Sunday, April 1, 2012

I wonder what will be in 100 years.


Friday march 30th, 2012 was my 10th week anniversary celebrating the beginning of the recovery of my body. I was waking up after three long years of illness. That Friday, I went about my day like any day but something felt different.  There was a bit more oxygen in my muscles, my mind was clearer, my heart was lighter.  When the time was drawing near to bedtime I realized it was the first, almost normal day, I had in three years.

It was an incredible feeling as my body and mind started to feel a new sense of wholeness.  I felt elation and gratitude as one day led into the next realizing that my main concern was not on my health but regaining a lost life. I was rejoining the circle of life in a way that I so desperately missed.

In October of 1009, I received a call from my rheumatologist that my blood count was extremely low.   My doctor feared that I had internal bleeding and so I began the testing process.  My nightmare began when the doctors could not find out why this was happening.  Added to this new issue my kidneys began to decline, I developed a distinctive rash on my legs, my autoimmune system was going haywire causing infection after infection, a lump surfaced on my arm, tensions was rising, testing and testing, blood infusions were numerous, biopsies and yet no answers.  My body was failing yet there were no answers.  The doctors at the mayo Clinic in MN finally diagnosed me with two rare diseases, cryoglobulinemiua vasculitis, in July 2010, along with a host of other complications.  During the course of the next three years I fought for my life.  After two separate rounds of chemotherapy,  I’m starting to face each new day with a smile of hope for a future of wellness.

It has been 13 years now since I let go of my former life when autoimmune diseases attacked my body.  It began with Lyme disease, fibromyalgia, chronic fatigue syndrome, rheumatoid arthritis, raynauds, thyroid disease, anemia, hormone imbalances, just to identify the main diseases.  I was living a healthy lifestyle, eating right and exercising at the time.  Most people called me a health nut.  In fact, my career was in health, fitness and nutrition.  What was the benefit I often ask myself? What causes disease to attack a seemingly healthy body?  Why did I have to let go of all the things I loved so desperately? Why was I always sick, so weak, in so much pain and never able to regain my strength long enough to reenter the life I once knew?  My husband and I tried every conceivable treatment to help my body regain strength and wellness but to our disappointment, it never happened.

Just when I thought my medical condition could not get any worse, to my utter surprise my health desperately decline in 2009.  We knew that I was seriously ill, my disease was life threatening and there was no allot that was know about my condition.  It was frightening not knowing where this rare disease was leading me.  This fear is one that millions live with every day.  A whole new world opened up to me when I found other people living with rare diseases on social media sights all around the world.  Now I sit day after day in conversation with this new world.  I know that I can make a difference in at least one person’s life by sharing my life experiences living with chronic illness and learning to cope with my rare diseases.  I will share my stories, my knowledge and my struggles along with my confidence and courage to live my life as rich and as full as I believe is possible.

I have learned so much about life on this journey living with daily illness and count my blessings that I view my live with a cup that is always full.  I can honestly say that I am fortunate to have been removed from the merry go round of life, to have had the opportunity to look within myself and see what I call the quiet voice of my soul.  I’ve embraced the philosophy of the east and honor myself in spite of the fact that my body is ill.  I have learned that I am not my body and I will do everything I can to understand what I can do to heal what hurts.

This is a brand new chapter and a powerful one for me.  I’ve been told I’m in remission, whatever that means.  Basically my doctors do not know enough about my illness to tell me what tomorrow will bring.  But, I do not need to know about tomorrow because my focus is on today.

There is so much that is unknown, in this year of 2012, about these mysterious diseases that are affecting society.  So many children are suffering with no treatment.   Why?  Is it the environment, global warning, toxins, fake food, pesticides, additives, preservatives, antibiotics, contaminates, medications, processed food, WHAT?  How have we gotten to this point?  How long will it take society to clean up this toxic world?  The question is actually what we do not know.  Where do we start undoing the damage done to this once pure and clean world?  We are progressing in this 21st century but how long it will take before we end this epidemic threatening the lives of society, zapping our life energy needed to maintain an average life.  It have been said in Buddhism, it takes a thousand life times to undue all that we have created within to rediscover our true selves.  How long will it take mankind to clean up our toxic world and restore health in the human body?

I just ask myself these questions because I’m not a scientist, a doctor or and educated person that would understand things beyond ordinary living.  I know the basics of clean living and it hadn’t worked for me.  There are too many other factors that clearly are out of control.

