Monday, December 5, 2011

Tis The Season To Give
Join Sisters Against Lupus and our community partners as we
give HOPE this holiday season.
 Saturday, December 17th from 9am to 9pm
 
 
Homeless Feeding
Homeless individuals will be picked up and brought in to receive a hot meal, toiletries and coats to keep them warm this winter season.

Toy Drive
Children from local shelters will be brought in to shop for toys. Parents will also have an opportunity to select a toy to wrap and give to their child.
 
FACT: In 2010 there were 8,937 individuals either on the streets, in shelters or in transitional housing.  24,000 become homeless at one point each year in King County.
 
HOW CAN YOU HELP? Join us in our mission to raise 200 COATS and TOYS to brighten the lives of as many homeless families this holiday season. 
 
 
 
  • 1st Set a goal (example: 10 coats, 6 toys)
  • 2nd Share this information with your friends, family, church and coworkers via email, text, and Facebook. Let them know why you are doing this and how they can help you reach your goal.
  • 3rd Collect coats and toys then contact us to arrange a pick up or kindly drop off at any of the locations below.    
TOGETHER, we can make a difference!!
 
Volunteers Needed: If you are interested in serving food or distributing coats and toys, please email info@sistersagainstlupus.org
 
Drop Off Centers:  Please drop off new or gently used coats and new unwrapped toys at the following locations and times:
 
Tabernacle MB Church  2801 South Jackson Seattle *Tuesday –Friday 9AM-5PM
Babalu 1723 North 45th Street  Seattle  *Thursday-Saturday 7PM-1AM
Saigon Palms 101 Southwest 41st Street Renton *Saturday 8PM-1AM
Munch Bar  505 Bellevue Square  Bellevue *Sundays 8PM-1AM 
Life's Salon 7629 Rainier Ave So Seattle *Tues - Fri: 9AM - 7PM Sat: 8AM - 5PM

Tuesday, October 11, 2011

LOVE IS THE CURE!!!

Question,

How do you picture your wedding day?   

Maybe visions of all your family & friends united together toasting and celebrating your union, laughter filling the room with bouquets and boutnerrs being tossed. A celebration ending with a pile of gifts. All for you,  perfectly picked, from your wedding registry, right??

Envision this twist..... Wanting your wedding day to be more than a celebration of you, but to bring awareness to a disease that is fastly spreading and effecting your brothers and sisters.  Finding a way to Band the community together to create an atmosphere of LOVE. As your guest come together to celebrate God’s gift of marriage, they can begin to Believe, Love is the Cure!.... Well, for the groom Sean and Bride Kim, LOVE truly is the CURE.   

 
Sean & Kim didn’t register at Nordstroms for toasters or cutlery sets. Instead they showed their support in SALs  mission to spread awareness, find a cure, and support Lupus Survivors.  They selflessly asked family and friends to give to Sisters Against Lupus in lieu of wedding gifts.  It is rare to find people who can cry with you while offering you a lifting hand up, but that is the core of this beautiful couple.  Neither of them have Lupus or have family members effected by it, but as Sean puts it "We're all brothers and sisters in God’s eyes". 

 For Sean & Kim, showing love & compassion for others, is second nature.  So on their wedding day, it was no surprise this day exemplified LOVE in every form.  Some can emphasize with struggle & offer a tissue to absorb the pain, but readied action is rare to find. Sean & Kim acted by sharing the most important day of their life to spread Lupus awareness and to raise money for a cure.  


From the depth of our heart, Sean & Kim we thank you for showing us love in action, love that transcends boundaries and finds the cure for Lupus!  Thank you for being a living example of His love.  Thank you for going against the grain of the “traditional” wedding.  Thank you for having a servants heart.  Thank you for sharing your love, with all who love the both of you, of whom God has made one. 


WE LOVE YOU!!!
 
"You are the cure; you are not a victim you were perfectly placed in an imperfect position so that the strength you have been given would be the prescription

You are the cure; you stand when others have fallen, you believe when others have forgotten, you inspire, you are a fighter, you are faithful, you are strong.  You are a survivor

Because of you I stand and we can stand together

You are not alone; you are the cure

Survivor" 
         ~Sean Goode

Sunday, September 25, 2011

10 BACIS FACTS ABOUT LUPUS


Lupus is a complicated disease. 
Whether it has been suggested you may have lupus, or you have a definitive diagnosis, you should know these 10 basic facts about lupus.

