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Vaginal and Vulvar Dryness & Pain

 

Sexual Desire (Libido)

 

Practical Strategies: Where to Start

 

Sexual Activity & Relationships

 

Hormones & Treatment Decisions

 

Hormones & Treatment Decisions

 

Safety Questions

 

Getting Support

Finding Your Style

Dressing a Changed Body

Weight Changes & FLuctuating Sizes

Comfort, Side Effects, & Personal Needs

Shopping, Budget, & Overwhelm 

Suncare During Radiation Treatment

As a general rule, you don’t want any sun exposure on a treatment site while receiving radiation treatment. Always check with your radiation oncologist before using sunscreen if you are undergoing radiation. Your doctor may not want you to put sunscreen because the skin is prone to injury.

General Sun Protection Tips During Cancer Treatment

Use a sunscreen that is specially formulated for your face that delivers both UVA and UVB protection in a broad spectrum SPF 30 or higher.

Apply sun protection daily and liberally – a dollop about the size of a golf ball – to all exposed skin, such as the lips, ears, scalp, sides and back of neck, and exposed chest.

Get in the habit of applying sun protection every morning, about 20 to 30 minutes before going outside, and reapply often – about every two hours.

Remember that you’re still exposed to UVA/UVB rays even in the shade.

Stay inside during the intense-sun hours of 11 a.m. to 4 p.m. Though remember: If you’re indoors, windows offer no protection against UVA rays.

Don’t forget to wear a hat – preferably one with a wide brim of about three inches.

Remember:

Put your sunscreen under your makeup. (Apply sunscreen first). SPF numbers aren’t cumulative. If your moisturizer and foundation both have an SPF of 15, it doesn’t mean that you’ll have a protection of SPF 30.

UVA and UVB rays:

UVA

UVA is long-range ultraviolet radiation that has the ability to penetrate deep into the skin, causing immediate tanning, premature skin ageing and can play a role in the development of certain skin cancers. UVA is not readily absorbed by the ozone layer – about 95% gets through.

UVB

UVB is short-wave ultraviolet radiation that can penetrate the epidermis and is responsible for delayed tanning, sunburns and most skin cancers.

A large portion of UVB is absorbed by the earth’s ozone layer – only 5% reaches the planet’s surface.


Source: Health Canada

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Cancer runs in my family — it has affected six out of eight siblings, my mom, my aunt, my grandmother, my cousins, and even my niece and nephew. But I’ve never let it define me. I don’t even like to use the “C” word — I call it “the unwelcome intruder.” It infiltrated my body and so now we’re just working on getting it out of there. I don’t allow it to control me or have authority over my body.

Throughout my treatment, some things have stayed constant in my life, and this grounds me. I’ve kept working, because I love my job and it gives me a sense of normalcy. My children are there for me — I’m a single mom of four kids, 22-year-old triplet daughters and a 24-year-old son. I love going on walks with my little nine-year-old Havanese and reading psychological thrillers.

My faith has been another constant source of strength. When I had a recurrence of the unwelcome intruder, I prayed a lot. I was like, “I can’t go through this a second time. Lord, what are you doing?” And I received a message saying that this was not a journey I was to take alone — that this was going to be a community-based journey for me. I have a habit of isolating myself, especially during times of struggle. Thanks to this message that came through, I’ve been staying connected and sharing my journey, especially through the women’s connect group at my church. We all go through struggles in our lives, and my hope is that by sharing mine, it’ll help people to see their own challenges in a better light and to know they’re not alone or stuck. I know there’s an end to this.

It wasn’t just my church community, either. Once I decided to overcome my habit of cutting myself off from others, I was surprised at how vast this community travelled. More and more people outside of my church, outside of my faith, have come to walk alongside me. They send texts, stop by, bring me meals, go for walks with me, and even attend appointments. It has been really uplifting, encouraging, and inspiring. I feel held and supported.

This community extends to Look Good Feel Better (LGFB) as well. Losing my hair was a big thing for me. I cried and cried for weeks on end in anticipation. I just turned 61, but I don’t feel old —and I didn’t want to look old, or sick. My hair started falling out just two days before my LGFB workshop. I felt really shut down. I almost didn’t go. But I’m so glad I did, because the workshop really helped me get through it. 

I loved how the volunteer talked about hair loss — so calmly, so casually. She’d rip off her wig, put on another, and then switch to a bandana. Something opened up in me when she was doing that. It felt so freeing. I realized I was no longer stuck to my hair, and that it was okay that it was gone. My hair falling out felt like the end of the world for me, but the workshop helped me realize that hair is just hair. It doesn’t define who I am. This new perspective changed the entire trajectory of my journey. The workshop gave me my life back, basically. It was so empowering. As a bonus, I’ve been having a lot of fun with wigs, trying different hair styles and colours.

My positive mindset has really helped me through this journey. Prayer, connection, community — these have been instrumental. And I really do treat this as a journey — not just a medical, physical journey but also a mental, spiritual, soul-deep transformation. I don’t have to worry about the unwelcome intruder in my body because that’s what my medical team does. My responsibility is to make sure that I’m staying as healthy as possible, physically and mentally. I’m not just focusing on the cancer, but on making myself better. 
 

Cleansing and Moisturizing

Skincare Ingredients and Treatments

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Choosing Head Coverings

Care and Maintenance

Special Considerations

Scarf Styling and Techniques

Still have questions? We cover these topics and a LOT MORE in our workshops.

