Archive for the ‘Personal Activities’ Category

Coping With The Holidays

Posted by Kelli on December 21st, 2009


Coping With The Holidays
By Kelli Ellis

I am my own worst enemy. Like many others with Fibromyalgia and Chronic Fatigue, I find the holidays a highly stressful and painful time of year instead of the joyful and happy time it should be.   I am too focused on the perceived expectations of others instead of the reality of my limitation and restrictions..  I know many of us want to accomplish what our bodies are simply not capable of, so we have to adjust our outlook and re-evaluate our priorities. The holidays are all about spending time with those we love most – keeping time and energy for what we hold most precious and dear. Doing so will help reduce the stress and thus the pain and emotional issues that crop up at Christmas.

Pace Yourself.. 
When you think “I’ll just  visit 1or 2 more shops, go up 1 or 2 more aisles, wrap 1 or 2 more presents, bake 1 or 2 more trays of cookies or do that 1 or 2 more things.” – Don’t! Stop before you get to that tired or hurt point. Don’t deal with a fibro or cfs flare, prevent one.

Decorate, but not too much..

  • Have a smaller tree with few decorations.   I have invited over the nieces in past and we made an afternoon of putting up the tree.

  • Have someone put up the outdoor lights.
  • Get a nativity scene that is pre-made as one unit and/or lightweight, so you don’t have to lug many pieces.  I have a smaller plastic Precious Memories one (which the kids love to play with) and a small water fountain of Joseph, Mary & baby Jesus.
  • Celebrate

  • Choose carefully to go only to 1 or 2 holiday parties, don’t accept every invite.

  • If you can, spend time with those you hold dear, not those who will cause stress.
  • Plan ahead how long you plan to stay and stick to it.
  • Always keep a supply of regular meds on hand, in case.
  • Delegate

  • Pass on some of the holiday chores to others so that while everyone shares the joy, they also share responsibility.

  • Cooking

  • Share these responsibilities or making an easier selection.

  • Do a pot luck dinner.
  • Choose a one dish dinner to limit the number of dishes.
  • Choose easier recipies.
  • Prep or make whatever can be done beforehand and refridgerate or freeze.
  • Keep to your normal eating habits as much as possible & do not overdo it on sweets and other foods.
  • Baking

  • Do a holiday cookie/snack exchange.

  • Bake cookies in stages – many recipes require overnight in the fridge.
  • Cheat – buy your cookies.. I know, not the same, but nothing’s the same anymore, is it?
  • Shopping

  • Online/catalogs/mail order gifts.

  • Gift cards & gift certificates.
  • Plan ahead, make a list & write it down.
  • Organize your trips into several short shopping trips.
  • Shop in the morning, or later in the evening when the crowds are thinner.
  • Start early – once I started on Dec 26th.
  • Take regular breaks to rest.
  • if you use a mobility device (cane, crutches, walker), take it with you even if you don’t need it yet
  • Use a shopping cart for stability, to carry parcals & outterwear.
  • Use a coat check if your mall has one so you don’t have to worry about your jacket.
  • Get salespeople for help if you can find them.
  • Always keep a supply of regular meds on hand, in case.
  • Wrapping Presents

  • Wrap using gift bags & tissue paper.

  • Take advantage of on-site wrapping services – many are for charity.
  • Holiday Cards

  • Do them well ahead of time like October or November,

  • Make labels so you’re not writing address after address, if even it’s ony the return address.
  • Above all – KISS! Keep It Sweet and Simple!

    Posted via email from Kelli’s Posterous

    Good Day

    Posted by Kelli on June 20th, 2009

    Today was a good day, physically speaking. Today was the Lacrosse Day of Champions for my step son’s Lacrosse League. Rob coaches 2 teams & is the House League Director.

    My day started very early, so last night I was in bed before 9:30 – unheard of when I’m not crashed out. This morning I rolled out of bed at 6:10am – amazing accomplishment considering I don’t normally get up til noon. Got dressed & packed up & out the door to get the van we were renting for the day. Finished at the Rental agency by 7.30. Head up north to the arena ( I live 20km/12mi from the arena) to drop off the other half. Off to pick up my stepson & grab breakfast & back to the arena by 9.30am. Help unpack the van.

