From the category archives:

C'est MOI

With Invisible Illness Week wrapping up, I was determined to blog again (as promised) & what better way than to do the meme created for the event. These 30 queries have been 3 days in the answering but I hung in there because awareness of illnesses & issues that are so often not recognized, much less understood, is crucial to the well[ish]-being of those living with them. For a better understanding of what I’m living with & the journey therein, be sure to read my first IIW post: What’s getting in YOUR way?

  1. The illness I live with is: still undiagnosed
  2. I had a doctor once & she charged on a sliding scale. Ruling out what she could, she admitted I need more extensive testing which, of course, we couldn’t afford. Instead, she taught me about Myalgic Encephalomyelitis (also known as Chronic Fatigue Syndrome) & Fibromyalgia — convinced I had at least one, if not both — & helped me learn more about supplements.

    My=muscle / algic=pain
    Encephalo=brain / myel=spinal cord / itis=inflammation

  3. I was will be diagnosed with it in the year: I become insured
  4. Knowing a diagnosis would leave me essentially uninsurable, my one doctor & I didn’t pursue our well-founded suspicions. Further knowing a diagnosis alone wouldn’t help if it couldn’t be followed up with care — welcome to a healthcare system that’s been broken a long time — we just sought to alleviate symptoms, never imagining I’d still be doing so 15 years later.

  5. But I’ve had symptoms since: childhood
  6. I didn’t start putting the pieces together til my mid-20s but, by then, my Chronic Daily Headache was nearly a decade old. A key revelation came as I researched migraines; the overwhelming head pain that comes above & beyond my always present headache. They often present abdominally in children & I’d been treated for “stress” stomachaches in my youth.

  7. The biggest adjustment I’ve had to make is: brain damage
  8. My struggle to function is a chicken or the egg quandary. The dysfunction stems from my brain misfiring & misunderstanding its own information as my body uses up any energy it manages to generate trying to function, leaving my brain vulnerable. Our minds & bodies are designed to restore themselves regularly but mine can’t thus they degenerate.

  9. Most people assume: I’m exaggerating
  10. How could a headache last well over two decades? You couldn’t possibly have it every day! How could you not remember your childhood?! Surely you mean you just don’t remember it well!? Given that I too would love to better understand how such things are possible, if anything, I understate. Declarations without explanations are frustrating from both sides.

  11. The hardest part about mornings is: trying to move
  12. It’s admittedly better now that we have some semblance of a bed. After sleeping on the floor for years, our sofa-bed is an utter God-send. Having someplace to sit during the day also rocks but getting to that point can be tricky. Not only is my sleep not as restorative as it should be, it actually creates extra pain since I can’t maintain the needed support for my parts.

    “Taking time to rest improves the rest of our time.”
    ~ Dorian Rhodes ~

  13. My favorite medical TV show is: House
  14. While I love sarcasm & brilliance run amok, Greg House’s determination is especially appealing. He’s dealing with chronic pain, fighting to differentiate his legitimate need for drugs from drug-seeking & not letting other people’s agendas stop him. His determination to solve each case leaves me hoping I’ll one day have a doctor that fights that hard for a diagnosis.

  15. A gadget I couldn’t live without is: my MacBook
  16. Macelangelo, as he’s known, is my connection to the world at large. I’ve been without a computer too often; most recently, before moving to Palm Springs 2 years ago. My physical world is just too damn small without the interwebz. I have no local support, no personal transportation & no other means of staying in touch with family or friends.. nor would I have as many friends!

  17. The hardest part about nights is: sleeping
  18. It’s hard to get to sleep, harder to stay asleep & hardest to get enough sleep. With me being tired all the time, you’d think sleep would come easier but, since it doesn’t, I’m all that much more tired. Vicious cycle, anyone? To add insult to injury, between my brain’s misfirings & being woken by pain that occurs if I stay in one position too long, my sleep’s not deep enough.

  19. Each day I take __ pills & vitamins. thirteen[ish]
  20. Until I can avail myself of healthcare, meds are rare & I can’t currently afford all the supplements I need. The non-negotiables though are a couple Beano before meals, a multi-vitamin at breakfast, Cranberry capsules with lunch & dinner, daily detox, plus a Melatonin at night. I also allow myself constant ibuprofen one week a month & am rationing my last Rx of Vicodin.