Now I’m awake again, able to think clearly and process new information, I am learning so much about social media, how it is connecting the dots between sick people around the world, patients like myself, the medical industry, legislation and research.  It is and endless web of people meeting people, and that continues into not only medical issues but every aspect of life.  It’s exciting to watch and I pray that the lines that are connecting the dots will someday bring us to a better, cleaner and healthier world.  I want to engage my energies into this powerful grassroots movement in hopes to create awareness to this complex mystery of health.  It is my intention to empower those living with chronic and debilitating diseases to observe themselves as a person of wellness not just a broken body. Through mindful awareness, we can live a life of wholeness in ways that some many never have imagined.  The Buddha once said, ‘what you think you become”.  I will not become disabled in my mind or in my spirit.

The miracles that will take place within the medical field in the next 100 years are beyond my comprehension. I imagine cruelty to animals will be extinct, we will swim in crystal clear waters, the food we know of today will no longer be contaminated with poisons that destroy our immune system, pesticide will be a  term no longer in existence, the emphasis will totally be on wellness not illness, the medical field will be one of solidarity with holistic care being in the forefront, our bodies will be clean.  Is it is possible?  All things are possible in and through God but what about in the hearts and minds of mandkind?  Will the global connection of all beings someday lead us to a healthier life style where disease is nonexistent? I wonder.



Friday, March 30, 2012

30 Day Health Activist Challenge Post

I just wanted to tell you about a new activity I'll be doing this April. The Health Activist Writer's Month Challenge hosted by http://myhealthshare.org. I will be writing a post a day for all 30 days. I hope you'll join me in writing every day about health. It's going to be a lot of fun and I'd love to see what you have to say about each of the topics, too. All you have to do is be able to start posting once April rolls around. Looking forward to writing with you!

Tuesday, March 13, 2012

Rethinking the loss of oneself.


This is the first short blog I am posting as I catch up on the last 15 months of my life living with Cryoglobulinemia.


It's important to realize that everyone is entitled to a pity party as situations arise in our lives especially when illness incapacitates normal living. The poor me attitude gets us no where. It simply boils down to two choices. Either you say, these are the cards I've been dealt and no matter how bad they may look I'm going to  play them the best I can, or you give in to letting your mind take you to dark places of negativity. What are your chances for happiness then.  I chose life, freedom from doom, possibilities for tomorrow.  I do understand that the human body can only withstand a certain level of stress and eventually the nervous system breaks down causing emotional issues. I've been there in my most difficult years which have been many. In situations like this I agree we may need either counseling or medical intervention or perhaps a crazy night out with a bunch of friends. These times don't have to last forever.  They are just brief moments in time that we learn to rise above if we choose.
First let go of all the negative things that rattle the mind, that being the things that remind us of loss. Then restore our minds with the opportunity of inventing "a new me". There is a Buddhist saying, "You become what you think". I have learned to rethink the new me. Because my state of "wellness" has changed that does not mean that I have changed. I am still the same person with physical limitations. Notice I did not say my health problems. So important. I can not let my physical limitations stop my life. As a sit quietly and let go of the loss,  pain, frustration,  fear, and allow the past to leave my mind and my energy body I now can open myself up to new possibilities. I once was, by title, a personnel trainer, body builder, athlete, yoga instructor, sales associate, sales manager, landscape designer, nutrition counselor.  That does not determine who I am today.  Today I am free from titles. My door is open and the breeze continues to bring me friends, teachers, mentors, opportunities, love and the ability to see that I still am Me but my exterior has changed. I will always be a devoted wife, mother and nanny but my first priority is finding the peace and joy that enthralls me to become a better me. In my lowest times I held desperately onto Hope but now my visceral reaction has become Determination. 
I am determined to find answers for others suffering with this rare disease Cryoglobulinemia. I will find support and help lead the way to a community just for our disease.  Sitting alone at home with a rare disease is frightening because you know you aren't going to get a set of text book answers.  You may not get answers at all. Finding a doctor who understands a rare disease is a big undertaking. Finding an approved treatment is almost unheard of. But we never give up hope.

 We may be Rare. But we are Strong.


Sending healing thoughts to all.



