april watts, au naturale, butter n jelly, charlene brown, coco lea, crochet designs, dc natural hair, go-go, H street festival, house music, mini me, mz sixx, paul wharton, releaxed, weaves, wigs

Mini Me: Natural Hair Model-H Street Festival

My mini me was a model in the H Street Festival Day held Sat in Washington DC. She was representing Coco Lea Crochet Designs ( Designer, Annette Williams) and Sophizticated Ladyz Hair Salon ( Celebrity Stylist, Charlene Brown 1010 H Street, NE-2nd Level, Washington DC). The H Street Festival is an annual street festival designed to showcase the unique qualities of this vibrant Washington, DC community. The event is a part of the revitalization strategy to bring attention to the developing arts and entertainment district at the eastern end of the H Street NE corridor. This year’s festival includes more than 30 musical and dance performances, an art car exhibit, two live performance stages that are produced by the Rock & Roll Hotel, a fashion show preview of DC Fashion Week, face painting, rock climbing, basketball games, carnival games, free popcorn, cotton candy, and dog tag making, a fully-loaded Hummer display, luxury car displays, free health screenings, crafts, and international foods.

The night before I co wash mini Me’s hair with conditioner, coconut milk, and honey. After co washing and moisturizing I completed a “faux hauk” look by using Butter N’ Jelly styling aid and applied 3 pony puffs along the center of the head with a 3 strand twist out in the front.

Charlene accented the faux hawk with a braid that wrapped through out the head-still spot lighting the natural hair style.




Milaki Conner applied the makeup ( the lighting wasn’t good in these pictures, however the make up was FLAWLESS and age appropriate).


Next up was the show!!!!! Mini Me ROCKED!!!!!! It had begun to rain, the runway was wet. She adjusted, kept the beat when the music changed mid walk, and gave the photographer what they wanted at the end of that runway. She RIPPED THAT RUNWAY!!!!!! I was very proud of her and was gleaming from ear to ear.. She almost made me wanna adorn my stilettos and rock out for old time sake ( lol..lol).




Mini Me met Paul Wharton ( model coach and member of the Dc Housewives Cast). He gave me lots of advice, advised me to keep mini me in the modeling game because she is a natural. He also said he could feel her confidence and she was a natural beauty ( yeah!).

We also had a opportunity to network with April Watts ( a multi-talented performer best known to audiences for her work hosting television and radio programs in the Washington, DC metropolitan market including her current gig on Magic 95.9 (radio) and WHW Rock ( indie talent showcase Produced and Hosted by April Watts)

I didn’t get an opportunity to capture additional photos. Along with being the mom-anger I was also assisting behind the scenes. There were some fierce models rippin the runway- BUT Mini Me was the ONLY CHILD/TEEN NATURAL!!!!! I love the fact that despite all the straight hair, weaves, and wigs she didn’t feel pressured to “look” like them. She said to me “Mommy, can you do my hair and make it big? ” I admire my munchkin for staying true to herself and rocking HER WAY! I love…love…love.. that my mini me looks up to me and I ‘m her role model. She is so much like me ( her smile, her personality, her confidence) – everyone that meet her in person always say ” she really is a mini you!”

Mini me brought along a friend for moral support ( I ended up putting her to work..lol..lol..). After the show we walked up and down H street looking at all the vendors, and the food that was available for purchase. Despite the rain and the cool weather it was a great day!!!!


S/N: With the festival being held in DC I was expecting to hear Go-Go the entire day-that wasn’t the case- there was a DJ there ROCKING HOUSE ( my 1st love).. WHEW it was giving me FEVER!!!!! Almost made me think I was 21 again partying at Nell’s.

Disclaimer: These images may not be reproduced, copied, transmitted or manipulated without the written permission of Mz. Sixx. Use of any image as the basis for another photographic concept or illustration (digital, artist rendering or alike) is a violation of the United States and International Copyright laws. All images are copyrighted © 2011 – Au’Naturale by Mz. Sixx.

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I’m walking for Lupus!

