Tuesday, February 9, 2010

IEP's and Tongue Twisters

Turn-it-Around-Tuesda
y

How Much Wood Could A Wood Chuck Chuck, if a Wood Chuck Could Chuck Wood?

Good Question...I honestly don't really care. But sitting in the the small group, at Braden's IEP meeting yesterday, I began to wonder how bright our supposed "leaders" really are.

Do people really ponder questions like a wood chuck chucking wood, then make up a funny rhyme about it?

Anyways....Sometimes at these IEP meetings I have no choice, but to 'zone out', because they can get overwhelmingly exhausting.

As we were discussing the modifications of behavior and social skills part of the IEP, Neurofibromatosis came up in the discussion.

We had talked about our 'condition' at the beginning of the year and I even gave each of the teachers a wonderful print-out provided by The Children's Tumor Foundation, that explained the 'NF child' in a very descriptive, beautiful way. (thank you CTF for this) But it seems this print-out got lost, and the teacher just wanted to ask ME, the mom, some personal questions about how NF impacts Braden's life. (I was thinking "hmm this meeting is supposed to be 45 minutes...The ins and outs of my son and the way NF is a part of that would never be explained in 45 minutes! Like a spider's web....delicate and complex").

The teacher's began to joke about Neuro-Fibro-ma-tosis, in a light hearted, very unoffensive way. In fact, I kind laughed inside of myself at their ignorance. "Wow, that's such a long word and hard to say." One teacher said. Another said, "Yeah, kinda like a tongue twister, try saying it 3-times fast!" "Neurofibromatosis----Neuro--fibro--moy....ohhh DARN.....That's sooo hard to say!!!", the teacher said. And me, being me, finally gets to say the response I have been waiting for ....since I began blogging (and Thriving)........ "Think it's hard to say? Try Living with it!"

The room feel silent. The playfulness was over. How does NEUROFIBROMATOSIS impact Braden's Life ? Let me sum it up for you. It makes him stronger (not weaker), He learns different than other children, so help teach him, he loves different than other children, but still needs the same encouragement, he is soft spoken, so listen better, he may need to be told over and over to do something...but eventually--He'll get it, so praise him!

NF impacts our lives in so many ways, but only negatively, if we allow it. We have chosen, as a family to keep as much bad out....and to seal in as much good as we can. We focus on the good times, the happy times, because we know, there will be plenty of bad.

We are constantly "turning it around"...and finding something good....Because in life that's what you need to do. If you focus on the bad---that's all you will get.


Monday, February 8, 2010

Motivational Monday

I try to respect my doctors, I really do. When I go the the Dr, I respectfully listen to what they have to say. But lately, I have to wonder if some really know what the heck they are talking about.

Neurofibromatosis isn't THAT rare. 1 in 3,000 people are affected with NF in some form. Which makes me wonder why there aren't more Drs who know how to treat the symptoms that come with NF.

I actually had one DR recently tell me that my NF should not be causing me any pain...Ok maybe it should NOT, be, but it IS! She went on to tell me, that she would not prescribe me any pain medications because her past patients had taken advantage of her. So round and round we go.

It's like I am trying to change a dirty diaper with one hand tied behind my back. The job, however tough it may be, CAN be done. There ARE solutions and ways to do it....I just need to find them.

I have an MRI that diagnoses me with hydrocephalus. I have NO history of EVER abusing narcotics. And....I am very obviously in pain....and my Dr doesn't give a damn. "The only thing I can do for you, is UP your Topomax, Kristi."

(I take 100 mg of Topomax nightly and have found no change in my headaches. All I have found happening is blurry vision, my hair falling our and I'm dizzy and hell)

I ask this "doctor" about sending me to a pain management clinic and she tells me that there are none available in our city. I swallow hard, and close my eyes.

What does one do, when no help is available? Where do you go? Well....You just keep searching for that one place or person who CAN help you. I found that place in The National Institute of Health. They know about my headaches.....I have Drs there who listen...who care. I hope one day, I can participate in research for NF and headaches. Until then, I won't give up....give fighting....keep THRIVING.

Thursday, February 4, 2010

Thriving Thursday (Guest Blogger)

Having a rare genetic disorder puts you into a whole different world. You meet people you wouldn't have met, if the illness had not been a part of your life. For that, I feel like Neurofibromatosis has been a blessing. So many lives, so many families, touched by NF. I am thankful for each of the friendships I have made, on my journey.

Thanks to FaceBook, I met Michael Forbes. A 40 something single guy, who touched my heart. His personality and brilliant writings drew me in almost immediately.

He's just a guy, who is out there, fighting the good fight, but with that THRIVING attitude that pushes him to the top! I am proud to call Michael a friend and proud to have him a part of my THRIVING with NF blog!

Today, he tells and inspiring story of overcoming addiction, fears, and depression. Something we all deal with on a daily basis. I connected with this story and felt the pain Michael had to deal with and I am proud of him for being brave enough to share his story.

Please leave him some love, and let him know what you think!

