Showing posts with label Schwannomatosis. Show all posts
Showing posts with label Schwannomatosis. Show all posts

Thursday, October 4, 2012

Part II - Let's Put on Our Superhero Gear: The Cape

It's here! Without further adieu...

The latest flare rudely interrupts a day out with family and later a pain jolt nearly rockets me off the sofa  into the ceiling. I am called as if from my body's pager alerting it is time. Pain has arrived once again. It waits for no one and on it comes. Part of the body tenses and breathing turns rapid. I gulp breaths or even hold my breath, awaiting the next pain tremor.

Nerve Pain 101 A slideshow from WebMD.com explains nerve pain in detail, its triggers, conditions that cause it, treatments, etc. 

For me, worry mode begins. I wish I was more chill, say more into meditation or prayer mode. I am trying but my concentration breaks too easily. My thoughts invade like this: "If I have this surgery or that surgery will I finally be better?" or "Time is lost each day. I want to work and I can't!" or the often-times tear-inducer "What about my goals and dreams... Everything, it seems, is gone! My real life has just stopped. The first half of my thirties... Poof!" Talk about a magic trick!

Will I rest tonight? Who knows... Staring at the clock, hour after hour tends to go by, swallowing pain pills every three to four hours. People marvel how I can take pill after pill tiny tablet to capsule without water. I marvel how my liver and my body overall can last this long on such a routine of high doses of opiods accompanied by anxiety and depression medication. I've been taking a dose of hydrocodone off and on pre- and post-surgery since I was 18. I have had to up the ante now the past three to five years given my pain has surged like something from a fireworks stand on the Fourth of July. We're not talking sparklers either!

Day after day of pain, a patient - at least me - is on HIGH alert like after you go see a scary movie or a political thriller - (one of my favorite genres) you are a bit more jumpy or on edge. At least the day after thinking about it. Around every corner, every bend, even sitting in a dark corner, down a secluded hall... For me, I'm propped on the couch, my usual MO, and the burning will come followed by numbness so intense I have to drop the book, magazine or iPad immediately. Fire. Alarm. The surge of pain in my arm is hot, a fire blazing into my hand. Then as quickly turns numb, unfeeling, the fire is out.
Later, another jolt of pain arrives and the ol' body winces with each passing voltage in the knee, back, shoulder, or neck. Instead of body jolts, I want my life jolted back... brought back, a shred of recognition. Something. A flicker of hope... Yet, I know I have a long way to go from where I stand but it is a shorter distance from where I stood months, years ago.


Writing in general makes me feel alive, so starting this blog, The Healing Redhead, has been a blessing this year. I wished I did have more stamina to do more fiction, more of my book or more of my hobbies like exercise, cooking/baking, and crafting. It can get frustrating when I have so many interests and ideas and my body will not cooperate, support me. But that doesn't mean I can give up, right? Right? I can't hear you!

That is where Pinterest.com comes in handy. I may not feel like hiking in Yosemite today (first, I need to get in shape a bit) or even hiking local hot spots, a favorite pastime, but that doesn't mean that the California dream or weekend hobby is lost forever. I surely hope not! I have always wanted to see Yosemite for myself because of Ansel Adams' work. His photographs have always mesmerized me and the way John Muir wrote about the area has motivated me to put this beautiful postcard destination on my ultimate bucket list! I gotta go! Every time I see a photo it reinvigorates my spirit and determination!
Yosemite National Park 

Yo, how could you NOT want to go too?

For years, I have had New Zealand on the list as well! I mean it's hard to resist. I could talk to friends, family and even [blush] strangers about Christchurch and its surrounding beauty. I was INTO NZ! Its tourism board should SO cut me a check. I could go on and on! I even had honeymoon plans and no honey! How funny is that? I really wanted to go! Then, I saw this special on (of ALL things!) a shopping channel {blame my Mom!} about Vienna, Austria. Shock: I didn't buy anything! I did come away with an absolute LOVE of Vienna and its overall aesthetic beauty and its history, architecture, and performing arts. All from a shopping channel. I KNOW! CRAZY, RIGHT? It's not the History Channel by no means but it gave me enough nuggets of info that I started my own discovery of Austria. So move Vienna up that bucket list, y'all! New Zealand got put on the back on the plane, so to speak.

It is so important to have a few dreams you hold close. If you aren't sure what you want, Pinterest.com may be perfect for making a Dream Board or Bucket List Board or an In the Future Board. It can be small items or big items or a combo of the two. I even include a board of supplies, helpful gadgets, facts, inspirational quotes that might be helpful for people with chronic pain. You are welcome to check it out! Find it located on the "The Healing Redhead" board on my Pinterest account. Repin all you like! Remember: You can check out my Pinterest site any time. Just click the big red P to the right. ***If you have a favorite chronic pain product and/or recipe, e-mail me and I will feature it on my Web site and on Pinterest. Of course, I'll give YOU all the credit!*** Just e-mail: lesliee30@gmail.com.