  21. Regarding alternative treatments, I: love yoga
  22. Yoga is what got me working again, five years ago now. That job lasted until a fall onto my back which the doctor then recommended yoga for. :wink: The breathing & stretching remain part of my coping arsenal but I long for the day I can return to yoga classes. I also know full well that massage & acupuncture make a positive difference but am unlikely to have such options.

  23. If I had to choose an invisible or visible illness, I’d choose: neither
  24. Seriously, if there were a choice.. but I digress. If I had to choose a disease, I’d opt for just about anything less debilitating. That’d be doubly handy as many visible illnesses are. While it can be nice to “not look sick,” I’m not sure it makes up for the reactions using a motorized cart in a store gets me. Meanwhile, I have been treated better since using a cane.

    “Given the choice between the experience of pain and nothing, I would choose pain.”
    ~ William Faulkner ~

  25. Regarding working and career: I miss people
  26. My various jobs have each tapped into my creativity in some way & “working” online fortunately does as well. What my online projects can’t provide is the wonderful randomness of the public. Not that there’s a lack of people, obviously; I mean, here you are (& thanx) yet I miss the unexpected interactions, the smiles & hugs, the people-watching, my customers.

  27. People would be surprised to know: how difficult tasks are
  28. I’m continually surprised by the complexity of the simplest things. I’ll be doing something I’ve done before but not remember how. I’ve accepted that I don’t remember things but simple tasks should be doable by rote, no? Instead, I’m constantly relearning everyday routines. Shoe-tying, egg-boiling & other such mundanities require way too much concentration.

  29. The hardest thing to accept about my reality has been: thinking
  30. As a student of thought/collector of ideas/lover of concepts, I mourn the unfettered ability to think. Because I do still drink deep of all that I can, as I’m able, the loss may be as invisible as the illness causing it yet my brain often shuts down altogether. I truly believe God is in the details so the blurrier my thinking is, the more disconnected I tend to feel.

  31. What I never tho’t I could do while ill but did was: be consistent
  32. My fear of being unable to follow through hasn’t kept me from attempting to, mind you. I have a blog that’s been on an unplanned hiatus since January, am halfway through last February’s HaikuWriMo at deviantART, seem to be collecting unfinished poems & posts.. to name but a few attempts. However, there’s hope for, even when I couldn’t really write, I kept up on Twitter. :eek:

  33. The commercials about my illness: are aggravating
  34. Mine is as yet unnamed but the various possibilities are addressed & I resent the implication that a pill will fix me. This is yet more rampant online where, amidst all the support sites & articles, lie (pun intended) those proclaiming cures. The only thing I can be sure I have is autoimmune dysfunction which needs funding for research, not incomplete treatments.

  35. Something I really miss doing since I was diagnosed is: dancing
  36. I never did get the dance lessons I wanted but it would be harder yet to have an actual skill set & not be able to use it. Despite being untrained, dancing was once my therapy with dance clubs providing escape. It’s been over five years since my last dance — lost to the music & the crowd — which led to being carried off the dance floor & ending up bed-ridden. :neutral:

  37. It was really hard to have to give up: constant coffee
  38. Rest assured, your coffeesister still allows herself one a day. It is a health drink, after all. Although coffee’s been my constant companion for as long as I can remember, my compromised health can’t take too much of a good thing. Hot beverages being a therapy I can’t live without, my morning coffee’s followed-up with black tea then green & I wrap up my day with herbal.

    You don’t have to be still with a hot beverage for it to be therapeutic but you’ll be better off for every pause you let it create. (from Finding friendship, drink IN hand)

  39. A new hobby I have taken up since my diagnosis is: letting go
  40. Letting go of guilt, chores, the rest of that to-do list or whatever threatens my time &/or sanity thus health is freeing as well as necessary. My time is spent on self-care rather than self-doubt if not bogged down by more than I can possibly do, much less guilt over what’s not done. To-do lists are a lot looser now; I do things not only as I get a chance but if I get a chance.

  41. If I had one day of feeling normal I would: dote on my Hunny
  42. Setting aside the question of what the Hell normal is, the thing I resent not being able to do day after pain-wracked day is take care of my husband even a fraction of how well he takes care of me day in & day out. I’d love to be able to put his needs first for a change, not that they never are but mine inevitably rear their helplessly needy head. He so richly deserves a day off!

