Cancer Treatment

Overcoming the Trauma of Having Cancer

“My past is an armor I cannot take off, no matter how many times you tell me the war is over.”

“My past is an armor I cannot take off, no matter how many times you tell me the war is over.”

Tomorrow I will walk through the doors of the Lurie Cancer Center as I have many times before. This routine has become all too familiar. Over nine months of treatment mixed with numerous other visits and hospitalizations allows me to walk the halls of Northwestern with ease and eerie familiarity.

It starts with a visit to port draw to get my blood drawn. This is hands down one the hardest part of the visit for me. Hours before my appointment I begin preparing for this by applying a numbing cream to my chest port—a small device surgically implanted into my chest that helps deliver medication and make for easier blood draws during treatment.

For many cancer patients, our port devices stay in long after our cancer treatment—sometimes for years because of the risk for potential relapse.  Until then, it requires routine flushes by a medical professional. While showering or getting dressed, this protruding bump in my chest is a constant reminder of my treatment and the fact that my journey is far from over.

Next, I will wait to see my oncologist and get the results of my latest blood work. I will hold my breath as she palpates the lymph nodes in my neck, chest and lower body. I pray that I hear the words, “Everything looks good. See you in a few months.” Yet I also try to mentally prepare myself for the potential ‘what ifs’. Will I need another repeat scan? What if my blood work is off?

Many people believe that going into “remission” means victory—that one has defeated their disease and they have moved on to recovery. Surely, remission marks a major turn in cancer care, but it is more complicated than simply being done with cancer treatment.

The following is a vivid glimpse into the reality of being a cancer survivor.


Imagine you're going about your day, minding your own business, when someone sneaks up behind you...

You feel something press up against the back of your head, as someone whispers in your ear.

"Sssshhhhh.... don't turn around. Just listen. I am holding a gun against the back of your head. I'm going to keep it there. I'm going to follow you around like this every day, for the rest of your life."

"I'm going to press a bit harder, every so often, just to remind you I'm here, but you need to try your best to ignore me, to move on with your life. Act like I'm not here, but don't you ever forget... one day I may just pull the trigger... or maybe I won't. Isn't this going to be a fun game?"

This is what it is like to be diagnosed with cancer. Any STAGE of cancer. Any KIND of cancer. Remission does not change the constant fear. It never truly goes away. It's always in the back of your mind.

Please, if you have a loved one who has ever been diagnosed with cancer, remember this. They may never talk about it or they may talk about it often. Listen to them.

They aren't asking you to make it better. They want you to sit with them in their fear... their sadness... their anger... just for the moment. That's it.

Don't try to talk them out of how they are feeling. That doesn't help. It will only make them feel like what they are going through is being minimized. Don't remind them of all the good things they still have in their life. They know. They are grateful.

But some days they are more aware of that gun pressing into the back of their head and they need to talk about it. Offer them an ear.

Source: The Teal Society, @thewombtangclan


No Evidence of Disease, Lingering Trauma

There is no timestamp on trauma. There isn’t a formula that you can insert yourself into to get from horror to healed.
— Dawn Serra

In the US, 1 in 2 women and 1 in 3 men will develop cancer in their lifetime. It is often said there are four phases to dealing with cancer; diagnosis, waiting for test results, treatment and the period following treatment or remission.

Thanks to advances in treatment and early detection, more people than ever are becoming cancer survivors.  As survivors, it’s often understood but less often spoken about that the assault to our bodies and minds as cancer patients extends far beyond our last treatment cycle.

Remission itself brings reassurance and a sense that period of calm and recovery is now within reach. You have been given a second chance to rewrite the rules and try living differently with greater appreciation. In truth, remission does NOT mean you are all clear. Instead, remission the hope that your active cancer treatment is about to be a closed chapter in your life. It means finding a way to move forward while still under routine monitoring for potential relapse.

 Life goes on and relief flourishes after you are told you are in remission. Then, a few months go by and the next appointment looms on the horizon. The cycle of dread and worry repeats. This cycle repeats over and over for the first few months and sometimes up to five years or more after you are diagnosed.

