womens health – The Lupie Chick Project

au naturale, aunaturale, lupie chick, lupus, miss naturale, miss sixx, mz sixx, natural, natural hair, womens health

I Shaved My Head Because of Lupus -2 Year Lupus Anniversary

July 16, 2013July 15, 2013 The Lupie Chick

Today (July 9th) was my 2 year ‪#‎Lupus‬ Anniversary and the first day I’ve worn my bald head out in public (that wig was killing me softly). I woke up with a tear in my eye as I realized what this day was. Thoughts of how much #lupus has taken from me….. then my family ( you all) left comments on my note and I realize just how much #Lupus has given me. Mister ( my lupus as it call it) has removed some people from my life and gave me some wonderful new friends and supporters. You guys are awesome and I appreciate each and every one of you. Thank you for allowing me to celebrate and be me unconditionally! This day, July 9, 2011 forever changed my life.. ‪#‎lupiechick‬ ‪#‎bald‬ ‪#‎hairloss‬ ‪#‎NoWig‬ ‪#‎IRock‬ *I played in a little paint (makeup) this morning* and you KNOW I’m in ‪#‎purple‬ from head to toe and rocking my #lupiechick bracelets

Watch the video as I shave my head (because of Lupus)

Subscribe to my Youtube Channel http://www.youtube.com/user/allwayzalady

Follow The Lupie Chick on Facebook

https://www.facebook.com/TheLupieChickProject

acne, affordable, african american, au naturale, aunaturale, lupie chick, lupus, miss naturale, miss sixx, mz sixx, natural, natural hair, womens health

DIY Homemade Green Tea Lemon Sugar Scrub

July 4, 2013July 5, 2013 The Lupie Chick

INGREDIENTS

1 cup Sugar ( white sugar or brown sugar)

2 tbsp Extra Virgin Olive Oil

2 tbsp Raw Honey

1 tbsp Lemon Juice

3 tbsp (brewed) Green Tea

CHECK OUT THE YOUTUBE VIDEO

Benefits of the Ingredients

Lemon – A natural source of Vitamin C; an ingredient commonly used to lighten sun and age spots and even out skin tone; a natural astringent that tightens pores and brightens the complexion.

Sugar – A natural exfoliator; a natural source of glycolic acid which evens out skin tone, cleans pores, and improves overall skin texture by removing dead, dull skin cells.

Olive Oil – High in Vitamin E which soothes and heals skin; a natural moisturizing ingredient often used for its anti-aging benefits.

Honey – A natural humectant so it locks water into the skin keeping the complexion hydrated; the antibacterial properties benefit acne-prone skin by reducing breakouts.

Green Tea– Green tea contains catechins, which are natural anti-bacterial agents that suppress acne-causing bacteria. As well, the anti-inflammatory action of green tea helps reduce any swelling caused by acne. Green tea also contains Vitamin B and Vitamin C. An adequate amount of Vitamin B, especially B12 is key for skin regeneration. Vitamin C is essential in the production of collagen, a protein which enhances the firmness of skin and helps your skin repair itself.

As a face scrub: This scrub is ideal for people who suffer from breakouts and acne as all of the ingredients is highly beneficial to acne prone skin. Lemon tightens pores and evens out the skin tone, sugar removes dead skin cells and cleans pores, olive oil heals acne scaring, and honey prevents future breakouts.

To use, apply to clean face in gentle, circular motions. Be cautious of using on open wounds as the lemon may sting. Leave on for 7-10 minutes and rinse with cool water.

As a body scrub: Apply to body, paying extra close attention to elbows, knees, feet and hands (nails and cuticles especially) and rub in circular motions for 3 to 5 minutes. Rinse. Enjoy the silky softness of your smooth skin.

<a href=”http://www.bloglovin.com/blog/9741415/?claim=n3thzthdmd3″>Follow my blog with Bloglovin</a>

au naturale, aunaturale, lupie chick, lupus, miss naturale, miss sixx, mz sixx, natural, natural hair, womens health

#HAWAC My Niece.. My Sister.. My Best Friend

April 8, 2013April 8, 2013 The Lupie Chick

I grew up the youngest of 5 children. I was the baby and often treated like a baby. I wanted to baby someone. Have someone to play with and have tea parties with. When momma said ” who did this?” I wanted someone else there to take the blame lol..lol.. All of my childhood friends had younger siblings. I never told anyone, but I was down low envious of them. I always wanted to be someone’s big sister, be that someone to be looked up too, and with whom I could teach and share life’s experiences with. OK, lets be honest.. I wanted someone to boss around and split kitchen duty with **insert evil grin**…

My niece, Tamecca and I are 15 months apart. We lived in the same home, went to school together, and shared some of the same friends (she was friends with my friend’s younger siblings). Growing up, we DID NOT GET ALONG . I’m not sure if it was sibling rivalry or just us being stubborn, but I don’t recall too many “fun” times growing up with my niece. I could not boss her around, and she damn sure wasn’t going to help me with my chores. We argued A LOT, it wasn’t fun to always be on edge and for some reason we were never in a good place with each other. ** insert hand on hip and side eye** BUT anyone that knew us KNEW if you mess with one it was going to be hell to pay!

Fast forward to adulthood. We have a GREAT relationship. We’ve made so many phone calls to each other to share good news, bad news, and just news. I will never forget the call I made to my niece on July 15, 2011, the dreadful phone call I wish I could take back. I called my niece to tell her I have Lupus. ** insert dead silence** because it was dead air for about 45 seconds…She tried to be brave and tell me it’s OK, but I could hear the hurt, and fear in her voice as she struggled to find the words to comfort me. My niece was the 2^nd person (to my husband) I told I have Lupus. I would call her before taking any meds or to get advice relative to my treatment plan. I would call (and yell) when I was frustrated, in pain, and being a big a$$ baby. She never allowed me to feel sorry for myself or willow in pity. Her famous line “ you know grandma (my mother) didn’t play that, she worked hard so we could have, she beat cancer, you can’t give up, the doctors don’t always know what they are doing!” ..lol..lol..The calls I would normally make to my mother (who is a retired RN, who is battling Alzheimer’s) I was now making to my niece! Had she become the little sister I always wanted. The late night call I received from her after she read my blog-her yelling telling me I just took her on an emotional roller coaster crying and laughing at the same time-How could I do that to her!! lol..lol..

In times of financial strain I’ve never had to ask to borrow money, she always volunteers to give, even if it meant borrowing from someone else to give to me. We have so many things in common in our adult life-growing up- it was Toni & Tamecca (us), both of our 2^nd children are girls my daughter A’Yianah & her daughter Anya ( get it.. both names start with an A, and both of our 2^nd children are girls, AND they are 16 months apart in age). We both became grandmothers for the first time together (2 days apart). I remember being really mad (I think I was 12 or 13 yrs old) at her because I wanted her to call me “Aunt Toni” lol..lol.. and I was really MAD that she refused! Lol…lol… Now, she often calls me on the phone and say “hey Te Ta” in her cheery “what cha doing voice”.

I still remember the day she announced that she successfully earned her RN nursing degree-the pride I felt was unbelievable. I was shouting “SHE DID THAT” YOU BETTER WERK!!!!! ..I was calling everyone (including people who didn’t know her to BRAG about what my niece had accomplished). Finally tears of joy!!! Something to celebrate J

The late night-early morning conversations about life, family, kids, fears, joys, lows, highs, with no judgment-are PRICELESS !!!!! We cry together, we laugh together, we pray together. I love my niece sister. I’m proud of the relationship we have now, I have my sister, my niece, my best friend, my ride or die, all rolled up into one!

Love you niecy-sissy poo 🙂

au naturale, aunaturale, lupie chick, lupus, miss naturale, miss sixx, mz sixx, natural, natural hair, Uncategorized, womens health

#HAWMC Long Hair Dont Care… Short Hair Dont Either

April 5, 2013April 12, 2013 The Lupie Chick

Lupus Related Hair Loss

Lupus hair loss can be caused by the disease itself, as the immune system destroys hair follicles, or by medicines such as prednisone and immune system-suppressants—in which case hair loss often stops once the medicine is stopped. Hair may fall out in strands, or in clumps with the slightest pull, and sometimes it just thins out and gets very fragile and breakable.

According to the American Academy of Dermatology, an average person loses anywhere from 50 to 100 strands of hair each day. This may seem like a lot but keep in mind that it’s normal to lose and re-grow hair. However, when you aren’t seeing any re-growth, then it’s typically a sign that you may have an issue with your hair.

Most people don’t even notice the 50 to 100 strands of hair that they usually lose every day. With systemic lupus, the situation can be very different, with the loss of hair much more dramatic and noticeable.

It’s not a secret that I recently experienced hair loss after my most recent flare up. I didn’t speak about it much as it was happening, but on March 15, 2013 after months of shedding, loc’s breaking off, and obvious balding around my edges, I decided to BC aka Big chop.

I went to see my home girl Camille, Owner & Natural Hair Stylist at Noiree Salon in Silver Spring, MD and had her to take it off. She seemed a little hesitant, saying that she would take me shorter but I didn’t have to BC. I said NO- I’m ready- TAKE IT OFF! In a matter of 5 minutes my two strand twists were laying in a pile on the salon floor.

The previous year, I suffered hair loss and had my cousin April cut my bra strap length hair into a Diva cut.

