Monday, November 28, 2011

Is It Cancer? MPNST and Neurofibromatosis




No one wants to hear the word Cancer directed at them, or anyone for that matter.  But for those of us with risk factors, we must realize the possibility of it happening.


Neurofibromatosis carries with it a number of issues; neurofibromas,  pigment changes in the skin, skeletal anomalies, and learning disabilities.


Although neurofibromas are benign tumors, malignant peripheral nerve sheath tumors (MPNST) sometimes occur. MPNST, in the past also referred to as “malignant schwannoma” or “neurofibromosarcoma,” and can occur in the general population but is one of the hallmark complications of NF1.


MPNST, typically forms from unexpected growth of a preexisting neurofibroma, particularly a plexiform neurofibroma, the first symptom is typically unexplained or sudden pain, in the area in or around existing tumors.


Symptoms may include:

  • Swelling in the extremities (arms or legs); the swelling often is painless.
  • Difficulty in moving the extremity that has the tumor, including a limp.
  • Soreness localized to the area of the tumor or in the extremity.

The thing to remember is that just because you have a higher risk in developing cancer, doesn't mean you will.  Being aware of your body and noting to your doctor any changes you notice is key in staying healthy, and catching things early.  Be aware of your tumors...how they feel and what they look like.

What is MPNST?
MPNST is also referred to as malignant Schwannoma, neurofibrosarcoma, and malignant neurilemmoma. This type of cancer usually develops in young or middle-aged adults, more often in men than in women. The average age of MPNST patients is between 29 and 36 years. About half of all cases of MPNST develop in people who have Neurofibromatosis.
http://en.wikipedia.org/wiki/Malignant_peripheral_nerve_sheath_tumor

Treatment?
To treat these tumors, a patient sees an oncologist and a neurosurgeon.  Also, patients can benefit  from being treated by medical teams that specialize in soft-tissue sarcoma tumors. Treatment of MPNST often involves several steps, depending on the location of the tumor, type of sarcoma, other patient circumstances and overall health.


Types

  • There are three main types of treatment for MPNST. These treatments are surgery, radiation and chemotherapy. Doctors often use all three types in combination to create specific individual treatment plans for a patient.

*Surgical Removal

  • The most common treatment for malignant peripheral nerve sheath tumors is surgical resection. Resection of tumors involves the removal of the tumor and surrounding malignant tissue. The doctors analyze the edges of the area removed, and if cancerous cells remain, they remove a little more surrounding tissue. This continues until the tissues the doctors remove are clear of cancer cells.

Radiation Therapy

  • Radiation is the use of specifically directed ionized radiation in a medical setting. Radiation is a common treatment for these tumors, and is often very effective at different stages. Preoperatively, radiation can reduce the size of a MPNST, making surgery easier for the doctor and therefore reducing the time spent under anesthesia. Radiation helps doctors achieve clear borders without having to cut out more tissue, which is very important when the tumor is in a peripheral area such as an arm or leg. Clearing the borders without going deeper often saves the patient from an amputation. Radiation can also destroy cancer cells that surgery couldn't remove.  (Radiation is sometimes used as a "last resort" with people with NF, because it has been studied that Radiation can make the symptoms of Neurofibromatosis worse.  Your doctor will decide what is best for YOU and your situation

Chemotherapy

  • While chemotherapy is not particularly effective at treating localized MPNST, doctors often use it to treat cancer that has spread to other areas. Chemotherapy, taken either orally or intravenously, involves taking medication that kills cells.


I didn't want to start the week with a negative post that scares people, but MPNST happens....And the more you know about it, the better chances you will have at catching it sooner.

MPNST is rare...But if you arm yourself with knowledge, IF it does happen to you, your outcome will be much more positive.

Even when it's scary....Even when it's overwhelming...A Positive Attitude is key in fighting ANY battle!  Remember, it's E.A.S.Y. to THRIVE; EDUCATE yourself-Watch your ATTITUDE-SHARE your stories-and YIELD to the possibility that anything is possible!

THRIVE ON!


Friday, November 25, 2011

Black Friday

We got up bright and early today...Got in the car and raced to be first in line.  Surprisingly...We found a parking spot, nice and close!

As we walked through the doors, we saw the crowds swarming.

No...We weren't at Target, Wal-Mart, Khols, or Sears....Today was "Chemo Day".

We spent our morning on the 7th floor of the Children's Hospital.

