Hello Mighty Family n Friends 🖐
How are you all today
I do hope you are warm n tucked up inside if its anything like the weather in The UK today very wet and windy 🌧🌫
This week is international Trigeminal Neuralgia day on October 7th . As you can see by the picture the colour is Teal.
It is one of my rare diseases and by sharing this with you I'm trying to raise more awareness.
There are other facial neuralgia's but this is the most common rare one. 🤷♀️🤦♀️
I also have glossopharyngeal neuralgia too, I'm so lucky 🖐🦓
The best part is they make the names so hard to pronounce .
Why!!!!!!!!
Its face pain, its already hard to talk why make the disease name unpronouncable!!!!! 🤦♀️🤷♀️REALLY
The pain is like being hit in the face by a baseball bat or a train or an electric shot. Again n again. Over n over . For hours or minutes.
Pain meds don't work as its nerve pain. Only anti seizure meds work which come with a whole host of side effects and don't always work for each person. It never takes the pain away.
There is no cure.
Thanks for listening guys
Love n hugs Tj 🦓🥰🤗💜💙🧡🐕🧚♀️🦷
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