Sunday, February 26, 2012

Rare Disease Day - February 29,2012




Handprints Across America

There are nearly 30 million Americans living with rare diseases. We want to see you and how Rare Disease Day is spreading across the United States. We invite you to print out this flyer with the Rare Disease Day logo and to take a picture of you holding it up anywhere in the US. We will post these pictures in a gallery on the Rare Disease Day US website. View what has already been submitted.


http://rarediseaseday.us/take-action-now/handprints-across-america/

Empowered patients are coming together around the world to help bring reform to our healthcare industry.  Please read.  http://e-patients.net/

If you or your loved one has been diagnosed with a Rare Disease then join in and fight for awareness, education and  research. Open your eyes and see the connectivity happening today on our social networks.

Join me today!



Thursday, February 16, 2012

ULTRA ACT FOR RARE DISEASES 2012

A QUICK READ
Information on the ULTRA ACT now be addressed in congress. You can easily vote.

The Unlocking Lifesaving Treatments for Rare diseases Act of 2012, or ULTRA, H.R. 3737, will improve access to the FDA's Accelerated Approval process for very rare diseases, provide a more predictable regulatory process, bring down development costs, and spur investment in the development of treatments. Additionally, ULTRA requires the FDA to use the best science available, ensuring treatments are safe and effective and reach patients sooner. 

With the introduction of ULTRA, the EveryLife Foundation will begin to build Congressional support for this important legislation. Most importantly, we thank Representatives Stearns and Towns for their leadership and support of the rare disease community.

http://www.curetheprocess.org/ultra_act


Marianne Vennitti
https://www.facebook.com/groups/318304641519371/
Cryoglobulinemia Vasculitis Organization

RARE DISEASE DAY -


Want to get involved in Rare Disease Day? Just open the link and tell your story or post your photo. If nothing else just look and read about all the others with a Rare Disease who are also fighting for their lives. Alone we are Rare. Together we are Strong.

www.facebook.com
Raise awareness for patients living with Rare Diseases



Marianne Vennitti
Cryoglobulinemia Vasculitis Organization

RARE DISEASE DAY VIDEO


This is the Official Video for Rare Disease Day. It's awesome.
www.youtube.com
February 29, 2012 marks the fifth international Rare Disease Day coordinated by EURORDIS and organised with rare disease national alliances in 25 European co...


RARE DISEASE DAY - WHAT YOU CAN DO FROM HOME


MY suggestion for today for Rare Disease Day is an important one and easy to do.

Click the link below, fill in the information, and your done. By signing this form you will become an Ambassador for Rare Disease Day and you will be supporting NORD for all that they do for us to bring awareness to Rare Diseases. This will also bring exposure for Cryoglobulinemia Vasculitis because you will be asked what organization you are associated with. We have signed in as a Partner. They know us know. LET THEM HEAR YOUR VOICE!

It will only take a a couple minutes to fill in your name and organization. Please fill in Cryoglobulinemia Vasculitis Organization for yourself and all those who suffer with our disease. Thank You *Marianne*
rarediseaseday.us
Rare Disease Day is about realizing the similarities among all individuals impacted by rare diseases. By working together we can raise awareness and create a global impact. Whether you are an individual or part of an organization, we want you to show your support by becoming a Partner or Ambassador.

RARE DISEASE DY FEBRUARY 29TH, WHAT YOU CAN DO FROM HOME


Today I would like to bring your attention to Letters to the Editor for Rare Disease Day Awareness. This is a sample letter you can print out and send to the editor of your local newspapers. Click the link and open the first link, letter to the editor.

http://rarediseaseday.us/take-action-now/press-kit/

If you have extra time browse through this page and see all that we have been supplied with to do our part for Rare Disease Day. Along we are Rare. Together we are Strong.

Marianne
Cryoglobulinemia Vasculitis organization

RARE DISEASE DAY - MAKE A DIFFERENCE FROM YOUR HOME


Write Your Reps

Information is provided for you to search for your representatives on this page. THIS ONE IS REALLY IMPORTANT!

As part of Rare Disease Day, we would like to take the opportunity to reach out to Congressional Representatives to educate them about rare diseases, but we need your help! Every voice is important in this process and together we can make our voices heard. If legislators are more informed on the issues they will be able to make better decisions for the constituents they serve.
...See More
rarediseaseday.us
As part of Rare Disease Day, we would like to take the opportunity to reach out to Congressional Representatives to educate them about rare diseases, but we need your help! Every voice is important in this process and together we can make our voices heard. If legislators are more informed on the iss...

