SCA Awareness Fund Donations
Individuals that have made a contribution to the cause. Thank you for your contribution, with your help we can make a breakthrough!
New Vision Enterprises, California
Diabetes Awareness
November is American Diabetes Month, a time to communicate the seriousness of diabetes and the importance of diabetes prevention and control. For years, the American Diabetes Association has used this month as an opportunity to raise awareness of the disease and its serious complications.
In 2009, the Association launched a national movement to Stop Diabetes® – with the audacious goal of gathering the support millions of Americans to help confront, fight and most importantly, stop diabetes.
With nearly 24 million children and adults in the United States living with diabetes, and an additional 57 million Americans at risk, there is no time to waste. One out of every three children born today will face a future with diabetes if current trends continue. Diabetes is not merely a condition. It is disease with deadly consequences. Drastic action is needed from everyone. How will you Stop Diabetes?
Types of Diabetes
Before people develop type 2 diabetes, they almost always have “pre-diabetes”—blood glucose levels that are higher than normal but not yet high enough to be diagnosed as diabetes. There are 57 million people in the United States who have pre-diabetes. Recent research has shown that some long-term damage to the body, especially the heart and circulatory system, may already be occurring during pre-diabetes.
Type 1 diabetes is usually diagnosed in children and young adults, and was previously known as juvenile diabetes. In type 1 diabetes, the body does not produce insulin.
Insulin is a hormone that is needed to convert sugar, starches and other food into energy needed for daily life. Only 5-10% of people with diabetes have this form of the disease. With the help of insulin therapy and other treatments, even young children with type 1 diabetes can learn to manage their condition and live long, healthy, happy lives.
Type 2 diabetes is the most common form of diabetes. Millions of Americans have been diagnosed with type 2 diabetes, and many more are unaware they are at high risk. Some groups have a higher risk for developing type 2 diabetes than others. Type 2 diabetes is more common in African Americans, Latinos, Native Americans, and Asian Americans, Native Hawaiians and other Pacific Islanders, as well as the aged population.
In type 2 diabetes, either the body does not produce enough insulin or the cells ignore the insulin. Insulin is necessary for the body to be able to use glucose for energy. When you eat food, the body breaks down all of the sugars and starches into glucose, which is the basic fuel for the cells in the body. Insulin takes the sugar from the blood into the cells. When glucose builds up in the blood instead of going into cells, it can lead to diabetes complications.
During pregnancy — usually at around 28 weeks or later – many women are diagnosed with gestational diabetes. A diagnosis of gestational diabetes doesn’t mean that you had diabetes before you conceived, or that you will have diabetes after giving birth. But it’s important to follow your doctor’s advice regarding blood glucose (blood sugar) levels while you’re planning your pregnancy, so you and your baby both remain healthy.
Symptoms:
Type 1 Diabetes
- Frequent urination
- Unusual thirst
- Extreme hunger
- Unusual weight loss
- Extreme fatigue and Irritability
Type 2 Diabetes*
- Any of the type 1 symptoms
- Frequent infections
- Blurred vision
- Cuts/bruises that are slow to heal
- Tingling/numbness in the hands/feet
- Recurring skin, gum, or bladder infections
*Often people with type 2 diabetes have no symptoms
The Toll on Health
- The death rate from diabetes continues to climb. Since 1987, the death rate due to diabetes has increased by 45%, while the death rates due to cancer, heart disease, and stroke have declined.
- About 60-70% of people with diabetes have mild to severe forms of nerve damage that could result in pain in the feet or hands, slowed digestion, sexual dysfunction, and other nerve problems.
- The rate of amputation for people with diabetes is 10 times higher than for people without diabetes.
- Two out of three people with diabetes die from heart disease or stroke.
- Diabetes is the leading cause of new cases of blindness among adults.
- Diabetes is the leading cause of kidney failure.
Cost of Diabetes
The American Diabetes Association estimates that the total national cost of diagnosed diabetes in the United States is $174 billion. Direct medical costs reach $116 billion, and the average medical expenditure among people with diabetes is 2.3 times higher than those without the disease. Indirect costs amount to $58 billion (disability, work loss, premature mortality).
