Sickle Cell Camp A Great Success

Camp Crescent Moon Celebrates Its 45th Year in Pacific Palisades Operated by numerous volunteers, the president and CEO of the Sickle Cell Disease Foundation of Southern California said she would like to start an endowment fund to help further finance the camp. An extra boost of laughter, excitement and outdoor education filled Temescal Getaway Park this week as Camp Crescent Moon celebrated its 45th year with its annual session in Pacific Palisades. It is considered the nation's first and oldest summer camp for children with sickle cell disease between the ages of 8 and 14, and many children from Los Angeles and around the country attend. It's partnered with the Sickle Cell Disease Foundation of Southern California. On Monday, President and CEO Mary Brown said they have about 85 campers participating this year, up from 80 in 2011.  "We lose about 10 percent of the children due to the illness," said the camp's director. Sickle cell disease which changes normal, round red blood cells into cells that can be shaped like crescent moons. Sickled cells can get stuck and block blood vessels, which stops the oxygen from getting through, causing infections, pain, and even stroke and anemia. However, many people are able to have a very good quality of life by learning to manage the disease. Amanda Shelton, Kimberly Washington and Lisa Washington, former campers now counselors from the L.A. area, said they are functioning sickle cell adults and enjoy coming back to teach the children about the disease. Portia Ragin, a camp counselor who comes from Atlanta, GA, said her father has sickle cell disease. "I just feel like I'm giving back to everything that affects him every day," she said. Brown said they have 47 staffers at the camp, which includes a medical team of volunteer nurses, doctors, social workers and counselors - some with sickle cell disease and some who do not. She said the counselors volunteering with the disease are called "palanca," which in Spanish means sacrifice. It costs approximately $100,000 for the camp to use the park for a week in the summer, Brown said, and they rely on cash and in-kind donations from their contributors. A charity auction was held earlier this month at Amoeba Music in Hollywood to benefit the camp. "We're on a shoe-string budget," she said. "I'd like to get a $5 million endowment for the program. We put a lot of effort into this project to make it happen. It's served as a model for other sickle cell camps." For more information about Camp Crescent Moon and how to donate and volunteer, visit their website. What a Wonderful experience for campers and staff. Donate your money, time, and energy to one of the oldest organizations for clients with Sickle Cell Disease. matthew.sanderson@patch.com .

EXPRESS YOURSELF

There are many moments throughout our lifetime that we are confronted with the desire to fully express how we feel. For the Black Male this is a daily paradox. As a male with SCD we get that double whammy because we feel dependency is a sign of weakness, yet we depend so much on family and friends to get us through our crisis.  Most of us grew up depending on others. As SCD became more prominent, the SCD community found a need to put in place pediatric clinics which would advocate care for us until we reach young adulthood. (17-18). Once we hit that threshold we look at our self as being grown and try to handle our illness in a compartmental area of our life. Some of us find that we are not able to handle the patchwork of our health plans, medical services and our daily routines.  In fact, it is difficult to find any adult programs that are focused on the transition from pediatric care to adult care. Sad but true, even if a program is available we have to take responsibility and get there.

In contrast, in the 1950's when I was an infant there was very little knowledge of Sickle Cell Anemia. There  were very few programs at all, if any.  Pain meds were sparingly used in crisis.  Transfusion therapy was non-existent. The patient and his mother were probably sent home from the doctor with some sort of iron shot and told to give aspirin every 4 hours, making the blood even thinner. You see, most of the time we were diagnosed as anemic, nothing beyond that. Generally, the only comfort if in crisis was constant rubbing of the joints involved, singing, television and comforting dreams.  What I've learned today is these attempts to minimize pain were the beginning of psycho-social behavioral modifications.  So let's give parenting the credit for being ahead of science. 


Despite the progress made towards pain management over the last 40 years, there is still a gaping hole between what is known to work and what is given to the patient with regards to pain management. The issues that complicate a more collaborative approach to pain management between patient and the medical community are, community concerns, emergency room responses, appropriate medications, accurate information, curricula development and fear and concerns of the patient. We need to express ourselves in raising awareness to pain management throughout the health care system and sub-systems each and every time we encounter them.

Was hospitalized for 3 weeks this past stay. I had pain that was not only Crisis related but also intensified by the need to have my shoulders, elbow, and to say the least my right knee replaced due to Avascular Necrosis. Ha! Ha! Which one is first? I have to look at our disease as a testament to our strength and Gods Blessing. How we feel allows us to live through these critical times even when we feel all is against us. We must communicate, (Social Media and the ability to get our word out through these mediums is a powerful tool.) Be Strong and Positive and let that sense of humor SHINE! Join my blog @ 1chanceonly-bigdaddy54.blogspot.com I thought this was a good poster... Take a look. https://www.facebook.com/photo.php?fbid=319934218076135&set=a.148627608540131.33233.135851093151116&type=1&ref=nf

CAMP CRESCENT MOON WORLD GAMES

This is my favorite time of the year. School is out and camps begin. I'm not talking about the Mitt Romney or the Donald Trump kids type camp. Not even scouting camps. I can remember going to Scouting Camp and almost coming home each year calling myself a failure because I never stayed the full amount of days due to crisis pain, too much excitement and chills from swimming in the lake. I would be devastated. Kids would tease me and say I was a "Weakling" then the rumors would start about the length of time I had to live. The bet was from 14-18 years old. Each year I celebrated their loss bet; however some children, including myself, have been scarred emotionally for many years.
   
