I know that everything brought forth to this website is supposed to be original material, but I have stumbled upon something so great, that it needs to be shared with as many people as physically possible. As a result, here is the virtual book tour with Toni Bernhard – regarding …
Read More »When The Doctor Says It’s Endometriosis
Seven years ago, I remember sitting in my doctor’s office when I first heard her say, “I think you may have endometriosis.” At that point, I only knew two things about endo: 1) it has something to do with scar tissue and 2) it can cause infertility. Surgery was scheduled …
Read More »Your Body Knows Best!!
Greetings and Salutations to all my Fight Like a Girl members!! I hope you are all feeling well. I have been a bit under the weather (yes I know you are stunned by this shocking revelation! LOL!). Last week I decided to go to a cardiologist because my blood pressure …
Read More »Dealing With Naysayers
Today my feelings were hurt as a result of another person’s actions towards my illnesses. This is fairly common in my world, much to my dismay. You see…a large portion of the common public still view fibromyalgia and chronic fatigue syndrome as forms of mental distress. Some have been known …
Read More »Seeing the True Beauty
Let’s stop being such a self conscious nation and let’s look into mirrors and see what is truly there: the beauty everyone else can see but that we must discover for ourselves.
Read More »Annie’s Story (Fibromyalgia and CFS)
Being as I am a new phenomenon to many of you (!), I figure I should at least introduce myself and what I plan to be writing about for The Fight Like A Girl Club. My name is Annie Martin. I am 23 years old. I have been mysteriously ill …
Read More »Fighting Liver Disease Like A Girl
Right now, I am less than two weeks away from a partial liver transplant. I am 29 years old. Finding out you have any life-threatening disease is scary (to put it mildly), but finding out you have a disease that carries the stigma of cirrhosis… well, let’s just say it …
Read More »Dani’s Story (EDS – Ehlers-Danlos Syndrome)
I suffer from EDS. I am both Hypermobility type and Vascular type. Can I get a “WOO HOO!” for winning the dysfunctional genetic lottery? LOL! It is a horrible disease; the Hypermobility type caused me a great deal of pain. I suffer from numerous subluxations and dislocations. Every joint is prone to it. I have intense pain, swelling, skin discoloration etc…I am hypersensitive to barometric pressure changes and can predict weather better then any meteorologist I have ever seen on TV!
Read More »Newly Diagnosed With Lupus…So Now What?
I can remember having lupus symptoms like joint pain and extreme fatigue as far back as six years ago. For many of us Lupus has always been a silent disease until that day we are struck with a severe flare up. The road has been rough, but I'm glad to finally know my health status after being in the dark about it for so many years!
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