MARIANNE VENNITTI
CRYOGLOBULINEMIA VASCULITIS ORGANIZATION
CVO - ASSISTANT DIRECTOR
MRSMVENNITTI@GMAIL.COM

Monday, February 13, 2012

NEVER GIVE UP - EVER


I'm excited to share the good news.

This morning I received a call from my oncologist telling me that my blood test for Cryoglobulinemia Vasculitis came back NEGATIVE.  This means that the LAB TEST was unable to detect any Cryoglobulins in my blood. It does not mean there aren't any. It does mean they have reduced enough to give me a negative reading. And that is great news.  I actually have had 3 incredibly awesome weeks and I feel like my body is getting stronger and healthier. I still don't know what tomorrow will bring with all the complications but for today I finally  have made progress after living with constant fear for the last 3 years and living like I was dying.

Never ever did I feel I would think about tomorrow.
Never did I think I would see normalcy of any kind.
Never did I think I would see joy in my husbands eyes.
Never did I think my body could recover.

So today I offer you a RAY OF HOPE for wherever you are on your journey

Never ever give up.

RARE DISEASE DAY FEB. 29TH AWARENESS Hand Prints Across America


This week I will be posting ways you can participate in Rare Disease Day right from your home.

Today's post for RARE DISEASE DAY FEBRUARY 29TH, 2012 is:

                         HANDS ACROSS AMERICAN 

Simply open the link, print out the flyer, take your picture with the flyer and post it to the link provided.


Next, post that same picture to Cryoglobulinemia Vasculitis Organization Face Book page.  

You support is needed to help save lives, and to insure that treatment is found.


Saturday, February 11, 2012

Marianne Vennitti on BroadCause

Marianne Vennitti on BroadCause:

'via Blog this'

Be Aware. 1 in 10 Americans is afflicted by a Rare Disease. 75% of these people are children.

Cryoglobulinemia Vasculitis is a Rare Disease
- CVO - Assistant Director

Home

I been lost again for the last year because I've been sick. New symptoms, no answers, more weakness. I'm inside my house more than not because of my Rare Disease Cryoglobulinemia Vasculitis. Cold weather causes my blood to jell causing life threatening complications. People like me need support and answers why there aren't more things being done for Rare Diseases. One out of every ten Americans has a Rare disease and 75% of us is a child. Be Aware. I currently am an advocate for Cryoglobulinemia Vasculitis Organization and all Rare Diseases. Please watch.

http://wherearethecures.org/am

Find me on FaceBook at Cryoglobulinemia Vascvulitis Organization.
Assistant Director


Saturday, August 27, 2011

LIVE EACH DAY LIKE IT IS YOUR LAST


Let me give a quick update on my health issues since February.  Kidney failure, heart disease, vasculitis and severe anemia have all been unexpected problems this year.  Because my immune system was so compromised I was seseptable to infection. The complicatons included phenumia, ear infections, herpes of the eyes, vertico, blurred vision, tinitus (constant  ringing in the ears). This all led to anxiety and panic attacks. While all this was taking place I also was receiving regular blood transfusions due to the anemia. My energy level was about 2 on a scale of 1 to 10. In April my doctors determined that I would have to start chemotherapy  again.  This time it would be more intense then last August.  On April 29th I began  treatment of  high doses of steroids and Rituxan. This was followed with 5 days of oral Cituxan chemotherapy. If I thought I  was sick prior to the chemo was I ever in for the biggest surprise of my life.  It only got worse.  I felt as though each and every chemo pill I swallowed was killing me more and more each day. The panic attacks were controlling my life.  The fear was mind boggling.  Each day felt like my last. My world was ever so small just lying on the couch day after day waiting for some kind of relief. The doctors were not offering me the hope I was looking for. I needed to do my own work if I was going to find the hope I needed to survive.

