Thread:EmmaRN/@comment-35236548-20180620031035/@comment-35564866-20180621150034

Thank you so much, both of you💞 It means a lot to know there are prayers and good thoughts being sent out into the Universe from you, for me 🤗

Pam, I’m sorry you deal with the ocular migraines too. I know we talked about migraines before. I’ve had the Chronic intractable type since 2001. They started when I was in College getting my BSN. Just boom, out of the blue and sometimes followed by seizures. I’ve had too many head injuries from the seizures- I swear it always happens on concrete. I get the Botox for migraines now, it’s 32 shots around the head and neck area every three months. It’s decresed them to about 10 per month though, so it’s much better than the way it used to be.

I just try to take each new symptom and not freak out about it. Lupus effects so many of the bodies systems. As long as my kidneys stay healthy I’m okay to deal with the other symptoms.

Talou, the hardest thing for me, the part that makes me angry I suppose is a better way to put it- is I can no longer work as a Nurse. I miss it so much, it was a huge part of my identity. That took awhile to fully accept, and sometimes I still am not so good at that part.

I’m off to do some gifting and visiting. I still have to finish this latest event 👍 Thank you both from the bottom of my 💗 you two lift my spirit, and I’ll say it again- it means so much and I’m so appreciative for your friendship and kindness🌹 Have a wonderful day. Hugs, Em