I’ve learned part of living in remission is learning to manage the fluid emotions of joy and gratitude intermixed with the feelings of guilt, shame, anger and fear. Post-cancer life is often interwoven with moments of empowerment followed by a somber reckoning that this way of life has become your “new normal.” There are periods of immense joy and elation that come with the news you are “in remission.” Then there are long periods of waiting and worrying if the next visit to the doctor will bring more freedom or news of a potential relapse.  There are countless daily reminders of what you have been through and the reality of what could be around-the-corner.

Guilt

At times, I’ll be the first to admit I often feel a sense of guilt when it comes from my cancer treatment. Guilty for being able to receive one of the latest advancements in cancer treatment (immunotherapy) and surviving when so many others who were diagnosed after me, some younger than I, have since died. Guilty for going on about my cancer journey long after my treatment has finished. Guilty for not always remembering to be thankful and seize the day. And guilty for all the trouble and worry I put my loved ones through.

Anger

Some people (myself included) become angry after treatment. Some struggle to get past the trauma, while others learn from it and use it as a catalyst to live life in a completely different way. Any traumatic life event that you go through will leave scars and people survive in different ways. Chemo and radiation save our lives, but they also cause a hell of a lot of side effects, including secondary cancers and painful, lingering side effects like neuropathy and gastrointestinal issues.

Feeling Broken

For most cancer survivors, the first year in remission is often the most difficult This is because when you’re in remission, it finally hits you that you literally almost died and spent the majority of the last year fighting for your life. It’s a startling realization to take in and fully process. When you’re going through treatment, you’re in survival mode—too sick and tired to actually realize what’s really going on. Remission lends the opportunity to reflect on the good and the bad. Getting diagnosed and treated for cancer can leave you at times feeling broken, helpless and largely distrusting of your body. In my experience, remission at first turned my survival mode into a state of hyper-vigilance where any unusual symptom made me flip out and almost convinced I was in the throes of a possible relapse.

Cancer survivors are tasked with carrying on with their lives by learning to adapt to a “new normal” that comes with being in remission. We must rediscover who we truly are under all the layers of trauma our cancer treatment may have caused. We must learn to find our footing and move forward amidst the shifting sands of fearlessness and fear, confidence and worry, relief and calm, certainty and uncertainty. Our sense of cautious optimism grows with each disclosure that our cancer has not spread and there is no evidence of disease. Over time, we learn to breathe a little easier, while the fear is always there—it seems to move further and further to the back of our minds.

Addressing and understanding the emotions you are experiencing as a result of cancer or any disease is difficult. It’s painful. But I’ve come to learn and accept it’s entirely necessary to heal. Seeking out community—a therapist, friend or family member, or a support group of others who have experienced similar trauma like cancer—is a crucial step in recovery. I’m hopeful that in time I will be able to transform this horrible, traumatic experience from an endless stressor into a source of strength.

Overcoming Fear with Gratitude

One way I am trying to overcome my anxiety and lingering fear regarding my treatment is by expressing daily gratitude. The latest research in neuroscience shows that when we practice gratitude we are actively rewiring our brains and naturally boosting our serotonin levels. According to neuroscientist  Dr. Alex Korb, all we need to do is simply ask, “What am I grateful for?” No answers are necessary. Just searching helps.  

Some ways to practice gratitude:

  • Keep a gratitude journal.

  • Tell a loved one or a friend something you appreciate about them.

  • Look at yourself in the mirror and think of something you like about yourself.

  • Sit in a quiet place and think about when something went well. How did that feel? Practice that feeling every day for a week.

  • Next time something bad happens consider 5 good things that happened as a result of this event.

  • Write someone a thank you note.

  • Write it down, talk about it, think about it, re-live it, meditate.

 

It has been said that trauma creates change you don’t choose; whereas healing creates change you do choose. There is a great transition from patient to survivor. I believe the journey from patient to survivor begins with patience. We must be patient with ourselves and give our bodies and minds time to heal from all the trauma we have endured. Healing comes moment by moment and one breath at a time.



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Sources:

  1. Cancer Truths- The Teal Society  

  2. '1 in 2 people will develop cancer in their lifetime'- Medical News Today, 2015

  3. The Upward Spiral: Using Neuroscience to Reverse the Course of Depression, One Small Change at a Time  by Alex Korb, PhD

What I Learned a Year into Remission

May 1st, 2019 marked 1 year in remission from Stage 3 Classical Hodgkin’s Lymphoma.