The 4th Annual Baltimore Walk for Lupus

Druid Park in Baltimore

September 24, 2011

2:00pm-5:00pm

As you may know, lupus has a personal face for me. I was diagnosed earlier this summer and currently battle this disease on a daily basis. After hearing about a 19 year old young lady with a 4 month old child losing her battle to Lupus, it has driven me to stay healthy, bring awareness, and push for a cure. Living with my own personal struggle remind me that we have so far to go in battling this disease.

To do my part, I’m walking on September 24, 2011 to raise money. The money will go to the Lupus Foundation of America, DC, Maryland and Virginia Chapter (LFA-DMV). LFA-DMV provides free education and support services to lupus patients and their families. Money will also go to support research, because they believe, as I do, that one day this awful disease will have a cure.

To reach this year’s goal, and my personal goal, I need your help. You can make a secure online donation through my personal website. Click here on this link to make a difference in the lives of as many as 320,000 people (80,000 patients and 4 of their closest friends/family members.) If you do not wish to make a donation online, simply click here, fill out this form, make a check payable to LFA – DMV Chapter, and mail the check and the form to our offices at: 2000 L St, NW suite 415 Washington, DC. When your donation is received, it will be credited to the total on the Walk’s webpage.

Making a difference starts with just one step. So, walk with me in spirit as I walk through Druid Park to raise money and awareness.

Thank you in advance for taking that step with me.

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Mini Me Updo for Picture Day

Today is school picture day for mini me.. She has in 2 week old twist (she’s been swimming in these twist over the holiday weekend-hense the fuzzies).


She styled her hair herself by applying a lil shea butter creme, leave in conditioner, a few dabs of aloe vera gel on her egdes,and a couple of bobby pins. She grabbed a few sections, twisted them to one side-secured with a boby pin, and fluffed the lose twist.


Yesterday it rain cats and dogs.. Her friends were running because some of them had just gotten a relaxer.. She was ” strolling” along and loaned her hooded jacket to a friend. the friend said: ” You don’t need it? ” Her response: ” Naw, I’m natural.. my hair loves the rain” Get it mini me!!!!!


These images may not be reproduced, copied, transmitted or manipulated without the written permission of Mz. Sixx. Use of any image as the basis for another photographic concept or illustration (digital, artist rendering or alike) is a violation of the United States and International Copyright laws. All images are copyrighted © 2011 – Au’Naturale by Mz. Sixx.

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Venus Williams and Sjogren’s Syndrome

Venus Williams a seven-time Grand Slam singles champion, pulled out of the U.S. Open yesterday and said she has Sjogren’s syndrome.

Venus said in a statement issued at the Open in New York and reiterated today on ABC’s “Good Morning America”

“I’m really disappointed to have to withdraw from this year’s U.S. Open. I have recently been diagnosed with Sjogren’s Syndrome, an autoimmune disease which is an ongoing medical condition that affects my energy level and causes fatigue and joint pain.” She added: “I enjoyed playing my first match here and wish I could continue but right now I am unable to. I am thankful I finally have a diagnosis and am now focused on getting better and returning to the court soon.”

Sjogrens Syndrome– What is it?

Sjogren’s (SHOW-grins) syndrome is a disorder of your immune system identified by its two most common symptoms — dry eyes and a dry mouth.

Sjogren’s syndrome often accompanies other immune-system disorders, such as rheumatoid arthritis and lupus. In Sjogren’s syndrome, the mucous membranes and moisture-secreting glands of your eyes and mouth are usually affected first — resulting in decreased production of tears and saliva.

Although Sjogren’s isn’t life-threatening, it is an incurable condition where the immune system starts attacking glands that produce tears and saliva instead of fighting infection, according to Arthritis Research U.K. Around a half- million people in the U.K. suffer from the condition, which is usually diagnosed in women between the ages of 40 and 60. The American College of Rheumatology’s website said between 400,000 and 3.1 million people are affected in the U.S.

The exact trigger of the disease isn’t quite clear, Mizutani said {Wesley Mizutani, a rheumatologist on staff at Orange Coast Memorial Medical Center}.”That’s the million-dollar question,” he said. “We don’t really know. There’s probably a genetic component, certainly, but there’s more than that.”Certain antibodies are associated with Sjogren’s, but it seems to need a trigger, like a viral or bacterial infection, for the immune system to go awry.