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Application Techniques

Foundation and Base Makeup

Eyebrows

Eye Makeup

Lip Care

Makeup Hygiene and Safety

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Nail and Hand Care

Is treatment impacting your nails?

Find help in our Nail Care Workshop.

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Post Surgical Products

Prostheses Basics

Fitting & Clothing Tips

Nightwear & Sleep Support

Care & Maintenance

Skincare During Radiation

Nipple Appearance Options

Access & Financial Help

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Find resources and community in our Bras & Prostheses Workshop.

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By Adriana Lombardo

I went for chemotherapy at Princess Margaret Cancer Centre once a week for two years.

The first time I went I didn’t realize I’d spend a full day there. I didn’t know what to pack at first. I brought along one water, a granola bar, and a book to my first chemo appointment.

Soon afterward, the nurse explained to us that although you may have a “set-time” for blood and chemo, it doesn’t necessarily mean that that is when you get called in. She told us that it takes a while for the blood results to come back and once they are cleared by the nurse practitioner, then chemo gets ordered.

Once chemo gets ordered, it’s a matter of the pharmacy making the order, which takes time.

From that day on, I always made sure to pack my favorite items that I always kept on-hand – not only for chemo, but wherever I went during treatment.

Crackers & Other Dry Goodies

I was on steroids for two years and a bit.

It was brutal during my intensification phase (30 weeks of high dose steroids) where I usually had heartburn or nausea and needed to munch on something dry to feel better.

Crackers were my go-to and always a staple item to have in my bag because I just never knew when I’d get the steroid munchies.

Other dry, salty goodies like popcorn or even bread, made it a lot easier to keep my hunger at bay most of the time…seeing as I was hungry all the time.

Let’s be honest, I always carried some sort of food on me whether it be sandwiches, rice, or leftover pasta.

I would whip it out of my bag and set myself up with a mini picnic.

Different Hats

I had purchased a wig at the Wig Salon at PMH but I only wore it twice because I preferred to go bald and just wear hats out of comfort.

I purchased pretty much every single hat in that store and then some!

I liked carrying around different style hats to change into whether at the hospital, at an appointment or while I was out.

At one point of treatment, changing hats for me was like changing shirts and never knowing which to wear because I just had too many options…yup, that was me! But hey, it’s not like I can’t transition them into everyday hats now that my hair is back.

Chapstick & Moisturizer (LOTS OF IT)

I expected skin changes as one of the side-effects, but because it was the winter time, I had extra chapped lips and extra dry hands. I had to reapply my Chapstick at least three times within the hour and constantly moisturize my hands to prevent them from cracking.

Water

While taking steroids, I found it extremely difficult to keep up with any hydration because everything tasted like metal to me, but I knew I’d regret it if I didn’t try and force myself to drink because then it would lead to other problems…if you know what I’m saying.

At least carrying the bottle with me would encourage me to drink it, not only because it made my bag heavier (motivating me to finish it), but also because it stuck out of my bag, so I knew it was always there right in front of my face.

Sunscreen

Anyone and everyone should always make sure to apply some sort of protection to their skin.

I never thought that I’d start wearing sunscreen during the winter months, but I had to once I learned about all the risks associated with sun exposure during chemotherapy.

As much as it scared me, it put me in place knowing that I needed to constantly reapply it, even if I was just driving around in the car.

Now, it has just become a habit of mine to always apply it in the morning and carry it in my bag to reapply it throughout the day. The small travel size options, or the ones that come in the Look Good Feel Better kit are a great size to have on you.

Antibacterial Soap/Wipes

“Disinfect everything!” are the words that stuck with me throughout my entire treatment.

The nurses made it very clear that germs loved me at this point – being immunosuppressed and all.

I was susceptible to catching anything, so I had to make sure that my hands and any surfaces were always clean.

It was embarrassing at first, having to disinfect tables at the mall in food courts if I went to buy a coffee with family or friends, being extremely cautious in public bathrooms, and even if I was having a picnic at parks…people looked at me funny but I knew I had to be careful. Maybe my actions remind them of the pandemic.

I grew used to the idea of being “safe,” and embraced what I was going through when I had to do it.

If people looked at me funny or stared, I’d smile and say, “I know, right!? How can someone fighting cancer and going through chemo look this great bald?” or “I pay my oncologist big bucks to look the way that I do.” *wink*”

People thought I was ridiculous, but what did I care. I was going through this, not them, so there was absolutely no need for it to bother them in any way, shape, or form.

Just learn to laugh about it and then people will laugh with you.

Books/Magazines & Entertainment

You need to pass the time somehow. During treatment, I grew to love psychology and self-help books. I found them to be quite insightful at this point in my life. I was already going through a life-changing experience, which made me begin to question everything, so I decided to take that time and re-evaluate my whole life and give it a makeover.

Plus, I always had my cellphone on me for social media, games, and texting.

Make sure to carry around things like books, magazines, or crossword puzzles, because you’ll find you’ll have a lot of time on your hands while going to treatment or other appointments. You might as well make the most of it.

Vitamins/Medication

I always found myself to be out and about at the point when my medication or vitamins were due. I found it a lot easier to just carry them around in a cute little makeup bag that I had purchased solely for that purpose. That kept everything safe, clean, and in a place that I knew would always be in my bag.