May 1st, 2019 marked 1 year in remission from Stage 3 Classical Hodgkin’s Lymphoma.

In the depth of winter, I finally learned that within me there lay an invincible summer.
— Albert Camus

A year ago I got the call saying my latest scan showed there was no cancerous activity in my body. I officially made it to the other side of my diagnosis, but I still had 4 months of chemo left.

A year into remission, I’ve found hardest part of remission is simply being. During treatment the goal is to reach remission but once you do, you’re often left feeling...okay now what? What do I do next? Resuming your old ways seems impossible. So ...much in your life has changed. Some things for the better. Some for worse.

My cancer journey has taught me accepting the changes— both positive and negative are part of healing. Healing is a paradox. It’s a constant push and pull between watching your appearance drastically change while celebrating any progress you make towards healing. Because all these bodily changes indicate something very powerful is happening, right?

I had big plans to celebrate my first year of remission. I planned to run in my first 5K at Northwestern next month. But as I started to train and push myself to get into shape I soon realized my body isn’t ready…YET 😉

So this year I may walk the Northwestern’s Cancer Survivors’ 5K instead of run but I’ve decided any positive change is PROGRESS. Instead of pushing myself to accomplish lofty goals, I’m giving myself grace. Grace to not push myself so hard and enjoy the healing process one day at a time.

Healing is becoming whole again and that wholeness comes in many forms. We are shaped by our positive and negative experiences. But I’m slowly learning it’s how we find balance that truly makes all the difference.

Today, I’m so grateful to be able to enjoy dinner at home with my family. We’re counting our blessings and hugging each other a little tighter tonight. I hope I am fortunate to count my remission by the number of years but until then I am learning sometimes all you can do is not think, not imagine, not obsess. All you can really do is take a deep breath and have faith it will all work out for the best.



If you want to donate or join me next month for the Northwestern Cancer Survivors’ 5K please visit my team site: https://secure2.convio.net/nmhc/site/TR/Walk/EVE_LCCWALK…

Thanks for your continued prayers and support!

Scanxiety: 6 Ways to Cope

“Every three to four months I get a wake-up call that my life has taken an unexpected turn. Believe me, there are daily reminders of how different I am now; but scan time is big time scary time, mentally. It takes living with cancer to yet another l…

“Every three to four months I get a wake-up call that my life has taken an unexpected turn. Believe me, there are daily reminders of how different I am now; but scan time is big time scary time, mentally. It takes living with cancer to yet another level of heighten sense of mortality and anxiety. So MANY thoughts and what ifs course through my brain. SO hard to shut it off.” – Katie Edick, METASTATIC AND MAKARIOS.


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One of the hardest parts about cancer is the waiting. Waiting for results. Waiting for answers. Waiting to know if you’re in remission or the fight is still raging on.

 Going through cancer treatment is like being on a giant emotional roulette wheel that spins you around for a few days and then shoots you out the other side. Land on red, you’re in for another trip to Cancerland; land on black, you have three more months of freedom  until your next scan. Couple that with my tendency to pass out from needles/ stress and you have a recipe for some serious scanxiety. Fortunately, my life-long battle with anxiety has taught me some good ways of coping with such gut-wrenching uncertainty.

Here are 6 ways to cope with scanxiety:

 

1.       Sometimes, the unknown is the greatest cause of our anxiety. Cancer treatment brings a new level of uncertainty to your life. If you are unclear about anything from what to expect during the scan, to when and how you can expect to receive your results, or what those results might mean, don’t be afraid to ask your doctor. I’ve found having a clear understanding of what you may or may notexperience allows you to be better prepared and often helps calm your mind.

 

2.       Distraction is often the best antidote for anxiety. Before my scan, I make sure to watch some funny videos or clips of my favorite movies. I also listen to music while waiting for my appointment to help relax my mind and shift my mindset. After my scan, I do my best to stay active and preoccupy myself with work, or exercise or household projects. Yoga and walking meditations are some of my favorite ways   to stay active when I’m not able to do more strenuous exercise like running.