To my unexpected surprise, with my strong faith, trust in God, my best friend and husband Chris, my awesome family and close friends I began to regain my strength.  I started having what I call "peep a boo moments" when I felt very brief glimpses of relief.  Half way through my treatments I began to feel hope again.  There was hope stirring in my soul and determination brewing in my spirit.  I recall on one particular day when I felt a change in my attitude.  I knew I had to beat this sheer craziness I was living. Hour after hour I repeated in my mind and sometimes out loud, "I am happy, I am healthy, I am one with the Lord." My attitude began to change. I insisted that my husband change his attitude.   We weren't going to look at every little set back as the end of the world and possibly the end of my life.  We were going to change our minds and change our lives.  I have a statue in my Zen garden that reads, "what we think we become".  Did I think I was going to die? Sometimes I did. I saw my future as just one health issue after another. I was excepting the fact that this was the only life I would ever know again. My body and spirit became helpless. I lost hope because day after day things became worse.  Of course if you have never experienced losing control of your body, mind and spirit it definitely is a frightening journey. It was time to change my attitude and change my life.  By the Grace of God I began to rise above this torment. Moments of relief and healing turned into hours and then into days. My test results began to improve along with my energy.  Yesterday, August 26th was my last treatment. I walked into the treatment room full of energy and hope knowing in my heart I have been given another chance to live my life with a vibrant healthy body and spirit.  Never question the resilience of the human body, the power of the mind and spirit.

It is our responsibility to walk away from every challenge in life with a powerful new positive attitude. Know and believe that in each and every hurdle we encounter there is a wealth of knowledge we receive to carry us through our next pathway.  Never allow the  difficult times in your life determine your  future.  They are the stepping stones to your future happiness.

If you or anyone you know has Cryobolbulinemia Vasculitis please contact me on this blog.





Sunday, July 31, 2011

MISSING SINCE FEBRUARY

Hi to my fellow bloggers. I'm redesigning my blog template today and plan to start posting again hopefully by tomorrow.  It has been since February since I have been here due to a variety of complications with my health. For the last month or so I have been catching up on life, getting things back in order, sorting, filing, cleaning, organizing.

I am happy to say that I am in the Waking Up Stage again and having been here many times over it takes time to reconnect to ever aspect of life.  Although it is a slow process it is a welcomed stage to be journeying through.

Thursday, February 24, 2011

WAS I GRANTED A MIRACLE?

It has been a long time since I have written. To my surprise I had several setbacks this years. I have been back and forth to doctors since I last posted. In January I was admitted to Cooper Hospital with a new health issue, congestive heart failure and a weakened heart muscle.  When I left the hospital I  ended up with pneumonia.  It's taken a lot to get back on my feet. I believe first in God and second in myself so I know I will always get through the crisis. 


My daughter is delivering our first granddaughter on Friday. That is our 5th angel. That in itself has kept me treading hard through the storm.  Although I do believe the Lord is the one who carries me.


I prefer not to read blogs that give tons of details so I will get right to the point.  This rare blood disease (Cryoglobulinemia)that I now live with has been quite a challenge since it has been a very cold winter here in NJ.  I can not be exposed to cold temperatures. Therefore, I have become a hermit. Friday I was supposed to start six more five day treatments of chemo.  I have to admit that I was not handling the time frame very well with my new grandchild on the way. Six rounds over the course of five months is a long time to be down again.  I'm almost standing and I feel the bowling ball coming at me to knock me back down.


Two days ago I called my oncologist to find out the results of my  blood test. He was testing to determine if I still was in remission. It came back negative. My doctor was sure it was going to be positive. Everyone is aghast.  Chemo is cancelled for Friday and I wait until all the doctors confirm that this is really possible.


What is it? Faith, hope, prayers, a real miracle?  Does God really test us to our limits? Does this strengthen our faith so we can spread the good news of the Lord and give others hope? Is it just part of the cycle of life. Good verses evil. Nothing last forever. Why? Am I more courageous today? You bet your butt I am. Do I want to spread hope, reassurance and inspiration? Definitely. Why is life so difficult? Why so many challenges?  Did God make this life so difficult so we would search Him out? Or does life just have it's ups and downs. 


How come some people just seem to breeze through life without any real tragedy?  I've always considered myself a selfless person having compassion, lending forgiveness, searching harder and harder for my higher power? At the same time witnessing my shortcomings.  And yet I have had more than my share of serious struggles through my entire life? Why?


As I sit and ponder and question I sit in awe that I may have been granted another miracle. Do me realize all the miracles we receive in life?


I pray today you receive at least one small miracle or at least you feel the spirit enter your heart.


Love and blessings to all,


Laughingnana 

Wednesday, January 26, 2011

JOY IN THE MOMENT



HOW MUCH DO WE MISS??????????????????
CREATION
SOMETHING I LOVE...PHOTOGRAPHY


SIMPLICITY


BEAUTY




Noticing all things that bring me joy.