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**Copied with permission from Michael Forbes http://www.nfonroute66.com**

Changes contain powers that transform how we live. After 44 years, I have learned this valuable lesson and now accept the shifts in the paradigms of my life. Yet, I didn’t consciously acknowledge the growth changes bring until June, 2002 during a doctor’s appointment. I hid in the addiction of nicotine.

At times, the throbbing the pain in my leg was so excruciating that I wobbled while walking. I was discussing with my specialist a proper course of treatment for the plexiform, having finished a years worth of MRI’s, CT Scans, and other assorted tests. The results all negative followed a typical pattern. Tumors bother me for a period of time, I get a battery of tests, and the pain magically stops.

After the exam, I stood behind a curtain getting dressed. Her voice hovered over the white tatted top. “Have you dealt with the psychological aspects of having Neurofibromatosis?” I told her no, yet knew most of my issues related to NF and life were emotional.

I left her office at University of Chicago Hospitals and lit a Marlboro inhaling the disappointment. I walked around the campus, stopping at 57th Street Books and an Asian Noodle restaurant. The immediate point I had to deal with was a constant pattern. Another NF complexity without an answer. The psychological question altered my life when August arrived.

Sure one doctor said he could remove the tumor and was gangbusters to anesthetize me and perform his Jekyll style of medicine. I thought his ego was over inflated and said no. I feared losing my leg, which a second surgeon suggested. On top of that, I had to consider my out of pocket expenses since my health insurance declined more then they paid.

As a child, I remember endless doctor visits, exploring treatment options. I started walking at age 2 and talking at 4. Even this young I felt different. After corrective hip surgery, doctors advised me to stop bicycle riding and playing soccer, because contact sports could cause permanent damage. They also confirmed my previous mind-set.

Given the changes and additional rejection (even the school district declined requests to test me for learning disabilities,) thrust upon me in 13 years, I disappeared into the addiction of nicotine when a friend and I decided to buy a pack of cigarettes at a local pizza restaurant. Neurofibromatosis sucked and adults told me to just breathe through the pain, be normal, and fearless.

Cigarettes provided solace. Their comfort intensified as I entered puberty. My body changed more compared to others, when mosquito bite sized tumors formed along with my facial and pubic hair. Peers teased me about my large head and instead of defending myself, I hid in the hazy fog of cigarette smoke. Even my sin sticks were hidden under the eaves of a local church rarely entering my house.

The other aspects growing up were typical. I became friends with other king sized squares, worked, and dated. I valued this transformation. NF remained the harder one to accept. I believed facial disfigurement would strike me at any time and was scared, rarely discussing it, since I had to be fearless according to adults.

My late teens and early 20’s were easier. In college, I explored various majors earning a degree in Behavioral Science. I worked as a case manager serving the disabled. My identity remained hidden helping others. Peacefulness continued to be found in packs of twenty. Each working day I’d be outside at 10:30, 12:30, and 3:00, feeling blissful for seven whole minutes, while I toked my 100mm friend.

Cigarettes stood by my side as I consumed Barium for CT scans. Cigarettes were there after I spent two hours in a claustrophobic MRI machine. Cigarettes were there for the happy negative results I received. Cigarettes were there when my health plan denied payments. All I had to say was, “God I need a cigarette,” and my savior appeared with the flick of a bic. I desired to quit and accept Neurofibromatosis once and for all.

The warm sunny days of August 2002 finally arrived and a singles camp in Saugatuck, Michigan. From the moment, I pulled up to the sandy – tree lined grounds, magic was in the air. Several morning groups were offered, and since my specialist felt I could benefit from the therapy, I chose massage. This involved exposing my tumors, which made me uncomfortable, especially in front of strangers. Yet, I risked ridicule and enrolled.

A dimly lit cinder block hallway led to the massage rooms. Whiffs of lemony pine aromatherapy scents filled the air and I entered the men’s locker room. The time had arrived to either show off my tumor-ridden body or continue hiding. I put on my blue/gray swimming trunks and slid across the sandy tiled floor into the massage room.

As I entered, quiet new age instrumental music echoed from a cassette player. Several sheet covered tables stood in the center with chairs around the edges. My inner child came out upon seeing a light green sheet with turtles imprinted on the percale. I had these sheets when I was young and keep a souvenir pillowcase from the set in a box of childhood memories. I choose this table as my own and ran my hand across the sheet releasing the memories of being six.

One the first day, the group leader handed out several papers, asked us what we desired, and took questions. I discussed NF referencing the tumors inside my body. After a demonstration on face and neck techniques, it was the participant’s turn. Two gentle kneading hands flowed over my face and neck that morning as my partner touched me sending me into a hypnotic trance. The turtles provided comfortable safety that week of learning a full body massage. No one ran and people wanted more information about Neurofibromatosis. The highlight of getting a massage arrived though by Paige, a woman separate from the massage group.

