An Open Letter to the Doctor Who Gave up on Me

Jan 7

Posted by

I know I’ve already published 2 new blog posts today, but I have to share this incredible post by a newer blogger I’ve been following. I know everyone with a chronic illness will relate.

Life with an illness

Dear Doctor,

Before I start, I want you to know I’m not even mad. You’re not the first or probably the last to turn over my case. The moment that you gave me the pity look, and said “you will never get better, you will have a feeding tube the rest of your life, and I can’t help you.” Tears immediately welled up in my eyes, and my stomach sank to my feet. That was the worst feeling, when you gave up on me. 

View original post 283 more words

About abodyofhope

I do not know why it is that we must wade through tragic circumstances to find truth. We nearly drown! But under the water, there are pearls. I hope in writing this blog, more will come to the surface. Over the past 15 years living with chronic pain, patient advocacy has had a powerful effect on my life through meeting so many remarkable teens, women and men: SURVIVORS. These individuals are HOPE personified. I wish to honor them in the same spirit they have encouraged me to press on. Eight years ago, I became bed-bound from a variety of secondary chronic illnesses. A procedure meant to help the pain condition I had been managing for several years- went bust #BIGTIME. Over the years, my entire life has changed. I have changed, but I am still striving to live my best life possible. Along with sharing inspiring pieces about spiritual wellness and finding quality of life inside of ongoing illness, I also share health research, awareness information, poetry, memes, art, and this blog is also an attempt to put my own pieces back together. Welcome to A Body of Hope, and thank you for visiting. [Complex Regional Pain Syndrome/ RSD, Postural Orthostatic Tachycardia Syndrome (POTS), Dysautonomia, Chronic Intractable Migraine, Cluster headache, Trigeminal Neuralgia, Occipital Neuralgia, Hypersensitivity to Sound & Light, Fibro, CFS/ME, Cerebrospinal Fluid Imbalance......blah, blah, blah] >>> P.S. My headgear is protective for pain. I just rock it hard ;)

Posted on January 7, 2018, in Uncategorized. Bookmark the permalink. 2 Comments.

  1. Lifewithanillness | January 7, 2018 at 2:27 am

    Thank you so much for reblogging!!! 💛

    Liked by 1 person

    Reply

Leave a Reply

Fill in your details below or click an icon to log in:

Gravatar
WordPress.com Logo

You are commenting using your WordPress.com account. ( Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. ( Log Out /  Change )

Cancel

Connecting to %s

A Complex Life

Living with Complex Regional Pain Syndrome

Get More Resilient

Our resiliency has limits, but we can always become more resilient.

Dr. Jen Gunter

My Life: Beauty Love and Chaos

Blog, Poems and Short Stories by Becky Allen

DeltaLifes.com

HEALTHY LIFE & SUCCESS

Tea With Jennifer

Living Grace, one day at a time...reflections on life, love & laughter

Fightmsdaily

Living life with a chronic illness is definitely not easy. But I do my best to push through all the barriers this illness puts in front of me! In my heart and mind, I believe maintaining a positive outlook on all situations in life will carry us through to much better times! I hope you find the information that I provide both helpful and inspirational!

Miss Diagnoses

Life with assorted ailments

Health News

Pain Management Specialist in San Diego & La Jolla

Pain Specialist treating Intractable Pain & Treatment Resistant Depression

Twilight

( writer )

Survivors Blog Here

Keep Moving Forward

How to Get On

#OneGoodThing Daily

Surprising silver linings in caregiving, food, art, style, travel, and more!

Sue Spitulnik

Writing, Sewing, Travel, and Thoughts

Whidbey Acupuncture + Herbs

Dr. Kent Herbal

Speak Truth

Doss Doc's

Father Figure for Hire

Young, Hip and Bionic

%d bloggers like this: