Go safer and go green – Go the Melaleuca way – or make your own stuff and SAVE

In February, I joined Melaleuca Wellness Company as a preferred customer. They make safer, natural products.  Preferred customers shop every month on the website, and save.  They even give you twenty loyalty dollars for the first 6 months, which means you get free products.  And the products are amazing.  I like the Renew body lotion, and so does my niece, who has eczema.  I use it because ever since my last back surgery in 2010, my back has been itching like crazy, and Renew lotion is the only product I’ve used that stops the itch.  I was so happy I joined Melaleuca, and when I think of the two years I spent in needless discomfort, I mentally kick myself .  The vitamin supplements are awesome, as well.  I can’t really swallow horse pills, which is what you get when you buy them at Walmart or somewhere else.  These vitamin supplements are broken down, so I swallow two multivitamins and 4 calcium pills every day.  Which is a lot better than gagging and choking on a horse pill.

We have all heard the horror stories.  Johnson & Johnson uses formaldehyde in their products.  Shampoos and conditioners off the shelf have a lot of cheap ingredients that make your hair feel clean, but they are not exactly safe.  Environmental cancer is possible.  Olivia Newton-John’s daughter had a childhood friend who died of it.  It happens.  The toxins are real.  And they are deadly.  Remember those Mr. Yuk stickers they gave us in school to put on products that were poisonous in our homes?  The poison was not necessary then, and it isn’t necessary now.  A friend from high school told me she makes her own laundry soap.  Tide laundry detergent, Lysol, bleach,  and many others are REGISTERED PESTICIDES.  I don’t know about you, but that both disgusts and scares me.  If you google it, there are lots of ways to make your own natural laundry soap.  It’s not expensive or time-consuming.  Quite the opposite, really.  I have it on good authority.

If you are interested in joining Melaleuca or just learning more about it, leave a comment below and I’ll put you in touch with someone who will take you from there.  And if you do the business part of Melaleuca, you will even make money or even replace an income.  If you want to rake in more, and stay home with the kids and live greener lifesyles, this is a great opportunity to do that.

Things I’d Like To Do Someday

I love the saying in the image above – the truth in them is universal, because it goes for every single person in the world, no matter who they are, or what their background is.  Writing is basically all I need to do these days (other than obligations like to family and friends, etc).  I can see it all in my mind now:  I will write and all the pieces will fall into place as I go.

Here is my list of things I’d like to do SOMEDAY:

1.  Sponsor a child.  I am not picky about the country, but I’d love to the opportunity to go visit said child as well.  I’d love to get to know him/her on a more personal level.  Compassion, it seems, is my specialty.

2.  Keep on bringing more and more awareness to pediatric cancer.  I will never stop caring about this.  Ever.  I will keep fighting until my very last breath.  I’d dearly love to visit St. Jude’s and other hospitals.  I’d love to meet the people I’ve met online since I started advocating for this.  Maya Thompson and Melinda Marchiano, this means you!

3.  Go to Disneyland with my family, and watch my niece’s face light up when she sees Mickey Mouse,

4.  Meet the celebrities that I love – to thank them for sharing their gifts with the world.  The list includes Sarah Michelle Gellar, Olivia Newton-John, the cast of Glee (especially Darren Criss, Chris Colfer, Kevin McHale, Lea Michele, Dianna Argon, everyone on the show, really), Johnny Depp (I am curious to see what he is really like, especially since I took a “Which Celebrity You Should Marry” quiz on Facebook and my result was Johnny…  Weird?), Howie D of the Backstreet Boys, Kristoffer Polaha (though probably not him because I’d cry at his pure loveliness), Taylor Swift, Jodi Picoult, Amanda Seyfried, Meryl Streep, Emma Stone (we’d have so much fun together), David Boreanaz, Allyson Hannigan, James Marsters, Joss Whedon (to thank him for the loveliness that is Buffy the Vampire Slayer, my favorite show EVER), casts of both Grey’s Anatomy and Private Practice, the list goes on and on and on!

