Skip to main content


Today is International Occipital Neuralgia Awareness Day! 

What is Occipital Neuralgia (ON)? 

“Occipital neuralgia (ON) is a condition in which the occipital nerves, the nerves that run through the scalp, are injured or inflamed. This causes headaches that feel like severe piercing, throbbing or shock-like pain in the upper neck, back of the head or behind the ears.” - The Facial Pain Association. 

ON is rare, some numbers suggest 3 people per 100,000 develop it. 

There is no cure. 

A bit of my story with ON: I was diagnosed last year with Occipital Neuralgia (ON), though my symptoms first showed up in 2020. ON is very painful. My symptoms are electric like shocks and stabs to the back of my neck, head and behind my ears and tip of my ears. I also at times have a continuous burning ache on the back of my head and ears. My neck and back of my head feel like it is in a vice grip. I also have a crawling sensation. The pain level from ON can be very chronic at times and debilitating. My pain is thankfully not constant however. It flares and the flares can last anywhere for a few days, to weeks, even months. In a flare, the pain tends to be constant. My triggers, can be from anything such as touching my neck, the back of my head, and ears. Brushing my hair, pulling it into a pony tail, or sleeping on a pillow, wearing a hat or hoodie can also be incredibly painful.

Today is International Occipital Neuralgia Awareness Day, but for those who have this condition or loves someone with this condition, ON is every day. There is no cure. That’s why awareness is so important on today and every day. 

For more info on ON check out The Facial Pain Association (FPA) and the Occipital Neuralgia Foundation


Occipital Neuralgia Foundation: onfsupport.org

Follow The Medical Zebra on Instagram! Scan the QR code below!




 

Comments

Popular posts from this blog

Angel

  Many people don’t understand the depth of virtual friendships.  Virtual friendships are real friendships. Just because they come about from connecting with someone online doesn’t make them less of a friendship.     Those of us with rare chronic illness, our virtual friendships are formed from the chronic illness world itself. You connect with those who already understand what you are going through. These friendships are special. The chance of coming across someone in person that has the same rare condition, is rare like the condition itself.  Because of that, these virtual friendships are that much more meaningful and impactful. They touch your heart and life.   Angel.  When I think about her I always think of three things. Butterflies, makeup and how much I thought her name fit her.   We met through a support group for Trigeminal Neuralgia. The funny thing is she messaged my identical twin asking for advice and looking for someone who wou...

Disabled and Loved

ID for accessibility: Photo of couple lovingly holding hands.   There is a myth that needs to be broken.  That myth is that people with a disability and chronic illness shouldn’t fall in love or be in a relationship.   I have had chronic health conditions since my childhood. In my teen years my conditions became more severe and multiplied, I developed the rare condition of trigeminal neuralgia (though I would not receive my official diagnosis until almost a decade later).   I remember the fear that struck me, "Who would want to be with someone with so many health conditions and who may not even be able to kiss them?"   From an early age, I was taught I was a burden and undeserving of love. I was a "burden" to my parents, my pastor, my Sunday school teacher, and even to a supposedly loving god.    Once my health conditions started showing up and getting worse, I was then a burden to a future spouse, if I should even date or find someone who wanted t...

Scars To Your Beautiful

I wished I could put into words what it feels like emotionally and mentally to be a chronic illness patient.  Some days, it’s just a routine of taking your medications, going to your doctor appointments, pain, fatigue medication side effects etc. Some days it’s just normal to not be normal. Other days, like for me today, I’m crying.  I’m crying because yet again, I’m facing another health battle. There’s a sting to this battle though. Because I have faced it before and well, thought I had won. Even my doctors called me a success story. And even used my case at a teaching conference. I held on to those words and was damn proud of myself for winning against this yet another rare disease. And one that left me with visible scars and insecurities.  When you are a chronic illness patient, sometimes you get used to being sick, but please don’t mistaken that with being okay with being sick. Maybe some individuals are. Maybe I’m just not accepting of the fact that I have chronic i...