This time, I was ready to “let it go” (in my Keyshia Cole voice). My TWA has changed my looks. Co workers barely recognized me when I returned to work, and attendees of my event Cupcakes & Cocktails were surprised at the short hair. I rocked a TWA continuously for 7 years back in the 90’s, but most of the people that I socialize with today had never seen me with short hair.

I’m still a little self conscience about the bald spots (especially my edges) – but as we all know-sometimes its part of the process (shrug shoulders).

Beginning today I will document my journey as I take steps to re grow my hair (specifically my edges). I’m not seeking to grow my hair a certain length, I just want to re grow the balding spots.

488252_10151145642073809_749906445_n

Check Out These Helpful Tips To Assist With Regrowing Your Hair

Vitamins & Supplements for Hair Growth (Biotin)

Few people are actually deficient in biotin, which occurs naturally in bacteria in the gut. Nevertheless, therapeutic doses of biotin – also called Vitamin H or B7 – are necessary to achieve benefits in hair health and rapid growth. It is difficult to overdose on biotin – many supplements come in 500 microgram capsules.
Biotin is useful for those who want their hair to grow faster: some claim it can even reverse premature greying if the greying is caused by marginal biotin levels. Biotin can be taken alone or in conjunction with other B-vitamins. The latter may be a good idea if you lead a stressful lifestyle – B vitamins help to prevent stress, which is a cause of hair loss!

Natural Oils that can be used to help promote regrowth

Peppermint and Rosemary are commonly used to regrow hair, but must be combined with other oils like olive oil or coconut oil (also good for hair regrowth)
Castor oil and Jamaican Black Castor Oil are often used for regrowth because of their thick quality and ability to thicken the hair. Jamaican Black castor Oil

If your hair loss is mild, try a new haircut

You don’t have to BC like I did (that was my personal preference). Long hair is weaker than short, so consider a shorter ‘do’ with layers to hide thinning or bald patches.
Wash fragile hair with baby shampoo, and use a leave-in conditioner with sun block
Products like Shea- butter and sesame oil have natural UV filtering properties. And while many hair products claim to protect hair from the sun, unless they have a SPF rating or contain a known sunscreen ingredient, these could be just marketing claims. If you plan to be out in the sun for more than an hour, the best hair care tip is to wear a stylish hat or scarf.
Avoid adding more stress to your hair from using curlers and alcohol-based styling products, which can irritate sensitive skin.

Rock Your Good Hair

Hairpieces and extensions can be added into thin areas to create a fuller look. Just make sure that these aren’t too tight, because tension on weakened hair also can lead to hair loss.
Wigs come in a wide range of styles, colors, and lengths. Your stylist can custom cut the wig to match your face (and personality). And don’t forget your scalp! Keep it dry to prevent chafing, and remove the wig occasionally to allow your skin to breathe.

Whether you decide to go with a wig or a new hairstyle, remember that there’s no wrong way to deal with hair loss. Everyone has a different comfort level; it should be an individual decision. Stay tuned as I document my attempts!

If you have lupus and are losing hair, do NOT experiment with over-the-counter hair loss treatments. Talk to your doctor about treatment options.

#HAWMC, au naturale, lupie chick, lupus, miss naturale, mz sixx, natural, natural hair, spoonie, support, Uncategorized, womens health

Day 2: #HAWMC 5 Ways to Fight Like a Girl For Lupus

April 3, 2013 The Lupie Chick

Sometimes when dealing with chronic illness, you’re inner you says FIGHT, the outer you don’t know how or where to begin. It can all be a tad bit overwhelming, and at times confusing. Below are my top 5 tips to FIGHTING LIKE A GIRL FOR LUPUS!

Step 1: Acknowledge It!

First we have to acknowledge that we have an illness before we can take a step in any direction. Though symptoms of Lupus differ, people with them are united by the denial, anger, fear, hope, and acceptance and other feelings they bring. At diagnosis, feelings of grief and loss had consumed me. I felt that Lupus was restricting me from the things I enjoyed; no longer able to attend cabarets (because of the loud music and the migraines), it was summer, and I was unable to attend barbecues, crab feasts, or hang out at the beach/park with my children and grandson. I felt inadequate, isolated, and withdrawn from family, friends, and the MC/SC community. A month into my diagnosis, I took to YouTube and posted a video. Instantly, when I acknowledged my disease, and stop acting sick, people stopped treating me like I was sick! I buried my grief-stricken feelings, and haven’t looked back!

Step 2: Claim Your Power!

Ask yourself a question. Are YOU ready to “Fight Like A Girl”? By claiming your power you pledge to stand strong and fight against Lupus. You declare that you have a power within that will help prevail against weakness and that if by chance we fall while struggling to stand we will not feel guilty but reach out to our Lupie sistas & brothers for help! I pledge to do all this and believe we can because we have claimed our power!

Step 3: Find Your Social Media-Family!

