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Always Winter but never Christmas I’ve been in this mental place before and know how scary it feels. Having Epilepsy can be a lot to manage and cope with. Personally I’ve found it helpful to connect with people online and share experiences with them. Helps me feel less lonely. Sending you love ❤️
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An #ArmLift procedure known as #brachioplasty can improve the dreaded appearance of #bingowings . #PlasticSurgery
harleystreetaesthetics.com/procedures/bod…
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Ace fab funny sad emosh rocket-tastic.
Loved it. Another great soundtrack too. #GuardiansoftheGalaxyVol3
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Brain Ablaze I talk about it with people I trust but would love to meet people in New York who live with it
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Always Winter but never Christmas I totally hear you. I first joined a zoom call probably 7 months after my diagnosis. I didn’t turn my camera or mic on out of nervousness, but it was nice to listen to other people share and know I wasn’t alone. It’s 100% ok to go at your own pace. Now I feel comfy to share more
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Brain Ablaze I’m on it right now and I’m finding my combinations of medicines to be strong. I’m going to speak to my doctor to ask if it can be lowered or we can lower one of my medicines.