January 3-9, 2019 Vol. 85 No. 22 www.spokesman-recorder.com
PRST STD U.S.POSTAGE PAID TWIN CITIES MN PERMIT NO. 6391
THE VOICE OF THE AFRICAN AMERICAN COMMUNITY SINCE 1934
By Sheletta Brundidge Contributing Writer
B
Race & Hair Wrestler’s shorn locs expose more than outdated rules
See OPINION on page 5 for more on this issue
Realities of living with sickle cell By Charles Hallman Contributing Writer One in 2,400 are born with sickle cell disease (SCD) in the U.S. As one of the most common inherited blood disorders, it is widely misunderstood. Last month, the Minnesota Sickle Cell Coalition — comprised of patients, doctors, healthcare providers, and advocates — co-sponsored a Sickle Cell Disease Stakeholder Forum at Sanctuary Covenant Church in North Minneapolis. Approximately 60 healthcare professionals and others attended the Dec. 10 event to not only help improve care for those afflicted by the disease but also to increase awareness of the disease, screening and healthcare disparities. SCD is a group of inherited red blood cell disorders including Sickle Cell Anemia (Hgb SS Disease), Hemoglobin SC Disease, and Hemoglobin Sickle Beta Thalassemia. People with sickle cell disease produce abnormal hemoglobin (Hgb S), which can interrupt blood flow and prevent oxygen from getting to important parts of the body. This can cause many potential health complications, including extreme pain, risk of stroke, and pulmonary hypertension. “Pain is what I have been born into,” Isaiah Lane, who has SCD, told the MSR. It has historically been seen as a childhood disease because those stricken typically did not live to adulthood. Yet, according to a 2013 Harvard study, the average life expectancy for persons in the U.S. with SCD is 38 years for men and 42 years for women.
SMALL BUSINESS SPOTLIGHT Aromas of hibiscus and chai fill the air as you walk through the doors of the Heritage Tea House & Café located at University and Western Avenue N. in St. Paul. Run by Raeisha Williams, the tea house first opened its doors in December 2017, although it’s been a dream of hers for quite a while. Offering a full menu of healthy soul food options, tea and liquor, the tea house’s couches and tables provide a wide array of seating choices and a comfy atmosphere to those who want to enjoy a relaxing meal or just some tea. Photographs of Williams’ family are scattered across the wall of this cozy spot where locallymade African crafts are offered for sale on the back wall. The MSR sat down with Williams (RW) for a Q-and-A session about the tea house and the legacy she’d like to leave behind. MSR: What inspired you to become a business owner? RW: My mom and grandma. For as long as I can
Rae Blaylark
Photo by Charles Hallman
While state and national health experts report a longer life expectancy, it still remains an incurable, often unbearable disease. “I’m 30. I live with SC disease,” said Brianna (her last name withheld by request). “I have near constant pain. When I don’t have pain, it is a memorable day.” Those afflicted are not only burdened with shortened lives of pain, they face uncertainty in communities that are ill prepared to provide unbiased care and support. The national Sickle Cell Disease Coalition recently released its 2018 State of Sickle Cell Disease Report Card focused on four major areas: access to health care, training and professional education, research and clinical trials, and global issues. According to its report card, there have been initiatives around the country that have ■ See sickle cell on page 8
lack communities across the country watched in disbelief as a Black New Jersey high school wrestler was forced to either cut his dreadlocks or forfeit a regional match. A video showing Andrew Johnson having his hair and his heritage chopped off at a match last month went viral with more than 20 million views on social media. Andrew, a student at Buena Regional High School, had a cover for his hair that he had worn in previous matches; however, Alan Maloney, a White referee, said it wasn’t good enough. Instead, he started the clock, giving Andrew minutes to comply. Wanting to compete, Johnson begrudgingly allowed team personnel to cut his hair. He is seen crying and visibly shaken in the viral video. “I don’t care what the rules are,” said Lindy Vincent, co-host of “Two Haute Mamas” podcast on Minnesota’s WCCO Radio online. “If someone is doing that to my child, I’m going down there to speak up for him. I’m not just going to sit in the stands and watch him be humiliated and wronged in such a horrific way.” The incident hit close to home for Vincent, because like Johnson, her son Dylan has dreadlocks and plays sports for Breck School. She was shocked to find out that Andrew’s parents, Charles and Rosa Johnson, were in the stands. “For that official to just take some scis-
Andrew Johnson Submitted by Johnson family sors to his head like she was chopping down a bush outside the front door of her home broke my heart. There was no feeling in it for her. She had no compassion for this child. She looked like she didn’t have a care in the world.” Added Vincent, “This whole incident says a lot about the criminalization of Brown skin and Black culture. This official didn’t just cut off his hair, she chopped off his humanity, as well.” Vincent was among many across the country who expressed outrage. New Jersey Governor Phil Murphy said he was deeply disturbed by the story. Olympic wrestler Jordan Burroughs, ■ See Wrestler on page 9
Be Better Foundation
honors victims of gun violence “I want to give my condothe 31st, which was her birthlences to the Flowers family day,” said Flowers. He told the MSR, “I don’t because I know exactly how “Often, we think, ‘That want her [passing] to be in it feels,” said Hayden. Boyd’s brother, Al Flowkind of thing doesn’t happen vain. Anybody who dies with to me.’ But nothing precludes gun violence should always ers, Jr., has taken the personus from being a victim of vi- be recognized, and I want to al tragedy as inspiration to olence,” said Minnesota State use this as an opportunity. work for well being in the Senator Jeff Hayden, whose Our family has a lot of pain, community. 25-year-old sister was killed but we can lift that hurt for “Little Man, as we call him, in a crossfire July 23, 2016 be- others who are in the pain.” ■ See Be Better on page 8 tween rival street gangs. Having already established the Taylor Hayden Memorial Foundation to End Gun Violence in her honor, Hayden was present Dec. 22 at the launch of the Tarvanisha B. Boyd “Be Better” Foundation at Sabathani Community Center in Minneapolis in honor of another victim of gun violence. Veteran activist Al Flowers created the “Be Better” Foundation in honor of his own tragic loss — the shooting death of his 24-year-old daughter Tarvanisha Boyd on Dec. 20, 2014 during an argument in her Georgia home. “This is always a tough time for [the family] from the 20th, when we lost Tarv, to Al Flowers, Jr. (left) and John Thompson Photo by Antanisha Spears By Dwight Hobbes Contributing Writer
HERITAGE TEA HOUSE & CAFÉ
remember they’ve been business owners. They coowned a floral and African gift shop on 38th and Nicollet for most of my childhood. Just being there with them, helping them with floral design, running the register inspired me the most. Also, seeing the difference between business owners and workers and how the success paid off. MSR: Why a tea house? RW: We knew we wanted to be small, we knew we wanted to be intimate, we knew that we wanted to have things that we loved, and my family traditionally has loved tea. Oftentimes people don’t think of tea as African American culture, but it is. There are so many articles that date back to the early 1800s where affluent African American women-owned tea houses. So just continuing that tradition is sort of re-emerging that tradition of tea houses owned by African Americans — it’s actually happening nationwide.
Raeisha Williams
Photo by Chris Juhn
■ See sBs on page 8