                                                                         
The areas in my body begin burning, jolting, and misfiring. It seem like the Devil's work and I never remember signing a contract with that red monster. The pain zaps in my back and in my leg. After being so patient, I am about to lock horns with that pain scale or whoever seems to be in charge of it. Day after day after day I am met with excruciating pain. I might get a break in between but you know The Pain with a capital P will be back you just don't know when...
It does happen. I finally let loose, l let the tears fall. I may seem strong in public at the doctor's office, grocery store, running to the pharmacy, and generally with people I exchange conversations with at the check-out stand, restaurant table, or at the occasional trip to the yogurt shop. It is a quiet sob and the wetness on my cheeks is cold against the forward motion of the standing fan, oscillating, oscillating. I would never put an enemy through this kind of pain... Well, except that ONE gal from high school... Kidding, only kidding. Seriously, no one should go through this. No one. When nerve pain strikes, it is mind-blowing, the color red, the word blazing, the word unrelenting... It is real & it takes everything a patient has, physical and mental, to endure its wrath.

With Schwannomatosis, the condition (www.ctf.org/) I have, tumors press on and against nerves & that is what causes my nerve pain along different parts of my body. I am wondering, how many tumors I actually have in this 5'9 frame of mine? Yet... Do I really want to know? Doctors have always shielded me from the big number and focused on the case at hand. That's when there's a plus side to the invisible nature of my condition. I don't have to know EVERY detail. I need to be concerned about the ones hurting me and the ones that might turn malignant although I've been told the chances are low that will happen. I still think it is important to stay on top of things and keep going to my doctors and surgeons on a regular basis and do my scans. Although, it is my most dreaded chore.

                                                                               

I press my fingers at different points on my body, searching like a physician or perhaps the TV crime show coroner who investigates a body looking for answers posthumously. Yes, I just said THAT! Wanted to make sure you were listening... or still reading! {wink}

I press just below my hip bone, a-ha, a possible growth. That explains all the pain around my right leg -- one of the areas of pain. When I am in pain, I tend to need quiet around me and I am still, quiet myself. The television cannot be blaring with yet another episode of Law&Order, its special theme song and signature "dun-dun" it is so famous for around the world. Even as much as I love hearing the lil' nugget of pop culture go by, I have to focus on my body and the pain. Instead of hearing the two single notes and breaking into a grin, my teeth clench and my body braces for the next attack. I can't afford a smile right now. If I stay still sometimes, I feel as though... ZAP! ZAP! Two different areas. Zap! In my hand. I feel as though I will be rewarded. With no pain. Not the case this time. Holding still doesn't mean anything for me. It just psychologically helps me make it through the tough nerve zaps, the ones that shoot and arc through my body as if something is chasing it, hunting it down much like so many of the "perps" in Law & Order Criminal Intent, SVU and my new favorite, the British Edition on BBC-Television.

                                                                             

It can be so difficult living day-to-day with these pain conditions, caring for our own families, if we can, dealing with the guilt if we can't, and going to doctor appointment after doctor appointment, scheduling, getting the bills, refilling prescriptions, and just living day-to-day.
My nerves overwork themselves each time in the big waiting room and the little waiting room because you never really know what Dr. _ is going to say or prescribe this time around. I try my best to read or text, distract myself somehow, but I'll be honest, it rarely works whether I have the 8:15 a.m. appointment or the 3 o'clock. I tap my feet and wait for the nurses each time to read the names from the plain folders like we, the patients, are award receipts (how ironic) and later in the little patient room, I'm staring at the plain white door and waiting, waiting, waiting for it open... Then, Viola, the door finally opens! Hooray, by then you feel it is time for a party or cocktail or mocktail at least. You've waited so long.

                                                                       
Even though we might have unforgiving illnesses we still need to make time for laughing, relaxing, working toward goals (big and small), and loving life -- even if that means just a mocktail or a trip to the craft store, that's something! So, even if I didn't see that Law & Order because of my pain I can catch a show spin-off or DVR one, no problem. It's not very hard to find that show on TV! Ha! So, please just spend some quality time with those you love & with yourself. You have to spend that awful time in pain, too, right? You know when the pain triggers and emotions get the best of you. Don't begin to resent yourself. The worst possible thing we can do is give up on ourselves. We might not be able to pursue certain dreams right now but that doesn't mean we can't dream at all, daydream, brainstorm, pin, read, rest, watch, and best: DO at least a little... Enjoy a hobby. Travel to your favorite hideaway or a new place with a beautiful vista, your Vienna, your Yosemite! It doesn't even have to be very far away. There are quite a few places locally I want to see and experience in the coming months. If I do 'em, great! If not, they're on the list for next time! Go at your own pace & have fun! Fingers-crossed, it's a pain-free adventure!

Saving the World
with Capes n' Tiaras
(via Pinterest)
There's a quote I spot every now & again about owning a tiara and a cape and if you had those two items (and wear them!)
YOU COULD / CAN RULE THE WORLD! Some days our capes go missing or we leave the cape at the cleaner's but most of the time you know what? We just have to strap on those invisible capes and do the best we can. We're strong! We battle the beast of pain & chronic illness regularly... And NOT just one month out of the year! This is a 365 days, 7-days-week, 24-hours-a-day (better-believe-it) condition! We have battle scars to show for it! But we are not quitters! We want life, we're in it! So tiaras & capes, why the heck not! Even with invisible illnesses, We Can RULE the world!
Who's with me?