  43. My illness has taught me: to slow down
  44. Perhaps my insomnia since childhood was a symptom of a more compromised system than yet known. Filling those extra hours over the years provided a distraction. By not slowing down, I kept from having to face how I really felt. I could contend being too ill to continue college was just the result of overdoing. All I had to do was find a better balance, right?!

  45. One thing people say that gets under my skin is: get well soon
  46. While such well-wishers are well-intentioned, which I do appreciate, the implication that I can “get well soon” belies the reality of my situation. I’m not even sure I’ve ever been well & can’t count on ever being well, dealing as I am with not just chronic but debilitating health issues. Thus, when someone who’s known me for a time uses this phrase, it feels dismissive.

  47. But I love it when people: insist on helping
  48. Innate self-reliance makes it hella hard to ask for help yet I need it. If someone helps without being asked, much less insists on doing something for me, it’s an unqualified gift; I’m able to avoid the extra pain & save a little energy while not putting anyone out. It’s an acknowledgment — as much as a reminder to me — that I need help but, moreover, that they understand.

  49. My favorite [concept] to get through tough times is: the yin-yang
  50. The yin and yang represent all the opposites found in the universe; each having within them the seeds of their opposite state, that is, sickness has the seeds of health, health contains sickness, wealth, poverty, etc. None can exist without the other &, to the extent we experience anything, we become capable of experiencing its opposite. Seek that seed in every circumstance.

    “Don’t curse the darkness – light a candle.”
    ~ Chinese Proverb ~

  51. If someone’s diagnosed I’d like to tell them: your illness isn’t you
  52. Our bodies — being physical — are but part of our circumstances. They & their maladies may effect who we become, as any external force can, yet who we are at our core is up to us. Just as my smile, though initially noticed due to my overbite, is remembered instead for its warmth; whatever your body’s putting you through is distracting but temporary, don’t lose yourself to it.

  53. What surprised me, living with an illness, is: it doesn’t get easier
  54. As fatalistic as that may seem, I’m not saying there’s not improvement in the illness itself or my ability to cope with it. However, the understanding that I could get worse again at any given moment is a constant. My condition has roller-coastered year after year, I don’t know what I’ll be dealing with moment to moment, having my life held hostage doesn’t get easier.

  55. The nicest thing done, when I wasn’t well, was: remembering me
  56. It’s natural to meet silence with silence but some remember my many silences aren’t by choice, won’t shrug off yet another absence, remember what I’m struggling with & reach out despite my inability to. Quotationaries to blogging, a shout-out into the voids can spark the energy needed or bridge the neglect. My love to all who’ve checked in if I haven’t tweeted for a time.

  57. I’m involved with IIW because: understanding leads to progress
  58. From the empathy we with invisible illnesses can share to the better understanding we can foster in those who know us to a clearer picture of the health issues that are a possibility for all of us therefore the true state of our so-called healthcare system, each epiphany paves the way for progress. Seeing these invisible struggles, how do we all not seek to ensure care?

  59. The fact that you read this list makes me feel: grateful &..
  60. I’m overwhelmingly grateful: Grateful that my blog still gets readers (given how much my illness interrupts its flow), grateful you care enough to be here, grateful my experience may make a positive impact & hopeful. My hope is that you’re taking something you can use away with you & that you’ll return. I hope to keep sharing & learning from each other — tell me something I may not know in the comments — for, together, we can change the world.

(|_|*cheers*|_|)
“Joy is your sorrow unmasked. And the selfsame well from which your laughter rises was oftentimes filled with your tears. The deeper that sorrow carves into your being the more joy you can contain.” ~ Kahlil Gibran

PS: Here’s a sampling of others’ “30 Things..”

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{ 12 comments }

Whatever it is, don’t let it.. not completely anyway. We all have things we’re putting off & issues that are holding us back. The damn dirty deal of it all is that we don’t always have a choice. Now, don’t get me wrong; we always have a choice but sometimes all we can choose is our attitude. The simple truth is that we can’t do anything & everything we want, much less when we want to but we sure as Hell can do what we can do. That may seem oversimplified but too often we’re so caught up in what we can’t do that we neglect to do what we can. Rather than focus on what’s not done (poor, unfinished blog posts), we have an opportunity every day — any given moment — to act. Our actions need not be big, just purposefully taken.

