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Turmoil ensued in my life following this declaration of my inadequacies. Secret, closed door meeting followed...the pathways between cubicHells were abuzz. I lost sleep. OK, I exaggerate a bit (when HAVEN'T I?!?). But there WAS a lot to find out and prepare for if I really WERE going to publicly announce my inadequacies to my employer and not simply drift out to the freeway with my cardboard sign.
AKA, REQUEST FORMAL ACCOMMODATION AS PROVIDED UNDER THE AMERICANS WITH DISABILITIES (ADA) LAW.
So, due to the secretive nature of all government agencies (and my own, frank paranoia of such), I really can't say much more about my ADA request here (not even in sarcasm and jest, should this blog be pulled into court at a later time!), but I WILL inundate you with trivial information about my PAIN. Aren't YOU the little luckies, my preciouses?!?
I met in person with my neuro ARNP (I know?? How odd I would actually SEE a provider versus Internet medicine!), who I shall hence forth refer to as the Always Really Nice Practitioner (ARNP), on Tuesday of last week to complete the reams of paperwork necessary when making a formal ADA request (I then rented a U-Haul and had the reams couriered to my office)...and, to discuss this never-ending pain I am having in my shoulder/neck/arm on the RIGHT side of my body (left side has always been the bad girl rebel, so Ms. Right side has become a mystery). I held her captive (hostage really) for a very long time as we hashed over papers, then what has worked, hasn't been successful, and what I am WILLING to try in combating this pain (and my willingness waxes and wanes on any given day).
Thanks to Jane (you know who you are!), I was carrying with me the suggestion of trying a TENS unit (Transcutaneous Electrical Nerve Stimulator) for pain management, since the pain seems to be localized to my right side/arm (yeah, I KNOW the picture up there is of ECT...electroconvulsive therapy, not TENS...but it's really just a matter of electrode placement now, isn't it?!?! LOL). My ARNP didn't flinch or bat an eye at this request and promptly filled out a prescription for it (anything to shut me the he!! up, no doubt). She also weighted down my prescription load with a script for massage therapy and Lidocaine dermo patches (I'm rather surprised there wasn't also a script for a dog muzzle, but whatever). We are staging a grand assault on my pain...I hope it doesn't hear us coming and try to change its militant tactics in advance.
I've got a physical therapy appointment this coming Wednesday with my favorite PT person, Madam Z, who will wire me up for sound with a TENS unit I can borrow for two weeks to see if it has any effect on my pain level. If it does, I can then petition my Almighty Insurance Company to PURCHASE a unit for me or bite the bullet and buy my own if they say "no". Failing those two options, I suppose I can storm chase and try to position myself for lightening strikes to my body, which I wouldn't necessarily be OPPOSED to if this pain keeps up without relief! And, who knows, a good "jolt" of lightening might also work as ECT for me AND improve my mood...win/win all around if you ask me...but, YOU didn't. LOL
Alrighty then...I have no more strength to continue pushing my anger through a small hole (whine) about my pain issues. Thank you again, Blindbeard, for inspiring me to write this post (just saying that to be sure everyone despises YOU for sparking my whining rant rather than thinking little, old me could have POSSIBLY thought this up on my own!). And now, I think I will go hop on the deck and flop like a fish (Sponge Bob fans will get that reference)...
**BTW**
What in the heck is WRONG with BLOGGER right now?!? This is the second time this week I have attempted to write a post in which BLOGGER eats part of it without warning!! I can't retrieve it, can't pull up anything via autosave, etc...unfortunately, large chunks of my witty humor have vanished and the recreation just isn't the same. GETTING MIGHTY TIRED OF THIS, BLOGGER...FIX YOUR SH!+ PLEASE...
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5 comments:
I am traveling over to my new blog list occupant due to the witty way she tackles her condition. I am alarmed at this pain MS sufferers seem to graduate to. I have always thought I was lucky to have what might be described as chronic fatigue syndrome if you are feeling nice or phantom disease if not which does not cause you any pain. In fact you just feel weak and if you don't stop working you get weaker, and then you may get some hallucinations about separating from your body which is a sign to go to bed and stay there. Your eyelids might even weakly stick when you blink. Your body might start feeling like a big slab (corpse). The terror is what bothers me, wondering if I can stop my free fall with relaxing exercises and deep breathing and I promise myself bed rest bed rest no matter how boring. Mary Jo who has been diagnosed with MS but now some of her doctors wonder is not blogging now, because she has pain and exhaustion. Do you know her, so you are taking her place until she gets back to blogging because she is very witty also and I miss her. Gerry
I know you all just thought I was being lazy (I am) or just terribly distracted (I am that too), but Blogger has done that to me twice now. I have been attempting a post for 2 weeks now that just disappears after every brilliant thought. And being lazy and distracted, those thoughts don't come easy.
Good luck with your new PT Tens unit and not working so many hours.
Good luck Cheese with your ADA request. I know your rant was serious but somehow your ranting makes me feel better. I look forward to hearing about your experience with the TENS unit.
Whine all you want. It's better out than in, right? I've done my own bit of whining too. Mine's not pain related, but I feel your pain. Hugs.
I will be anxious to see how your ADA request turns out.....you have every right to complain and whine....good luck to you...
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