A survivor’s journey.

Our breast cancer survivor role model for October, Allison Kelly.

Our most beautiful role model for the month of October, Allison Kelly.

Six years ago, Allison Kelly was turning 40. With no family history of breast cancer, she had very little anxiety about scheduling her first mammogram. She did all the right things like monthly self-breast exams and yearly check ups at the doctor. And, to add to her sense of ease, Allison nor the doctors ever felt the slightest lump during her exams. Then everything in her life changed in an instant. “My mammogram lit up like a Christmas tree,” Allison recalls. “There were two tumors growing and my results were triple positive.” Allison, married with two young children who were just three and seven at the time, had a lot of big decisions to make.

Allison and her doctor’s decided on a treatment consisting of a lumpectomy, radiation, and chemotherapy. The treatments lasted a year and a half. “I can go on for hours about that hell,” Allison lamented. Then, while sharing her story, Allison paused for a moment and said, “You know what’s funny? When I started the chemo, I thought the hardest part would be losing my hair. It was my signature — my thick, long, curly hair. Turns out that was the easiest part. Chemo was a bitch.”

To get her through it all, Allison relied heavily on her strong network of friends. “Thank God for friends and family. They were my support.” They walked side-by-side with her in her first Avon walk, while she was undergoing chemo. Friends brought meals, helped keep her spirits up — one even broke into her house and cleaned it while she was sick during her treatments. It was encouragement from friends and family, especially her husband, that helped her get through each day. She described him as a stoic man who picked up all the pieces when she was sick, but who never let her lose her sense of humor. “He could always make me laugh,” Allison smiled, “even on the worst days.” Allison also drew support from her Oncologist. She recalls telling her Oncologist, “Just help me see my kids through high school.” Her Oncologist looked her straight in the eyes and firmly stated, “You’re going to live to be a grandmother.”

It took Allison a year after her last treatment to finally feel normal again. Allison went about her life, working, raising money for breast cancer research, and spending time with her husband and children. And, not one to be beaten, Allison continued walking in Avon walks. To date, Allison has participated in 8 walks, and will be walking her 9th in 2014. One year Allison was going to walk two walks, one in DC, then one in October in New York with her family. But when October came, Allison was too sick to travel or walk. Her family in New York walked in her honor.

A few years passed and Allison approached her five year remission anniversary. “For my five year anniversary on 12-12-12, my husband planned TWO parties. I’ll never forget it.” Her doctor’s assured her she had beat cancer — she was given the all clear. Glad to put cancer behind her, Allison scheduled a follow up mammogram two weeks after the party. She recalls how, in the early stages of her cancer, days seemed like years when waiting for results. “There was one point I went for five weeks without knowing if I would live or not.” However, when speaking of her first post-remission mammogram, she recalls her complete lack of worry, “I walked in there not worried one bit.”

Then, she got the results. It wasn’t good. The cancer had returned. Luckily it was caught early, but her doctors told her chemo wouldn’t work this time. In February 2013, Allison underwent a nine hour double mastectomy and reconstructive surgery then went on to spend three days in the cardiac ICU. Allison spent weeks sleeping in a recliner at home as it was too painful to lie down in a bed, but, in typical Allison fashion, she kept her positive attitude and sense of humor, posting hysterical quips about pain meds to her Facebook page. Allison has a third and hopefully final surgery scheduled this month. Allison described the surgery as “intense” and “painful,” but, she would do it again in an instant to know that she probably won’t have to face breast cancer again.

Allison is our role model for Breast Cancer Awareness Month. She is a force to be reckoned with, but warm and sweet at the same time. Her personality is infectious. Her eyes are full of light and kindness, yet at the same time, you immediately sense you would not want to throw down with Allison. Cancer didn’t stand a chance with this gal.