 

3.       Focus on your breathing. During my test, I keep my eyes closed the whole time and focus on my breathing. Fast, shallow breathing increases anxiety. I make sure to take a big deep breath and hold it, then slowly breathe all of the air out of my lungs. Once I get that breathing down I add a mantra. A powerful mantra I love to use is “I am (breath in, pause, long exhale) my breath”. This helps me quiet my anxious thoughts and stay more present.

 

4.       Remind yourself this is only temporary. Worrying can be a great distraction but it really never solves anything. Worrying my cancer will return or that it has returned robs me of precious moments. Moments where I’m still very much in remission...so why waste that time worrying about something that may or may not be true?  Worrisome thoughts will arise but I do my best not to entertain them for long. Instead I try to shift my focus to the things I can control each day and make those my priorities. I remind myself to be grateful I’ve reached remission, no matter how long it lasts.

 

5.       Prepare for the worst but visualize the best possible outcome. Scanxiety often feels like a rollercoaster of hoping for the best but preparing for the worst. Creating a strategy for the worst-case scenario can give you a better sense of control. Cancer often makes you feel powerless, but creating a basic action plan just in case can help you regain your power as well as help you maintain a more optimistic and resilient attitude.

 

6.       Your mind is more powerful than you realize. Visualization and guided imagery have been shown to improve your mood, control symptoms or side effects and even boost your immune system. Imagine yourself receiving great news after your scan. Allow yourself to experience the feelings of relief, gratitude and elation. Think about these things as though you are remembering them. Seeing it in your mind’s eye can give you the reassurance you need to overcome your scanxiety.

 

Remember, while we can’t control what is happening to us in life, we are always in control of how we respond to what’s happening.

 

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To the Doctor(s) that Misdiagnosed Me:

Throughout history, doctors have often been looked up to as gods for their ability to heal others. But even the best and brightest people make mistakes. Upon graduating from medical school doctors take a Hippocratic Oath professing to “first do no h…

Throughout history, doctors have often been looked up to as gods for their ability to heal others. But even the best and brightest people make mistakes. Upon graduating from medical school doctors take a Hippocratic Oath professing to “first do no harm”. But in certain cases, it is believed by many doctors that it may be better to do nothing rather than intervening and potentially causing more harm than good. As patients, here are 5 things we would like you to remember before you diagnosis us.


To the Doctor(s) that Misdiagnosed Me:

In my 30 plus years on this planet, I’ve been the unfortunate witness to the wide spectrum of care that exists in the medical field. As a cancer survivor, and after personally dealing with several chronic medical conditions myself, as well as both my daughter’s and husband’s serious medical conditions (heart surgery and brain surgery), both which required almost immediate life-saving surgical intervention upon diagnosis, there are 5 important things that I would like you to keep in mind when diagnosing a patient or a member of their family with a potentially life-threatening illness.

1.    We are beyond scared. Please be patient and kind. We may be just another patient on your schedule or a last-minute appointment that got added to your day, but please keep in mind patients often seek out the best medical experts when we are in life or death situations. We are scared for our lives. We want reassurance and false hope if necessary, to get us through this difficult time. Please remember to see us as fellow humans first. Patients second. 

 

2.    We are more informed patients thanks to Google and other online resources. Thanks to technology, I now walk around with 24/7 to my complete medical history for the last 4 years of my life. I have access to every blood test, scan and test result you can think of. I also have access to medical research articles and you’d be surprised by the valuable medical information you can get from Facebook and other online support groups filled with other’s going through similar health struggles. Please respect my ability to research my medical condition and listen with an open mind to my concerns regarding my health.

 

3.    By the time we are coming to see you, we have likely consulted with numerous other doctors and specialists. As moms and wives, we are often the ones in the family who are often on the frontlines of our families’ medical struggles. We manage the appointments and research the best doctors and specialists we feel can best help us. Please see as us more than as an unnecessarily worried, anxious, stressed ‒or worse a hypochondriac, a person who has an irrational underlying fear or belief of having a serious disease without medical evidence to back up their symptoms. Sometimes fears are valid. Sometimes it is CANCER or the worst possible scenario so all options should be explored until a valid theory is reached.  Sometimes symptoms can’t be explained with routine tests.  Please take the time and have the patience to get to the root cause of my issues, rather than simply prescribing me a prescription and calling it a day or dismissing my concerns as simply “in my head” and that “I’m simply stressed or depressed” and should seek out some ways to reduce my stress levels.

