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

SCD-- Where They Are Headed and What They Are Leaving Behind ( A Series Of Discussions)

My sister in law, who happens to be President & CEO of The Sickle Cell Disease Foundation of California was in town attending "The Second National Conference on Blood Disorders in Public Health".  After talking to her my question was, where was SCD research headed and why was there no studies showing advances in Stem Cell or Bone Marrow transplantation.  Her reply was SCD is going Global.  That's where the action is; "New Born Screening".  Consequently, in this posting I will talk about an abstract presented during this session and what it means to adults with SCD.

ABSTRACT #1 (BS8-5)

Clinical Predictors Of All-Cause In-Hospital Mortality In Patients With Sickle Cell Disease in United States-First Reported Results From A Nationally Representative Sample.

RESULTS

In 2007, a multi site study of 166,084 admissions with a diagnosis of SCD was conducted. Males represented 37.5% of SCD related hospitalizations. There was a total of 844 deaths reported in the above admissions with an all-cause in-hospital mortality rate of 0.5%. Of these, 420 (49.7%) were females. These are astounding odds that SCD patients face when they are admitted to the hospital either through pain crisis, acute chest syndrome, and or development of sepsis. Intubation, as a cause of death occurs primarily after the patients organs began to crash in ICU.  In conclusion, the authors propose that early and targeted aggressive therapy based on the presence of these factors should guide the management of hospitalized SCD patients for improved mortality.

MY COMMENTS

As I write this, it makes me wonder why so much money, time and effort is put into research that we already know the answers to.  Fifty years of studying SCD has yet produced viable outcomes or protocols for hospitals to use in assessing patients with SCD.  It pains me as one who's had all of the above diagnosis; death still affects about 50% of those patients admitted with these diagnosis. By the grace of God and the relationships I have with my doctors allows me to post this blog today. 

One of the factors I did not see them discuss is how much of a contributing factor the amount of  pain meds a patient has taken prior to their ER admission. I pose this question because in 2005 I had an episode where after days of self medicating I wound up on a ventilator with Acute Chest Syndrome for almost 10 days.  Many SCD patients do not have the support group I had who could inform the ER doc of what types of pain meds I was taking, how long and the dosing.  This is important information that can go unnoticed and cause mortality.  My sister in law believes the lack of advocacy in the ER by a parent, family or friend to fully disclose pain medication usage causes an alarming amount of unwarranted deaths to those with SCD.   

In conclusion, we must communicate with our physicians (Hem/Oncs) the need for adequate and timely protocols for patients presenting with pain crisis as an underlying symptom of high mortality. What do you think?

Help Support Sickle Cell Camp For Children

I recently wrote about adding more content to this blog. Camp Crescent Moon is the oldest Sickle Cell Camp in the US. What's so unique is it has survived all of these years because of corporate contributions and individual donors who understand the hardship SCD presents to our youth.

My eyes were opened to barriers faced by our youth when I worked in Philadelphia, PA in the Pharmaceutial industry and visited the clinic and hematology floor at Chilren Hospital. What I noticed were children who wanted to enjoy camp with children who are like them. So, below is a link which will allow you to give support to "Camp Crescent Moon".

http://www.firstgiving.com/fundraiser/patriceragin/campwalk