BRAIN TUMOR STORIES MATTER

 

Hello!

 

This December is my 4-year craniversary & I can vividly recall this exact time of year (October) four years ago being the scariest three months of my life. I had my surgery on the calendar 12/12/19 and I instantly felt REAL anxiety for the first time. The kind of anxiety that made my heart race, and my hands shake, made my breathing shallow, stole my ability to concentrate and focus, and led to sleepless nights. When I did fall asleep I would have nightmares about bleeding out on the surgical table, or a big earthquake happening that would make my surgeon screw up (I live in California so this is a legit fear!).

 

I can't tell you how many times I cried in the shower alone, how often I prayed in bed trying to convince myself I'd be OK, and how many times I rehearsed my story to tell those I loved that I was confident and ready to do this so they didn't worry about me or look at me differently. In the eyes of all, I was strong and fearless, and with my will to survive I was ready to fight; however, trapped in my mind I was a total mess.

 

I share this not to scare anyone because it really is much better to be on the healing side of this diagnosis. I share this story to remind you that if you are scared, in pain, sad, mad, angry, confused, or not fully aware of what's to come YOU ARE NOT ALONE! I went into this surgery with not a single symptom or deficit. This was an incidental finding six years prior that changed my life forever and technically saved my life in the eyes of medical professionals.

 

I invite you to connect with me, you will be glad you did! I tell people in my zoom groups all the time, I never wanted to be a warrior, yes I am going to fight and not give up on this journey but it is EXHAUSTING. I can and I will do what is needed but what I want is a hug, a safe place to fall, and companionship from people who get it because I'm exhausted trying to explain this journey to people who look at me like I'm complaining or I should move on.

 

For all these reasons Meningioma and Brain Tumor Companion exists and I am here to support you in any way I can. I realized a year post craniotomy that I could let the diagnosis get the best of me or I could make the best of my diagnosis. So here I am, constantly moving this community forward, helping others in any way possible.

 

Lastly, I'd like to give a huge shout-out to Dr. Daniel Kelly at St. Johns Hospital in Santa Monica, CA. He is a stellar neurosurgeon, his team is tops, and look at that beautiful cut and shave. He is known for the keyhole entry, and I am forever grateful for his skillset! #StrongerTogether #braintumor #braintumorsurvivor #braintumorawareness #support #supportgroup #meningioma #anxiety #fear #notalone

COMPANION MARIA'S STORY

My journey began when I received the life-altering diagnosis that the unbearable trigeminal nerve pain I was experiencing on the left side of my face for almost a year was due to a large skull-base (petroclival) meningioma. After craniotomy and gamma knife treatment, I attempted to return to my pre-crani life, only to find myself hitting a major wall. About a year into recovery, I found this group, and it has provided invaluable support, unconditional acceptance, and friendship. I only wish I’d found it sooner! Angel creates a safe space, supportive interaction, personal engagement, and kindness unlike any other I have found online. Before finding this group, I did not know anyone who suffered from my condition and I felt lost. I feel lucky now to be a part of the community she created. 

 

*Maria splits her time in both Miami and Philadelphia. I want to honor her one-year anniversary with the BTC community which was October 3rd, 2022. She has participated in 21 sessions thus far and we have supported her through the good and bad days. We love you Maria and we thank you for all the support you give back to our other members. ❤

WE NEED YOUR HELP!

 

Please take a moment to help us raise money for the Ivy Brain Tumor Research Center in Phoenix AZ in honor of our beautiful companion Maki who is a 7-year glioblastoma stage 4 cancer survivor. Recently she was diagnosed with two new tumors and is battling this condition yet again, she is on chemo daily until... You can help be the change and here is how!

 

1) Sign up to walk/ run/ or participate virtually with our Brain Tumor Companion team at the Head for the Cure 5k in Phoenix, AZ on Saturday, October 29th, 2022. Enter code BTC and your registration is free! Register by clicking here!

2) Start your own fundraiser once you do join. Ask people you care about to support you!

3) Give a gift and donate today! It's easy every $5 helps. Click here to make your tax-deductible donation.

 

Thank you in advance for your help and a big thanks to all who already contributed. We are so close to our goal, please help us exceed it!

❤ ❤ ❤

Follow ​​on:​ Facebook​ I Instagram​ I YouTube

​Website:​ Brain Tumor Companion | Meningioma Companion

Blog: My Life A Year Post Brain Surgery

Copyright © 2022 Brain Tumor Companion LLC | Meningioma Companion All Rights Reserved

 

*The information provided in this newsletter is not to be perceived as medical advice, simply information that is shared by brain tumor peers. Brain Tumor Companion | Meningioma Companion is not contracted or paid to promote any of the people, companies, or groups that are shared on this platform. 

Los Angeles, CA, USA
424-239-9366

Follow: Brain Tumor Companion Meningioma Companion

Share on Facebook

Visit: Brain Tumor Companion Meningioma Companion