 

4. “Statistical improbabilities” exist. I’m one of them. As a cancer survivor, I’m a walking medical statistic and so is my daughter and my husband. No matter how outrageous my claim or statistically unlikely based on your initial assessment, realize that the human body is a mysterious and complicated machine and although you are extremely well-educated and highly trained, even the best doctors overlook symptoms and miss diagnoses. Please dig deeper and don’t settle for the first, easiest explanation you come across. If something doesn’t make sense, please continue to investigate.

 

5.    I’m trusting you with my life or the life of my loved one.  As humans, most of us are on the cusp of life and death all our lives and may never realize it. But as a mom to a child born with a congenital heart defect, a husband who had a serious brain malformation and now as a cancer survivor myself, I understand first-hand how fragile life can be. However, I also believe in miracles and the incredible power of people like you to help fix our broken bodies and uplift our spirits by giving us the power to have hope even in our worst times. Hearing you or someone you love has a life-threatening diagnosis is almost indescribable. But as a patient, what matters MOST are the words that come next. I’ll never forget hearing the words from my Ear, Nose and Throat Specialist on November 27, 2017:

You have Hodgkin Lymphoma. This is a type of cancer that starts in your white blood cells which are part of your immune system. However, this is extremely treatable cancer. Even curable in a lot of instances.

When I first met with my oncologist who specializes in my type of lymphoma cancer. One of the first things she did after explaining my diagnosis, was to compassionately look me in the eyes, hold my hand and tell me, “My job as your doctor (and a mother myself) is to cure you.” I believe her conviction at that moment was instrumental in helping me have the courage to go through with pretty aggressive 9 months of cancer treatment. And thankfully I did because I’m now in remission, largely to my doctor’s clinical trial and the trust we established during my initial consultation. Please remember that you are giving more than a diagnosis. You are sometimes giving a life-changing label, one that once spoken out loud by an esteemed medical professional can be quite unforgettable and even damaging‒ whether or not it is correct. Please also be careful with how you explain our diagnosis. As a patient and the mother of a patient, I want the good, bad and ugly. I want to be prepared by educating myself on all possible outcomes so I know what to expect. And remember, if you don’t tell me, I’ll probably just look it up on online anyway.



The Hippocratic Oath:

I swear by Apollo the physician, and Asclepius, and Hygieia and Panacea and all the gods and goddesses as my witnesses, that, according to my ability and judgement, I will keep this Oath and this contract:

To hold him who taught me this art equally dear to me as my parents, to be a partner in life with him, and to fulfill his needs when required; to look upon his offspring as equals to my own siblings, and to teach them this art, if they shall wish to learn it, without fee or contract; and that by the set rules, lectures, and every other mode of instruction, I will impart a knowledge of the art to my own sons, and those of my teachers, and to students bound by this contract and having sworn this Oath to the law of medicine, but to no others.

I will use those dietary regimens which will benefit my patients according to my greatest ability and judgement, and I will do no harm or injustice to them.

I will not give a lethal drug to anyone if I am asked, nor will I advise such a plan; and similarly I will not give a woman a pessary to cause an abortion.

In purity and according to divine law will I carry out my life and my art.

I will not use the knife, even upon those suffering from stones, but I will leave this to those who are trained in this craft.

Into whatever homes I go, I will enter them for the benefit of the sick, avoiding any voluntary act of impropriety or corruption, including the seduction of women or men, whether they are free men or slaves.

Whatever I see or hear in the lives of my patients, whether in connection with my professional practice or not, which ought not to be spoken of outside, I will keep secret, as considering all such things to be private.

So long as I maintain this Oath faithfully and without corruption, may it be granted to me to partake of life fully and the practice of my art, gaining the respect of all men for all time. However, should I transgress this Oath and violate it, may the opposite be my fate.

Translated by Michael North, National Library of Medicine, 2002.


Sources:

The Hippocratic Oath

https://www.nlm.nih.gov/hmd/greek/greek_oath.html

Myth or Fact: Is "First Do No Harm" Part of the Hippocratic Oath?

https://www.thoughtco.com/first-do-no-harm-hippocratic-oath-118780




Hair Today. Gone Tomorrow.

My hair loss journey from Stage 3 Classical Hodgkin Lymphoma, a type of cancer that starts in white blood cells.