Asking Allison to share some final words of wisdom, Allison spoke of finding local support even beyond friends and family. She received from INOVA tremendous help from a local organization called, Life with Cancer. “They helped me with how to talk to my children about what was happening to mommy, and three things were key. One, it’s not your fault, two, it’s not contagious, and three, I’m going to look funny.” She also said her friends used the free scheduling service, Take Them a Meal to help schedule meals for the family. But, her biggest piece of advice was to get a mammogram. “I shouldn’t have had cancer. I didn’t fit the profile. That 10 minutes of discomfort saved my life.”

During the month of October, we will be again participating in Pink Hair for Hope, which has helped raise over $2.5 million dollars to date for cancer research and advocacy programs. Through this program, pink extensions can be added to your hair for $10, with the proceeds going to breast cancer research programs. We will also be donating $1 from every haircut in October to the local organization, the Tigerlily Foundation. And, kicking it off, we are hosting a Pink Hair for Hope night on Thursday, October 10th from 6-8 PM.

Your action item for this month …

Jonathan and I have been asked on several occasions this question: “What got you into pediatric cancer fundraising? Do you know someone who has cancer?”

Honestly, we were pretty oblivious to pediatric cancer prior to 2007. And I mean oblivious as in ‘head stuck in the sand because you just don’t want to know about such awful things’ oblivious. But in 2007, a friend told us about Taylor Love. I still have the email and vividly remember watching the video for the Loneliest Road Campaign. At the time, our first born was not even a year old. It hit us so.very.hard. What if this was our child? The sorrow and desperation we felt was immediate – and we both said, “what can we do to help?” We started by holding our first ever cut-a-thon to “cut out” neuroblastoma, the rare pediatric cancer with which Taylor was diagnosed at just 18 months of age, and have held six annual cut-a-thons.

Fast forward to 2010. I wanted to re-connect with a mother I’d met on a cloth diapering network. I had been meaning to reach out to her as I wanted to get our kids together for a play date and I felt awful that I hadn’t even met her newest, then 6 month old Casey. The email I received back made my heart stop and my eyes immediately fill with tears. Her son, at just 6 months old, was diagnosed with atypical teratoid rhabdoid tumor (AT/RT), a rare form of brain cancer. He was undergoing extremely toxic treatments of chemo as there was no drug or therapy formulated specifically for babies. So toxic that she would have to wear gloves to change his diapers as his urine was toxic. Casey fought his battle with pediatric cancer until he was 14 1/2 months old. I can’t write anymore about Casey because I will start crying (again). Please read his CaringBridge site to learn more about the wonderfully cute little baby boy, Casey Kropf.

So yes, this is the really, really bad stuff — the stuff no one wants to talk about because it’s kids and it’s so awful. This is the stuff I tried hiding from for so many years. But the truth is, it’s real, and it is awful, and if we DON’T talk about it, nothing is going to get done. 

About that same time in the summer of 2010, we learned that Taylor Love, who was showing No Evidence of Disease from the neuroblastoma, was diagnosed with chemo-induced leukemia. Yes, you read that right — the very chemo she was given to cure her of neuroblastoma gave her a secondary cancer. Taylor has fought both cancers and is in school living a mostly normal life. But she and her parents live in fear every day of several scary thoughts: will the cancer return and what long-term effects did treating her cancer have on her body?

Unfortunately, our list of “do you know someone who was diagnosed with pediatric cancer” didn’t end with Taylor or Casey. In late 2011, we learned that a client’s 2 1/2 year old daughter, Ava, was diagnosed with Pre-B Acute Lymphoblastic Leukemia, or ALL. Little Ava has been undergoing chemo since 2011, and has six more months to go. And, just about three weeks ago, a long-time friend shared that her 2 year old, Kate, was also diagnosed with ALL. Pictures of Kate from just three weeks ago show a healthy, happy 2 year old. This is a startling contrast to the photo that her mom Lindsay posted today of a newly bald Kate, recovering from a fever and bone marrow biopsy in a hospital bed. This one hit me especially hard as Lindsay and I were pregnant at the same time — I with my third and her with her first. Again, this could be my daughter.