What color is YOUR cape? As Pinterest attests, Glitter is A color! I think I like midnight blue! How about you? **Men, you gotta improvise! You got the cape! Maybe stellar shoes, or a hat that is a show-stopper! Tell me in your comments below. I would LOVE to hear 'em!

Let me just say... Awareness week may be over, but that doesn't mean we stop. If we want the stigma to change we need to educate and make Invisible Illnesses visible by showing the world WE ROCK & that we ARE visible. We need to make our stories visible. So... on days we don't feel good, let people help. I've noticed with my Mom if I tell her how I feel in terms of the pain scale (1-10) she understands better than me saying, "The nerve pain is acting up again." Plus, it helps me to quantify it and compare whether my pain was worse or better than the last pain surge. This may not work for everyone but it is something that can help some patients connect and/or reconnect with friends and loved ones.

While we are communicating that message, fasten that cape & tiara!

It's going to look fabulous on you! Remember, we ROCK!

Before I go, I have song that is special to me that I find inspiring as writer, patient, and simply, as a person. I hope you enjoy it and find some truth nuggets within! It is called... The Cape & its by legendary Texas singer/songwriter Guy Clark. Thought it was a bit apropos given our whole theme here and a perfect way to close this two part series. --The Healing Redhead

Guy Clark singing "The Cape" live with Verlon Thompson in 2010

Saturday, September 15, 2012

Let's Put on Our Superhero Gear!


SPECIAL FEATURE for Invisible Chronic Illness Awareness

Introduction
Last week was Invisible Chronic Illness Awareness Week! Below is part one of a two-part article on the *zap* of chronic pain and how we, as patients, continually *POW* give it all we got! To a patient with invisible illness the symptoms and realities are very VISIBLE to us. Ironically, I would have posted this last week but I dealt with my own set of chronic issues... I kept going though and I give you this two-part special. After all, awareness might last a week but we live with our conditions 24 hours a day, 7 days a week, 365 days a year. No holidays. In fact, I did miss celebrating Christmas last year with my extended family because of my nerve pain due to my Neurofibromatosis type III or what is called Schwannomatosis (www.ctf.org/). So, it is a very true fact this kind of illness makes for many sacrifices, challenges, prayers and silent moments, and for me, a chance to tell it like it is. That's why I have The Healing Redhead Web site, to give co-chronic healers a hand and give those around us a glimpse in, if just for a second, and to focus on a life that is very real and so often misunderstood. It can even be a teeth-grinder at times, as you will soon see... in Part II.

Thanks for stopping by!

Part I

Zap! Sting!

Bam!
It might happen one day.
It might happen over a period of time.
It may happen again and again and again and you don't have a specific name for it.

Poof.
It's a sneaky one that invisible Illness! It can make its way in and out of your life and back again as quick as that guy you dated who loves commitment so much (read sarcasm). Over time, little by little, the signs start to reveal themselves. A fall. A mysterious pang here, no it's there. Then, a surgery goes awry. Then another. Pain itself starts to escalate as does your anxiety. Before you know it, months pass or maybe a year or more... you've been left without a career, hobbies, and even the home you own has a for-sale sign and you live with family now.

Symptoms related to invisible illnesses are often complicated so much so even David Blaine and David Copperfield can't make these illnesses visible with their powers. The patient's symptoms lay hidden under the surface and hidden from those around them -- family & friends to doctors & dates who can't tell a single thing is going on unless that person speaks up, winces or complains. See, the symptoms manifest largely on the inside, hidden from view, and the person suffers in mostly silence, especially during a flare-up or spike on the pain scale. Invisible doesn't mean out of the way and taken care of; if anything this person is more vigilant. They are at the doctor more, the MRI scanning bed, and off to get blood tests. It is sort of like flipping the inside out and seeing what the story is telling us. The worst thing anyone can do is ignore symptoms and refuse to go to the doctor. To me, that's putting one foot in the grave. I have a family story to back me
up. But that's later. An another story entirely.

Speaking of family... brothers, sisters, parents, and extended family sometimes don't believe us and what we go through on a daily basis. Friends, too, may not understand and may even leave our side. Others may try to "fix" us and when that doesn't work they too will find other "cases." If this is something you deal with, I have a great book titled, "Why Can't I Make People Understand" by Lisa J. Copen. She says it to the reader straight, not a lot of fluff. But that doesn't mean Lisa isn't compassionate. She is one of our best resources as patients of chronic illness and as warriors of invisible illness. This book really helped me and I go back to it from time to time when someone might say a thing not too friendly or just not thinking. This author helps us step back and put things in perspective. I like her because she's an insider who knows what this journey is like so she's not writing about stuff she hasn't lived or seen. It's is as authentic as it gets.