Let’s take action together as I explore my somedays along with my invisible illnesses. The reason I blog is to share my experiences, that others may learn from them too, & the reason I don’t blog as often as I’d like is my wonky health. I’ve borrowed an interview of me by Alex Fayle from his fantastic site, Someday Syndrome, as it addresses what’s in MY way & I’m sharing it here — now — because today is the beginning of National Invisible Illness Awareness Week. The recent push for Health Care Reform has prompted me to share more about my own health so I will be posting yet more this week but hope my answers below reach you in a way that impacts your own perspective & perhaps even the healthcare debate.

invisible LOLcat, not really ~_^

  1. Describe who you are, how you live and what you do in one sentence. (e.g. Alex is a former procrastinator who uses his visionary ability to uncover hidden patterns and help people break the procrastination obstacle so they can finally find freedom and start living the life they desire.)

    Dorian aka coffeesister is coffee for the soul; brewing up help, health & happiness from a simple, stimulating & sustainable life while offering life lessons, potential perspectives & empathetic encouragement to all takers for that’s why we’re here: we’ve all been lent to each other.

  2. Name one moment in your life when you threw a pity party for yourself and the reasons why you felt you weren’t able to achieve your goals. Were you feeling stuck? Had you felt you failed? What wasn’t working in your life?

    I’ve had chronic pain, in one form or another, throughout my life but that didn’t prepare me for being bed-ridden by my late-20s. I’d gallantly pushed on despite migraines, chronic daily headaches, tendinitis, mild scoliosis & asthma for over a quarter of a century — even keeping a job through what was presumably mono, despite having to drop out of college. Then.. No amount of willpower nor sense of urgency nor the strongest determination could make up for the fact that I was debilitatingly weak, constantly tired, painfully sore & cognitively spent.

    We (fortunately, I wasn’t alone; thank you, Dave) were building our first home, finally working in theatre & newly living near my family (another God-send) yet I felt like I was alternately missing out or ruining it. Although I’d always had bad bouts with my so-called health, none of the tricks I’d learned over the years were working. Employing everything I knew about sleep, diet & exercise simply gave me bouts of functionality. My world had turned around & I was left with a new reality in which I not only had few enough good days but fewer answers.

    Being starving artist types who live paycheck to paycheck, insurance had just never been an affordable option so my doctor could do little more than guess once what tests we could afford offered no answers. With symptoms like tiredness, grogginess & confusion as well as nothing but the likes of “Chronic Fatigue Syndrome” to point to for an eventual diagnosis, I was treated by most people as if I had a psychological disorder instead of a physical one. That’s when the party really got going because I too began to wonder.

  3. Even our lowest moments fulfill a need in us or express our desires. When you threw yourself that pity party, what did you hope to gain? What need did you fulfill?

    My life hadn’t been particularly easy so, for a time, I took a much needed break. You know, the ol’ “if you can’t beat ‘em, join ‘em” routine. The more rest I got, the more bouts of functionality came my way & that Dave-person even managed to get me my own computer so things weren’t bad per se if still not forming a life anything like I’d ever envisioned or known. As I shared recently on Twitter; surprisingly enough, being horizontal does get tiresome.

    Dave & I believe that it’s important to be content in your life, regardless of circumstances, but just as important to not be satisfied. Thankfully, I wasn’t. I do love to think & it may have become increasingly challenging to do so but I’d certainly had plenty of time to do so anyway. The computer was used for research as my doctor had pointed me in the likely directions — speaking of which, Fibromyalgia Awareness Day was just last week — & the conclusions eventually started adding up.

    When life stops us dead (or at least forces us to play dead), there’s a reason. When there’s no discernible cause for the hiatus from life as we know it, there’s a damn good reason. Not only did I need to reassess my current situation, it was high time I found the throughline for my nearly 30 years. I recognized I was still very young, despite feeling very old, & had always been wise for my years so I’d equally not felt the need for in-depth retrospection & long since known myself quite well. Looking at my own life with a fresh perspective was a challenge & a gift.

  4. Tell us what you did to break up the pity party. What actions did you decide to take? Did someone help you buoy your spirits? Push you along?