Once set off, the system can’t really be fixed — but certain steps can be taken to mitigate the symptoms for the vast majority of patients. Keeping eyedrops and a bottle of water nearby are two such easy measures. Brushing after every meal and otherwise good dental hygiene are a must.

More extreme measures can also be taken, from anti-malarial to autoimmune suppressant drugs.

But, Mizutani pointed out, it could be worse. “If I had to choose an autoimmune disease to get, Sjogren’s would be one of the milder ones.”

I’m sending prays and positivity to Venus Williams, like my friends and family have told me ” God is Able”

Get well soon-

Love you Venus xoxoxoxoxoxo

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Mini Me First Day of School -2011

Wow, where did the summer go? School finally re opened for mini me after Hurricane Irene. Every year since she entered kindergarten, I always took mini me to school on the first day. We would go to Starbucks, have our coffee beverage and a pastry and talk about the importance on staying true to yourself and not getting mixed in with the wrong crowd-aka- Mean Girls. I was super excited about our yearly tradition *squeals*, mini me had alternate plans {insert gas face}. She politely informed me that she was riding the bus on the 1st day { gasp}! The Bus!!!! what about our Starbucks date? What about tradition? Her response- we can do it tomorrow-followed by ‘ Moooooooom- I want to go with my friends on the bus” {insert face crack}.

She is a few months away from officially becoming a “teenager” she is ready to say “I’m 13”. Is this what I had to look forward too- my mini me dissing me to hang with her friends {sad face}. I tried to act like my feeling wasn’t hurt, and I managed to capture a few pic’s.

She is coming into her own style and has discovered MAKEUP! {screech}. Now she is asking for her own make up and brushes, double ear piercings, and teenager earrings ( the larger style hoops- I told her only teenagers and adults wear them- well she is banking on a pair for her 13th b’day)



whew, she is JUST LIKE ME- and I’M NOT READY!!!!!!! I wish I could turn back the hands of time- when she was 5 or 6 years old and she pranced around in my heels, my jewelry, and tried her best at imitating me. NOW she wants to WEAR my heels, and jewelry to school!!!!!{ locks the drawer on everything!}. I think she is trying to give me a run for my money on her perfected model walk {she has a show coming up September 17th} she can rip that runway- Just Like Her Mama {lol…lol..}

Natural Hair Looks

Mini Me Hair– Mini Twist – sides pulled up, “hump” in the front

Mz. Sixx- 2 french braids in the front, 3 strand twist-out in the back ( 3rd day hair)

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Coping with Lupus Headaches



I have begun to suffer from Lupus headaches. These are not like the average headache, pop a Tylenol and it go away. These are more on the end of migraines. My head feel like its splitting, pounding, piercing, throbbing and aching all at the same time. Followed by a spinning sensation like a tornado and a feeling of nauseous and sometimes vomiting. Typically these headaches start mid day and lasting hours into the evening. Thus far, I’ve been taking Ibuprofen to treat these headaches, but most of the time the only relief I get is from rest. I turn off the lights (make the room as dark as possible), turn off the TV, and go to sleep.

I’ve been told that one of the ways to help prevent headaches or migraines is to understand your possible triggers. In order to do this, health care providers often recommend using a migraine diary (also known as a headache diary). This is a tool that allows you to clearly capture, in a standardized way, how often you get migraines, how severe they are, and the possible relationship to physical, emotional, or environmental factors. There are several down able diaries, electronic diaries, and headache diary apps(s) for (Iphone, Ipad, and Droid Mobile cell phones). * They make apps for everything* lol…lol

I’m trying to avoid harsher treatments and drugs such as Plaquenil and prednisone to treat these headache episodes. This seems to be the first drug of choice upon complaint of the headaches. I prefer natural alternatives therapies such as exercise, diet supplements, meditation, special diets and maintaining a strong support system. I’ve also been told that conserving energy by setting limits on how I spend my time is helpful. Fatigue is a common complaint for lupies. Listening to your body’s signals by resting or taking short naps during the day can help reduce the occurrence of lupus headaches.

