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Real members of MyLupusTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
A MyLupusTeam Member asked a question 💭
Crawfordville, FL

Has anyone been told they have hae type 3?

October 24, 2015
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A MyLupusTeam Member

I was not told a type of SLE, but I wasn't having a flare at the time of diagnosis. Type 3 just means your immune system is malfunctioning in a different way. Your antibodies attach themselves to antigens, but then the cells are deposited in joints and tissues. That deposition causes inflammation and other symptoms.

October 25, 2015
A MyLupusTeam Member

Hae is not Lupus. It stands for hereditary angioedema.

October 29, 2015
A MyLupusTeam Member

I am a RN so I just told you what I know. Ask your doc to explain it better or ask if you can have an education appt with a nurse

October 25, 2015
A MyLupusTeam Member

Very helpful,
Did your MD tell you this?
How, and what site, can I find out more info.
I'm deteriating very quickly, health wise. Now I have CARDIAC PROBLEMS. I have 10 out of the 10 symptoms of an imminent Heart Attack or a Stroke !! Very scary
I appreciate your helpfulness.

October 25, 2015
A MyLupusTeam Member

Thank you, never thought a Nurse Educational Appointment? Very Smart idea.

October 25, 2015

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A MyLupusTeam Member asked a question 💭

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