It's the pain, struggle, and symptoms all encased in the human body for no one to see. It's waking up each morning and knowing getting out of the bed and to the bathroom will be the first of several, if not many, challenges of the day. The shower has become less of a relaxing, comforting getaway and more of an overwhelming hygiene routine that wears me and my patience out (you too?)! But at least this patient is clean and smells nice! In most cases, I don't speed right through and dry my hair like during my previous life. It's hard for me too because hanging out with wet hair is one of my biggest pet peeves but right now I have to slow my pace and deal with it. I'm pretty out of it energy-wise after my shower so I may just try to comb out part of my hair or pull it back in a clip until I regain some energy to continue. I don't know about everyone else out there in ChronicLand but I am still amazed (after a few years) by how a semi-warm shower can leave me zonked, so tired, out of energy. If you feel the same way, talk to me.

POW!-erful option
Combing, drying, and styling are for the experts! I see the celebs & reality "stars" go get their hair and makeup done and think, nope! They should do their own makeup & their own hair and

give their beauty and fashion pros to the cancer hospitals and housebound patients with invisible illnesses! Great idea, huh? At least there should be a program like that! I think a great name is: Dr. Glamour or The Dr. Glam Squad! *Tell me what you think of the Dr. Glam idea in the comments section!

It disappears then reappears like that rabbit in a hat or the coins behind your uncle's ear. The pain gets trickier, more surprising every time. The symptoms always seem more intense, more complex, a grand puzzle with constant moving pieces. Some physicians are part of that working puzzle while others are less willing to help The Chronic Pain Patient and turn them away. I want to see chronic pain centers become more integrative and not just rely on pain pills and surgeries as answers. These centers and the doctors who serve this particular population, in general, need to be more holistic in their service toward patients -- no matter if it's MS, Neurofibromatosis, or Crohn's Disease. I've been enlightened on this subject by reading "The Chronic Pain Solution: Your Personal Path to Pain Relief" by Dr. James Dillard. It was a fascinating read and one that gives real solutions to patients, solutions that make sense and provide inspiration. Dillard covers a large gamut of topics, including activites, diet, and how readers can develop their own pain control plan. I highly recommend it.

Stay tuned for Part II coming soon...


**I was not paid to recommend the books featured in the blog post.


 ©The Healing Redhead


Sunday, September 2, 2012

Take a Byte... Umm... Bite of This Cute Cupcake

Been checking out various cupcake recipes on Betty Crocker online today and found this cutie for back-to-school! Celebrate a job well done in the classroom (teacher and/or students) with mini versions or this size:


A+ Betty Crocker -- The Web site offers a fun feature where you can fill in up to three items from the pantry and *PrEsTO* it will build a recipe! How cool, right? I thought so. And if you love coupons, you will LOVE Miss Betty! www.bettycrocker.com

As for my cool-for-school selection is that the cutest laptop or what? Bet it is delicious too! I'd definitely take a byte... ummm... bite of that computer! I just love that it is an apple cupcake -- perfect for September-October... Let the fall baking begin! Yay! I started my own festivities this weekend with a 12 oz. pumpkin latte from Starbucks. I even got inspired to create a pie board on Pinterest. I will post a link when it's ready. FACT: Do you know that I have never made a pie in my entire life? That just will not do anymore. I want to start making PIES, dang it! It's a bucket list entry -- it's that important! I really don't want my pain from Neurofibromatosis to get in the way. If my pain can stay within reasonable limits and my energy can hold on here and there for some solid afternoons, we might just be in business, as they say. See building endurance and keeping my energy up (without 12 naps a day) is my current challenge. I would love to be able to bake a pie or two, a batch of cupcakes, and yummy pumpkin bread (a family favorite). We will see. I'm excited about the possibilities, though. I want my body to cooperate SO BAD yet like so many in similar circumstances know it can be disappointing season to season, putting up with constant aggravation, sadness, and missed opportunities. It is nursing those quelched hopes -- big and small -- that finally bring the tears. It is something hard to admit but it is true.

With chronic pain, much of it is out of our control. We do what we can and the rest we have to
deal with day to day and sometimes minute to minute, watching that timer like a nervous, first-time baker...waiting for that delicious cookie to rise.

Nerve pain is the the hallmark of Schwannomatosis or what I call NF 3. Don't tell any doctors or researchers. Heck, do! Why didn't they just call it that? Anyone know? Anyway, nerve pain, especially this brand, listens to no one. I mean NO ONE! It is the ultimate devil, the robber of life, the arch-enemy. I think you get the picture. Just ask anyone who has it. It is as haunting, even more so, than anything you find on Oct. 31. Let me make myself clear: the pain is scary, the people with the condition, like myself, ARE NOT! The adjectives that describe nerve pain are telling: stinging; jolting; radiating; numbing; burning; zapping; and more... The list could fill a large billboard. But I'd rather see a billboard photo of cute cupcakes (like above) or an ad for Dancing With the Stars' hottie Maks! Oh, don't act like you don't know WHO I speak of! Mr. Chmerkovskiy! (Brief side note: Good thing the contestants of Bachelor Pad did not get his last name at the Spelling Bee last week! Who knows how long that bee would have lasted! Those poor child judges.