My hair loss journey from Stage 3 Classical Hodgkin Lymphoma, a type of cancer that starts in white blood cells.

My hair loss journey from Stage 3 Classical Hodgkin Lymphoma. Diagnosed in November, 2017. Currently 9 months in remission and counting thanks to immunotherapy and AVD chemo. Learn more about my treatment here.

My last chemo was August 9, 2018. I was notified I was officially  in remission on May 1, 2018 prior to completing my full 6 cycles of chemotherapy.


One of the most difficult parts of the cancer journey is watching your appearance or the appearance of someone you love drastically change before your eyes. Watching my reflection slowly change was one of the most painful parts of my cancer journey, particularly losing my hair, because once my hair began to go, everything became SO REAL.

When clumps of my hair started to fall in the shower, I watched in horror as the amount slowly gathered by the drain. All my life, I have been blessed with thick, beautiful, healthy hair. I never in my life did I ever think I would ever have to worry about losing it… but there it was slowing going right before my eyes. 

Where at one time my hair was so thick, I could snap a rubber band just with the sheer weight of my ponytail, now there was nothing I could do to stop the growing patches of my scalp that were beginning to show.  I tried makeup to cover my growing roots from my last color months before my diagnosis. After all, I was going to lose my hair, what was the point of a touch up now?  My hair was becoming a mess but it was the least of my worries. I knew in my heart holding onto it was a losing battle.

“Mommy, are you gonna lose all your hair?”

As a woman and a mom of three young children, losing my hair was one of the most gut-wrenching things I have had ever tried to explain to my children, particularly my youngest twins who were 3 at the time.

Once you find you or your loved one has cancer your thoughts immediately go to hair loss. Pictures of chemo patients you have seen in movies and on TV float through your mind. I know because it went through mine.

You start to search for all the remedies to counteract hair loss: Castor oil. Cold Caps. Extra biotin supplements. You cling to stories where others went through chemo and were fortunate to go through treatment and not lose all their hair.

I thought preparation of some sort was definitely a necessity. Once my diagnosis was confirmed, I got a couple books for my children to read to help them understand what our life was going to be like and most importantly what mommy was going to maybe look like for the next few months. One of the best books I got for my young twins was “Nowhere Hair” by Sue Glader which offers a  wonderful way to explain hair loss to young children.

As much as I knew I could deal with my changing appearance by wearing hats and wigs, I knew mommy’s changing looks could be scary for my children so I wanted to be compassionate and considerate of their feelings too. I thought it would be best to let nature take its course and not try to do too much to prevent my hair loss. I decided I would shave my head if it became absolutely necessary, but I was hopeful that my thick hair would be able to weather the trauma of treatment.

Before I began treatment I had shoulder length thick wavy hair. Before I began my immunotherapy treatment I decided to cut it as short as possible, while still being able to pull it back into a ponytail.

During my three infusions of Keytruda prior to chemotherapy, I was fortunate not to experience any hair loss. The only hair loss I can attribute before I began chemo was likely an effect from all my scans prior to being diagnosed and then during the staging process. 

The Hair Loss Begins

Most hair loss for patients having the AVD or ABVD chemo regimen like I had for my Stage 3 Classical Hodgkin’s lymphoma significantly increases by the 4th chemo treatment.  I definitely noticed my hair loss picking up at that point. Many other lymphoma cancer survivors report hair loss starts after the second chemo treatment. I’ve also heard of people would did not lose all of their hair even with several cycles of chemotherapy.  Other patients with RCHOP chemotherapy report different patterns of hair loss. Some people just reported extreme thinning. I believe I would classify as extreme thinning because I never ended up shaving my head during treatment. Once it got bad I started wearing wigs and had fun experimenting with different hairstyles.

The worst of my hair loss from stage 3 Hodgkin Lymphoma. This is the aftermath of 3 cycles of Keytruda immunotherapy plus 6 cycles of AVD chemo. 6 cycles = 12 individual chemo treatments.

The worst of my hair loss from stage 3 Hodgkin Lymphoma. This is the aftermath of 3 cycles of Keytruda immunotherapy plus 6 cycles of AVD chemo. 6 cycles = 12 individual chemo treatments.

A look at some of my different wigs.