    I’m still working toward more thriving than surviving but it’s crucial not to miss out on life along the way. No matter what you’re going through, your psyche’s still capable of laughter, your heart still responds to beauty & your soul still needs to be fed. I continued Stage Managing intermittently despite ending up in a practically comatose state after each show, teaching myself how to use this new body & mind in the process. That also allowed me to work with teens which was my first vocation. Staying connected to my passions kept me sane & combining them kept me going for the teen volunteers were learning what I did (but no longer could do on my own).

    Feeling somewhat like myself again, it was time to fill in the blanks. Both the figurative ones, such as what I had been doing to my health all these years, & the literal ones, like a malfunctioning brain, had to be addressed. Everything we experience is a collision of perspective & circumstance so fundamental change, especially to the point of restoring health, relies on understanding how each came about. I asked the people who knew me best (w/mug raised to that Hunny o’mine & me mum) comparative questions about my symptoms, frame of mind & any other differences they’d noticed past to present. I kept a “brain book” — like a journal but far less interesting — to track my thoughts since my gray matter was no longer reliable. I used the scientific method to ascertain what caused which & which worsened when. It doesn’t matter what’s not working or how you may break, the human spirit can dominate but it will triumph if you do more than mend the cracks; rebuild (we have the technology).

  5. Can you look back on that moment and tell us how you felt when you did decide to take action? What results came about from your decision to take charge and move on?

    Empowered. I tell you what; did I mention empowered? All the best things in life are active. Just as you can’t steer an anchored ship, you can’t create change until you make changes. Sure, some of them will be wrong.. YAY you! Mistakes mean you took a risk, you tried. We can’t learn without mistakes. A societal majority has misrepresented success. Success is NOT not failing, has nothing to do with what you do, even less to do with what you own & everything to do with who you are. The key to discovering who I was, as it is with all of us, was to discover my mistakes. It wasn’t that I blamed myself but that I knew I’d missed something because, when I hadn’t taken action, my body had been forced to. However healthy you may be, heed your body’s messages. It knows what it needs.

    I was so used to pain it didn’t occur to me as I was growing up that it wasn’t normal. We really do acclimate to whatever we don’t know isn’t typical. In turn, we don’t know what it is that’s atypical so we don’t talk about it. Other, equally damaging things in my life have also fit that pattern. I came to realize that I hadn’t just been in denial when it came to my health but was in denial about being in denial. Upon figuring out that constant pain wasn’t a common phenomenon, once I quit self-medicating with alcohol in my teen years, I was no longer covered by parental insurance. When I couldn’t conveniently avoid the pain & play at normalcy that way, I assumed instead that my pain was just worse than most people’s. Rather than face that there were indeed people without any, thus recognizing pain as a problem, I allowed myself to believe it was only severe pain that was considered a warning sign & downplayed my own.

    I’d been downplaying quite the collection of symptoms over the years. It had become habit so as not to worry others & I’d lost track, no longer noticing the progression. We can give ourselves no better gift than to take stock periodically. If all’s well &/or we’re comparatively improved, we feel appropriately grateful whereas, if the comparison doesn’t hold up, we can take appropriate action. In order to function from day to day, it can be important not to keep a constant watch on the big picture lest we get overwhelmed. Be sure to install multi-paned glass in the picture window of your life so you can focus on each pain pane as needed then be sure to step back now & again for that telling big picture. At nearly 30, I finally stepped all the way back for the first time & discovered not just a slew of random symptoms but a myriad of related symptoms all pointing to one thing: autoimmune dysfunction. It wasn’t a specific answer but it was the key to fighting back.

  6. Everyone has a Someday problem hiding deep inside, even little ones. What variety of the Someday Syndrome do you currently harbor? What would you like to achieve but haven’t yet?

    “I’ll do that (insert someday here) when I feel better.” The sad fact is that I very often must wait til I’m feeling better which is precisely what makes this Somedayness so insidious. Anything we need to legitimately consider in our daily lives can all too easily become more habit than prudent. When money’s especially tight, we become wary of spending it. My energy is like a constantly devalued currency in an unstable economy. Its value will plummet without warning &, the next thing I know, the simplest task had far too great a cost. It’s human nature to steer clear of actions that have negative consequences; the more difficult something is, the more reticent we become. When it’s not only difficult but likely means you won’t be able to do anything else for a time, that reticence becomes procrastination.