There are more kids — an acquaintance on a yahoo group lost her 11 year old Stephan to a brain tumor. Our friend’s nephew lost his battle with leukemia at age five. A friend’s neighbor also lost their 5 year old son to leukemia. Isabella Santos, whom we heard of through a client and friend, lost her battle with neuroblastoma last year — she was just 7 years old and had been fighting for five years. Now we are up to eight children, and that’s just children in my circle of friends and doesn’t include the many others I read about daily.

After having our eyes open to this epidemic the last several years, there are a few things that have really stood out. The first is that most of the folks out there doing the fundraising and trying to spread awareness are the parents and families of those directly affected. This just isn’t right. They have enough on their plate – it’s our duty to relieve them of that burden. Second, childhood cancer, to us, isn’t rare. We’ve heard the words “proportional funding” and “rare” often in this world of childhood cancer — this needs to change. These kids need more funding; childhood cancer isn’t rare (at least not anymore).

Here are some of the hard truths about childhood cancer from The Truth 365:

  • Of the $5 billion of federal funding allotted for cancers, pediatric cancers receive only 4% of those research dollars.
  • Pediatric oncologists spend 60% of their time fundraising as there is not enough money to keep research flowing for these kids.
  • Childhood cancer is the leading cause of death of children under the age of 5.
  • One in 330 children will be diagnosed with cancer by the time they are 20.
  • Each year, there are 13,500 children diagnosed with cancer.
  • Incidence of invasive pediatric cancers is up 29% in the past 20 years.

  • In 20 years the FDA has initially approved only one drug for any childhood cancer.
  • The average age of death for a child with cancer is 8, causing a childhood cancer victim to lose 69 years of expected life years; a significant loss of productivity to society.

  • Childhood cancer survivors are at significant risk for secondary cancers later in life.
  • Cancer treatments can affect a child’s growth, fertility, and endocrine system. Child survivors may be permanently immunologically suppressed.


After reading this post — and let me warn you, the post is, with every right, edgy — we decided we weren’t going to call our September community outreach “Childhood Cancer Awareness Month,” but instead, “Childhood Cancer Action Month.” What one or two things can you do this month to help these kids? We’ve got some ideas for you, and many of them don’t cost a dime, but will have a profound impact as you spread information about pediatric cancer.

First, here’s what we are doing:

  1. We will be donating $1 from every haircut in September to The Arms Wide Open Childhood Cancer Foundation.
  2. This year, instead of a cut-a-thon which only lasts one day, we wanted to do
    Gold Hair for a Cure

    Gold Hair for a Cure

    something that people could participate in for the entire month. Similar to the Pink Hair for Hope campaign, we are launching a Gold Hair for a Cure campaign. Come and have a SO.CAP gold extension added to your locks for just $10 and we will donate 100% of our profit to finding a cure for pediatric cancer. When people ask why you have a gold hair extension, tell them about Pediatric Cancer Action Month! (And, we have contacted SO.CAP USA to see if they can make this a national campaign. We’ll keep you posted!)

  3. We will be asking every person checking out if they would like to add $1, $3 or $5 to their ticket to be donated to pediatric cancer research funding.
  4. I am hosting a Silpada fundraiser this month. I am donating 100% of my profits from this fundraiser and am raffling off free jewelry for those who order. Need gifts, want something for yourself and want to help? Easy! Shop the fundraiser here.