You see in the 60's, camps had no idea of what was required to treat children with different diseases like SCD. Most Black Scouting Camps (in the south) had no doctors, counselors, teachers, etc. who were able to care for a camper who may have become ill. You had minimum staff and minimum equipment.
   
Going to SCD camps now, although under-funded, is a lifelong benefit in psycho-social behavior and coping skills which enable our children to live fuller lives. My children have been campers, volunteer counselors and administrators at Camp Crescent Moon (Sickle Cell Disease Foundation of California) since they were old enough to attend. Each year has been a labor of love for my family. Their appreciation for Sickle Cell Disease continues to grow.
   
Kids who attend camp look forward to meeting their peers who have SCD. They know they won't be bullied or teased because of their disease, unlike the humiliation I experienced 45 years ago.  They know the doctors, nurses, counselors, staff and all who volunteer without pay for that week are there because they love them and not because they sympathize with them.  Looking at each year's photos and hearing the wonderful stories warm my heart to no end and reinforces the importance of Sickle Cell Camps.  You see when I was growing up I had nothing to compare my Scouting days with. Suffice it to say, Black Scouting presented me the opportunity to grow into a young adult much like SCD camp does for the new generation of Sickle Cell Patients.


During the remainder of the summer or throughout the year you may have an opportunity to support your local state Sickle Cell Foundation.  Take the time to look at some of the photos or listen to testimonials and you will be convinced that this cause is worthy of your support.   http://1chanceonly-bigdaddy54.blogspot.com

WORLD SICKLE CELL DAY-JUNE 19

Continuous outreach is the only way we will gain momerntum and find a cure for SCD.


What can you do in recognition of this day?   Maybe give blood at the Red Cross.  Talk about SCD at your Church or a group setting.  Visit someone in the hospital.  Whatever it is, know that it will be appreciated.

World Sickle Cell Day

In the year 2008, the GeneralAssembly of the United Nations adopted a resolution which determines sickle cell disease as a public health problem and one of the world’s foremost genetic disease, requiring heightened awareness and activism, diagnosis and management. The result of the resolution was that June 19th was declared as World Sickle Cell to increase awareness of the condition all over the world.
The World Health Organization (WHO) has started work on a war footing to promote a world wide agenda to address hemoglobin dysfunctions.
WHO has made a commitment to:

• Recognize that sickle cell disease is a major health issue.
• Increase awareness of the world community regarding sickle cell disease.
• Eliminate harmful and wrong prejudices associated with sickle cell disease.
• Urges member countries where sickle cell disease is a public health problem to establish health programs at the national level and operate specialized centers for sickle cell disease and facilitate access to treatment.
• Promote satisfactory access to medical services to people affected with sickle cell disease.
• Provide technical support to all countries to prevent and manage sickle cell disease.
• Promote and help research to improve the lives of people affected with sickle cell disease.

World Sickle Cell Day

The World Sickle Cell day is celebrated across the globe with special emphasis in African Nations and Asia. The celebrations include a press, media campaigns, music shows, cultural activities, and talk shows.
Since no known cure exists for sickle cell disease, the main goal is to prevent further complications due to sickle cell disease. The main emphasis is hence on educating medical professionals, care givers, and associated personnel about prevention, research, and resources to minimize the complications due to sickle cell disease. Hence June 19th is devoted mainly to spread awareness, through talks, seminars, pamphlets, literature and consultations.


Taken From: AltiusDirectory.com

NFL 49ers Draft Cam Johnson Who Has Sickle Cell Trait

I received this link from the advocacy group, "SickleStrong". Thank you for this article.

Cam Johnson wants to be treated like any other draft ready college football player. Certainly his hard work indicates he deserves being rewarded fairly. Yet, this is not the case. Why? You see the NFL General Managers have done their risk assessment and can make the case to draft players like Cam at a lesser value using the SC Trait as the reason to draft him in a lower round and pay the lesser rate. Economics aside those of us in the Sickle Cell Community should applaud this young man for his commitment, hard work and pursuit of a life long dream. May God continue to Bless him and let us lift him up in prayer.

The link below is the San Francisco 49'ers press release regarding the 2012 Draft. Read some of the comments regarding opinions about Sickle Cell Disease and traits. There are many differing opinions from a lot of ignorant people. We need to educate and advocate as often as we can in order to clarify and remove barriers associated with SCD.


http://www.ninersnation.com/2012/4/29/2986396/49ers-draft-picks-cam-johnson-sickle-cell-trait