More about my long-time friend Nichole.

So it’s been a little bit over a day since my friend Nichole passed away. In the end, she had no longer been able to take the various medications that had sustained her for as long as they had — she became severely allergic to so many of them, and attempting to desensitize even in the safest ways possible caused her kidneys and liver more damage, chief among those medications being the gene modulator Trifakta that had helped her stay out of the hospital for as long as it had. She painlessly and peacefully passed away surrounded by loved ones with her hands being held as she crossed over, and with absolutely no suffering. Although I do wish that she had been able to live longer than the thirty-nine years she did (which is actually kind of impressive in terms of longevity with cystic fibrosis), I wouldn’t have wanted her to linger if she were suffering prior to her passing. I’m glad that I was able to tell her that I loved her and would always remember her before that, though, and know that she received that message from me in addition to all of the other messages that her friends left her and her husband when he posted to Facebook informing us that she wasn’t doing well and did not appear to have that long — days — left. She left behind a young daughter.

I had known her for almost the entire lifespan of my youngest son, who is a bit older than her daughter.

So I’m losing one of my friends. This just sucks.

One of the people that I’ve known the longest online, who has cystic fibrosis, is expected to pass away in a day or two due to liver and kidney failure from the medicines she had to take for… wait, well, the whole cystic fibrosis thing. I haven’t heard anything other than her husband informing her friends that she is probably going to pass away that day or tomorrow. I’ve known her so long, and we go back so long, when Bub was an infant on my lap. He’s almost thirteen years old now, and our friendship is the length of time of one Bub.

It’s still amusing that my interactions with the cystic fibrosis community are measured in Bubs.

…okay, to be completely honest, I do still find it a bit hilarious. He’s like a measuring cup, I swear.

Even though part of me wants to see her fight and her health improve, I don’t want to wish that on her if it means pain and suffering on her part. She wants to become stardust when she passes, and it sounds like she wants to travel the galaxy (I would too if I were in her position, because that sounds fun). At any rate though, I’ll always remember her, and I made sure she got that message from me while she was still alive.

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