    I take a few minutes to watch the Peanuts play (those are the little anklebiters) & then off to be girl friday (even tho it’s Saturday).. Most of the next few hours was spent between doing some in-house tasks & sitting down to read. Oddly enuf, I was *still* doing good.. No pain, no fatigue.. So, at 11.30 I drop off my step-son & get my lunch. I come back by 12 & eat while Rob’s on the floor coaching the Novice kids.. He’s just bouncing off the walls in enthusiasm.. I had to run (yes, run-or as close as I can get to a run) to the change rooms to get an Ice pack for an injury – twice (yes, twice) When his game finishes, I head out to pick up his lunch while the third novice game is on to see who wins. I’m back shortly after 1pm & decide to head to his parent’s place for a nap.

    So I’ve been a busy body with bits of activity & bits of no activity, but no real “rest” periods, not like my doc wants (I’ll explain rest to ya’ll another time).. But I’m still not having pain.. & not the devastating fatigue of the CFS.. What I haven’t done by this point is taken my meds… at 12 noon, I am supposed to take my codeine contin – 12 hour release that I take at 12 noon & 12 midnight.. So, no wonder when I wake up form my nap & I’m sore and achey and still & starting to hurt.. *this* is when I realize I haven’t taken my meds. Of course, where are they – the arena.

    When I get to the arena Rob’s ready to go.. immediately loads up the van & off we go – no real time for me to take anything.. with a detour to Dollaramma & I fergot about my meds again.. So I don’t get my meds until dinner – we hit the Keg on the way home and while waiting in the bar for our table, I take them.. 5 of ‘em.. ya, that’s a small chunk of medication. But interestingly enough, I’ve started to feel better after I had gotten moving around.. And interestingly, My leggs didn’t ache when I got up from sitting at dinner like they normally do.. When I sit for extended periods, like a social chatty dinner that lasts almost 2 hours, then ya, the leggs are usually difficult to get moving..

    So, now we’re home, the van’s unpacked, I’ve got the overnight info for parking the van cuz we’re not going to take it back tomorrow morning. I’ve gone on FaceBook & Feed my virtual roses.. I’ve done a blog post & now writing this one at almost 11pm and I am still going.. Where’s Rob? Crashed out on the bed. But I am heading to bed soon too..

    But it’s been a good day… Am I gonna feel it tomorrow? Unfortunately, yes.

    Categories

    Posted by Kelli on May 24th, 2009

    The sole purpose of this post is to create, and potentially modify categories for this Blog. Initially, I had this categorized list.. Three columns, each with the appropriate title.. That was until I realized, well, I needed a new category.. I don’t have room for 4 columns, so I gave up on that idea . I’m just gonna put ‘em in alphabetical order and then add later as needed.

  • Ability/Disability, Allergies, Alternative Medicine, Alternate Treatments/Medications, Articles, Assisting Devices, Auto-immune disorders, Awareness Ribbons, Anger
  • Behaviour
  • Chemical Sensitivities, Chronic Fatigue Syndrome/ME, Cognitive Limitations
  • Depression and Mental Health, Disability funds [CDN], Disability funds [US]
  • Endometriosis, Exercise, Emotions
  • Fatigue, Fibromyalgia
  • Goodsearch.com, Grooming, Gender
  • Hypo/Hyper-Active Thyroid
  • Intro, Irritable Bowel Syndrome
  • Legislation [CDN], Legislation [US], Links
  • Medications, Memory Impairment, Music
  • Non-medical
  • Pain, Personal, Personal Activities, Physical Limitations, Physicians, Possibilities, PuppyDog
  • Quotes
  • Relationships, Research, Restless Leggs Syndrome, Rest
  • Spirituality/Faith, Spoon Theory, SleepSupport, Stress, Supplements
  • Tips, Twitter
  • Vent
  •