Further published studies suggest that when additional costs for gestational diabetes, pre-diabetes, and undiagnosed diabetes are included, the total diabetes-related costs in the U.S. could exceed $218 billion. The cost of caring for someone with diabetes is $1 out of every $5 in total healthcare costs.
For more information visit, American Diabetes Association.
Resources: American Diabetes Association
Breast Cancer Awareness
What is Breast Cancer?
Breast cancer is a type of cancer where cells in the breast divide and grow without normal control. About 85 percent of breast cancers begin in the mammary ducts, while about 15 percent arise in the lobules [3]. Tumors in the breast tend to grow slowly. By the time a lump is large enough to feel, it may have been growing for as long as 10 years. However, some tumors can be aggressive, and grow much more rapidly.
It is important to understand the difference between invasive cancer and ductal carcinoma in situ (kar-sin-O-ma in SY-too). These are discussed below
Invasive Breast Cancer
Invasive breast cancer occurs when abnormal cells from inside the lobules or ducts break out into nearby breast tissue. This allows the cancer cells to spread to the lymph nodes and, in advanced stages, to organs like the liver, lungs and bones in a process called metastasis.
Breast cancer may grow from a tiny tumor to a larger one, later traveling to nearby lymph nodes, then distant ones. Finally, it may spread in other parts of the body. Cancer cells can also travel from the breast through the blood and lymphatic system early in the process when the tumor is small [4].
Ductal Carcinoma in Situ (DCIS, non-invasive breast cancer)
When abnormal cells grow inside the milk ducts, but have not spread to nearby tissue or beyond, the condition is called ductal carcinoma in situ (DCIS). The term “in situ” means “in place”. With DCIS, the abnormal cells are still “in place” inside the ducts. DCIS is a non-invasive breast cancer (you may also hear the term “pre-invasive breast carcinoma”). Although the abnormal cells have not spread to tissues outside the ducts, they can develop into invasive cancer.
Both men and women can get breast cancer. For more on male breast health, see Breast Facts for Men.
Who Gets Breast Cancer?
What are the estimated numbers of new breast cancer cases and deaths in the United States for the year 2010?
About 207,090 new cases of invasive breast cancer will occur among women in the United States during 2010 [5]. And an estimated 39,840 women will die from breast cancer this year. Also, about 1,970 men will be diagnosed and 390 men will die of breast cancer during 2010 in the United States [5]. In addition to invasive breast cancer, an estimated 54,010 new cases of in situ breast cancer will occur among women in 2010 [5]. (Breast Fact References)
How does breast cancer affect…
- African Americans
- Ashkenazi Jewish Women
- Asian Americans
- Hispanics/Latinas
- Native Americans
- Lesbians
- Older Women
- Younger Women
- Pregnant Women
- Men
Early Detection
Getting regular screening tests is the best way for women & men to lower their risk of dying from breast cancer. Screening tests can find breast cancer early, when it’s most treatable.
Make a Difference
Imagine life without Breast Cancer. Get involved. There are millions that can die from this disease in the next 25 years, so we must continue to fight to save lives.
Ways to help save lives:
- Make a monetary donation
- Find a local race for the cure
- Become an Advocate
- Participate in an event
- Find an Affiliate
- Join Circle of Promise
- Hold a Passionately Pink for the Cure Fundraiser
- Purchase with a Purpose
This article written in honor of two survivors that play a major part in my life: Shirley B. (mother) & Rose B. (sister in love). I have watched these two exemplify true strength and courage. My mother has fought the battle of Cancer and is a living illustration that if you don’t give up, you can win against this deadly disease. Also, Rose is fighting a good fight against this disease as I write these words. I am overjoyed to get the wonderful updates from her husband, & my Big Brother, Rod.
I encourage every woman as well as men to do a monthly self-exam. Women make sure if you are age 40+ and if you are under age 40 and have a family history of breast cancer or other concerns about your breasts, talk to your doctor about when to start getting mammograms or other tests and how often to have them.
Resources: Susan G. Komen for the Cure
Sickle Cell Disease: 100 Years Later

- Phyllis Thomas
In 1983 the House of Representatives unanimously passed a resolution, introduced by the Congressional Black Caucus, asking President Reagan to make September National Sickle Cell Awareness Month. The president signed the resolution in August of the same year.