I’m starting my headache diary today, a gluten free diet, and hopefully I can figure out what or who (lol..lol..)are my triggers . If you have any advice- please share ….

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Lupie Emotional Roller Coaster

Who knew that revealing to the world that I have Lupus would take me on an emotional roller coaster? I still remember having written the post 4 days before I released it. I would read it every day, and become nauseous at the thought of releasing it. On Friday [August] the 13th, I decided to finally publish it. As soon as I hit publish, I was panicked and tried to figure out how to delete it. Before I could delete the post, it had already gone to my yahoo groups, and emailed to my blog followers it was too late! Immediately my phone started ringing, emails, text, tweets, were all coming in so fast that I turned my phone off, went to the bathroom and cried. I got my composure, grabbed a hot cup of green tea and came back to my desk- 5 minutes later a co worker came over and hugged me [ I forgot that some of my co workers follow my blog] tears instantly started streaming down my face. Friends and followers told me how emotional they were reading the post. Some were so emotional that they couldn’t talk- that’s why they took to text and email. I thought to myself “why were YOU so emotional” I didn’t get it. I didn’t think much more about it, until later that evening when the tweets came in and people were crying and asked if they could forward my post. I found myself getting depressed.
“Why did I write the post” I asked myself over and over. I wasn’t ready to be the face of Lupus- or was I? People started asking me more questions about Lupus. Some had never heard of Lupus and some only knew it as the disease that Toni Braxton has. I started to explain as best I could, provide an explanation for the condition of my skin, and my inability to move sometimes. Most were very compassionate, and then something happened. I no longer was Mz. Sixx or Sixx (mc/sc club name), or Au’Naturale (my Twitter name), or Toni (child hood nick name), I was the helpless natural haired lady with Lupus. People started treating me as if I was sick. I know it was all heartfelt, and came from a place of love- but it made me a crying mess and I felt like a burden to people. Now every minute was about Lupus. Here comes the babying “ how are you”, “are you feeling OK” “sit down”, “lay down” “go home”, AGGGGGGGGHHHHHHHHH!!!!!
I had wanted to make a you tube video with me actually speaking on it, but I felt like I had nothing to talk about [Up until this point I had only created picture slide shows]. Well today was going to be different- I needed to get a few things of my chest. My hand was hurting to bad for me to type- so I came home, grabbed my lap top, sat on the floor and just started to speak. I didn’t edit it, apply music, and make it “cutesy”. I wanted it to be raw- because that’s how I was feeling at the time.
Click Here to watch Video
This experience has made me reflect on who I am. Among the many hats that I already wear, I just added one more – “The Lupie Chick”. I’m realizing that I have to be selfish [in the instance] and make myself a priority. I’m the star on the team of “ME”. Some won’t like it- but guess what? I don’t like having Lupus either [shoulder shrug]. I have to listen to my body and not push myself being what I can handle. I will not give in the “pity parties” that some have invited me to join. I will not be treated like a helpless baby, and I will not hide. I will LIVE and ENJOY my life until the wheels fall off-and all the wheels must fall off before I stop [insert fist pump]!
[climbs off the roller coaster]
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Hello-I’m a Lupie Chick

Repost
Where do I start…
My Name is Mz. Sixx and I have Lupus

that was very hard for me to say 😦

Face Fully Made Up w/ Dermablend

Some of you are familiar with my skin troubles that I’d been experiencing for over a year. I would try different things, some worked for a while, and some never worked at all. Growing more and more frustrated and embarrassed by my skin, I went to get my prescription re filled for a facial cream my dermatologist had prescribed to me. Hoping that would be my saving grace.

Partial Makeup
As I began any normal day, I went to CVS hoping to come out with a tube of some magical cream that would clear up my adult acne (the diagnose I’d previously been given). The pharmacist informed me that my prescription required authorization. When he called to get authorization- the dr. instructed him not to fill it and have me come in his office. I thought to my self- “great, he gonna give me the sho nuff good stuff to clear this up”. I made an appointment to see the doctor the next day- never mentioning it to my husband or friends- I wasn’t the least bit concerned. I went to work late so that I could see the doctor and drop my prescription off as soon as possible.