We are not alone! There are 1.5 million lupus survivors in the United States. Facebook, Twitter, Instagram, and LinkedIn have hundreds of different groups and pages dedicated to raising awareness and support for Lupus. On Facebook, you can do a search (in the search box) for the keyword Lupus. A list of Lupus support groups & pages should appear. On Twitter and Instagram the way to find someone is to search for a hashtag mentioned in a tweet/picture post. All the people who have used those hashtags will appear-you simply “follow” and most will “follow back” Some of the common hastags to search for are: #lupus, #LupusAwareness, #spoonie, #butterfly, #ChronicIllness, Together we share our pains and sorrows, our joys and pleasures. Whatever we experience we can learn to share it and fight it together!

Step 4: Become an educated Patient!

Whenever I get a new symptom, like a rash or chest pain, I say to myself, “Its Mister (aka “my Lupus”) begging for attention. No need to worry. No need to check it out. It’ll go away in a few days.” At times, this is probably true. But more often, a new symptom needs to be evaluated and perhaps treated so it doesn’t become a life-threatening event. I will post on one of the support groups that I belong too and/or I will turn to Google. It’s imperative to our health that we become “hands-on” patients and educate ourselves. As patients we cannot just depend on our doctor to tell us everything. We have a responsibility to our health and well-being to do our own research! Find out the current medical news, keep a food/illness diary (this helps to discover what foods trigger symptoms-check out this app), look up alternative medicines, talk to other patients and find out what works for them. Some great Websites to visit are: Lupus Foundation of America, WebMD, MayoClinic.com, John Hopkins Lupus Center, Alliance for Lupus, NIH, and Life with Lupus.

Step 5: Sharing is Caring!

You’ve heard it before: “It takes a village”, “Two heads are better than one”, Each one can reach one! So reach out and help someone else begin the journey to overcoming Lupus. It can be scary, but 9 out of 10 times, there is someone who can relate and/or has experienced something similar to what you are dealing with. Together we can stand strong!

The informational content of this article is intended to convey general educational information and should not be relied upon as a substitute for professional healthcare advice.

au naturale, aunaturale, lupie chick, lupus, miss naturale, mz sixx, natural, natural hair, womens health

Day 1 #HAWMC Why I Write

April 2, 2013 The Lupie Chick

I am super excited to be taking part in the Health Activist Writer’s Month Challenge which is being hosted by WEGO Health! The entire month of April will be dedicated to sharing our stories as well as educating and raising awareness!

Day 1 #HAWMC Why I Write

Initially, I had a blog relative to natural hair. I LOVED talking about natural hair, and offering advice & tips as to how to care for natural hair. Au Naturale by Mz. Sixx was my baby. I had gained followers, was getting offers from companies to host giveaways, & meetups – I was on to something. In 2011 Lupus creped his ugly head into my life. I could no longer keep up with blogging, attending social events and was lost as to what was happening to my body. After being diagnosed, I was stumped as to how I would tell my friends and family I finally had a reason for the scarring on my face and the extreme exhaustion. I took to my blog and posted Hello-I’m A Lupie Chick.

That was the first time I had actually said the words “I have Lupus”. Wow, the response was overwhelming as most of my friends and family was not educated or aware about Lupus. The inbox messages, text, emails began to be too much. First, blogging about Lupus was a “relief” and a way that I could provide my friends and family with updates. There were moments when I felt like I was complaining or no one was reading. Months had gone by without any posts, because I didn’t want to burden my followers with my Lupie Chick issues. I started to receive tweets stating that they were about Lupus because of my blogging and interactions on social media. There were a few people in my life who suffered in silence and they were speaking through me and the blog. WHAT A BURDEN THAT WAS FOR ME TO CARRY. Additionally, I was still posting on the natural hair blog. It was too much, What if I said the wrong thing? What if I felt like saying F*uck it-would I offend someone? Would I receive hatful messages because someone didn’t like my post? How can I keep up the pace with informative content on two blogs? I came to realize that I’m human; I’m not a robot that you can switch off and on. I don’t have to blog daily or weekly. I have feelings, emotions and a voice that I refuse to silence to spare anyone else’s feelings.

In March of 2013, I combined both blogs- Au’Naturale by Mz. Sixx and The Lupie Chick = Naturally Lupie. I write to be a voice and a face to a little known invisible disease. I write in a conversational way….my grammar isn’t always correct, I occasionally use slang and or profanity-not to get attention, but because that how I speak to my friends or that’s how I’m feeling at the time. I didn’t want my blog to be a text book encyclopedia type of blog. I didn’t want my blog to be a repeat of every other natural hair blog. I wanted my blog to tell the struggle and be a pillar of strength for the weak and weary. My blog is the little thing in your head saying “yes you can and YOU WILL”. I’ve always been loud and in your face type of person (some say obnoxious)-I’m not the whispering type…so why start now? Mister (my Lupus) is loud and obxinous too- when he wants attention he show up on my face and my hair. He has tried his best to take my beauty and silence me. Most recently, I’ve had to cut all my hair off aka Big Chop the day before a huge event I was hosting to celebrate women, as a result of a Lupus flare (talk about loud and obnoxious). The hair loss has left me bald around the edges and nape of my head. I posted about it on Instagram w/ pictures, and guess what- I received 36 comments where other Lupies have or had experienced the same thing.