A look at some of my different wigs.

Making the Most of My Hair Loss

Through the first part of my chemo, I made the most of my hair loss by wearing slouchy beanies and winter caps because my chemo treatment started in February in Chicago. However by midway through my treatment around May I knew I was going to need to consider starting to wear a wig.

The changing weather made wearing hats uncomfortable. I decided to look into my insurance benefits to see if they reimburse for a wig and surprisingly a wig was a covered benefit.

It’s important that hair loss in chemo takes many forms than just the hair on your head. It means hair anywhere is up for grabs. Leg hair. Eyebrow hair. Nose hair.  Even those pesky other hairs women get. Which meant less shaving for once in my life. Sweet victory!

After having long, thick hair all my life one of the greatest blessings is now how must faster I can get ready. And how much money I can save on hair styling products because now I can share them with my husband.  Always a silver lining.

Going through cancer has taught me time and again that even our most difficult seasons can bring many blessings if we know where to look. Sometimes, when we hardly recognize the face staring back in the mirror, that’s okay. It’s okay when that happens because I believe it means we’re in the midst of transforming into something better.

Losing my hair has helped me gain a new level of self-confidence. Never in my life did I ever think I would proudly rock this short of hair. I thought for sure I’d stay in my wig for months. But, as of right now, I’m also enjoying rocking a lot of hats too.

Hair loss is a journey for everyone, regardless if you are the patient yourself. It’s important to do what you feel is best, when you feel it is best. I learned there is no magic time table. But thankfully, I also learned hair grows back pretty quickly.

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 Hair Loss Resources for Cancer Patients

Real-hair wigs can cost thousands of dollars and are often only partially covered by health insurance, but there are ways to get wigs for FREE:

  • American Cancer Society: To support cancer patients undergoing chemo, the American Cancer Society offers brand new FREE wigs at wig banks and cancer centers around the country. Click Here and go to the “About Us” tab for resources in your area. Or call 800-227-2345.

  • Cuts Against Cancer: This nonprofit organization and foundation is dedicated to creating and donating free Medical Wigs for women and children who cannot afford to purchase a Real Human Hair Medical Prosthesis. For a FREEwig for anybody facing hair loss from any type of cancer living anywhere in the world, Click Here.

  • Friends are by Your Side: Celebrity hairstylist Martino Cartier founded this charity to help cancer patients get FREE wigs through a network of hundreds of salons across the US, Canada, Mexico, England and Australia. Click Here to see whether there is a salon in your area.

  • Lolly’s Locks works with wig providers across the country to connect cancer patients in need with high-quality wigs. Created in honor of Lolly Toll, who lost her life to cancer in 2012. Lolly understood the relationship between looking good and feeling good, and it was her wish to help those who could not otherwise afford a stylized wig. Click Here

  • EBeauty Community Inc.: Provides FREE wigs for cancer patients undergoing chemotherapy treatments. They also have a national wig exchange program through which you can donate wigs you no longer need to others who do. To request a wig or donate one, Click Here

  • HairToStay: This nonprofit offers need-based grants to offset the expense of scalp cooling systems for breast cancer patients in the US to minimize hair loss during chemotherapy. To learn more, Click Here

Good to Know

  • It takes at least six ponytails to make one wig. If your friends and family have hair to spare and want to help the cause, tell them about the Pantene Beautiful Lengths campaign that collects healthy hair to make FREE wigs available to cancer patients at the American Cancer Society’s wig banks. Donated hair must be a minimum of 8 inches long (measured from just above the elastic band of a ponytail to the ends). Click Here, or call 800-945-7768, for more details and where to donate.

Source:  https://breastcancerfreebies.com/wigs/

Books to help children understand hair loss from chemo:

“Nowhere Hair” by Sue Glader

Amazon link: https://www.amazon.com/Nowhere-Hair-Explains-Cancer-Chemo/dp/0984359168/ref=sr_1_1?ie=UTF8&qid=1549460550&sr=8-1&keywords=nowhere+hair

“Our Mom is Getting Better” by Alex Silver

Amazon link: https://www.amazon.com/Our-Getting-Better-Alex-Silver/dp/0944235859/ref=sr_1_1?ie=UTF8&qid=1549460629&sr=8-1&keywords=Our+mom+is+getting+better