The doctor enter the room and starred straight at my nose [insert gas face right here].

Naked Face- No Makeup- Its hard to see in the pics, but I also have a red bumpy rash
As soon as I noticed the way he was looking at me, I got scared. He began to “drill” me about what been happening to my face. He then said that my face had gotten worse since my last visit and he was concerned. CONCERNED– did he just say he was CONCERNED??? – I obviously knew my face had gotten worse- what started out as one dark spot on my forehead was now covering my nose and had spread to my checks. He did a biopsy on my nose area and took blood. I’m really anxious and nervous at this point. I’d only known people to need a biopsy when they thought they had cancer. That “c” word scares me to no end. I silently cried many days and nights, anxiously awaiting the results.
The nurse called me and asked that I come to the office as soon as possible. My first word was “WHY” what’s the problem?? She wouldn’t say. She only would say that we need to discuss treatment with you- TREATMENT??? TREATMENT FOR WHAT??? Now, I’m shouting and crying at the same time. She still wouldn’t reveal anything to me and advised that I come to the office as soon as possible. I’m sure anyone else would have ran to the office, I didn’t. I did not want to hear that I had cancer. Nope, I was convincing myself and saying Hail Mary as many times as I could over the course of two days. The doctor called me wanting to know why hadn’t I come to the office and when was I coming. (Sigh), I was being a real bitch- I just out right said. LOOK, I’M NOT PAYING YOU A CO PAYMENT FOR YOU TO TELL ME I HAVE CANCER- YOU CAN TELL ME THAT OVER THE PHONE! He said “who told you, you have cancer”? You don’t have cancer- but I need you to come in the office. I’m sure he said more, but I blanked out of the conversation when he said I didn’t have cancer. So I took my lunch break and went by the office. I was calm, cool, and collected- because I thought I had just dodged a death sentence.

As soon as he walked in, I began to apologize for being such a baby and bitch at the same time. He accepted my apology, and sat down, and asked me if I was familiar with Lupus. Lupus?? Ummm……..Not really- why, I asked. He hands me a bunch of pamphlets and goes on to explain to me that I have Lupus. Lupus is a chronic autoimmune disorder that can affect virtually any organ of the body. In lupus, the body’s immune system, which normally functions to protect against foreign invaders, becomes hyperactive, forming antibodies that attack normal tissues and organs, including the skin, joints, kidneys, brain, heart, lungs, and blood. Lupus is characterized by periods of illness, called flares, and periods of wellness, or remission. I have Discoid lupus erythematosus, which mainly affects the skin. The symptoms of this form of lupus include a rash on the face, scalp, or elsewhere. The rash may last for days or years, and can recur.

UPDATE: Initially I was diagnosed with Discord Lupus, I have since been diagnosed with Systemic Lupus. I now see Dr. Michele Petri  affliated with John Hopkins Hospital in Baltimore, MD. My dermatologist is Dr. Valerie Callender, who has 27 years experience treating individuals with Lupus

I said okkkkkkkkkk, so what I gotta do to get rid of it? He then said, he can treat the symptoms (from flare ups) but there is no cure. WAIT- STOP THE DAMN PRESS- DID YOU SAY NO CURE?? I rose up outta that chair and honestly I was MAD- the kind of mad, where you’re ready to fight. I’m not sure if I was mad at the doctor, myself, or the world, but I was furious, and I felt betrayed! (I know it doesn’t make sense-but that’s how I felt). After 20 minutes of asking multiple questions and answering questions, and FINALLY having a reason for the shortness of breath, the hot flashes, sweating, headaches, fatigue, anemia, gastrointestinal problems, weight gain/lose, insomnia, bouts with depression, and the skin rashes- it was making sense now. I went home and instantly went to the Internet so that I could educate myself on Lupus- 2 days later my brain was fried and I was full of questions.