THAT’S WHY I WRITE; to speak up and not suffer in silence or alone. I have had moments where I had no idea what to write and felt like I had no meaningful content left to offer. I have had moments where I’ve felt completely inadequate to try to offer hope to readers when I felt so helpless myself. I have had moments as recently as this weekend when I’ve felt like I physically didn’t have anything left to give. But I do- I have LOTS more to give and I will continue to write- not only for you but for ME!

healthcare, lupie chick, lupus, lupus Awareness, lupus foundation, neurologist, NHBPM, research, rheumatologist, web md, womens health

DAY 2: Advice For A Newly Diagnosed Lupus Patient #NHBPM

November 2, 2012March 3, 2013 The Lupie Chick

Being diagnosed with lupus can bring about a flurry of emotions. You may feel upset or nervous about what the new diagnosis means for your future. You may be angry at the idea that your life may change. You may even feel happy that after some time of not feeling well, you finally have a name for what was ailing you. Finally, your condition has a name. Each of these emotions is normal, and no reaction is the right one. In fact, you may feel all of these emotions at some time or another.

But beyond your emotional reactions, you may be wondering what your next steps should be. Below are some tips for moving forward after being diagnosed with lupus.

1. Get a second opinion. Before you begin your journey into chronic health care, you want to make sure you are heading down the right path.

I didn’t get a 2^nd opinion when I was first diagnosed. My dermatologist originally diagnosed me (I had the butterfly rash across my face, and lesions on my neck and under my breast). After she performed her examination she was “certain” it was Lupus and referred me to a rheumatologist & neurologist who ran additional test and confirmed that I had Lupus. Honestly, that was the best day of my life. It answered a lot of questions and FINALLY I KNEW that what I was experiencing wasn’t my imagination. After getting over the initial shock, I was ready to battle & WIN!!!!!

2. Bring a friend or family member to be an advocate for you. You may need to have some tests done and see many doctors in the beginning. Having someone else there to take notes, ask questions, or just be an emotional support is very important. It is normal to forget a question, or not remember important information after a doctor visit. It is also great to have a supportive person with you who can hold your hand, distract you, make you laugh, or just listen.

I have never had a friend or family member come with me to any of my appointments (well my husband has attended 2 or 3 ). There were times when I wanted “support” and then there were times when I was happy I was there alone. From my experience, I have found that when people don’t understand what is happening they can be very judgmental. Going through the motions and of trying to come to grips with everything- JUDGEMENT WAS THE LAST THING I NEEDED OR WANTED!

3. Start a notebook or a folder for your healthcare. Take notes and ask for copies of your test results. Take time to actually read your tests and learn what they mean, or ask your doctors. Keeping a record now is a great start. It’s always a much bigger job to back track and get records that you may need in the future. These records and notes can be helpful when you’re seeing multiple doctors, dealing with insurance companies, applying for disability, etc.

Yes, yes, yes!!!!! I started experiencing a “brain fog” and I would literally forget what someone told me only minutes previous. It’s imperative that you keep records and minimum keep notes or download one the apps on a smart phone that will store your medical records and or notes for you. I remember an incident when my rheumatologist had prescribed me a medicine that counter acted something the neurologists prescribed me, I ended up with massive migraines and I wanted to die (I was in that much pain). Once I gathered everything out of my cabinets, purse, and night stand, I went back to the doctor, showed them everything I was taking, and they figured out exactly what the culprit was. From that point forward I have kept impeccable notes and I always keep a record of my prescriptions ( dosages, strength, etc).

4. Do your research. After being diagnosed with lupus, you will soon hear all kinds of words that you may not have heard before. Names of medications, secondary diagnoses, and symptoms can be overwhelming and scary. A great way to combat this feeling is to learn as much about lupus as you can and get yourself familiar with the lingo. This will help empower you in conversations with doctors and nurses. When you know what they are talking about you can ask appropriate and necessary questions. WebMD is a great place to start on your quest to educate yourself. There are many articles, posts, and videos on the site that are very informative.

