understands.

    Again, I thank you.
    Betsy

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