Skip to content
As I live And Breathe

As I live And Breathe

A Woman's Journey With Rare Disease

Author: Nikki

I've been a rare disease advocate for quite some time. I have LAM (lymphangioleiomyomatosis) and TSC (tuberous sclerosis complex). My LAM is severe enough that I needed a lung transplant. Now my TSC has progressed to the point where I now need a kidney. I maintain this blog to raise awareness of my diseases, rare diseases, transplant, organ donation & discuss other important healthcare topics and life with chronic illness.
Posted on 10/26/201510/27/2015

HOT BUTTON: Hero Worship, Inspiration Porn, Pedestal Propping, & Tokenism

Posted on 10/25/201510/31/2015

Rebuttal: Why We Can Stop Government Funding Of Science: It Doesn’t Create Much Innovation/The Myth of Basic Science

Posted on 10/24/201510/24/2015

Food For Thought: Everything Doesn’t Happen For A Reason: An Examination

Posted on 10/23/201510/24/2015

Don’t Wait For A Time of Need To Know What You Need

Posted on 10/22/201511/09/2015

Worthwhile IndieGoGo for “Lungies”

Posted on 10/21/201510/21/2015

Changes to Lung Transplant Scoring – Will It Impact Me?

Posted on 10/20/201510/20/2015

What Matters

Posted on 10/18/201510/18/2015

The Power of Dreams

Posted on 10/15/201510/20/2015

Getting Fixed Up

Posted on 10/14/201510/14/2015

Turning A Corner

Posts pagination

Previous page Page 1 … Page 37 Page 38 Page 39 … Page 45 Next page
Create a free website or blog at WordPress.com.
As I live And Breathe
Blog at WordPress.com.
Privacy & Cookies: This site uses cookies. By continuing to use this website, you agree to their use.
To find out more, including how to control cookies, see here: Cookie Policy
  • Subscribe Subscribed
    • As I live And Breathe
    • Join 226 other subscribers
    • Already have a WordPress.com account? Log in now.
    • As I live And Breathe
    • Subscribe Subscribed
    • Sign up
    • Log in
    • Report this content
    • View site in Reader
    • Manage subscriptions
    • Collapse this bar