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My name is Lenora Sanders. I have a 14 year old daughter name Tiya who is a huge fan of yours. She is an entrepreneur and an honor student. She follows you on the internet and various social media outlets. You are an inspiration to young girls everywhere. My daughter is very opinionated and socially conscious much like yourself. She really hates bullies. She feels that to stop bullying, you must first empower the victim. Bullies know who to target and who will speak up. She has specially designed tshirts that hopefully will help boys and girls of all races to love the skin they’re in. we also created a bullying grou on facebook https://www.facebook.com/groups/1259393494075445/ Saturday 8/19 My daughter will be filming a Public Service Announcement about bullying and will be interviewing victims and their families. We would like to know if we can count on you to post the video on your various sites to spread the word about this growing problem? It would be greatly appreciated
Selena Gomez, I admire your concern for the hungry children.
I have been working on a plan and design of Hydroponics, Aquaponics, the only survivable future for this country, the children around the world, the environment, Please visit the website: http://aquaponicscal.info/
Affordable Healthcare if we stop eating the deadly toxic food. After viewing the website aquaponicscal.info I am hoping you will assist in finding a FUND RAISER.
Our government is doing almost nothing for the children, the future, the environment. The first lady's mission for healthy eating should not become a passing fad. My plan includes ' Community farming' from children's bedroom window to the neighborhood to a commercial AQUACULTURE entity that includes a full curriculum academy for the farmers children, solar and wind turbines. My design will accommodate the window to the field.
AIR IS FIRST, WATER IS SECOND, FOOD IS THIRD. FOOD HAVING NO NEGATIVE IMPACT ON ENVIRONMENT AND USING LESS WATER IS THE WAY OF THE FUTURE.
I've loved Selena since I was 5 years old and saw her as Alex, the spunky wizard on Wizards Of Waverly Place. Wizards Of Waverly Place was literally my favorite show and even when it was over my love for Selena didn't stop. After the show ended I still continued to support Selena and when her music started coming out with Selena Gomez & The Scene (omg feels) you know I was always jamming out to it xD and continuously supporting her throughout my childhood. 2 days before my 13th birthday I finally got to see my queen perform in person!! :)) I was so excited and when I heard the track for Revival start and saw the outline of Selena I literally started bawling my eyes out and screaming xD Selena has always inspired me and I've loved her with all my heart still to this day. (I'm 14 now :) ) Selena is my literal queen and she is so strong and gorgeous and so kind to everyone around her. I'm proud to call myself a Selenator and I could go on and on about how much I love Selena Marie Gomez but I'm sure people don't want to read all that xD (even though this is kinda long, ty if you read this far xD). But, I hope to meet her soon and tell her how much she means to me and and how much she inspires me in person!! Love you Selly!!!!!! <3
She inpired me with her heart, her unconditional love she has for everyone. I grow up with her, and learn to love myself "Who says you are not perfect" right? She is strong and beautiful inside and out. When i listen to her songs i can feel whatever she feels. She is a living inspiration. An angel send to us from God to make this world a better place. I learn from her that noone can bring me down. And to be myself. She has so much love inside her and i honestly dont know how is this possible.After everything she is been through, she rise above all that and she is stronger than ever.I m SO proud of her.
Hello my name is Frank Rivera- President of Sarcoidosis of Long Island, a rare disease non profit organization. I am instituting this plan for affordable mental health care as well as pro bono mental health care for rare disease patients as well as caregivers. I would like to see if you would like to be a part of this project. I am starting off on Long Island New York in November 2017 and have enough backing financial and organizational to hopefully go nationwide in March 2018.
Business Mission: Sarcoidosis of Long Island and Rare NY's mission is to empower the rare disease community, individuals, families, and youths to take control of their destiny and function productively by providing them with the necessary skills to realize their dreams, through counseling, education, social skills training, motivation, and participating in the treatment of abnormal behaviors to become successful.
Sarcoidosis of Long Island is prepared to introduce the following service to the market: Rare Disease Mental Health Facilitation: Rare NY is a non profit organization focusing on rare disease patients and caregivers including family members with mental/health issues. Our objectives are to: Provide counseling to individuals, couples, and families, face to face or online. Provide various therapeutic group sessions (i.e., bereavement, divorce, troubled children/youth). Provide health prevention and maintenance groups. Provide various disease-focused therapeutic groups. Many rare disease patients as well as caregivers worry about the physical demands of the rare disease and forget about the mental aspect of coping with mental diseases. Your mind is very important aspect to recovery. II.
BUSINESS SUMMARY: Industry Overview In the United States, the non profit industry presently makes dollars in sales. Research shows that consumers in this industry primarily focus on the following factors when making purchasing decisions: There are approximately 7,000 different types of rare diseases and disorders, with more being discovered each day 30 million people in the United States are living with rare diseases. This equates to 1 in 10 Americans or 10% of the U.S. population Approximately 50% of the people affected by rare diseases are children 30% of children with rare disease will not live to see their 5th birthday Rare diseases are responsible for 35% of deaths in the first year of life The prevalence distribution of rare diseases is skewed – 80% of all rare disease patients are affected by approximately 350 rare diseases According to the Kakkis EveryLife Foundation, 95% of rare diseases have not one single FDA approved drug treatment. Approximately 50% of rare diseases do not have a disease specific foundation supporting or researching their rare disease
Business Goals and Objectives Short Term: To start facilitating locally in Suffolk County NY to help local rare disease patients and caregivers find affordable or pro bono mental health counseling.
Goal 1: To continuously develop, strengthen, and improve services offered by the Non Profit Organization. Identify and develop strategic alliances with community human services and rare disease agencies. Identify and foster strategic alliances and networks with community medical group practices as well as hospital and Universities. Recruit Counselors(LPC), Psychologists, and clinical social workers. Identify and implement a pricing system two months before starting date. Arrange working capital for the initial phase of the turnkey venture.
Goal 2: To strengthen the Center's commitment to excellence. Continuously assess referral base satisfaction through the use of a referral base satisfaction survey. Continuously assess client satisfaction from three perspectives: accessibility, environmental factors, and treatment-related factors.
Long Term: To facilitate for the rare disease patients and caregivers of the United States affordable or pro bono mental health care. Improve the expected inclusive rate by 50% over the previous year. Increase all services offered through the Center by 80% over the previous year.
Please contact me for more details!