Here’s what you can do:

  1. Take a Crazy Hair Day for Kids’ Cancer flyer to your school and have your school host a no-cost fundraiser. It’s so very simple. Kids get to wear their hair crazy for a day and they bring in a small donation. We have a flyer for preschool and elementary schools, and one for middle and high schools. When other kids ask why their hair is ‘crazy’ for the day, it’s a *great* opportunity for these kids to share why. Don’t have kids in school? Take a flyer to work and hang it in your office kitchen. And if you are not a client of ours, take the fliers to your salon. Share with your stylist or the owner of that salon. Get them involved in promoting this amazingly easy fundraiser.
  2. Donate to any one of the many organizations helping kids battling cancer. Here are just a few great ones we know about or have donated to in the past: The Band of Parents, The Isabella Santos Foundation, Journey 4 A Cure, Arms Wide Open Childhood Cancer Foundation, and the DC Candlelighters. Please do not think any amount is too small. If everyone gave $1, these organizations and the children they serve would benefit tremendously!
  3. Participate in a walk or run, or triathalon.
  4. Get involved through a social media outreach campaign through The Truth 365.
  5. Watch the Truth 365 Documentary to learn more about the state of pediatric cancer.
  6. Write your Congressperson, and ask him or her to sign The Pledge. We need more than 4% of federal cancer research dollars going toward pediatric cancers.

Hopefully one of these will speak to you. These kids do not have a voice. They are busy fighting for their lives. Be their voice, take action for them.

Our August Community Outreach: Autism Speaks

Autism spectrum disorder (ASD) and autism are both general terms for a group of complex disorders of brain development. These disorders are characterized, in varying degrees, by difficulties in social interaction, verbal and nonverbal communication and repetitive behaviors. They include autistic disorder, Rett syndrome, childhood disintegrative disorder, pervasive developmental disorder-not otherwise specified (PDD-NOS) and Asperger syndrome. An estimated 1 out of 54 boys and 1 in 252 girls are diagnosed with autism in the United States each year.

Jonathan and I have several friends whose children have been diagnosed. Having witnessed their diagnosis as an outsider, we’ve seen the grieving stages the parents go through as they grapple through denial, anger, bargaining, depression, then ultimately acceptance with the disorder. We are oftentimes at a loss with what to say or how to help. It’s frustrating for everyone not knowing the true cause of the disorder. It makes parents question every little thing of the child’s past, all the way to conception, which leaves parents’ minds on an eternal treadmill of questioning thoughts — which for anyone can be exhausting. What we do know about children with autism spectrum disorder is that they are each amazingly gifted and unique. We know they are loved very deeply by their friends and family, even though it may seem at times that these same family and friends are exasperated. The truth is autism is exasperating. It’s also, at times, wonderfully incredible. As our friend said of her sweet, adorable son, “He teaches us something new about ourselves and about the truly important elements of life.”

We’d love for you to take a moment to browse through the Autism Speaks website. For the month of August, Salon Khouri is donating $1 from every haircut to Autism Speaks.

Our July Community Outreach – Keeping Our Kids Safe via The ART of Driving


Ashley Renee Thompson lost her life in a singular vehicular accident on June 10, 2003 — she was just sixteen years old. She was an advanced placement student, a competitive gymnast, and loved by her friends and peers. Her mother created The ART of Driving program in memory of her daughter to increase awareness among teens and parents of the unique risks faced by young, novice drivers and to impress upon them the need for improved training, increased supervised time behind-the-wheel, and increased parental involvement. The ART of Driving is also advocating for improvements in driver education for our youth and seeks to change the mindset of teens and their parents that tragedies like this “won’t happen to me”.

The ART of DrivingIt is our hope to help bring awareness to this organization. If just one parent or teen gains a new piece of knowledge from The ART of Driving that saves a life, then this will have been our most successful community outreach event to date! Please take a moment to Learn the Top 5 Reasons for Teen Crashes and Injuries, as well as an overview of programs offered through The ART of Driving.

For the month of July, Salon Khouri will donate $1 from every haircut to the Ashley Renee Thompson Memorial Foundation.

Our June Community Outreach – Help Us Bridge The Gap

FoodBridge_logoThis June, Salon Khouri will be donating $1 from every haircut to Our Daily Bread Fairfax in support of their Food Bridge program. Also, upon checkout, you can donate $1, $3, or $5 toward this program.

