Overwhelming gratitude
In support of
Lulu Locks and Kathy Gearon
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Lulu Locks and Kathy Gearon
Friends,
I don’t even know what to say. The help that you have shared us is going to have an enormous impact on my life. I’ll be able to pay off some medical debt, and upgrade my office so that I can work more/longer. Thank you so much.
Today I’m off for more blood work. I normally take three allergy medication’s, and had just startedanother one for mast Cell activation. It’s a bit of a funky one, I take these little vials of a concentrated medication three times a day and eventually will likely eventually be on
5 to 8. The on boarding side effects are great, and I was halfway through, and feeling many of the benefits already….. but then I learned that I needed to have a blood test either during Ring or just
after a flare. So, off all the drugs I go! Currently, I am red, covered in hives, my joints are killing me, and I can’t wait to get it over with. I can’t wait to be back on all of these awkward meds. Hopefully, I’ll be able to get back up to speed without all of the same side effects this time. For me, mast cell activation looks like swelling, redness, and the sensation of sand in my joints. yuck!
But at least I had a fun weekend of lots of histamines heavy foods and activities that irritate the crap out of me,
to just get it over with! Lol My list of things that I normally limit include: nightshades, corn, dairy, sugar, gluten, and hot showers. At the moment, I am incredibly uncomfortable, barely slept, laughing about it and very much looking forward to tomorrow being a better day.
love youmuch,
LuLu.
I don’t even know what to say. The help that you have shared us is going to have an enormous impact on my life. I’ll be able to pay off some medical debt, and upgrade my office so that I can work more/longer. Thank you so much.
Today I’m off for more blood work. I normally take three allergy medication’s, and had just startedanother one for mast Cell activation. It’s a bit of a funky one, I take these little vials of a concentrated medication three times a day and eventually will likely eventually be on
5 to 8. The on boarding side effects are great, and I was halfway through, and feeling many of the benefits already….. but then I learned that I needed to have a blood test either during Ring or just
after a flare. So, off all the drugs I go! Currently, I am red, covered in hives, my joints are killing me, and I can’t wait to get it over with. I can’t wait to be back on all of these awkward meds. Hopefully, I’ll be able to get back up to speed without all of the same side effects this time. For me, mast cell activation looks like swelling, redness, and the sensation of sand in my joints. yuck!
But at least I had a fun weekend of lots of histamines heavy foods and activities that irritate the crap out of me,
to just get it over with! Lol My list of things that I normally limit include: nightshades, corn, dairy, sugar, gluten, and hot showers. At the moment, I am incredibly uncomfortable, barely slept, laughing about it and very much looking forward to tomorrow being a better day.
love youmuch,
LuLu.
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