Comments on: Lupus Psychosis and Brain Inflammation

By: Laura Trask

Laura Trask — Sun, 15 Jan 2023 01:42:47 +0000

SLE is such a severe disease that I wish I never had. It has attacked my nervous system with painful neuropathy and guessing it’s had an impact on changing the person I am to the very core or characteristics. What makes me feel most crazy are the doctors that deny any of my symptoms they can’t actually see. So often it makes me want to just give up because each day is hard enough to endure with the pain and limitations alone.

By: Laura Trask

Laura Trask — Sun, 15 Jan 2023 01:42:47 +0000

By: April

April — Wed, 22 Dec 2021 13:56:03 +0000

I have had Lupus and many autoimmune diseases my whole life, had chronic migraines along with dizziness blackouts. 2 TIAs along with many other things. I have complained to Docs of seeing bugs, blacks spots, hearing voices, been diagnosed with vertigo. My go blury on me.
They just tell me listen to a radio or TV. I would love some other advice. I know am not crazy all the time. Lol! Is there any support groups in Houston tx area or doctors that specializes in this field? Thank you

By: Adel vasquez

Adel vasquez — Sat, 15 May 2021 17:04:30 +0000

How can I find a doctor that can help me find out if I have this.. I have sle lupus, I was diagnosed after two strokes and seizures. I battle my mental illness for already 2 years I had no idea it could be from lupus I thought it was only due to past life experiences I’ve had..

By: Cheryl Barban

Cheryl Barban — Wed, 28 Apr 2021 21:03:48 +0000

I have Severe anxiety, PTSD, migraines

By: Jeannie

Jeannie — Sun, 25 Apr 2021 12:06:14 +0000

I now have prism in my glasses. Lupus for 19 years affects my eyes

By: Heather

Heather — Sun, 25 Apr 2021 04:17:22 +0000

I have known I have lupus for 10 years now, accompanied with blood clotting disorder secondary. This explains a lot to me! I have severe anxiety.. and I have days where I feel completely, completely lost, sometimes almost dyslexic in speech and writing. A good nights sleep and I’m back like it never happened! I’m not happy I have to deal with it, but certainly happy I’m not crazy!

By: Cecilie Gardner

Cecilie Gardner — Fri, 16 Apr 2021 14:58:40 +0000

155 weeks sounds long term to me

By: Terry Wright

Terry Wright — Thu, 15 Apr 2021 02:01:31 +0000

I have been dealing with all this when i was diagnosed with lupus in 2009 i was treated with all kinds of medicine until they gave me something call diazepam and that clam my anxiety down and prednisone to keep the inflammation down i just thank God there was help to get me through

By: Debra

Debra — Sat, 27 Mar 2021 21:42:58 +0000

Wonderful article. My daughter experienced this and hopefully she will be open to reading the article. I assumed that was what was going on with her, but the “professionals” don’t seem to be able to do their job and treat her as a whole person.