With the down economy, many Fairfax families are struggling. Luckily, Our Daily Bread Fairfax is there to help. Our Daily Bread identifies and addresses the unmet fundamental needs of Fairfax area residents and empowers the community to help these neighbors maintain self-sufficiency. They are a volunteer-based organization focused on easing the plight of low income residents in Fairfax County, drawing volunteers from local faith-based groups, community organizations, local businesses, schools and universities.

We specifically are reaching out to help Our Daily Bread’s Food Bridge Program, which provides short-term food assistance to Fairfax County area residents who are struggling to make ends meet – helping them bridge the gap until they can achieve self-sufficiency. Needy families are referred to the Program by social workers, and generally receive assistance for approximately four to six months. Some clients receive emergency assistance once or twice to get them through a brief crisis.

Here’s how it works, with every haircut the month of June, Salon Khouri will donate $1 toward the purchase of a gift card for the Food Bridge program. Gift Cards allow Our Daily Bread’s clients to meet the specific dietary needs of their family, which many times includes managing specific food allergies. Grocery store gift cards also allow parents to make good nutritional choices for their children that include fruits, vegetables and dairy items that cannot be stored at the ODB panty. In addition, grocery store gift cards help Our Daily Bread’s clients to practice newly acquired financial management skills in getting the most out of every dollar they spend for food. Their Food Bridge Supporters collect and deliver either non-perishable food items and supplies or grocery cards to 30 of their Food Bridge clients each Sunday.

The goal of the Food BRIDGE is to take Our Daily Bread’s clients from a place of crisis to a place that is stable where food insecurity is concerned. Our Daily Bread helps their clients make good choices, teaches them how to manage resources and to go forward with new skills in being informed consumers.

If you would like to volunteer to help deliver food to families, please contact Christina Garris of Our Daily Bread Fairfax at 703-273-8829.

Crazy Hair Day for Kids Cancer – Help Us Spread the Word

Those of you who have been long-time Salon Khouri enthusiasts know our passion for helping children with pediatric cancer. We recently became aware of a grant program from Wella, the color line we use at the salon, called Hairdressers at Heart. This program will donate $10,000 to a salon’s charity of choice. I immediately emailed Mike Gillette, long-time pediatric cancer advocate and the guy behind The Truth 365 to share the information with him and to see if he had any ideas. As usual, Mike came up with a great idea that will not only help raise money and awareness for pediatric cancer funding, but also gets children directly involved in helping. The program is called Crazy Hair Day for Kids Cancer.

Here’s where we need your help. We are just asking you for help with two simple things:

  1. First, we need you to vote, daily, until May 15th, to help us win the $10,000 grant for The Arms Wide Open Childhood Cancer Foundation. Winning the grant will directly fund pediatric cancer research. Not many people realize that there is a severe lack of funding for pediatric cancers, particularly when compared to funding for adult cancer research. In fact, most drugs given to these little guys were developed for adults 20-30 years ago, and never tested on children. These kids need donations from grants and private donors to help them win their fight against cancer with tools made for them. These kids need current medicines designed for them to fight their specific cancers. Many children with cancer are oftentimes made more sick due to the toxicity of the drugs given to them to help them fight cancer.
  2. Second, if you have kids in school, or know someone who does, please see if your school would be open to having a Crazy Hair Day for Kids Cancer. It’s a simple, kids helping kids, no frills fundraiser. We have two flyers available that you can print and bring to your school’s administrative office. For more information on scheduling a Crazy Hair Day for Kids Cancer at your school, please email info@thetruth365.org. We have one flyer for preschool and elementary schools, and one for middle and high schools. Again, every dollar raised from your Crazy Hair Day for Kids Cancer fundraiser will directly fund pediatric cancer research.