I can’t say this ENOUGH!!!!! DO YOUR OWN RESEARCH!!!!!! I’m often asked for advice relative to Lupus. While I appreciate strangers, family & friends comfort level to ask me for advice ( treatment, & diagnosis), I refrain from giving medical advice. It’s not that I don’t care or I don’t want to share information, I’m NOT A PHYSICAN. Legally I cannot provide medical advice. I’m more than willing to share what has/hasn’t worked for me, but that information should not be used in place of a diagnosis or treatment plan. I have this disclaimer at the end of every post “The information included on this blog is for educational purposes only. It is not intended nor implied to be a substitute for professional medical advice. The reader should always consult his or her health care provider to determine the appropriateness of the information for their own situation or if they have any questions regarding a medical condition or treatment plan.” I encourage all of you to always consult with a physician before starting/stomping any Treatment plan, Nutrition (eating) regime, and Fitness plan. If you are looking for information and or support, outside of speaking with your doctor, I HIGHLY suggest that you become a member of the Lupus Foundation of America Chapter (in your state). The Lupus Foundation of America offers symposiums, teleconference calls, empowering events and the largest support group network.

5. Ask questions!!! Do not be afraid to ask questions, even questions you deem silly or unimportant. If you feel any kind of change in your symptoms, tell your doctor. I cannot stress this enough. You are a partner with your doctor in your healthcare. You need to take an active role. You are the only person who knows your body best, so if something feels off, say so.

You have to be your own advocate and cheerleader in this fight!!!!! No matter how minor the question may seem, ASK IT!!!! Make no assumptions!!!! Make sure that the doctor/nurses are listening and providing you with the approriate answers. You must be active and aggressive in your treatment plan !!!!

Tips Provided by Web MD ( my responses are highlighted in purple)

Until Next Time,

Live ~ Laugh ~ Love

¸.· ´¸.·*´¨) ¸.·*¨)

(¸.·´ (¸.·’ The Lupie Chick ™

Stay Connected
Instagram:@naturally_lupie
Facebook: www.facebook.com/mzSixx

Twitter: @lupieeChick & @AuNaturaleDC
The information included on this blog is for educational purposes only. It is not intended nor implied to be a substitute for professional medical advice. The reader should always consult his or her health care provider to determine the appropriateness of the information for their own situation or if they have any questions regarding a medical condition or treatment plan.

blog, Facebook, health, Instagram, lupie chick, lupus, lupus Awareness, mz sixx, natural hair, NHBPM, November, Twitter, womens health

Day 1: Why I Write About My Health #NHBPM

November 1, 2012March 3, 2013 The Lupie Chick

When I was first diagnosed with Lupus, I instantly took to the internet. I wanted to arm myself with as much information as possible. I was prepared to be over whelmed and immersed in everything regarding Lupus. I was alarmed by the amount of “repetitive” information that was available. Everything was a repeat and very “ text book” . I was clear what Lupus is (was), but I wasn’t clear as to how people lived with Lupus. What a day was like for a Lupie Chick ™. How Lupus affected friendships/relationships/marriages. How Lupus affected people’s mental state. How Lupus affected peoples emotional/physical/sexual health. I had LOTS of questions. I could not find what I was looking for; nothing was really answering what I wanted to know. (For me), I needed visual, clear, concise answer(s). Based on the lack of information available, I decided to write from my perspective and keep it REAL & RAW (no sugar coating). If I was in pain I wanted to describe or show pictures of the type of pain or the intensity level of the pain. I was going to show my bare face (without makeup) and talk about the scares, the nasty remarks, and assumptions people make about you when you have an invisible disease. I wanted to provide an outlet for my fellow Lupie Chicks™ to know that they were not alone and we could cyber space high five each other.

I will never forget my first posting telling the world, I Have Lupus; people were calling me with tears in their voice telling me I had taken them on an emotional roller coaster. I heard from friends I havent from in years (more than 10). It wasn’t my intention to make anyone cry or become upset, I wrote from the heart. I wrote as if I was speaking to my girlfriends or family. I’ve found that my ability to be open and my style of writing works for the type of platform I’m building.

I’ve started posting daily pictures of myself saying Hello /Good Morning to my fellow lupies. If I miss a day, people will inbox me on Facebook or text me and say “where is our daily picture?” I never knew that a simple picture would/could make someone’s day, or provide a little encouragement.

Not too long ago, I received a mention on Twitter that said “because of the Lupie Chick I know more than I ever thought I could or wanted to know about Lupus and the struggle”. I don’t know this young lady, never knew that she read my blog or tweets. I received a message from another young lady telling me “because of your blog I now know how to be a better friend “. I don’t get many (any) comments on my blog, and I wasn’t positive if anyone was reading my blog, UNTIL I get the random messages, text, or tags of people wearing purple, or mentions of “ The Lupie Chick”. Just the other day, my hands had swollen and I was in severe pain. I posted a picture on line and a young lady asks “what’s lupus?” I was in too much pain to type (reply) on my mobile, but I fought through and took a screen shot of the Lupus Foundation page explaining what Lupus is. Even in my mist of a challenge I was able to educate someone on this little known invisible disease. I’m so honored and humbled to be able to do what I do, and I’m MORE honored and humbled to my readers and audience who help spread awareness. I know that I will never stop writing, I will never stop bringing awareness, and I will never keep quiet – This is WHY I Write About My Health!

