My biggest point of starting this blog a few years ago
was to have my voice heard in the FHC community. FHC-
Fibrolamellar Hepatocellular Carcinoma is a rare form of liver cancer
that usually occurs in young adults. Because it is so rare,
finding others with it is like finding a needle in a haystack. And for
those who know me well, know I am a 11 year FHC survivor!
August 10, 2009 I got the sweetest comment here on my blog
from a girl named Jessy:
Jessy said...
Hi there!! I found your blog and wanted to introduce myself and share about my blog (www.canswercolumn.blogspot.com) because you're the only other person I've met with FHC and it just thrills my heart to finally meet someone else who understands completely my cancer (though I truly hate that you have it at all). I was diagnosed two years ago, five days before my twenty first birthday. Anyway, thank you for sharing your thoughts and pictures in a blog...YOU have totally inspired me today. :))
Sadly, Jessy lost her battle yesterday!!! :(
Jessy was the first of three with FHC to find me through my blog,
although I had connected with other FHC people elsewhere.
And you can tell by her comment how happy she was to find me.
I remember finding my first FHC person, the connection is one no one else can have unless you have been there. It's a feeling of feeling less alone!
As time went on, Jessy and I stayed connected off and on
through facebook. It was so funny when I looked her up
on facebook and sent her a friend request,
her accepting. In my message, I explained who I was, "You left a comment on my blog…ashley's art closet...I am a FHC survivor.....
Thanks for your comment, talk more with you later, just wanted
to make sure u knew the connection, have a great day!"
She confessed she was a little confused of who I was, being a blonde, but was so glad I reached out to her. I was strikingly busy finishing up my book but I watch her Facebook status from a far, she was living a busy life of treatments and planning her wedding, which she did in fact marry the man of her dreams. Oh to hear her tell her love story was just stunning, she too was a writer and a dang good one at that!
This summer when I became more active in a group called
Fibrolamellars of the World Unite, I added Jess.
Everyone who was in the group at the time racked their brain
to add those touched by FHC that they had come in contact with over the years. Jessy was so glad to be apart of the group. Only, I didn't know just how bad her health had really gotten. She came right into the group sharing her FHC story, just like everyone else in the group had done and was doing-each story is so different but has shinned such light to educate and help others. I could go on for days how people have been able to connect, pointing others to counselors, local groups, lodging paid for, meeting face to face another FHC person, sharing doctors info, treatment info, ask this question, take someone with you, and "oh, no they didn't" etc…!!!
I would see Jessy connecting with others. She was a true charm!
A very Godly woman, she had faith till her very last moment-
her husband even shared that with
the Fibrolamellars of the World Unite group
late last night. It just breaks my heart because if anyone
fought hard to find answers, healing she did.
She wanted more than anything to have children of her very own,
hers and her husbands. But just couldn't due to her health.
I know she is in a better place and will suffer no more,
but a piece of me knows she is mad as heck that she wasn't able to
prove cancer wrong here on this earth-she tried so hard!!!
My heart so aches and my thoughts and prayers go out to her family,
her husband, her friends, to anyone touched by her!
She was just awesome,
I will forever miss you JESSY
but never never forget you.
I too will live a life full of faith and possibility
just like you did my friend, lots of love!
click here
who-have-you-inspired-lately
to see the actually comment Jessy left me...
and to help you better understand the stress
in my life at that moment was me trying to fully
release everything in my book. Me and my sister
had talks about things we had been through together
that we had never talked about. Turning loose of thoughts
and feelings is awesome....very healing, which makes you
that much stronger!!!
Reminder: a portion of my first year sales of
Daddy's Briefcase:
My Journey through Liver Caner will be donated to FCF-
Fibrolamellar Cancer Foundation
as a part of the Ambassador Project.
Click here ==>
Proceeds donated to the FCF
to see my right up of offering my donation!!!
Or
here to see my story on the
Faces of Fibrolamellar.
Other
ways you can help FCF!
Also remember if you have read
Daddy's Briefcase
and would like to write a review do so
here.