As a person dealing with chronic pain issues 24/7, (my unscripted reality show) I have good days and not-so-good days and bad days. Fingers crossed with an upcoming medicine adjustment, I might be able to do more and actually sleep less. With that hope, I am making a list of Fall Fun Activities/Goals. You can do the same. Steal a few of mine, add a few of yours... Include them
below in the comments section! I love hearing from people! So when you have a good
day you can access the list and pick an item. Why not, right? If you have a significant other, children, extended family, etc., your list may look a lot different. Just remember to include 1-2 items for JUST YOURSELF. Like a massage. Too much $$? A lot of places run deals, so
don't automatically put the kibosh on pampering! Phone apps & newspaper & radio ads are
great places to start looking for % off.

My body is Ahhh-ing already just thinking about a SPA day.

With a new pain doctor working on my case and a hopeful spirit, I hope YOU & I, my reader, can enjoy autumn out and about... even if it's just a little bit. It is, after all, my favorite time of year!





A Few of My Autumnal Options
*Visit a pumpkin patch
*Make a pie from scratch
*Make seasonal cupcakes
*Visit craft store for inspiration
*Order festive dog collars for my fur babies
*Spend morning or afternoon at coffeeshop reading or writing at leisure
*Read political cartoons to offset the blistering candidate commercials
*Take autumn walk on cool, brisk day
*Enjoy tossing frisbee with puppy, Oliver
*Get a massage
*Enjoy a pedicure so my toes have autumn flair
*Go to local library & read magazines
*Make meeting of local writers group
*Visit church during off-hours to pray, listen
*Stretch right hand to strengthen mobility
*Try to journal with pen at times instead of with just computer (My left hand is at bit more difficult to write with given it is not my dominant hand. Journal with both and be
patient!)
*Last, but NOT least, make dog treats for "the kids."



***READERS, DON'T HOLD OUT ON ME! What are some of your favorite autumn treats? Don't forget: I would LOVE to hear your ideas and plans for fall.

 ©The Healing Redhead

Wednesday, April 25, 2012

Life Makes You Stronger, Period. {Part II}

In my last post I discussed the January 2012 article in Vanity Fair by Christopher Hitchens. I found this article discussing the ol' adage of "Whatever doesn't kill you makes you stronger" completely by happenstance just going through past tweets from a Twitter account I recently started to follow.
I'll be honest I was never a Hitchens' fan. When he passed away, though, I was amazed by how many people didn't know who he was -- at all. Like I said in my last post, on the day of his passing his book, "God is Not Great," became a #TT, or Trending Topic, on Twitter and people became angry, aggravated, and enraged but they didn't know the source of the #TT. Yes, it may not be a statement a person believes in but don't jump to the keys before you know the full story. It was a title of a book and also a epitaph of a man. It is my belief that whether you agree with him or not, you can't argue he made a lasting impression on American culture. He even made a lasting impression on me. That is why I write this today. I wasn't expecting to have an enlightening moment but it happened. Here I am to tell you about it...

Toward the end of the Vanity Fair article, Hitchens talks about pain in his arms, hands, and fingers while getting treatment at MD Anderson (MDA) in Houston. I can identify with this pain although I do not have cancer. I am treated at MDA for what is called Schwannomatosis. I have numerous internal tumors that pop up on my nerves throughout my body causing pain. That very pain oscillates from mild to maddening.
Most recently, I've had pain in my left shoulder, arm, hand, including the tips of my left fingers. It ranges from a burning sensation to a dull ache and from not hurting at all during the middle of the day to the point I feel as though my hand and arm are in a 300-degree oven or hotter.
This oven business usually happens between 9 p.m.-7 a.m. It's not the sizzling show you dream of as an adult singleton, let me tell ya!

"I am typing this [the article]" Hitchens wrote. "Having just had an injection to try to reduce the pain in my arms, hands, and fingers."

He went on to say that the no. 1 side effect of the pain is numbness in the extremities," filling me with the not irrational fear that I shall lose the ability to write."

There it is. My own worst fear right there in black and white. Staring at me, is it taunting me? I had a shoulder surgery now probably five years ago in Seattle at the University of Washington. After surgery I noticed my right hand was basically in a fist. When the surgeon came in for a post-op evaluation, he looked at me, my right hand, at me, my mom, my right hand. This kept up for what seemed like the length of an entire visit. Then, he finally spoke: "I'm not sure what happened." He shook his head. "The nerve probably just got stretched while in surgery."

Today, after two different rounds of physical therapy and just living life, my right hand is still not itself. It is no longer my writing hand or my hand to fork a salad or spoon my favorite chocolate ice cream. I use my right hand to pet my dogs, hold my iPad straight, and steady a book.
I will tell you it has damaged my self-esteem given that now I have this hand issue and my foot drop on my right side and a decade ago I had neither one.

Stretched nerve.

Cut nerve.


Surgery is hard enough, period. Patients, like myself, deal with the bumpy, pink scars masked by staples like tiny silver teeth in the skin so flat against the flesh it is as if each one is meant to be there from the beginning, at birth.

Patients mostly spend time worrying if the resected tumor(s) are benign or not. I know I do. In all my surgeries, though, all 20+ of them, the tumors have been benign. Very often this occurs in Schwannomatosis cases like mine. But these are tumors and they have their own rules. I have had two biopsies (which I think of as close calls) and each resected tumor from a surgery is tested. So even though I have been told it is very unlikely to be malignant, I remain skeptical. It can happen. It did happen with my father. [More on that in posts to come.] So, I continue to worry. I have reasons to worry.

