It has been a while since I wrote on my blog. I do not really know what to write recently of all the things that has been happening. But as of right now, I want to inform you guys that I am alright and will continuously going to be alright. :)
For a few months now, I have been nursing a bilateral pulmonary embolism for trying to get healthy as part of my new year's resolution. Which apparently is not good for me, or for any with Lupus for that matter. Although, I do not have that antibody that makes people with Lupus have blood clot. the antibody is called
Antiphospholipid antibody or APS. .By itself, APS is already an autoimmune disease, but it also comes out to people with SLE. So I am always checked it this antibody is out on my lab exams. My doctors have been checking and I do not have it, so they were wondering how I got my blood clot. But, as with everyone else new to having lupus, every day is a different day.
I have been getting my daily encouraging inspiration on instagram. I followed this bunch of people who also have Lupus. There is a lot of us out there. And all, fighting an invisible war inside us. There are good days, there are bad days. Well, hopefully, today is a good day for me. :)
And I leave you with a repost from someone, I forgot who. I will note it next time.
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I shared it on my facebook (which is private) but it came from this person.
Check them out. |
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