WHO'S THE BOSS?
There are so many things I wish I knew back when I was battling autoimmune ITP.  I wish I had someone to hold my hand and clue me in to the things I had to figure out for myself.
 
I hope I can be *that* person for you…
 
I’m going to be dedicating some blog posts to “The Things I Wish I Knew”!
 
What I wish I knew #1 - I'm the boss of me!
 
All joking aside...it is REALLY important that we realize our Doctor (GP, hematologist, etc) is our *partner*....not our boss!
 
I apologize in advance if I'm offending anyone here! I know some people feel *most* comfortable following *all* of their doctors "orders". I believe that western medicine conditions us to desire being told what to do.  When we agree (without question or concern) to do something someone in “authority” tells us, we are giving away our empowerment and our responsibility to ourselves.
 
Please don’t misunderstand…I am in NO way suggesting that you don’t take your doctor’s advice.  What I AM saying is that we DO need to take charge of our health and advocate for ourselves. We need to get comfortable asking questions, voicing our concerns, and making decisions together with our health care providers.
 
Personally, I might not be here if I had taken my doctor's recommendation to take 3 chemotherapy medications without having a spleen! I kept searching for other options and asking questions until I was comfortable with a treatment. It happened to be an alternative treatment.
 
I had an excellent relationship with my hematologist. He listened to me. I would go to my appointments with a pad of paper full of questions! He would answer all of them with compassion and grace. He knew my feelings about side effects from certain treatments (things that messed with my hormones & fertility). Together, we put them "at the bottom of the list". He partnered with me. When I chose alternative treatments, he respected me & kept monitoring my blood work even though Traditional Chinese Medicine was completely outside his scope!
 
It can feel scary at first, but it is so important that we advocate for ourselves!! Your doctor works for YOU! Don't be afraid to get a 2nd opinion or change doctors if you need someone who is more in alignment with your individual needs!

I would love to invite you to join my "Plarelwts, Plants, & Prayers" group over on Facebook.  It is a place where we can gather and offer encouragement to each other during our journey.  Click on the link below to join us!


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Meet Nina Cesena

 

Hi, I’m Nina!

I'm an ITP warrior, author, wellness coach, and woman of faith who believes that a diagnosis doesn't have to define the rest of your story. 

My journey with immune thrombocytopenia (ITP) began in 2003 with a platelet count of just 2,000, years of treatments, and eventually the removal of my spleen. After years of battling autoimmune disease, I reached remission—but I also discovered that healing was about much more than simply getting a diagnosis behind me.

My own journey led me to dig deeper into nutrition, stress, gut health, reducing toxic load, targeted supplements, essential oils, mindset, and faith. I became passionate about understanding not just what we can do to support our bodies, but why it may matter.

Today, I share what I've learned with other ITP warriors and people navigating chronic illness, helping them discover practical, whole-person ways to support their health and well-being.

I don't believe wellness is about finding a magic answer or doing everything perfectly. And I don't believe that ITP has no known cure means there is nothing you can do.

There is hope. There are choices. There are things we can learn and ways we can care for ourselves along the journey.
Most importantly, I've learned that healing is a journey—and you don't have to walk it alone.

I'm here to help you find hope, take empowered steps, and discover what's possible for your own healing journey.


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