I was the only person in my coed cabin taking massage. On the evening of August 6 the women talked me into massaging them. After an hour it was my turn. Three women took turns massaging me. Paige went last and with a rhythmic pattern caressed my neck to deeper levels. After a couple hours of sleep, I awoke. Consumed by overwhelming sadness, the pivotal June question my specialist asked surfaced. Had I ever dealt with the Psychological aspects of having Neurofibromatosis?

In the early morning moonlit hours, I sat in an outdoor sanctuary crying. I watched deer feeding on vegetation, felt the light–dew filled breeze on my skin, and heard the crackling waves of Lake Michigan meeting the shore. I started a transition by questioning myself about my life, feeling a new connection in body, mind, and spirit. The compassion of this Unitarian camp, its community, and land catapulted me to a new level of consciousness. Four days later, I left a new man, seeing Neurofibromatosis in a new light, grateful to Paige’s massage, and to God. I was ready to confront my addiction. On November 4, after taking a smoking cessation class and joining a support group, I drew in my last smoke while walking my dogs. After 27 years smoking finally stopped stunting my growth.

Today, my life has become a wonderful and amusing journey. New choices always appear and I have a spiritual connection to the universe. God has always watched over me, including those early years when my cigarettes were buried on church property. Now I am blessed to be me, liberating the scared child, accepting the powers of change, connecting with others, and looking for my soul mate. Neurofibromatosis is finally part of who I am. Only its symptoms need treatment.

© Michael Forbes 2009

Wednesday, February 3, 2010

Whiny Wednesday

Yeah, I do it every time....I push and push until things kinda just explode. I tend to look at things backwards, from the end result first and maybe that's my problem. But I just want what I want --when I want it!!

Yesterday, I found myself welling up with frustration....and no matter how much I tried to control it...I was bound for the edge, no matter what. In fact, I had huge rolling boulders pushing me towards the edge the entire day.

From the leaky washer, the van breaking down, vomit in the car seat, and cancelling an important appointment...the day was just horrible.....I found myself building up with this enormous amount of frustration and tension, and I didn't know what to do, or how to escape it.

Most of my posts are positive and uplifting...but today---forgive me, I just want to whine :)

After the van thing, the puke thing, and the appointment thing--I used our friends other car to get a few things done that needed to (THANK YOU TERRY) and had some time to think and sort out my craziness.

IF the van had not broken down....I would have had to take a puke covered Brooklyn to Bailey's appointment....so maybe God was working in some way there....? I don't know, the brighter side of things was where I was trying to get myself.

By the time I had gotten home from running around, Bailey had thawed dinner, made sure everyone's homework was done, bathed Brook and had the other kids get their chores at least started.

My bad day vanished right before my very eyes, as my children surrounded me with hugs and kisses...proud of their accomplishments. Even though sometimes, I find myself at the edge...something always pulls me back. And if I happen to fall crashing to the bottom....I can always start over with a new day...A new perspective.

Today is better and I am thankful for that-

Monday, February 1, 2010

Motivational Monday

"I wish to be a Princess, and to see the castle!" Rachel said as her eyes lit up up with excitement.

Lora and Kathy talked to Rachel about where the castle was, and how you need an airplane to get there. The other kids circled around Rachel, like hovering vultures, waiting for a meal.

The wish granters needed to hear Rachel say it....."I WISH TO GO TO DISNEYWORLD!!" She screamed. Our awesome wish granters then talked to us about the technical side of all this and handed me some paperwork, as the kids opened up some gifts.

I was already soggy with tears....I can't imagine how the rest of this wish is going to go.

I sat and watched as the kids tore into their gifts. After all the birthdays and just having Christmas, this was sure a treat! I was so amazed at the thoughtfulness in picking these gifts out...they were perfect!

Rachel opened up a official Make-a-wish Barbie doll, Brooklyn got a Little People Airplane and Riker got a read-a-loud story book. The older kids got gift cards for Target...which we will save to buy goodies for the plane ride!

The wish granters (Lora and Kathy) and I visited as the kids talked about the gifts and about the upcoming trip.

This was an awesome time to help someone understand Neurofibromatosis and its affect on our family. NF doesn't just affect those diagnosed with this life-long monster....Everyone in the family feels the pain from it.

I hate knowing knowing that there is nothing I can do to make my kids better. No cure, no treatments. The progression of Neurofibromatosis, is steady and cruel and I hate every second of it.

But in that moment, while telling Kathy and Lora all about NF, I looked over at my children and saw them happy. They didn't care about NF. In fact, they never really do. I am the one who stresses..I am the one who worries.

So even while NF may take part or all of my daughters sight, cause tumors to form in and out of her tiny body, cause learning disabilities and limit her motor abilities-SHE is the one who is teaching me to go beyond the diagnoses and see past it.

Lora and I have been in contact since her visit with us, and our trip to Disney World is set. March 22nd, out family of 8 will venture off to Florida to stay in "Give Kids the World" resort. We will visit theme parks and have fun...taking NF and squashing it, for a week.
This is the very first vacation for our family, so we are very excited. Make-A-Wish has already blessed my family so much, I can't imagine what is in store for us.