Until Next Time,

Live ~ Laugh ~ Love

Stay Connected
Instagram:@naturally_lupie
Facebook: www.facebook.com/mzSixx
Twitter: @lupieeChick & @AuNaturaleDC

The information included on this blog is for educational purposes only. It is not intended nor implied to be a substitute for professional medical advice. The reader should always consult his or her health care provider to determine the appropriateness of the information for their own situation or if they have any questions regarding a medical condition or treatment plan.

Atlanta, aunaturale, autoimmune, diabetes, domestic violence, healthy, Iyanla Vanzant, life, lupie chick, lupus, lupus Awareness, majestic divas, mz sixx, peace, purple, womens health

Are you living in PEACE or PIECES??

October 19, 2012March 3, 2013 The Lupie Chick

Painting by Yvette Crocker

Yesterday I spoke to an ex (whom I haven’t spoken to or seen in more than 17 years). He seems so broken dealing with a lot of heath issues (specifically diabetes) and the lost of his immediate family members. He had been dealing with a lot of guilt from situations that occurred during our relationship and had remained in that moment. Listening to him made me realize that we have life choices. We can live in PEACE or PIECES! I realized that I choose peace while he had chosen pieces. Yes, I know it is very difficult and hurtful to lose all of you immediate family members, and it’s also difficult to live with an illness (the same illness that had taken the lives of his family), BUT you have to choose PEACE. Choose to deal with whatever is before you and GO THROUGH IT (not around it).

I think back on all the test that I’ve had to take to have this testimony I speak about today. I have no shame and no silence. I survived sexual abuse, domestic violence abuse, the challenges of being a teenage parent, betrayal, mis fortune, financial instability, unemployment, and now fighting for dear life to beat Lupus. I FOUGHT and will CONTINUE to fight EVERYDAY for the rest of my life. We all have a responsibility to live our best life (whatever that may be). I know that everything that has happened to me happened for a reason to make me realize just how AWESOME I really am. I’m much stronger than I ever knew or imagined I could be. Do I have fear-of course I do.. but I have taken lemons (my fears & life challenges) and turned them into champagne (success)! This is MY LIFE- and whatever the devil has taken from me- HE CAN KEEP IT- BECAUSE MY GOD HAS SOMETHING BETTER FOR ME!!!!! I choose to live in PEACE!

To all of you that read this post- I ask you- how you will live the rest of your life? In PEACE or PIECES????

Until Next Time Fam

Live.. Love.. Laugh…

The Lupie Chick™

Stay Connected
Instagram:@naturally_lupie
Facebook: www.facebook.com/mzSixx
Twitter: @lupieeChick & @AuNaturaleDC

aunaturale, autoimmune, cardio, divaGetFit, exercise, healthy, lupie chick, lupus, walking, womens health, work out

Get past the excuses!

August 2, 2012March 3, 2013 The Lupie Chick

** In my Sunshine Anderson Voice** “I’ve heard it all before-all the excuses why you (me) can’t work out. I’ve decided to get up off the cough, bury the excuses and get moving!!!! My body is going down and it’s time for me to pick it up!!!!! I’m tackling my destructive habits, done with the pity party, and instead of investing in spanx (I’ve been known to wear 2 pair of spanx at one time-pretty much cutting off my circulation and the ability to wobble or drop it low lol..lol..) I will invest in work out gear and equipment.

I went for a brisk walk yesterday for the first time since being diagnosed with lupus (July 2011). I told ya’ll that every time I make up my mind to workout-mister ole evil ass creep in. On my way home-it started raining, more like storming.. ok.. I’ll do the Zumba on the wii,**no excuses** mid way home, migraine was coming on.. NOPE-whipped out my peppermint essential oil and was rubbing my temples like my life depended on it ** no excuses**-Guess what?? I got home-it had stopped raining, and my migraine was fading to black… ITS ON!!!!!!!

I put on my T-shirt, leggings, and sneakers and hit the pavement.

** Please note the Lupus T-shirt, Lupus Bracelet, and purle shadow-#LupusAwareness EVERYDAY**

Showing support to Running For Lupus with the “L” Hand Sign

When I was through I was a sweaty mess.. But I was ecstatic that I completed DAY 1 workout and didn’t cave into any excuses!!!! Below is my stats from the workout-using the sports tracker app on Android

The Top 6 Exercise Excuses and How to Beat Them

Just like everyone else, people with lupus need to exercise regularly or engage in some kind of movement, and most people with lupus can take part in some form of activity.

We all know that being physically active makes you healthier; you’ll sleep better, feel happier and more energetic. But when it comes time to actually get out there and start moving, many of us have a long list of excuses not to exercise — too little time, too little energy, or we simply don’t like to work out.