Salon Khouri will be donating $1 from every haircut the month of May to The Arms Wide Open Childhood Cancer Foundation. We would love for you to make donations in the amount of $1, $3, and $5 at checkout as well! Also, if your little one would like to stop into Salon Khouri to have a little pink, blue or purple Eufora Creative Streak sprayed into their hair for their Crazy Hair Day, we’d love to help them out at no cost! The spray washes out and is non-toxic. Just give us a ring at 703.273.7878 to let us know you are coming by. And, if your school agrees to do a fundraiser, let us know as well. We would love to send a stylist out to help make kids hair crazy, again, at no cost!

Crazy Hair Day for Kids Cancer

Crazy Hair Day for Kids Cancer

Update 5/25/2013:

We were so thrilled to be invited to Let’s Talk Live to share information about Crazy Hair Day for Kids Cancer. You can watch the video here.

Our April Community Outreach is ….

Some of the piggies from Polyface helping mix the compost.

Some of the piggies from Polyface helping mix the compost.

Growing up, I didn’t think about where my food came from. And sadly, I have to say the same about my twenties. Then, I started a family, and pregnant with my first child, I started to question everything I put into my body. Where did it come from? How was it grown? Was it sprayed with any chemicals? I began to venture out, starting small. I watched a documentary called Fresh, and was blown away by a guy named Joel Salatin. The way he argued his points and explained his passion for sustainable farming draws you in. His vocabulary is eloquent, and his speech is lyrical, forcing you to want to listen. You can see a glimpse of it here, but if you just search Joel Salatin on YouTube, you can find a plethora of interesting videos from Joel. I began ordering meat from his farm, Polyface Farm located near Charlottesville, VA. Polyface delivers to various host sites in Northern Virginia on a monthly basis.

After baby #2, I discovered Fields of Athenry on a Saturday afternoon drive with the kids while Jonathan was busy at the salon. I met the owner, Elaine on our visit there. She shared a lot of great information with me, but what I remembered most was her caring nature. One of her chickens had just had baby chicks. She showed my children and let them hold one of the chicks, then explained how they hatch. She also took them outside and had one of her girls set us up with feeding the baby lambs. I quickly made visiting FOA farm a Saturday tradition that summer, taking the kids to see the animals and learn about where food comes from as well as picking up delicious, fresh meats for the week.

Feeding chickens at Chicama Run Farm

Feeding chickens at Chicama Run Farm

Through my continued exploration of Virginia farms, I signed up for CSAs (Community Supported Agriculture), finding a winter CSA through Moutoux Orchard. (It’s now a year-round food club). Rob at Moutoux grows the most delicious, chemical free peaches I have ever eaten. I discovered another farm from a friend right next to Moutoux called Chicama Run. Dana, the owner and operator of Chicama Run is an amazing woman. I am not even sure if amazing is a big enough word to describe Dana. She cares for her farm, for her family, and for her community. She truly, truly cares about what you feed yourself. She shares a ton of great information on her blog and Facebook page. A great part for the kiddos about visiting her farm is being able to feed all the free range chickens!!

If you haven’t guessed yet, our April community outreach for Salon Khouri is to introduce you to some of these wonderful farmers. Earth Day is later this month and we can’t think of a better way to celebrate than thanking these guys for helping care for the earth through better, smarter farming.

We will also be donating $1 from every haircut this month toward a scholarship to help send a lucky individual to a Polyface Intensive Discovery Seminar where Joel helps teach others sustainable farming practices. If you’d like to donate, you can do so through our Community Page.

* updated 5/25/2013, in lieu of sending someone to the Polyface Intensive Discovery Seminar, we donated to the Farm to Consumer Legal Defense Fund.

Have you got some spare change?

Our March community campaign is to help raise money for the Kids Helping Kids Stop Hunger drive. Please take a moment to watch this brief video to learn more. We are so very encouraged and inspired by these little guys doing what they can to help others!

[youtube https://www.youtube.com/watch?v=dK6la8b97tc]

Please remember to drop your quarters in our collection jar at the front desk. We will also donate $5 from every kids haircut in March to this worthy cause.