Chemo Days are always a mix of emotions.  Bailey says these days are her favorite day of the week.   I love my days with Bailey too, but tend to hold my joy, until after we hear what her counts are.

Today they were low.  Which explains Bailey's symptoms. (Dizziness, blurry vision, headaches, nausea)

Low Counts, doesn't always mean that we skip chemo...It just means we watch for worsening symptoms.  It's a numbers game...A frustrating game of "wait and see".

Bailey just goes with the flow...No complaining, no whining.  Always smiling...Always positive.  She has a true 'thriving' spirit and knows that sometimes, she has to experience a period of pain, to get to where she needs to be.

How are YOU, when things don't go your way?  When you experience a fork in the road?  Do you whine, complain and let the world know how unhappy you are?  Who are you when no one is watching?  Who are you when EVERYONE is watching?

I know for me, when I find myself complaining to the world...Everything I do from that point is negative.

Do yourself and everyone around you a favor....And try smiling when you want to cry.  Try saying something nice, when somebody says something mean.  I know it isn't easy...Just just for one day, live, breathe, and speak a Thriving Attitude...and see what comes from it.

THRIVE ON.

Thankfulness Continues...


I didn't have fancy plates, cloth napkins, or wine.  My turkey wasn't served on a polished silver platter...

We ate our food at a picnic table that is placed in my dining room.

As I looked at my kids (and hubby) slurping their food and wiping their mouths with their sleeves, I couldn't help but feel extremely grateful.

THIS is what I love about my family.  We are real.  We don't ask for much and we know how to enjoy the simple things.

Who could ask for more?

Wednesday, November 23, 2011

Thankfulness


thank-ful-ness Adj: The consciousness of being grateful for what has been received.



My Thankfulness List

*My Family.  I put this first, because without my husband and my children, my life would be meaningless-pointless-and empty.  The 7 people who live in my house with me have seen me at my worst....And they still love me.  They encourage me,e very single day...Even on the days when life just seems overwhelming and un-winnable.
-Specifically, my husband...who for whatever reason, loves me despite all of my "flaws".

*GOD.  Normally I would have put Him first...But without my family and the joy they bring to me...I HIGHLY doubt that there would be any sign of God in  my life.  God has also seen me at my worst.  He has seen me doubt Him, question Him, get angry with Him and even at times turn my back on Him...But yet, He is always there, ready for me to come back to Him.

*My Church Family.  There are those few that I have connected with on a deeply spiritual level.  You know who you are...I appreciate your encouragement more than I could possibly express with words. I LOVE YOU.

*Children's Hospital.  We met in July of 2010 and you embraced our family, and ALL of its medical needs without hesitation.  Your quick and thorough care of my daughter Bailey has been amazing.  You have touched every single member in my family in such a wonderfully positive way.


*Make-a-wish, Starlight Foundation, There with Care, FISH, Once Upon A Child.  Your organizations are priceless in the way they have touched my family.  You all give in selfless ways and we truly appreciate everything!

*Facebook/Blog.  This has been such a wonderful tool, to be able to connect with literally THOUSANDS of families who are dealing with Neurofibromatosis.  Three years ago, when I began the whole Thriving thing, I never imagined that it would become what it is today!  Thank you all for your wonderful feedback.  I hope that I can continue to represent A Thriving Life, and be an example of what it means to Speak and Live a positive attitude.


I wish all of you a wonderful, safe, blessed Thanksgiving.  
Thank YOU, for blessing my life with your friendship.

Thrive On!

Sunday, November 20, 2011

Sometimes it's About ME!



 Anybody who has a child going through some kind of long term medical treatment knows, that it doesn't just affect the child going to and from the hospital...It Affects the entire family.


While so much attention is focused on the ill child, healthy siblings can be faced with emotional challenges and need some help in navigating the impacts on their sibling as well as the stress placed on parents.


The Children's Hospital-Center for Cancer and Blood Disorders clinic in Aurora Colorado, has an amazing program  for siblings of patients going through chemotherapy and has touched our family, in a big way.



A few months ago, Riley got to spend the entire day at the hospital to talk about how SHE is feeling and make friends who just "get it"...She created a wonderful project that was supposed to represent "her"..and how she feels about her life.


A few weeks ago, Riley attended the "Color Me Mine" event.  


Not every hospital has this program, but if you have a child undergoing chemotherapy, it is definitely something you should ask about.