    I’ve always been an expert procrastinator. My saving grace being that I use my procrastination skills to stay open to unexpected opportunities; ready, able & willing to set everything aside as priorities change from day to day. Ultimately, this is simply mindful living — letting the moments take me where I’m most needed. However, with so little energy currency to spend at any given time & the added taxation on any action of additional pain, staying ready can become standing (or lying) still. Limiting our expenditures can turn into a pattern of not spending at all. “Better safe than sorry” has its place & one of the mantras I live by is “when in doubt, don’t” but, when it’s fear masquerading as doubt, then it’s time to do, damn it, DO!

  7. Examining your Someday Syndrome problem, what are you currently doing to resolve it and eliminate it from your life?

    Ever trade one obsession in for another? Quit a bad habit by replacing it? Stop making yourself sicker day after day by being afraid to do anything? ur doin it wrong! Going from one extreme to another leaves out a world of possibilities. Fear loves to parade around inside our heads all dressed up as doubt. Good ol’ doubt; so wise, so sane, just there to help. Fear, when legitimate, doesn’t hesitate; it knows it’s justified & rears its scary head. Thank God. It’s the reason we don’t typically open the door the killer’s lurking behind in real life. When fear’s feeling over-protective not to mention a bit controlling, it hides. Because of this prowess, the only way to catch it in the act is that taking-stock-thing.

    If I had to choose just one mantra, it’d be “coffee makes everything better,” which I’d then question because it would actually be “question everything.” We have to ask ourselves all the obvious “Why?”s then follow up with as many “Really?!”s as we can muster only to then ask my personal favorite, “So what!?” So what if it hurts to do that? It’s really not worth a little pain?? Why settle for less when you can have what you want??? I’ve been out of bed for a decade now & have learned a lot about keeping my body going while giving it the chance it needs to get healthier. Unfortunately, some good habits had devolved into bad ones thanx to my bossy friend Fear. Fortunately, I reached a point where I looked around & asked, “What the Hell?!?”

    The big picture was once again of a life on hold. Pane after pane revealed how miserly I’d become with my health. From simple things like not making myself an always coveted hot beverage when Dave wasn’t available because the back pain & aggravated headache seemed too high a price to no longer venturing far from home for fear of getting stranded as will happen when the wrong muscle acts up at the wrong time. Big change always starts with little changes so things like being the one to make our nightly tea are what started to get me back on track. My Grandma’s death proved my final boarding call for the “you created a life, live it already” train. Not only did I reflect on the first time she kicked me in the butt, that I might make more of my life, but I ended up spending time with her daughter (aka Momma) who equipped my butt with the things I’d need to get on with that life. I seldom answer Twitter’s update query, “What are you doing?” but — since returning home with vitamins my body can absorb, meds that do what my body can’t & my beautiful wooden cane, Chester — I could.

  8. Many people suffer the same problems you do. You’re not alone, and neither are they. What would you tell people in your situation right now to help them avoid what you’re going through?

    Any time there’s not a tangible reason for a day to be lacklustre (frustration, health issue, disappointment), something needs to give. If you can’t pinpoint a problem but can’t declare a good day, your soul’s trying to tell you something. Decoding soul-speak can be tricky; common messengers are dreams, new frustrations (especially things that weren’t previously frustrating), cravings (often occurring with health issues) & recurring thoughts. Small changes can provide a new take on things as each day’s choices bring a different perspective. If nothing floats to the surface &/or you’re not typically so self-aware, the key to unlocking a current discontent or needed change is to journal. Nothing orderly or defined, mind you, & you needn’t continue indefinitely. Just shake a few things loose with some free-writing first thing in the morning or last thing at night. If you find yourself staring at a blank page, e-mail random thoughts (try using a time limit) to someone you trust or even yourself. Act on new ideas, try new things, change things up every chance you get & you’ll find what’s lacking.. or accidentally fulfill it.

  9. If you could ask for one thing, right now, to help you overcome your Someday Syndrome, what type of help would you ask for? You might be tempted to provide a cheeky answer, but stop and think a moment about what would really help you.