Stop Hunger Now is an international hunger relief organization that coordinates the distribution of food and other life-saving aid around the world. The organization is driven by a vision of a world without hunger and a mission to end hunger in our lifetime by providing food and life-saving aid to the world’s most vulnerable and by creating a global commitment to mobilize the necessary resources.

Stop Hunger Now’s meal packaging program provides volunteers the opportunity to package dehydrated, high protein, and highly nutritious meals that are used primarily to support development programs and to save lives in developing countries around the world.

Can we introduce you to an amazing woman?

Minu taking care of herself and her heart -- working hard on the treadmill.

Minu just six months after open heart surgery

I was flipping through my Facebook feed a few weeks ago and saw a slightly blurry picture of a beautiful woman on a treadmill. I’ve shared the photo with you above so that you can hopefully see what I did. There was something about her smile and the happiness dancing in her eyes. She had a look about her like she was ready for an adventure and her demeanor is not just inviting you to go with her, but daring you to. My eyes then glanced at the text above the photo in the Facebook feed: “Who would have known my mom had open heart surgery 6 months ago! Amazing.”

I nearly fell out of my chair and I had to know more. I asked my friend if she would mind bringing her mother in for a little bit of well-deserved pampering at Salon Khouri so that I could talk to her and learn more about the woman behind the mischievous grin.

Minu is 66 years old. She’s been battling high blood pressure for over thirty years. Over the last several years, she has been struggling with bouts of severe depression. During a visit to her cardiologist in 2012, it was discovered that her left main artery was 98% blocked. The scan also revealed that her aorta was about to tear. This came as a complete shock to Minu and her family. Quick to take action, the family met with the Medical Director of Cardiac Surgery of Inova Fairfax Hospital, Dr. Alan Speir, who soon after performed open heart surgery on Minu to save her life. During recovery,  both of Minu’s lungs completely collapsed and Minu was placed in ICU where she fought for her life. But, as you may have noticed from Minu’s grin, she’s a fighter. Just six days later, Minu was on a path to recovery and was released soon after. She began cardiac rehab sessions every other day for three months, and now visits for follow-ups, and to show off her amazing shape!

A gift that Minu serendipitously received from having the surgery is that her depression is now almost subsided. We both chatted about the possibility of the lack of proper blood flow that could have been a major contributor to her depression. I asked her what she now does to remain healthy and she proudly replied that she exercises thirty minutes a day and lifts light weights to keep her heart and body in shape.

As you may know, February is heart awareness month. Last February, we launched a “color for hearts” campaign at Salon Khouri, donating $5 from every hair color to the American Heart Association’s Go Red for Women fund which we are again doing this year. I fell in love with Minu — her passion, her warmth, her teasing smile and playful eyes. We have nominated her as our role model for women’s heart awareness. Her story is remarkable and her determination is absolutely something that we can all be encouraged by.

Minu after a little pampering at Salon Khouri

Minu after a little pampering at Salon Khouri. Photo by Aliyah Dastour of Alimond Photography.

We love our clients and our community. If you ever have feedback on our salon or our blog posts, please always let us know.


Jennifer Elkhouri
co-owner, Salon Khouri

Have a heart for HART

Our January community effort is to raise money and awareness for a wonderful organization called Homeless Animal Rescue Team (HART). We adopted our dog, Bogart, from this organization in 2000. Our experience with them was amazing. The care they put forth for ensuring Bogart was going to a good home was impressive. We hope that we can help this organization out through our salon’s community giving project. Take a moment to browse their website. Who knows, maybe you will find a Bogart to adopt for your family!

Furry friends rescued by HART

Furry friends rescued by HART

For the month of January, we will be taking donations at the salon for HART. We will also be donating 10% from the purchase of all Jennifer’s Silpada sales as well as 10% from the purchase of all Wella products to HART. To purchase a piece of handcrafted, .925 sterling silver Silpada jewelry for this fundraiser, visit Jennifer’s site and be sure to select Homeless Animal Rescue Team as the hostess at checkout.