What is Sickle Cell Disease? Who does it affect? What are the Complications?
Black Professional Women (BPW) is bringing awareness to a disease that millions are affected with in this world. There are so many that are not well educated on this disease. BPW, has and will continue to be an advocate for Sickle Cell Anemia.
BPW is sharing the story of a lady who knows about this disease, Phyllis Zachery Thomas age 46 originally from Dallas, Texas resides in Fayetteville, Ga. is a mother of a 25 year old daughter, wife for 26 yrs. and enjoys reality T.V. & traveling. Phyllis worked over 10 yrs in the banking industry where she was forced to retire due to disability. Because she knows how difficult it is to fight this disease alone, she began to advocate for herself as well as others. Phyllis became an advocate of Sickle Cell Anemia. She took her life experience and saw that there was a need for support and education for those who are affected by this disease. SCD Soldier Network Inc. was formed to help bring education and advocate on behalf of those affected by sickle cell disease.
Phyllis wanted to share her story by letting people get an inside look at her battle with sickle cell and what led her to form the SCD Soldier Network. She was presented with an offer to co-author a book with Atlanta filmmaker, Dan Moore Sr, Sickle Cell Disease: 100 Years Later.

In this book, Phyllis takes us on a journey of her life with sickle cell disease. She takes us through feeling alone and isolated, how it affected her life, and why she became an advocate. Also she shares the stories of others who too are affected.
Phyllis also wrote a poem, what turned out to be the anthem for SCD Soldier Network.
I’ve been fighting this thing, for much to long
and I just can’t fight this on my own.
I’ve been trying to speak and my voice is too low
But if I can’t tell them, then how would they know
My backs against the wall, and I’m going down way to fast
If something doesn’t happen, then I’m not going to last.
They don’t understand, I’m about let it all go
I’m tired of being strong, and they don’t even really know
This thing is pulling on me, and I’m down on the ground.
I’m gonna need some help, to turn this thing around
I’m not facing this giant, all by myself
‘Cause God sent me soldiers, just to give me some help
They’re fighting for me, ‘cause at times I get weak
When the pain is taking over, I just can’t speak
I need some soldiers, in this battle with me
I need some soldiers, who will help them to see
I need some soldiers, in this battle with me
I need some solders, front line soldiers with me
Phyllis, I thank you for advocating and sharing your story with the world. May God continue to use you in lending your voice in the world wide efforts of Breaking Sickle Silence.
Breast Cancer Awareness: Sharing My Story
Breast Cancer, knocked on my mothers door 4 years ago. I can remember getting the call from my mother to tell me that she was diagnosed with breast cancer. I am glad I was standing near the bed for it was what broke my fall. I physically fell and so did my heart and spirit. My mind began to race as the tears flooded my eyes.
My Mom said. ” LaVida don’t worry I will be fine, baby please stop crying”. Finally, I said “Mom let me call you back.” I cried even harder and screamed God NO! My husband held me as I cried and he reminded me God does not put more on us than we can bare. I fell to my knees and began to pray. I picked up the phone and called my mother back. My Aunts and Uncles and my brother were at the house with her, given her the support she needed at this time. As she and I talked, I told her I will be there with you through it all. She said that the her Doctor wanted to talk to me aswell about what was going on with her and also for me to get checked out.
My Mom had a partial masectomy done. My Aunt and I were at the hospital from 6 a.m. until 8 p.m. Man was that a day that time seemed to have stood still or at least was ticking by so slow. She made it through the surgery fine and we were finally able to take her home. She slept most of the night, but I didn’t, for I walked to her bedroom door several times just to peek in at her and watching her sleep. I remember kneeling down at her bedside and praying over her. Asking God to heal her body and to keep us all strong through this.
After a week or so went by, It was time for me to go home. As a busy professional, I had to get back to my job. I left my Mom, but my heart and mind was with her and my body came home.