You know, how it's always said that 40 is the new 30? For me, left is the new right. I'm not talking politics. Hold on! I'm not even going there! I'm talking hands! That's why the burning and aching at 2 a.m. worries me more than normal. As a writer myself with goals to meet and dreams to achieve, I related completely to Hitchens when he said: "I often grandly say that writing is not just my living and my livelihood, but my very life, and it's true."
Hitchens also discussed how he is threatened by a loss of voice. I, too, came to that same point when a tumor was found pressed on my vocal chord just last year that caused my voice to quake. After surgery, I got an injection at MDA that was supposed to help my vocal chords and it did...for awhile. Then it faded, again. Just above a whisper, I tried to speak. Waitors and grocery store employees inquired about my situation: "What's with your voice? Are you OK?" I so had a good (evil) response for them. They probably did mean well or were genuinely curious but it was NOTB. I mean, really?

I again connected with Hitchens, who at the time of writing the story, was receiving temporary injections into his vocal folds. "I feel my personality and identity dissolving as I contemplate dead hands and the loss of the transmission belts that connect me to writing and thinking."

Dead hands.

Loss of the transition belts.

When I saw "dead hands" something in me halted. The what-ifs started...
What if my next surgery turns my hand numb and into a non-working utensil? No-longer functioning... I mean I would have never imagined my right hand having such a fate!
What if...
What if...
What if...
I have two semi-working hands but neither one can hold a pen or pencil and I no longer write or type?

I stopped myself again.



* * * * *

I can't let this control me. I definitely can't let it when I'm not even in there [in the hospital]. A few years back, I found a new perspective that works most days in my favor. Any day I'm not going to or not at the hospital or doctor's office is a good day.

Today is a very good day. Very little pain.

No visits for at least a month. Maybe longer.

I never thought I would have such experiences in common with such a man of our time. No, I could disagree all day with regard to his thoughts on religion and politics but when it comes down to the hospital room, we are simply human with the same fears who just try to survive in such an environment.
Unfortunately, Hitchens did not survive. He was, though, during his life able to share a common experience that touches all too many of us, including yours truly. Just like out here in the real world, in there, you need a voice and you need to be heard. That's why this article is so important in my mind.

As for the ol' saying, "Whatever doesn't kill you, makes you stronger..." Scratch that.

**New adage: "Life makes you stronger." Period.**

Ironically, I was checking out one of my favorite Web sites & someone else with a scholarly background weighs in on the saying. Does he agree or disagree with me? Find out here.

As for me, no matter what happens, writing is way too important of an endeavor to relinquish because of an illness. It is my passion. Has been for a very long time. I was a sophomore in high school when I knew I wanted to devote my career to writing. Even in grade school, I wrote short stories.

I will not let myself stop completely. Ever. There are famous writers who, sick in bed, wrote stories. Like Hitchens. Story after story. So, I can't let Schwannomatosis and its side effects put my pen down. Not now. I'll just order the newest version of the Dragon voice recorder and go from there. Until then, I plan to write, write, write.            

View the complete Vanity Fair here.


©The Healing Redhead

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Image 1: spreadshirt.com
Image 2: http://www.bn.com/

Friday, April 13, 2012

Life Makes Us Stronger, Period. {Part I}


I know Christopher Hitchens (1949-2012) made many people's blood boil for his views and promotion of the "New Athesism" movement. It's quite an understatement, really, because when he passed away his book, "God is Not Great," became a Twitter trending topic and for those who didn't know about the book and the author's death were riled up, to say the very least. I still remember the countless tweets like: "How can you say this?," "This isn't funny," "Is this some kind of joke?" and "Tweet if you Believe God IS great because He is!"

Maybe it's the intellectual in me but I felt sorry for those people who didn't get. It's not that I believe in the philosophy of Hitchens regarding religion but people should be informed enough to know the origination of a trending topic (an author's death) or be willing to look it up (too much to ask, I know, silly me!) before jumping on the tweet machine. So many probably haven't even heard of Hitchens and probably still don't realize that the #TT was a book title rather than a mere stunt of the day. I know it's still a disagreeable topic but there was someone behind it.

Even though we may not agree with someone's background, philosophy, or religion (or lack of) I still think there are chances, mere instances, to find something of value between the person and yourself. Finding this similarity or middle ground can be important -- at business meetings, family reunions, the coffee line and maybe even your own mini-van. Ha! There is much to disagree about in this world for sure, and for many people, including myself, *atheism is a "deal breaker," as Dr. Phil likes to say. But even so, I found something of a treasure when I read an article by Hitchens, one of the last he published, in the 2012 January issue of Vanity Fair. If you spend time with people, there are some likely gems to uncover. I hope the following, covered in two parts, will illustrate just that.


Without going into too much detail, I will tell you I have a genetic disorder called
Schwannomatosis (www.ctf.org/) and the physicians at MD Anderson in Houston have taken good
care of me the last two-and-half years. Before that, I was at the University of Washington-
Seattle. In reading Hitchens' article in Vanity Fair, it confirmed that he was a patient at MD
Anderson too. He was being seen there for esophageal cancer. Diagnosed in 2010 while on a publicity tour for a memoir, he began writing about his illness. It is in speaking of his
illness that I write about him today.