1 - Lupus is an autoimmune, rheumatic disease.
In lupus, the immune system of the body attacks its own cells and tissues. Specifically, the joints, skin, kidneys, lungs, heart, nervous system, and other organs of the body are affected.
2 - There are five types of lupus.
    * Systemic lupus erythematosus - affects joints and organs
    * Discoid lupus - affects the skin
    * Sub-acute cutaneous lupus erythematosus - characterized by a specific, non-scarring skin lesion
    * Drug-induced lupus - develops after a drug reaction
    * Neonatal lupus - affects newborns
3 - Ninety percent of lupus patients are women.
Lupus affects roughly 9/10 times as many women as men. Most often, lupus develops in people 18 to 45 years old. Though lupus is most prevalent among women, it also may affect men and children, as well as people of all ages.
4 - There are 11 American College of Rheumatology criteria for Lupus.
Lupus is differentiated from other connective tissue diseases, based on eleven criteria offered by the American College of Rheumatology for classification purposes.
    * Butterfly-shaped rash across cheeks and nose
    * Scaly disk-shaped rash on face, neck, ears, scalp, chest
    * Sunlight sensitivity
    * Mouth sores, tongue sores, inside nose sores
    * Arthritis pain in joints
    * Pain in chest and side when breathing or moving
    * Kidney problems
    * Neurologic problems
    * Blood problems such as anemia, low white cell count
   * Immune system malfunction
   * Antinuclear antibodies
It is recommended that if you have four or more of the eleven criteria, you should consult with a rheumatologist.
5 - Lupus diagnosis may be difficult.
Lupus is considered an unpredictable disease, with no two cases exactly the same. The unique pattern of symptoms associated with lupus has caused some to say that lupus is like a snowflake. No two are alike. There are several symptoms of lupus which mimic other rheumatic diseases (e.g., severe fatigue), making the diagnostic process difficult.
6 - Lupus treatment depends on symptoms and severity of symptoms.
Conservative treatment with NSAIDs (i.e., nonsteroidal anti-inflammatory drugs like ibuprofen) and plaquenil may be appropriate for lupus patients with non-life threatening symptoms such as joint pain, muscle pain, fatigue, and skin rashes. More aggressive treatment which may include high dose corticosteroids or immunosuppressive drugs is used when there are severe organ complications. The benefits and risks of treatment must be weighed by each patient and their doctor.
    * Lupus Treatment Options
    * Lupus Poses Many Challenges
    * Lupus Medications - What Are My Options?
7 More then 1.6 million people across the nation have lupus.
Approximately 70 percent of lupus cases are systemic. In 50 percent of those cases, it is a major organ which is affected.
8 - Certain races have an increased risk of developing lupus.
lupus is two to three times more prevalent among people of color, including African-Americans, Hispanics, Asians, and Native Americans.
9 - The majority of lupus patients lead normal lives.
With careful monitoring of lupus, and treatment adjustments as needed, most lupus patients lead normal lives. There may be some limitations and the disease may impose restrictions at times but with good disease management quality of life can be sustained. The worst adversary comes from within, when the patient loses hope, loses will, and gives in to frustration and depression.
10 - A rheumatologist is a medical doctor who specializes in treating arthritis and other rheumatic conditions, including lupus.
Your primary care doctor can refer you to a rheumatologist , or you can get an appointment through self-referral if your health insurance allows it. Evaluation by a rheumatologist is important so that a patient can develop a treatment plan.

Friday, September 23, 2011

Survivors Circle

Lupus Support Group
Saturday September 24th 10AM-12Noon
 
Time for all SALs to get together to encourage, educate and empower one another in our time of sisterhood, SO EXCITED TO SEE YOU ALL AGAIN!!!!
3 reasons not to miss out....
1. Daniel Jahn, CSCS, USAW, Nutritionist and Maximum Sports Conditioning expert will be in the building.
2. Healthy snacks and refreshments will be served.
3. You'll like this one!!!! We have few tricks up or sleeve to spoil and pamper all the survivors.

