@pattig09 - THANK you so much. Apologies for taking so long to reply. Information from labs is files on my computer and for various reasons, I use my phone v. coming to check files. I wanted to do so before responding. I'd never heard from the doctors of "Hidden Inflammation and Immune Dysregulation" or if I'd read it, do not remember.
I do not see a C4a blood test from the last two years. LabCorp is where all my tests have been conducted. It will be relatively simple to have this run again in hopes one of the docs involved will write an order for it.
My hopes are up - oddly, considering a higher number would indicate what it may be. I know from reading that some of my symptoms (activated lipedema) won't stop or so I've read. If tho' it helps my mouth and tongue and even slows the lipedema outbreaks, I'd be glad.
Do you think that the vaccines had any impact? I'm a strong believer in getting them - flu and COVID in the Fall - and do not want to have greater exposure.
You also mentioned that isolating allowed healing to begin for many symptoms. I had B-cell non-hodgkin lymphoma in 2007, with radiation that appears to have kept it away since tho' the ID doc believes it should be watched more carefully now because of long haul symptoms. I'm curious too to learn if what I believe is COVID toes in both big toes is what is causing the inflammation and ingrown nails. So far my (fabulous) podiatrist - only since COVID when the nails grew in - and I both thought it was possibly other causes. Now in hot weather wearing sandals with toes exposed and no foot sliding, we are flummoxed about anything other than COVID toes.
Are you willing to provide here more about how you have managed since knowing what you learned about the symptoms? If not, is there a way for us to, if I learn more about mine, to correspond directly with you?
Off to send this to various docs. With immense gratitude, @pattig09.
Joan
@jeindc Send me a private message here in the Long Covid group of Mayo for a deeper chat. Also, in my profile everything I've researched and solutions that worked for me are posted as linked to my actual symptoms. You may find reading my posts will provide data that could help.