5.  Visit Rome, Italy and the Vatican.  Have genuine Italian food.

6. Ride horseback along a beach dressed in white – leggings and a dress.  I dunno why the white is so important to me, but it is.

7.  Have a pack of shih tzus/Ewoks…  PURE HAPPINESS!  Guess I better start saving for a California King bed!  Oy!

8.  See a Broadway show.

9.  See unicorns.   They are real.   I just know it.  How?  The Bible says so.  All you naysayers, hush.  I don’t want to hear it.

10.  This one is really tentative, because I do not think I’d be brave enough to do it, when it comes down to it:  Visit a known haunted house.  Doubt I’d last even 5 minutes…   I am such a wuss!  But I’d like to try…

I might add to this list as time goes on.  In the meantime, what’s on your big list of things to do?

Gratituesday

Gratituesday is something that Kate Walsh, aka Dr. Addison Forbes Montgomery on ABC’s “Private Practice” does on her facebook fan page. Every Tuesday, she finds something to be grateful for, and all (or most) of her fans follow suit. I think it is a great idea. It reminds me of the Olivia Newton-John song “Grace and Gratitude.”

“All I have and all I feel / is all because of you / all I reap is all I sow / and love is our living proof / Thank you for life / Thank you for everything / I stand here in grace and gratitude / and I thank you / Seasons come and seasons go, / No matter what we choose / A thousand names / A thousand roads / All lead to one simple truth…”

One simple truth. And what is that? That we are loved so much more than we can ever imagine. By who? By the One who created us, of course. I’m not just talking about our parents, for we began before that. We come from a place so beautiful and so filled with love that it is a shame that this world can tarnish us and make us forget. And we do forget. Most of it, at least.

This Gratituesday, I can see my dream play out in my mind. I see myself typing and typing and typing, for so long and so fast, never slowing, like I am now, and then sending it out into the world. Only then will I sit back and wait and trust. And trust some more. I know what I have to write, or at least, I know most of it. The rest will come in time.

This dream I have was placed in me for a reason. It is my purpose in life. I believe it with all that I am; every single square inch of me tingles with it. Every day I get a little closer. At times I will become frustrated by the slowness of it, but when that happens, I just have to remind myself that things unfold in God’s time, not mine.

God is everywhere at once, whispering in our souls that we are everything to Him. He can attest to our worth, even if no one else does. We each mean something to this world. We each attribute to its beauty. We each have gifts no one else has, at least not to the degree we have them.

I am gratified by this encouragement. I am grateful for a million things at once, my life and everything in it. It would take forever to list them all. God’s love, my family, my friends, my dog, the freedom to dream, my health, the health of my loved ones, music (I am always, always grateful for music and that I can hear enough to enjoy it), books, the internet, my room, entertainment, America’s military, food, shelter and clothing, blankets,joy, laughter, quietness, rainbows, trees, writing, my mind (which frees me), faith, conversations, so on and so forth.

Right now, I am gratified by the peace of the moment.