So, clear your schedule and come (email us to arrange a ride if you need to be picked up) RSVP by emailing info@sistersagainstlupus.org or by calling             253-293-1699         

One of the top criticisms of those suffering with Lupus is the lack of support & resources.  It is our goal to offer a safe haven of Hope, Support & Empowerment to Sisters, Brothers, Children, & Families affected by Lupus.  Join us for a time to mingle with other Survivors with similar struggles and share testimonies and coping strategies.
Saturday, July 23rd from 10AM-12Noon.
Sundance Cabana
210 27th Avenue
Milton, WA 98354
(Exit 142 - Enchanted Parkway just outside of Federal Way)
RSVP: by email info@sistersagainstlupus.org or call 253-293-1699

If you know of anyone who can benefit from this incredible time of healing;
Emotionally, Physically and Spiritually
Forward this to a Friend

Tuesday, September 13, 2011

JOBTINI

Are YOU looking for a JOB? 
Join us September 13th, 2011 at Citrus Restaurant from 5:30-8 p.m. and meet with recruiters from REI, Comcast, Verizon, Seattle Times, Community Health Plan of Washington, Microsoft, State Farm, Spring Creek Group, Projectline Services, Acorn of Washington, University of Washington, Harborview Medical Center and more! Jobtini is free for all jobseekers. Bring a friend, colleague or family member!
Event:Jobtini
Date:Tuesday, 9-13-11
Location:Citrus Restaurant-Tapas  
Address:1001 Fairview N, Seattle,WA 98109
Time:5:30 p.m. - 8:00 p.m.
Attire: Business Professional 21 & over event. 
Price:Free for all jobseekers!
"WHAT IS JOBTINI?"
JOBTINI is a quarterly social networking event Colors NW Careers puts on and brings together professional candidates of color, recruiters, and hiring managers from top Northwest employers committed to workforce diversity.
 
SAL is proud to support Colors NW and is thankful to them for helping us to spread Lupus Awareness! We hope to see you there. Click on the link below and check out their website for additional information

Saturday, August 6, 2011

It's time to celebrate!!! August 20th @ Babalu

Join Sisters Against Lupus (SAL)for an incredible evening as we celebrate with two women; Yedit Bereket & Kawanna Perine and their accomplishments of spreading Lupus awareness, assisting survivors battling this illness & raising funds for research.

Sisters Against Lupus could not have made it this far without your prayers, love & support throughout this past year.   With that said, we want to say THANK YOU and we hope you join us in celebrating our first year of Spreading Lupus Awareness & Supporting Survivors and raising funds for Lupus Research!

Wear your favorite PURPLE attire in honor of Lupus survivors.
Survivors, who courageously battle Lupus everyday.

Together, We Are The Cure……Lupus MUST Die!!

Facebook: Sisters Against Lupus
Event page: Click 4 more info

Saturday, June 11, 2011

Survivors Circle - Lupus Support Group June 25th 10AM-12Noon

Do you have Lupus? Maybe you've lost a loved one to Lupus? Or you're interested in learning more about Lupus and how you can be supportive of family/friends living with Lupus?

If you live in the Seattle/Tacoma area here’s an opportunity for you to get involved with Sisters Against Lupus as they host "Survivors Circle" Lupus support group!

This group offers Hope, Support & Empowerment to Sisters, Brothers, Children, & Families affected by Lupus.
HOPE

Local Rheumatologist shares an indebt look at what Lupus is and offers hope with new medicines.

SUPPORT
Mingle with other Survivors with similar struggles and share coping strategies.

EMPOWERMENT
Gain inspiration from the remarkable story of Sisters Against Lupus Co-Founder Kawanna Perine. 
Sundance Cabana 210 27th Avenue Milton,  WA
(Exit 142 - Enchanted Parkway just outside of Federal Way)
 
RSVP by email to info@sistersagainstlupus.org 
or by phone 253-293-1699
 
We hope that you can join us for this time of healing; Physically, Emotionally & Spiritually.

Click HERE to view event our facebook invite to survivors circle

Tuesday, May 24, 2011

THANK YOU!!!

Hello Friends & Family!!

Sisters Against Lupus would like to THANK YOU for helping us set another record breaking year at the 5th Annual Walk To Cure Lupus Walkathon on last Saturday!! With over 200 registered Walkers Team SAL raised a total of $10,328!!!

It was a beautiful sunny day in Seattle shared by a few of our supporters: Seattle Seahawks Jordan Babineaux, David Loud from Congressman Jim McDermotts Office & those sassy little ladies of Sweet Mahogany Drill Team!!

Whatever part you played, we say thank you from the bottom of our hearts!! We are one step closer to finding a CURE!!!

Your Sisters,
Yedit & Kawanna


Seattle Seahawks Jordan Babineaux walked with SAL

Sisterhood

 BECOME OUR PAL ON FACEBOOK CLICK HERE, THEN CLICK LIKE!!!

Tuesday, May 10, 2011

May 10th is World Lupus Day!!

May 10th is World Lupus Day

Let's kill Lupus before it kills us!!