She began her chemotherapy and radiation. I recall her saying,’I know my hair is going to start to come out. But, before that starts to happen, I am going to just cut it all off.’ My mom had shoulder length hair, and she was willing to cut it off. Weeks went by and she began to get sick from the chemo and radiation. She ended up in the hospital with congested heart failure. Here I go again crying like a baby. I began to pray harder than ever before. God, my Mom is a fighter give her the strength to endure this, give us, the family strength to be strong for her.
After several more trips to the hospital, her body started to weaken. But amazingly her faith in God did not. There were times she would say she was tired, but would also would say I am not giving up though. I watched my Mom fight this, which gave me the strength to endure.
My mom is a 4 year survivor of Breast Cancer. If it had not been for the monthly self examinations and yearly mammograms; that knock on my Mom’s door from this deadly disease could have been a trajedy.
I challenge every woman to do self examines monthly. Get your yearly mammogram. If you can not afford to get one, call your local Breast Cancer society (Susan G Komen) and find out where you can get a free or reduced price.
We all can make a difference by donating money and/or our time. The main thing is to get involved. Be a volunteer, an activist or a walker/runner in a local race. But however you choose to get involved, just know that everything you do makes a difference. After all, without the support of people like you, we know 10 million people could die of breast cancer in the next 25 years. Susan G. Komen for the Cure® strives to raise funds and educate people in the battle against breast cancer through global events and legislative actions each year. Breast cancer is still killing and impacting far too many of our loved ones. So, how will you get involved?
National Sickle Cell Anemia Awareness Month
The month of September was designated as “National Sickle Cell Anemia Awareness Month” in 1983, 26 years of designation. However, sickle cell anemia has plagued many lives for years. Sickle cell anemia is a blood disorder that affects many in the world.
I am one of those many that it affects. Even though I have had my share of crisis with this disease. I created a motto for myself many years ago. “I have the disease, but the disease does not have me!” I have lived many years with that statement as my daily encouragement. But I could not have made it thus far without the love of God and the love of my immediate family and my SCA family.
As a busy professional, life can become a little hectic and can be very taxing on the body. However, I have learned over the years to listen to my body and my doctor. My life trials with this disease have helped myself as well as others. I take my life’s journey with this disease and share it with others who are fighting or fighting this disease with a loved one.
Still to this day there are so many people that do not have knowledge of this disease. It is not left up to just health professionals to educate others on the disease; as a defier it is us up to me to share my life with others that suffer from the disease as well as family members who are fighting alongside their love one. However, I am just one person it is going to take all of us as friends, as families, as a group as a whole to make this happen.
Most who know me, know that I am a very private person. However, this chapter in my life is an open chapter to the world. Some people want to ask me questions about it, but are scared to ask. Most say, “Well I am sure it is something that bothers you to talk about to others.” But my answer is, “ask me anything about the disease, for this is small contribution of educating others about the disease.” Also it helps someone else that may be dealing with something that I have already faced and conquered. My testimony may just be the foot-stool of hope to someone else.
So this month I challenge you to give hope to someone with sickle cell anemia by:
* Giving a donation to your local Sickle Cell Association (financial donations are tax deductable)
* Donate blood to your nearest blood bank
* Volunteering
Also I challenge you to empower yourself with knowledge of this disease. Together, we are a multitude.
I would like to share this poem that I wrote six years ago:
Life Endured But Not Denied
Living, hurting, confused and sad….feelings that have all been rolled up in to three words
Sickle Cell Anemia
What is this I wondered? Will I live to have children? Will I live to see my children grow up?
Will I live my life to the fullest? All those questions that filled my head, as I lay there in that hospital bed.
Pain and fever stricken body, lump in my throat, pain in my legs, and anxiety all in my head.
After all the pokes, tubes of blood, and intravenous pain induced drugs. Again the questions began to fill my head.
Is this something so big that will control my life forever? How can I get beyond this? Rise above it all? And get out of this hospital bed.
As I closed my eyes, and began to cry I heard a small voice that said “you will be fine my child”
From time to time I could not believe what my friend had said to me. But every time I overcame the test and trials of my once dreaded abnormality.
Just those simple words gave me strength to go on. Removing the hurt, the confusion and sadness.
Leaving me with living, healing, understanding, and happiness.
And not least to forget, two handsome children and a wonderful husband.
Finally understanding that my friend and I are much bigger than it.





