Tag Archives: steroids

When Lupus Hits

Standard

Sometimes the hardest thing about Lupus is not the disease, but the medication for the disease. I was coming down with a cold which means disaster for my body-think aches, fever, muscle cramps, fatigue, sore throat…all for a cold. So I had to increase my steroids by a lot…I mean a lot a lot and the return is what we call steroid face. A necessary evil. You feel better, but look worse as your face appears to swell overnight.

I am thankful to God for the medications needed to live and wish I was not so vain…but it does stink what it takes to stay healthy-it .is.hard.

On a positive note, I gained weight and my hair is growing. I feel better and less depressed so life is good today!

Medications Begin

Standard

The kidney biopsy went well and the results showed what we expected. The plan is to increase medication then taper down as hopefully the kidney function starts to improve and Lupus calms down.

https://www.tiktok.com/t/ZTRDpfBYw/

You can view the Tik Tok in the link above.

Getting the news was expected, but still hard as I am pretty sensitive to medication I think due to my small frame. I call myself a one-percenter. If it has a small chance of happening…even one percent it happens to me. Fever blister, infertility, hair loss, eye inflammation, dry mouth- me, me, me.

So the journey to start 25mg of steroids daily (a lot!! get ready moon face) and 2000mg of Cellcept…an immune system blocker so mask up begins today.

My kidneys are worth it!