    Ask me what I’m doing now & again. If I can’t answer, I’d better have a Hell of a reason. Simply put, everything I do has a physical price so I’m constantly weighing the cost against the return. Feedback provides such high return value as to make the cost consistently worthwhile. In turn, I have to be willing to proudly proclaim my accomplishments. Most people aren’t going to understand what a big deal walking to the store is, much less consider making coffee something to be proud of (unless I were 4 rather than 40), nor should they but I will. We don’t need reassurance to realize we’re doing something of value. What comes in handy though is prompting; we get a chance to remember what & why we’re doing whatever it is that’s uniquely ours with the irreplaceable bonus of knowing someone noticed. As much as I love to blog & — yes — tweet, the motivation does wane without feedback. Everything I do is done with the hope it’ll touch another soul so each & every response touches mine.

    I had set the goal of posting weeklyish to each of my blogs just before my current derailment so will be working my way back to that. Your feedback on any or all of them would be an immeasurable help & I encourage you to please share anything. Comment on the writing, format, theme, you name it, or just comment. ^_^ From the freshly brewed warmth & wisdom poured into every post at my primary blog, “Drink Deeply,” to the quotationaries — quotations w/commentary — “Dorian’s Demitasse” is filled with; I’m sharing what I’ve learned, my experiences & those I love with the intention of helping. Then there’s “Drink Deeply [of me]),” where I share just that: moi.

(|_|*cheers*|_|)
“Let us rise up and be thankful, for if we didn’t learn a lot today, at least we learned a little, and if we didn’t learn a little, at least we didn’t get sick, and if we got sick, at least we didn’t die; so, let us all be thankful.” ~ Buddha

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{ 5 comments }

What the Hell, right?

25 July 2009 C'est MOI
Drink Coffee

What’s with the 404s?! Yesterday, the whole site was gone & today there’s another missing post. Who’s running this site anyway!? Oh yeah, that’d be me; you know, the one typing this. Of course, I’m done typing now as it’s been published & is being read by you — thanx, btw! :grin:

My weekly[ish] tweet posts require editing to turn into the beautiful plethora of pics, videos, quotes & links they’re meant to offer. Otherwise, you could just peruse my Twitter profile. :wink:

The good news is, I’ll be editing… :arrow:

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Hang in there w/me?!

27 June 2009 C'est MOI
Computer Construction Cats

Thanx for your patience (hopefully ~_~) w/these weekly Twitter posts. Not only am I in the process of editing them but the intent behind them was to intersperse regular posts. *oops* Seriously tho’, they are meant to share the best tweets of the week: the links, photos, quotations & videos. The one below is the only one edited so far, the rest will return shortly — as far shorter & more enjoyable reads. :wink:

Meanwhile, we (as in RhodesTer & I) were blessed with an opportunity to switch apartments thus settling into the new one continues to keep me busy. … :arrow:

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Finding luck, conversation resumed

13 June 2008 C'est MOI

No matter how elusive luck is, we never stop seeking it &
can’t help hoping for it — nor should we. That watchfulness keeps us aware of opportunities & the hope gives us the courage to take chances. By believing in a bit of luck, we stay open to things beyond the sum of our experiences. [...]

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coffeeWHO?

8 April 2008 A bit TMI

Twitter asked me to “Share my story” & share I did. Of course, the story they wanted was why I use Twitter. Having recently answered how I use it on two different sites, the basis for my response was already written but I could have answered why with one word. I’d imagine most of the [...]

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Tagged on MYspace *_*

14 March 2008 C'est MOI

<– This is Sheryl or, at least, her current MySpace profile pic. Same difference, right? What?! There’s more to each of us than captured online!? I think I’ve captured myself rather well here at Drink Deeply, I’ll have you know! Of course, this hopefully decent but certainly accurate rendering of me becomes a more complete [...]

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Entertaining Nutty Touched Personable

14 January 2008 C'est MOI

There are any number of words starting with E, N, T & P — not all flattering — that could & may be offered up to describe me. The ones that together describe my personality though are Extraverted, iNtuitive (I’m not the one that cheated, ‘I’ was already taken by ‘Introverted’), Thinking & Perceiving. I [...]

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A simple reply ~_^

20 November 2007 C'est MOI

My, my; how two weeks can disappear when your eviction from one dwelling leads to van-dwelling til a new dwelling is miraculously found but none too easily won. Having faced the physical challenges, undergone the testing of our faith & confronted the philosophical conundrums; here we happily & unapologetically are.

If coffee’s my lifeblood, perhaps the [...]

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