This is how it happened…

Hello, world!  I thought I’d try this blog thing.  I am an aspiring novelist, who is a childhood cancer survivor (or as one of my celebrity role models, Olivia Newton-John, would say ” cancer striver”).  I was diagnosed with stage 4 neuroblastoma in January of 1983.  I was barely 16 months old.  My parents had noticed that I was walking funny, leaning on walls and furniture and falling down a lot.  My mom brought it up with a nurse at my regular check-up, and the nurse assured her that all babies fall down a lot when they first start out walking and it was probably nothing.  But it was something, as tests came back positive for cancer.  The tumor was attached to my right kidney, on my right adrenal gland to be more exact.  Right away, I was scheduled for surgery.  They had to postpone it, however, because I came down with a cold.  After this major surgery (during which they removed 50% of the tumor), I had another minor one to insert a Hickman line so the nurses didn’t have to poke me with a needle every time they drew blood or gave me chemotherapy.  Thus started 19 long months of chemo.  I also had 3 doses of radiation.  And then another major surgery, a “look-see” to find out where the tumor was at in terms of size.  In the 1980′s, they didn’t know a lot about treating cancer, and they knew even less about treating cancer in babies.  My doctors and nurses were just scrambling around, trying to save my life.  One day, my dad got a phone call from a doctor, who was crying.  The cancer had spread.  Later, they would find out that my lab results had gotten mixed up with someone else’s, but by the time they figured that out, it was too late.  I had two really bad ear infections that were overlooked.  I came down with a viral infection called encephalitis, and it attacked and damaged my brain stem.  My parents rushed me to the hospital because I was screaming and crying that my legs hurt and I had a really high fever as well.  Finally, I fell into a semi-coma, and during the next few days, my parents witnessed my body changing right before their eyes.  I was right-handed, but now my right hand was curling into my wrist, and my body was as limp as a noodle.  When I was released from the hospital, I was like a newborn baby again.  I couldn’t sit up or even hold my head up.  I couldn’t swallow, so I had to be nourished through an I.V.  Couldn’t talk or anything.

A month later, my brother Ryan was born.  I was delighted!  When my parents brought him home from the hospital, I was sitting on an armchair in front of the window waiting for them.  I got to hold the baby right away.  Ryan woke up and started crying.  Most of my hearing was gone (although no one knew this because I was smart…  I adapted to my new circumstances and taught myself how to read lips almost right away.  Fooled my parents for 2 1/2 years!), and so I didn’t know what he was doing.  I reached over and closed his mouth.  Everybody laughed.  They still chuckle about that story to this day.

I watched my brother, this new addition to my family.  When he learned how to crawl, I started scooting across the floor on my belly, eventually working up to my hands and knees.  And when Ryan began to walk, I started to get to my feet using furniture as a support.  My dad built me a little indoor ramp which helped me take my first steps independently since this happened to me.  My mom taught me to sign a little, though it was difficult since I could only really use my left hand.  And when I was 5 1/2, I got hearing aids.  My other brother Patrick was born.  Two years later, my little sister, Jacqueline, was born.  I was so happy to finally have a sister.

Sooner or later, my parents knew that I was going to need a back brace, since they radiated only half of my spine back when I was being treated for the neuroblastoma.  Half of my spine grew with me, and the other half didn’t.  They knew even back then that I would develop scoliosis.  Shortly after we moved to Cashmere, Washington, they noticed my back curving more and more.  Finally, they couldn’t wait any longer.  I, of course, being just 9 years old, didn’t understand.   I was just going by what was happening in the moment, and I just knew that I didn’t like it.  They put me on a stretcher-like thing, with two bars at the sides and one narrow strip of material down the middle.  I was so scared I was going to fall, despite of how many pairs of hands were holding on to me.  All I knew was that if I fell, I would be completely powerless to stop myself from being hurt.  And I’ve always been completely terrified of physical pain.

I was 14 when I had my first back surgery.  My doctors originally wanted to go ahead and fuse the whole dang spine, but my parents were a little leery of this, since no one could promise them I would still be able to walk afterwards.  Finally, one of my surgeons spoke up.  His name was Dr. Bill Bronson.  He and my dad had gone to high school together.  He suggested that they fuse part of my spine then, and later, they could go back in and do the whole thing if they really needed to.  He said that if we did do part of it now, chances are good that it might break down over time.  But it would buy me time.  And so that is what we did.  I was promised that I would be free of the brace eventually.  And so this is what we did.  I missed a lot of school during eighth grade, but I was able to graduate to high school with my class – the class of 2000.

