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The Lupus Foundation of America (LFA) is responding to requests from our Las Vegas constituency for more direct patient services in your community. To meet these needs, the LFA will be hosting our first fundraising Walk to provide the funds necessary to deliver these imperative services. The money raised in your community will stay in your community!
Our Lupus Walk in Las Vegas Nevada is in April
At: Mission Hills Park
551 E. Mission Drive
Henderson, NV
Saturday, April 26, 2008 9am-12pm
I would like to share with you about what The Lupus Foundation OF America is
trying to Do. The Lupus Foundation Of America is trying get an office here in Las Vegas we have doctors who will volunteer their time to help Lupus patients that have no insurance.
I invite you to join my team to help get donations so Las Vegas can
have an office for Lupus patients you can join my team or just donate
on to my page, if you choose to join the team and are able to have your family
and friends donate it would help us get to our goal a lot faster.
here is the link. This link explains even more
so on our cause.
"Click here to read more
information on the walk
and or join our team
or donate "
I do not think people out of USA can donate because of the exchange rate has to be converted. But those in USA can..
Please if you can pass this on to those who are in USA and who would like to help us.
Thank you Hugs Angela
I am glad you stopped in.
I would like to share with you about Lupus (SLE).
This is how my doctor explained to me about Lupus.
He said:
"It is terminal in the aspect that there is no cure,
and eventually most people who have lupus
die of complications caused by
an over active immune system."
We can live a long time having Lupus
because of the medications that they have
for us.
I was diagnosed with Lupus and fibromyalgia in 2004.
I also have the beginning stages of Osteoporosis.
In 1999 I was told I have ostioarthritis.
In these pages that you see in the directory below.
I share about my life.
I share about my belief in a Higher Power.
I share about getting sober and living through different kinds of abuse,
child abuse, spousal abuse.
I started writing these pages in 1999 in hopes to find my Birth mom.
I found her in 2005.
I wrote her a letter you can read it,
it is in the directory below
in the second row in the middle.
I share about how Lupus and Fibromyalgia changed my life.
I used to dance Ballet and Jazz from childhood on up to my mid 20s.
I let Alcohol and drugs take my life over, now having Lupus I am not able to dance anymore.
Life is like a roller coaster has many ups and downs.
With willingness to live life, and having a Higher Power in my life, my life is good today.
Below is the table directory of my writings and to read my story in book form.
I wrote a book called:
"Thank you God One Lady's Journey within."
My book has 21 chapters in it,
it is not published at this time.
My book has been out on line since October 2006,
to read my book.
Just click on the title in the directory below called :
My Autobiography it is in the second row in the middle next to (I found my birth mom.)
To read my other writings in the directory just click on the titles below that you want to read.
..
Angel
In The Park.
My Childhood
Letting go
with
Love.
My life
living with lupus
& Fibromyalgia.
We never Graduate
in Recovery.
My Earth
Angel
My Better Half
My Autobiography,
"Thank You God
One Lady's
Journey Within."
I found my Birth mom.
Thoughts on
God's
Will or Mine?
My first Marriage.
Praying for
the
Military.
My thoughts
on
War.
Angels That Care.
A group that helps
Child Abuse.
Add your
link.
My two Dear
Friends.
WOSIB
Angels.
My Net Angel
(Lynnie)
Dana
My Little
Angel.
Recovery
Stories.
Fun
Page
My favorite music,
& Vidoes.
My
Awards.
My dear friend Krys
has won
her Emmy.
More Awards.
Join me in chatting.
Insperational
Readings.
Come join
my Newsletter.
Come visit me at
Authorsden.Groups
I am in.....
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Visit LUPUS BUTTERFLIES AMONG US
Those of us who live with Lupus or FMS can have a normal life
we just have to accept Lupus
and live life a little differently then we used to.
Subscribe to Support for all Autoimmune diseases
Email:
Visit this group
~New Forum for FMS~
Add this banner to your site Click Banner to enter
"What is Lupus and Fibromyalgia?
Click here to find out.
To visit"Lupus Foundation of America." click here.
"New To Lupus click here."
"Click here to visit Welcome to Linkable.org"
Subscribe to LWLupus
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Make yourself at home.
Enjoy your stay here.
I would love to hear from you feel free to email me any time.
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