How can you get past the excuses and get moving.

Exercise Excuse No. 1: “I Don’t Have Time.”

During your TV shows, use resistance bands, or walk in place. Or use Tivo so you can skip the commercials and see a one-hour show later in just 40 minutes, That’s 20 minutes of activity right there. Better yet, turn off the TV and spend your newfound time working out.

Music-When we moved into our new home, we didn’t have cable for a week or so- we turned on the radio, I realized that most stations have an online presence so I could still hear my go-go and Biggie. I was moving and grooving all around the house.

Your exercise doesn’t have to be a formal workout either. Try making small lifestyle changes that help you move more: take the stairs instead of the escalator, don’t drive when you can walk, and get a pedometer and try to increase the number of steps you take throughout the day.

People who exercise regularly make it a habit. They haven’t bought any more time during the day than anyone else. What we’ve done is prioritize it. We find time for things we value.

Exercise Excuse No. 2: “I’m Too Tired.”

It may sound counter intuitive, but working out actually gives you more energy. Once you get moving, your fatigue will likely disappear.

You’re getting the endorphins [feel-good hormones in your body] to release, and you’re getting the circulation going — as opposed to coming home and crashing on the couch.

It may help to work out in the morning, before you get wiped out by a demanding workday. If you’re not a morning person, don’t worry, just work out whenever you feel the best.

Exercise Excuse No. 3: “I Don’t Get a Break From the Kids.”

Take the kids with you. While they’re swinging, you can walk around the playground or the backyard, or jump rope. Walk the kids to school instead of driving them. During their soccer games or practices, walk briskly around the field.

Use your family time for active pursuit. Go biking with your kids or just walk around the neighborhood with your children. When the weather’s bad, try active video games (Zumba, & Michael Jackson Experience are my favorites), dancing, at home work out videos ( my buddy told me that Julian Michael’s videos are the #TRUTH).

Remember that your fitness is good for your kids as well as you. When mom or dad is more fit, has more energy, the whole family benefits.

Exercise Excuse No. 4: “Exercise Is Boring.”

You should want it and feel good about it before you do it. And it should feel good while you’re doing it.”

So how do you get there? First, find an activity you love. Think outside the box: Join a sports league (I’m thinking about joining the kickball league next season). Or, if you love music, line dancing ( can you say wobble!!!!). There’s an exercise for everyone.

If it makes exercise more enjoyable for you, it’s OK to watch TV or read while you’re on the exercise bike or treadmill — just don’t forget to pedal or run.

Working out with a group also helps many people. Not everybody’s cut out to go on a six-mile run by themselves.To find a group, look at meetups ( meetup.com or simply recruit several friends.

Every once in a while, try something totally new. Mix it up so you don’t get bored.

Exercise Excuse No. 5: “I Just Don’t Like to Move.”

There are people who really enjoy not moving. They prefer to knit, read books, or watch TV.

If it’s sweating you don’t like, you can get a good workout without perspiring excessively.You can work out indoors, where it’s air conditioned. You can swim so you won’t notice any perspiration. Or, try a low-sweat activity like yoga.

If exercise hurts your joints, try starting by exercising in water. The stronger your muscles get, the more they can support your joints, and the less you’ll hurt. If you’re physical limitations is more serious, check with your doctor/coach who can help you figure out exercises that are still safe and easy to do.

If you don’t like to move because you feel too fat, start with an activity that’s less public, like using an exercise video at home. Walk with nonjudgmental friends in your neighborhood while wearing clothes that provide enough coverage that you feel comfortable.
Exercise Excuse No. 6: “I Always End up Quitting.”

Set small, attainable goals. Then you’re more likely to feel like a success, not a failure. If you exercise for five minutes a day for a week, you’ll feel good — and more likely to want to try 10 minutes a day the next week.

It also helps to keep a log and post it somewhere public (follow hash tag #DivaGettingFit on Instagram, Twitter, and Facebook).
Having an exercise buddy keeps you accountable as well. My buddy is my sista friend Gayna. She encourages me, provides LOADS of tips, and holds me accountable. Thanks BUDDY!!!!!

It’s harder to start exercising than to stick with it once you’ve got your momentum going. Start a healthy habit today… you will feel better and will want to continue your healthy lifestyle everyday!

If lupus has you on the sidelines rather than in the middle of the action, this new low-impact exercise program, designed specifically for people with lupus, may be “just right” for you. Guided by a licensed A.C.E. instructor who also has lupus, this DVD offers a gentle fitness routine that you can practice in the comfort of your own home. The goal is not to become a super model but to get moving—and to improve your well-being in the process. DVD, 27 minutes.

Disclaimer: All exercise plans should be discussed with your physician or exercise specialist in order to maximize results and minimize possible harm.