High school was, well, it was high school.  Full of teenage angst and tears and frustration.  But also a time of liberation.  For the first time in my life, I knew what it was like to really have friends I could count on.  These were friendships that lasted too, which was so important to me.  I never had anything like it before.  In the middle of my sophomore year, I became friends with a girl named Tammy who was in a grade above mine.  We were kindred spirits. When Tammy graduated, I became friends with a girl named Valerie, who was in my class.  We kinda bonded over the show Buffy the Vampire Slayer.  :)   I absolutely love that show.  It speaks to me, to my heart.  Buffy Summers was alienated because she was different.  I was too.  I understood the heroine completely, because what she was going through, namely the ostracization by her peers.  And I loved the fact that in Buffy’s world, the problems that teenagers face become literal monsters.  How many times had I wanted to just beat the crap out of my problems?  How many times had I just wanted to give up, but instead I pressed on?

“You have to be strong… The hardest thing in this world is to live in it.  Be brave.  Live…”  ~ Buffy Summers, season 5, The Gift

“Make your choice:  Are you ready to be strong?”  ~ Buffy Summers, Season 7, Chosen

After high school, I went on to get my AA degree at the local community college.  Fall of 2002 saw me moving into a dorm at Central Washington University.  I decided to major in English because I’ve always loved to read and write, and I learned at an early age that I could make myself be understood (because of my hearing loss, I have a speech impairment) if I wrote down what I wanted to say.  This bloomed into creative writing.  I lived in a dorm room by myself and got to be fully independent for the first time in my life.  I absolutely loved it.    I graduated with my Bachelor of Arts in June of 2004.  That summer, my back started acting up.  If I did a lot of walking, I would be in so much pain I couldn’t move.  This went on for a year.  In summer of 2005, I had my second back surgery.  Dr. Bill Bronson was my primary surgeon.  The work they had done before, when I was 14, was breaking down, just as they expected.  Dr. Bronson went in and fixed that one area.  I was in the hospital for about 5 days and then went home.  That night, however, I felt something give inside me and a burning pain started in my left thigh.  I didn’t know how much it WOULD hurt until the next morning, when I tried to get out of bed.  Oh my gosh, it was the worse pain I’ve ever felt.  Excruciating. I was like, okay, this is it.  This is the pain I’ve been expecting all my life.  My leg felt like it was on fire, if I had known what being on fire felt like.  I screamed and cried for 4 weeks straight, through 2 rounds of steroids.  They thought I had a pinched nerve.  Finally, I went in for x-rays.  Oops.  All the hardware they put in during the surgery was loose inside me.  I remember Dr. Bronson saying surgery had only a 60% chance of fixing it.  I just stared at him.  I was like, seriously?  But they finally went in and fixed it and I woke up without the burning pain.  The only thing was I had to wear a back brace for 3 months to help stabilize my spine.  Ugh.

After that, my back was fine for a while.  And then it started hurting in the morning when I sat up to get out of bed.  EVERY. SINGLE.  DAY.  It always went away eventually, within 10 minutes or so.  But while it lasted, it was excruciating.  Because it went away, I was able to ignore it for 2 years.  And then, finally last summer, I had the full she-bang done.  9 days in the hospital.  And then my parents started remodeling our house, to give me a room on the main floor.  I had fallen down the stairs multiple times before, and we all knew if that happened again, it wouldn’t be good.  Since I have a rod the length of my spine inside me, chances are that I wouldn’t survive another fall down the stairs.  And all the bedrooms were upstairs!  Last summer was very long and boring…  I was either stuck upstairs in my room or stuck downstairs.  I had a physical therapist come to the house.  I relearned how to walk.  But while I recuperated, I couldn’t go out and do stuff.  Thank goodness for a mail order library and netflix.  Without these two things, I would have surely lost my sanity.  And of course, my shih tzu, Buffy (yes, yes, I named her after my favorite show).

I have my room downstairs.  I have my dog.  I have my niece Aliza who is 2 (her daddy is my brother Patrick.  I absolutely adore her momma Angelica!).  I am pain-free.  And now it is time to get serious about writing!