We welcome your letters and thoughts regarding
lupus. If you have a lupus issue on your mind,
here's the place to tell us about it.
Letters
Submission Guidelines
Keep it short and sweet! You'll have more
chance of being published. When you email
your letter to us, you must include your name and
contact telephone details for clarification.
No pseudonyms are permitted. We will will only
publish your name and general location. If you'd
prefer to remain anonymous, we will definitely take
that into consideration after contacting you.
Pease keep your letters to a maximum of 200 words
and note that your letter may be edited for legal,
length or other reasons.
Letters
July 2010
I've had lupus since
I was twelve years old. I am now forty-two and
lupus has taken me on a loop. I've had my
kidneys removed, both knees replaced and a hip
removed as well. Now I use crutches or a wheel
chair to get around. I don't let lupus get me
down. I just look at myself as a blessing and
how I can help other people with the help of my God.
So I just want you to know I have lupus - lupus does
not have me.
Tesa
Perry
Washington
District of Columbia
USA
April 2010
I have been
diagnosed with Lupus for eight years and this is the
first real useful site I have seen. I will be
definitely be checking this site out and thank you
to those people who put this together. New Zealand
is a long way from anywhere and I sometimes feel a
little isolated. This website looks like it will
fill me in on all that is happening around the world
and will focus to the positive brave people with
lupus - stories we all need to hear about. Thank
you.
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