In the VF article, "Trail of Will," Hitchens discussed the ol' saying, "Whatever doesn't kill me makes me stronger." Not a big fan of the adage, the author finds it "increasingly
ridiculous."

I will say I whole-heartedly agree with that! As a chronic pain patient and a person living with a genetic disorder for the past 17 years that has brought on its share of surgeries, biopsies, CTs, PETs, MRIs, countless ER visits, and more medicine than I can keep contained in
one large travel makeup container, I feel it is anything but accurate. More like inadequate, aggravating, and obviously needs editing! Ha! So, whatever doesn't kill me will...
A) kill me;
B) kill you;
C) doesn't make anyone stronger, especially the patient in question. The patient
is only tired and in need of more sleep (except insomnia is a side-effect); and/or
D) Something else might (kill ya) in this day & age (too much red meat, too much sugar, too
much sitting, too much alcohol, too many carbs... It changes nearly daily!)

In his article, Hitchens starts off his article with a pair of philosophers to make his point, Friedrich Nietzsche, who apparently coined the lovely (not!) phrase, and Sidney Hook. The article ends up focusing a lot on Nietzsche and Hitchens tries to demonstrate whether the good ol' saying was relevant in the philosopher's life or whether it was just some pretty poetic German.

It is in the last half of the article where Hitchens talks about his own experiences that gave me a new way to think of my own. But first he relays his thoughts on the quote in question: "[...] I have slightly stopped issuing the announcement that 'Whatever doesn't kill me makes me stronger.' In fact, I now sometimes wonder why I ever thought it profound."

I found a certain quote of his regarding pain to be especially profound and it gave me pause: "It's probably a merciful thing that pain is impossible to describe from memory. It's also
impossible to warn against."

What do YOU, MY BLOG READERS, think of this?

Yes, patients do forget how painful the day after surgery is so that when the next surgery comes around he/she (she -- as in ME!) can do it again. Funny, how that works!

Same goes for the ladies wanting baby #2 or #3. Labor is a distant memory and that sweet bundle of joy is right around the corner, never mind the contractions (yeah right!) and the bliss (pain!!) of delivery.

Also, READERS: in a medical situation, are you likely to find out what the procedure is like
beforehand or do you like to wing it? Do you think "winging it" is the better approach? Why/Why not?


So Hitchens starts to speak of his stint at MD Anderson and that alone puts me in a place I don't want to be, a place where I think of my own pain, my own loss, my own future.

So... we will talk about it next time! Part II How I Reacted to Hitchens Words...

But first...
Question:
Do you think it is wise to educate yourself on people in the public eye that you
fundamentally disagree with in order to simply know who the person is and what they represent?
Or... Do you feel that if you don't like a person or fundamentally disagree with the person,
you ignore articles that feature the person and do not learn about their background even if he or she is a newsmaker?


Hitchens photo courtesy of: http://www.telegraph.co.uk/
Vanity Fair cover: http://www.vanityfair.com


 ©The Healing Redhead

Wednesday, February 8, 2012

So What The Heck is NF, Anyway?

You get the diagnosis and begin dealing with your new life as a person with Neurofibromatosis. Family, friends, co-workers begin to ask questions. You ask yourself the same questions: "How are you holding up?" The answer varies, truly, as much as the weather here in Texas. Downpour and tornado warning one day and sunny, breezy the next. Your body can switch like *that,* a lightning bolt spasm that makes you jump in your chair during dinner or flail and jump from the shooting pains you get every night at bedtime. It's a nightmare day and night at times.

So, before I tell any more tales about my NF experiences, I thought it made sense to give a tutorial of sorts (Don't leave! This is good, important stuff! Promise.) to help those who may not know about NF and for those family members and patients that need a reference guide or a refresher course. Awareness is key and knowledge is power, right? :)

My first answer to the headline question (So What the Heck is NF?) is don't ask Oprah Winfrey.* Second, it's not something you can answer in 2-3 sentences. And no, this isn't a razzle-dazzle fun post but it is a very important one because it gives insight into patient symptoms and promotes awareness of a condition that is rarely, if ever, talked about in families, in the media, in politics, or on Main Street. We need to change that.

*Oprah Winfrey spotlighted NF on her show and ended up getting the facts mixed up and telling
her millions of viewers false information about the genetic disorder. FYI: It is not the
Elephant Man's Disease, Ms. Winfrey.

NF 101 In Session


Cases of Neurofibromatosis are as varied and unique as the patients living with the genetic
disorder. Some cases are non-symptomatic or mild while others can be the complete opposite.
Family members can be similar in the type(s) of symptoms they share or vary greatly. NF can also show up spontaneously without any family history, and we will discuss that more in a minute.

Key: NF patients can have tumors on the inside of their bodies that press on nerves causing pain from mild to severe. Other NF patients have tumors, on the outside, on top of the skin,
often protruding and causing deformities. Patients with internal tumors can have troublesome growths removed surgically but this can lead to nerve damage and also deformities of varying proportions.