Reminder, this Saturday May 14th 9AM @ Alki Beach join us as we WALK TO CURE LUPUS. Invite your friends, family & co-workers to join us in the fight to kill Lupus.  Not to late to register, click HERE to get registered or shoot us an email at sistersagainstlupus@gmail.com and we can add your name to the list of walkers :) 

Shirts for the walk will be available the morning of the walk.  Donations can be made in advance by clicking HERE.   Also accepting money raised to go towards research until the day of the walk, so lets raise funds to kill lupus. 

Your sisters,
Yedit & Koopie

Saturday, May 7, 2011

Symptoms of Lupus

Because lupus can affect so many different organs, a wide range of symptoms can occur. These symptoms may come and go, and different symptoms may appear at different times during the course of the disease.

The most common symptoms of lupus are:

* extreme fatigue (tiredness)
* headaches
* painful or swollen joints
* fever
* anemia (low numbers of red blood cells or hemoglobin, or low total blood volume)
* swelling (edema) in feet, legs, hands, and/or around eyes
* pain in chest on deep breathing (pleurisy)
* butterfly-shaped rash across cheeks and nose
* sun- or light-sensitivity (photosensitivity)
* hair loss                                                                                                          
* abnormal blood clotting
* fingers turning white and/or blue when cold (Raynaud’s phenomenon)
* mouth or nose ulcers

Many of these symptoms occur in other illnesses besides lupus. In fact, lupus is sometimes called "the great imitator" because its symptoms are often like the symptoms of rheumatoid arthritis, blood disorders, fibromyalgia, diabetes, thyroid problems, Lyme disease, and a number of heart, lung, muscle, and bone diseases.  
Lupus is a chronic inflammatory disease that can affect various parts of the body, especially the skin, joints, blood, and kidneys.


Thursday, April 28, 2011

A woman is like a tea bag

~ You can't tell how strong she is until you put her in hot water. - Eleanor Roosevel

STOP saying "I can't make it through this trial, I'm not strong enough or why me??" Our trials are what makes us stronger & without them we would not appreciate brighter days. You are never giving more then you can handle so shift your attitude & see what happens. Today Know you CAN & WILL make it through ANYTHING!! 

10 Basic Facts About Lupus


Lupus is a complicated disease. 
Whether it has been suggested you may have lupus, or you have a definitive diagnosis, you should know these 10 basic facts about lupus.

1 - Lupus is an autoimmune, rheumatic disease.
In lupus, the immune system of the body attacks its own cells and tissues. Specifically, the joints, skin, kidneys, lungs, heart, nervous system, and other organs of the body are affected.
2 - There are five types of lupus.
    * Systemic lupus erythematosus - affects joints and organs
    * Discoid lupus - affects the skin
    * Sub-acute cutaneous lupus erythematosus - characterized by a specific, non-scarring skin lesion
    * Drug-induced lupus - develops after a drug reaction
    * Neonatal lupus - affects newborns
3 - Ninety percent of lupus patients are women.
Lupus affects roughly 9/10 times as many women as men. Most often, lupus develops in people 18 to 45 years old. Though lupus is most prevalent among women, it also may affect men and children, as well as people of all ages.
4 - There are 11 American College of Rheumatology criteria for Lupus.
Lupus is differentiated from other connective tissue diseases, based on eleven criteria offered by the American College of Rheumatology for classification purposes.
    * Butterfly-shaped rash across cheeks and nose
    * Scaly disk-shaped rash on face, neck, ears, scalp, chest
    * Sunlight sensitivity
    * Mouth sores, tongue sores, inside nose sores
    * Arthritis pain in joints
    * Pain in chest and side when breathing or moving
    * Kidney problems
    * Neurologic problems
    * Blood problems such as anemia, low white cell count
   * Immune system malfunction
   * Antinuclear antibodies
It is recommended that if you have four or more of the eleven criteria, you should consult with a rheumatologist.
5 - Lupus diagnosis may be difficult.
Lupus is considered an unpredictable disease, with no two cases exactly the same. The unique pattern of symptoms associated with lupus has caused some to say that lupus is like a snowflake. No two are alike. There are several symptoms of lupus which mimic other rheumatic diseases (e.g., severe fatigue), making the diagnostic process difficult.
6 - Lupus treatment depends on symptoms and severity of symptoms.
Conservative treatment with NSAIDs (i.e., nonsteroidal anti-inflammatory drugs like ibuprofen) and plaquenil may be appropriate for lupus patients with non-life threatening symptoms such as joint pain, muscle pain, fatigue, and skin rashes. More aggressive treatment which may include high dose corticosteroids or immunosuppressive drugs is used when there are severe organ complications. The benefits and risks of treatment must be weighed by each patient and their doctor.
    * Lupus Treatment Options
    * Lupus Poses Many Challenges
    * Lupus Medications - What Are My Options?
7 More then 1.6 million people across the nation have lupus.
Approximately 70 percent of lupus cases are systemic. In 50 percent of those cases, it is a major organ which is affected.
8 - Certain races have an increased risk of developing lupus.
lupus is two to three times more prevalent among people of color, including African-Americans, Hispanics, Asians, and Native Americans.
9 - The majority of lupus patients lead normal lives.
With careful monitoring of lupus, and treatment adjustments as needed, most lupus patients lead normal lives. There may be some limitations and the disease may impose restrictions at times but with good disease management quality of life can be sustained. The worst adversary comes from within, when the patient loses hope, loses will, and gives in to frustration and depression.
10 - A rheumatologist is a medical doctor who specializes in treating arthritis and other rheumatic conditions, including lupus.
Your primary care doctor can refer you to a rheumatologist , or you can get an appointment through self-referral if your health insurance allows it. Evaluation by a rheumatologist is important so that a patient can develop a treatment plan.

