Lupus is usually described in 3 ways:

Autoimmune Disease
Connective Tissue Disease
Chronic Disease

These are all true.

It is an autoimmune disease because the body is fighting itself. Instead of attacking foreign invaders  (bacteria, viruses), the body has targeted it's own tissues.

It is a connective tissue disease because tissue that the body targets, is connective tissue. Connective tissue is everywhere in the body: the joints, the blood vessels, the linings of organs, etc.

So when a person has lupus - almost anything in the body could be affected.

It is a chronic disease because it is incurable - not always life-threatening, although it can be.

~From the Missouri Chapter Lupus Foundation~

Links

Lupus Home Page at Hamline University

Lupus: Missouri Chapter Lupus Foundation

Lupus: Foundation of America

It has been my privilege to be a proud member of the Lupus Groupus. The lists educates, stimulates, cares, supports and give an outlet of expression to all those with lupus and lupus like diseases and their family and friends.

As in all  packs, sometimes they disagree. But the group encourages a free exchange of ideas and discourages personal attacks on any individual. This is an open forum.

As a member you will freely receive education, love and support.

There are many knowledgeable members in the pack, but it is always recommended and advised that you check with your personal physicians. 
This is a place where you will meet some very caring and compassionate people who will support you. You will become eligible to receive "Spoakles" from Spoakle Inc. Something you do not want to miss! Thank you ladies, for your warm, wonderful, glowing spirits!

As a member of the pack you may give whatever knowledge, love and support you feel you can give.

There are many different people in the pack. From all walks of life, nationalities and races. Some educate, some support, some care. And some express needs, and feelings.

I encourage you if you have the disease, have a family member or friend that does to come to the lists. I encourage you to join the  pack. Go to the Hamline University link listed above for all the information you need to join. If you have any trouble with doing this, please contact me by email, so I can assist you.

I have graciously been given permission to link to the following site, from my lupus sister, Rainwater. This site is still in the making, it is being written by the people who live with the disease, with their contributions to it. Every day it grows a little larger.

On the lists, we were talking about doing a book so that all people, even those without computers, can hear words from kindred spirits. This may possibly lead to that dream.

When I go to this site, I see myself in a lot of these writings. It is called "Living With The Wolf." If you do not know of the disease, you might not understand how to some those little four words, can throw you into a real panic and strike fear into your heart.

Imagine, my friend, that you have just suddenly, without any warning, fallen from a very, very great height. You have pain all over every part of your body, inside and out, you cannot move. Your mind is not clear, you are in a foggy daze, a drunken like stupor. You just want to lay there, it hurts to much to move, you have no balance to move with. But you do move, with the help of others, or a cane, or a brace, because all of this scares you.

So you dizzily, wobble, with unsure gait, slowly, rushing, you can't go any faster, no matter how hard you try, to your doctor.

Now imagine, the look you might have on your face when your doctor looks at you and says, "You will have to live this way for the rest of you life."


Lupus Mind

If you can imagine just a little of this, then you also understand a little bit about lupus.

If you have this autoimmune disease or one like it, I highly recommend that you go to this site and read what others have written. Add your own voice, if you are comfortable doing this. If you are struggling, at all, even a little bit, with the complexity of this disease, I plead with you to go there! You need to see that you are not alone, you are not the only one struggling!
 
If you learn from your suffering, and really come to understand the lesson you were taught, you might be able to help someone else who's now in the phase you may have just completed. Maybe that's what it's all about after all...
Anonymous

If you know someone with lupus, or you want to learn about this disease, that affects millions, but is hardly ever talked about, or fully understood, go to this site. Learn from my brothers and sisters that walk this path with me. And maybe it will give you a little more understanding of why I personally, for my own needs, had to journey to embrace the wolf.
 
      
LUPUS WOMAN
A loving reminder from Sheo that I am never alone.
Thank you my very special Sister/Friend




PLEASE READ
A new lupus book is being written
Dreams do come true.
When we all work together.





 


This site was created by Jenny aka Lilwolff
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