I slowly began to tell my family- starting with my husband, my kids, and my siblings. My niece who is a RN, said to me” I knew it, I was waiting on you to say something”. My sister said, she knew something was wrong because of my skin, but nonetheless I was going to be ok. I’m a fighter and I don’t quit. I’ve been debating whether or not I should tell anyone. Honestly- I was embarrassed. I no longer feel embarrassed or ashamed. I HAVE LUPUS DAMNIT! It’s not the scarlet letter, and I will not allow it to take over my life! I’m surrounding myself with other people who are living with Lupus, and educating myself as much as I can on the disease. My blog will now included my battles and victories as Lupus is now a part of life. I’m not going anywhere ya’ll and I’m determined to whip Lupus A$$
Disclaimer: NONE OF YA’LL BETTER NOT START TREATING ME LIKE I’M SICK, OR WE WILL BE BEEFING!!!!!! Love ya much!!!!!

Check out my natural hair blog: Au’Naturale by Mz Sixx for natural hair product advice, styling options, product reviews, meetups, giveaways, and general natural hair chatter!

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Monthly Hit Or Dis(aster)

Product: GVP ( Generic Value Product) Tea Tree Oil Lavender Shampoo ** Sally Beauty Supply Stores**

Price: On sale 2 for $10 ( reg price $7.49)

Size: 16 Ounces

Hit or Diss: HIT!!!!!!!!

Comparable product: Paul Mitchell Lavender Mint Moisturizing Shampoo

Product Info: Enriched with tea tree oil, Invigorating fragrance, Rich lather

Soothes scalp GVP Tea Tree Oil Lavender Shampoo is a moisture rich shampoo that hydrates dry hair. Enriched with tea tree oil, lavender and mint. Nourishes dry, thirsty hair, while adding body and shine.

I love this product. I accidentally purchased this product at Sally Beauty Supply, once I was home and realized my error, I figured I would try it anyway since it was on sale. I used it as a clarifying shampoo, and it worked wonderfully!!!! I wet my hair, applied a quarter size amount into my hands and worked it into my hair. A rich lather formed and I felt some “tingle” on my scalp. I repeated the process once more and rinsed with cool water. I then followed with my conditioning treatment and style.

Pro’s:

  • SAME ingredients as the Paul Mitchell Lavender Mint Moisturizing Shampoo
  • My hair was SQUEAKY clean-removing all product buildup
  • Price: GREAT value ( any 2 generic products for $10), regular price $7.49
  • Serves double duty as a great cleanser for make up brushes!!!!!

Con’s:

  • If you are sensitive to the smell of Tea Tree Oil, Mint, or Lavender-you may find this item offensive. ( After I rinsed the product from my hair, I didn’t notice the smell, but other reviewers complained of the “medicinal smell)
  • If you are “particular” about the ingredients in your shampoo- this one isn’t for you- it contains Sulfates.

** What products or methods have you tried? **

**Where they a hit or a dis(aster)?? Lets Dish**

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North Carolina Natural Hair Expo- June 11th -12th

What is “1 Loc, 1 Luv” North Carolina Hair Care Expo?

This is an exclusive collaboration of Bornatty Clothing (North Carolina) and Dreadz N’ Headz Natural Hair Center (Baltimore, MD). It is the third stop of the 8 – Statewide Natural Hair Care Expo tour, “The Exodus II”.

This serves as a “tickler” event for the North Carolina attendees in Raleigh – Durham. This Expo is comprised of various LIVE entertainment, artistic flare from surrounding salons, jewelry makers, lecturers who specialize in holistic health, mind, body, and spirit.

“1 Loc, 1 Luv” is an Expo bringing people together, families, and the communities of North Carolina, bringing more “flava”, and product volume to attendees looking to transition their lifestyles, chemically treated hair, and gain more information on the natural beauty that exists in the Black community.

This expo is a journey, and an experience, thus, bringing life into the colorful community and culture of North Carolina, taking responsibility for “our” people’s health, mind, bodies and spirits, on June 11th and 12th. Martone Evans (Owner and Founder of Bornatty Clothing) and Malaika Tamu Cooper (Owner and Founder of Dreadz N’ Headz Natural Hair Care Center) are committed to bringing an event like never before to North Carolina. This is authenticity at it’s best for families!
For additional information please visit the website: http://www.northcarolinanaturalhaircareexpo.com/