   
ENDLESS







WHAT YOU THINK YOU BECOME

WHERE ARE YOU? WHERE ARE YOU GOING?







Thankful for all that I have learned on my journey.





DO YOU BELIEVE? 
WHAT DO YOU BELIEVE?


INNOCENCE
DETERMINATION!










LOVE





CREATIVITY








UNITY
GOD



COLORS OF LIFE, VIBRANT!



JUST HAVE TO LOVE THE BABIES!










PEACE


CELEBRATION


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I've been missing for a month.

Good Morning Friends,

Although I feel like I have been to hell and back over and over again, I am thankful for the life I do have.  I watch how strong my children have become because of my health issues.  My son has this quoto on his FB page. "We cannot change the cards we are dealt, just how we play the hand"- Randy Pausch.

What an awesome quote. Remember it.  It's all about attitude.  Be a happy survivor.

When I notice how much my son (he's 20) has grown watching me go through years and years of illness, I feel assured that if anything ever happened to me, he has the right attitude to get through his own issues.

Let's all try to have a positive day today.  Think of the blessings in your lives. Pray for those who are less fortunate than us.

Tomorrow is another day so let go of the sorrow of today if that is what you are feeling and remember that tomorrow there is a new sun that will shine blessings on you.  Just be open to what is.  If your life is full of joy than be an angel friend to someone else and offer them your heart.

I missed a whole month of what happened but I will get back to it later.  I just felt inspired to share these  thoughts this morning.

love to all and blessings
marianne

Friday, December 31, 2010

LIVING THE LIFE I NEVER THOUGHT I WOULD HAVE

Outdoor ice skating in AustriaImage via Wikipedia
It's the last day of  the year 2010 and I went ice skating with my husband, grandson, and son-in-law. It's been to many years to recall the last time I was on skates but it was exhilarating, scary, and totally awesome. I intend on doing more and more exciting adventures this year as I continue on this one year journey. God ask us to do as the children do. Today I felt that inner warmth of completeness in body and spirit. My life has been so serious with all the medical nuisances. I want to feel the explosion of excitement without anxiety, fear or regret. Although I know I am still climbing mountains to stay well my attitude is completely different. Maybe it just hit me that I really am getting older. Time is flying bye. I want to really live my life with God as my source of courage and daily guide. 

DETERMINATION
FAMILY
JOY
This is me happy without the fear of tomorrow, no confusion or regrets. No self pity. No concern for anything but the MOMENT.

As I dragged myself through this week I knew I was working with a different power of focus.  My blood volume was very low and yet I focused on my goals, not my illness.  I battled through two strong training sessions with tears in my eyes knowing that if I envisioned the end result I was already there. I no longer want to be a prisoner to what may happen tomorrow.  Today I end this year with motivation to touch the stars and dismiss this inner turmoil of despair. 

I will touch the world with my courage and the world will touch me. I will be empowered to follow the self that I am meant to be.

With loving thoughts and blessings,
Marianne
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Thursday, December 30, 2010

Don't STOP believing in you.

So much has happened over the last month, mostly negative. No that is an exaggeration. It just feels that way in the present moment. I realized in my DETERMINATION I lost my focus on the one solid belief I have, that being God.  How easy it is to get CAUGHT in the turbulence of our emotions and worldly nonsense. How easy it is to lose sight on the center of our being. When you have been captured in the rapture of bliss and then suddenly it is missing you enter into hell on earth. AWARENESS!!!

Today I restart my journey with peace of mind in my heart knowing that what comes first is my presence to the moment. Without it we get caught in a web of misery.  I'm fortunate to have traveled on the path of contentment for extended periods in my life. How awful it is to be lost in the darkness of confusion and forgetfulness. 

I am thankful for the numerous teachers that have shared their experience of peace.
I am thankful that the universe sent me an angel friend from my past to help me through my mind games.
I am thankful for my son who has such clarity that within a brief conversation he can turn my whole emotional dilemma into rational. 
I am thankful for my husband, my hero.
I am thankful for those who have walked before me that continue to inspire me to never give up.

My mindset for today;
Be strong in mind and spirit and remember you are never alone. The Lord is with you. Take your mind off of you and put it on God and watch miracles appear.


Be Determined to make a difference. Be determined to be the change you dream to be.

Walk in the Light of the New Days sun and walk in peace.
God  be with you.
NaNA