Wednesday, April 20, 2011

THIS IS MY STORY ~Selam Bereket


I was diagnosed with SLE ~Systemic Lupus Erythematosus as a young adult at the age of 15.  Prior to being diagnosed I underwent a verity of different tests to determine what it was that I had.  I was constantly in and out of hospitals.  Every day was a challenge because I was so weak and unable to do much for myself.  I was extremely fatigue and couldn’t understand why my body was swelling when I didn’t have much of an appetite, I felt like a balloon ready to explode at any given moment.  After several months of testing, they determined that I had a severe case of Lupus.  The Lupus attacked my kidneys and I was face with two choices: to do chemo therapy for three years or to start dialysis right away three times a week.  It was hard to accept all that was happening to me but I decided to do chemo therapy instead of kidney dialysis.   
Emotionally I was drained having to go through this at such a young age; I was unable to go to school so I took time off.  I did home school until I was able to feel better, once I felt a little better I began going back to school part time.  Once I completed my treatment, my kidneys returned back to full function and I was able to live a more normal life, but with medications of course.  I was able to finish high school, attend Portland State University and complete a BS in Health Science with a concentration in Community Health and minor in Communications.   Growing up, I had a lot of ups and downs.  I remember countless times where I was unable to get out of bed, even the thought of lifting a finger was painful; every joint in my body ached extremely bad, it felt like needles and pins stabbing me (the pain was unbearable).
During December 2008, I started feeling ill; I woke up one morning unable to barley open my eyes because my entire face was swollen.  My sisters rushed me to the emergency room in which I stayed there for over two weeks.  I felt as if I was re-living my childhood experience again, when I find out that my kidneys were being attacked by Lupus.  I came home after being discharged only to come back the next week with my whole entire body being swollen yet again, I gained over 20 pounds in fluid.  A few months down the road, I started chemo therapy once again, this time only for six months.  Unfortunately this time, the chemo therapy was unsuccessful.  The next step was just to try high doses of immunosuppressive mediation (which I have been on many years), which led me to be more sick and left me going in and out of hospitals.  My kidneys were failing fast; in November 2009 my kidneys shut down and I immediately was put on emergency dialysis where a catheter was surgically implanted in my neck and ran to my heart to dialysis with.  With this catheter, you are not able to get it wet as you are easily able to get an infection and die from doing so.  I have had to surgeries to get a fistula in place (one to connect my artery and vein together, the other to bring it up to the surface).
Lupus has affected me in MANY ways, it is holding me back from living my life fully.  I am in constant pain each and every day.  I have been on prednisone (a type of steroids) for ten years, this mediation was what made my bones brittle and weak.  Taking prednisone for so long is how I had three compression fractures on my spine, which left me in inconceivable pain and at bed rest for months on end.  I am still currently on dialysis three times a week for four hours each visit.  I wish that there was an organization that directly could have helped and other lupus patients with any financial needs, support and education awareness.  While growing up, having an organization like Sisters Against Lupus would have positively impacted my life in a lot of ways.  By Selam Bereket

Click on the link below to register and/or donate:
  
CLICK HERE & 'LIKE' our SAL Facebook page