The HypoGal Website and HypoGal Blog "Plays It Forward So Others Do Not Have To Rewind."



I am Lisa.

I am a middle-aged average woman who is blessed to have a wonderful husband and incredible children.

Unfortunately, after the arrival of my second child, I was stricken with several rare diseases.

Life with a rare disease can be a struggle.

Obtaining a medical diagnosis for a rare disease can be frustrating, costly and confusing.

I find that once you are diagnosed with a rare disease finding medical information about the disease can be a challenge.

Numerous rare diseases have limited medical information.

The HypoGal Website contains information that can be helpful to those living with a chronic illness or rare disease.

The HypoGal Blog is about my experiences with several rare medical conditions.

As for my medical record, I struggle with Sheehan’s Syndrome, Relapsing Polychondritis, Diverticulosis, Depression, Pulmonary Emboli, Cervical Dystonia, and Fibromyalgia.

I am a real mess! 🙂

I could be the poster child for rare invisible diseases.

"It Is What It Is", and I choose to play it forward.

Click on the following link to read my HypoGal Story.

You can read more about daily life with a chronic illness on the HypoGal Blog

Please, Like, HypoGal on Facebook.