Friends

From the time I was properly diagnosed with late-stage Lyme, I have had a new lease on life...like I have been given another chance...a second life. Living is very valuable to me, and I try to take advantage of each moment, and know that there is a reason for each moment.I'm feeling a little lost because I don't know what I should do with my life, other than the most important job of being a...

We are Mother/Daughter Lymies. We do not take Lyme Disease sitting down. Check out our site at www.lymesucks.org.We stand for everyone knowing that Lyme is a serious illness, what to look for, and how to avoid it.Lyme SUCKS!

Father passed away with secondary liver cancer. We dedicate our blog to keep father's positive energy available for all in need of support. Join our team where we will do the same: sharing our cancer stories so you know you are not alone walking the difficult road paved with cancer.

I am disabled with CFIDS/FMS. My mission to help people advocate for themselves and take control of their health challenges. My goal is to reach as many people as possible and share my own personal tips, tools, and pain management experience. I admire people that are able to deal with chronic illnesses. I also admire creative people that help inspire all types of people. I enjoy reading blogs,...

I am 31 years old, and I have had Chronic Fatigue and Immune Dysfunction Syndrome (CFIDS) -- also known as Chronic Fatigue Syndrome (CFS) and Myalgic Encephalomyelitis (ME) -- for my entire adult life. I am not alone. It is estimated that more than 4 million Americans (and countless others around the world) suffer from this disease. I currently work full-time at a great job and appear young and...

I am a 61 year old retired Baker/Chef living on a small hobby Farm In Winona, Minnesota. Iam Currently Caregiver to my wife of 41 years. Jenny is in her 12th year struggling with cancer. Radiation, Mastectomy,Chemo-Therapy, Breast Reconstruction and Heart Surgery have been the norm for us for a long streach. Currently jenny is home on Hospice and I tend her needs.The purpose of my Blog is to...

I have had CFS /CFIDS / ME for over two years but am getting to grips with it now that I have a diagnosis. I have always worked, somehow, though had to find imaginative and flexible options. I love the sun and the sea and making myself healthy. I am very lucky to have a supportive partner. I live in Australia and am exploring natural ways to restore my body to full health.

I'm a 37 year old woman with severe CFS/ME (bedridden) who has also been diagnosed with Lyme.  I enjoy reading (or rather, listening to) audiobooks, photography, music, the outdoors, travel (back when I could), writing, and enjoying friends, family and my wonderful fiance.  

Well, I'm a Christian minister, a single mother of two very healthy & strong young men, a sufferer of CFS / ME for the past 23 years...sometimes homebound, sometimes bedridden, now back in life but 'not of it'... happy to be alive and happy to see my boys grown, but struggling every day to keep myself together physically while dealing with spiritual things in almost a parallel way. Way past...