NEUROFIBROMATOSIS
Encompasses a set of distinct genetic disorders (NF 1, NF 2, and Schwannomatosis) that causes
tumors, often benign (but not always), to grow along the nerves of the human body. Anywhere a
nerve is, a tumor can grow.

Key: NF can affect the development of bones and skin.
Key: NF can be inherited by a parent (50-50 chance) or maybe the result of a mutation in the
sperm or egg cell. www.ctf.org

Spelling Out A Diagnosis

Neuro*Fibro*Ma*Tosis

Or....

Neuro*Fibro*My Toe is Aching!

Or...

Neuro*Fibro*Ma (To Her Daughter): Find a Cure


I've made all the fun I want from a word and condition I want nothing to do with ever again
but am stuck with eternally until there is a cure.

Key: There is no cure for Neurofibromatosis.

Over two million (that doesn't include loved ones, caregivers, friends, etc.) people are
affected by NF across the globe. I find it staggering especially when fellow patients can' find the medical care (specialists) they need. NF is more prevalent than cystic fibrosis, Duchenne muscular dystrophy and Huntington's Disease combined. www.ctf.org

Amazing, huh?

Profile of NF 1
Called von Recklinghausen or Peripheral NF

1) One in every 3,000 births
2) Patients with NF 1 may have: blindness; disfigurement; dermal, brain, and spinal tumors; loss of limbs; cancerous growths; and learning disabilities.
3) Fifty percent of NF 1 patients have learning disabilities. The potential for learning
challenges is five times more common in the NF 1 community than in the general population.
A patient may show no signs or symptoms or 1-2 of the above. It is not an all or nothing
scenario with NF patients. Each person dealing with this condition has his/her own set of
challenges and difficulties, whether it is blindness, surgeries, or spinal growths.

Profile of NF 2
Called Bilateral Acoustic NF (BAN)

1) One in every 25,000 births
2) Patients may experience multiple growths on the cranial and spinal nerves.
3) Patients usually deal with tumors on their auditory nerves that affect hearing. Loss of
hearing in the teens and 20s is the tell-tale sign of NF 2.
4) Patients must deal with an increased risk of nervous system tumors.
5) Patients can have vision difficulties, including orbital tumors and cataracts.
6) For a person with NF 2, tumors grow on the eighth cranial nerve in both ears.


Schwannomatosis
Most recently identified

1) One in 40,000 births
2) Eighty-five percent of Schwannomatosis cases are sporadic with no previous family history and 15 percent of cases are inherited.
3) Chronic pain is usually the first sign of Schwannomatosis. It usually outweighs any neurological challenges. www.ctf.org
4) Patients do not typically develop canerous tumors.
5) About one-third of people living with Schwannomatosis have what is called Segmental
Schwannomatosis. Tumors are limited to a single part of a patient's body, i.e. section of
spine or right arm.

Neurofibro-get-your-tosis-together-and-get-out-of-my-body

I don't know know how many times I've said it or how many more times in the future, but at
least there is hope...FOR A CURE! Physicians are working. Researchers are working. Even some
patients are doing their part fund-raising, creating awareness in their own personal ways. We
fight through pain, exhaustion, the looks and stares, the side-effects of pills and the side-effects of NF.

Neurofibromatosis is here now... But NOT forever!

To donate to the Children's Tumor Foundation, Ending NF Through Research, go here.

 ©The Healing Redhead










Source: tumblr.com via Leslie on Pinterest

Friday, January 27, 2012

YouTube provides patients, families with NF resources

You've heard of The Cat Lady, the 100s of laughing babies made famous on YouTube, the countless furry friends doing tricks with a flying frisbee, piano, or even a plastic pool. What YOU may not know is that YouTube has its share of videos on Neurofibromatosis. Yes, NF! Some include patient stories while others detail physician descriptions on what we, as patients, have to look forward to in the future in terms of medical trials, latest science, etc. Of course, there are more graphic videos of actual fleshy tumors and even surgeries, but I didn't focus on that. There is enough information on NF -- even Schwannomatosis! -- that it can be a resource for patients and families to go to for information, for hope.

You can start out by typing in: Neurofibromatosis, Schwannomatosis, and then Children's Tumor Foundation. To give you an idea of what is available, I will feature -- from time to time -- a video I find on YouTube. Last night, I found one that tells a story of a husband and wife. The wife, Jill, calls Schwannomatosis the "intruder" that enters their lives and never leaves. It is a poignant and passionate talk told from the caregiver's prospective. When I saw it I knew I wanted to share it with you all. Warning: You may need a tissue or... two.

This talk allowed me to know there is someone else out there dealing with the same beast I am
-- every day. Because Schwannomatosis is so rare it is easy to feel alone at times. This talk
allowed me to see that others face the same obstacles I do (although I wish they didn't). The talk was honest, heart-felt, real. Take a look.

Here is the video.


It is such a powerful message. One that more patients & families need to hear.

You can access YouTube here.

Type in key words in the search box located at the upper right-hand side of the screen. Don't hesitate to make your own video & share your NF story with the world! Create more awareness!

The Children's Tumor Foundation Web site http://www.ctf.org/


©The Healing Redhead