Damn Pride (vacation tips)

risingpheonix1

photo courtesy of shouldersdown.com

Going on vacation can be challenging with autoimmune issues (even without wrangling kids). I have learned that to have the best experience, I have to sink my pride. Yes, I do feel a little guilty when I see other people with disabilities who do not ask for or use some of the conveniences or features I do, but I do these things so I can have fun with my family – the cost to my pride is nothing in comparison. In fact, I use some of these conveniences in everyday life for the same reason. Quality time with my loved ones trumps pride every day.

 

My packing list consists of the same as most people – and then I add:

  • Medicine: everyday meds, standard prn meds (pain, muscle spasms, migraines, acid reflux, sleep, restless legs, sry eyes, dry mouth), and “vacation meds” (OTC meds for common ailments like indigestion, motion sickness, other vertigo, constipation, diarrhea, immune support, sinuses, cough, vomiting, sunscreen, aloe for sunburn, benadryl, neosporin, lip balm). And anything else I can think of on the way out the door that might be unique on that day – plus a rather robust first-aid kit.
  • Support: cane, wrist braces, elbow wraps, ankle wraps, knee wraps, thumb stabilizers
  • Food: meals and snacks for every day, even to carry into events and on plane given food allergies and other dietary needs
  • Drinks: water bottles (usually a case if traveling by car, if not, buy there), sports drinks (for electrolytes, may have to buy at destination), liquid flavors
  • and then just adapting the normal things:
    • Clothes: easy fastening (minimal buttons and zippers), multiple matches, extra underclothes, minimal needs (ironing, etc), sun blocking, layers, socks for support, compression, and minimal irritation (diabetic socks without toe seams, etc.)
    • Shoes: easy on-off, various heel heights, support (not that much different from others)(in fact, I rarely buy shoes with buckles to fasten)
    • Bags: multiple sizes and types for carrying stuff on the go, with multiple ways of carrying them (shoulder straps, backpacks, hand carry), 4-wheel rolling, etc.

But where the pride comes in is using a wheelchair at large parks, asking for the disability pass for rides (hard to stand in lines or up/down stairs), and asking for things in accommodation – not too far from elevator, can they use sheets without detergent or special detergent (allergic to many), asking for no cleaning chemicals (allergic to many), etc. (Note based on recent events: I do not ask for the haunted room!)

This vacation, I went to an amusement park and did not get a wheelchair or disability pass. I have been walking 12,000 steps a day and doing wonderfully. I thought I was well enough if I took precautions. I was not. About half-way through, my back, hips, and knees started locking up. I took it easy, used my cane, sat in shade, wore hat, took multiple breaks – and still no good. We had to leave about 1 pm because the body gave out. Had I sunk my pride, used the wheelchair, and got the pass, we could’ve stayed longer there, and I also would still have been able to function the next day.

I do get dirty looks from people (we’ve discussed that before), but pride goeth before a fall. I fell. Not literally this time, although it does happen relatively frequently given my balance and vertigo issues, but my issues ruined the day and I had been looking forward to this vacation for quite some time.

My advice is screw the pride. Determine what is most important for you – spending vacation with loved ones or being embarrassed by energy-conservation efforts?

This also works in daily life. I use the disability placard even if I feel okay, because 1) I may not feel okay in an hour (or less) and 2) it conserves my energy to use for other activities. Saving a little here may be all it takes to be able to go to supper with friends. And I do work to keep myself in good shape. Part of that is knowing where to bend before I break. I believe that learning to conserve energy and being smart now may mean that not only do I see benefits in the short term (being able to go to more events or be more active), but it also adds to my long-term quality of life. It cannot be good to lock up my back daily. Maybe if I prevent that, maybe the back lasts longer. I don’t know, but I believe.

So damn the pride! I choose to enjoy life, not pain!

 

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