Breaking down the barriers and blushes

6 minute read time.
Breaking down the barriers and blushes

Last week we published the ‘why do I feel so guilty?’ blog exploring why we may feel guilty when living with, or being affected by cancer. Today we are talking about embarrassment because it’s often a feeling many people experience when it comes to talking about your body.

On the Online Community, we often see members posting about how embarrassed they feel to talk about parts of their body with friends, family and medical professionals. Embarrassment shouldn’t hold you back from getting the support you need so in this blog we’re sharing some of the discussions from our Community groups to help break down the barriers and the blushes of feeling embarrassed when being affected by cancer.

Embarrassment is described as a feeling of shame, awkwardness, and becoming self-conscious about something. Talking about your bowel habits and private parts shouldn't be a taboo subjects as they are all natural parts and functions of the body. The Community is an embarrassment free zone as it’s a space for you to talk about things that are concerning you. 

“I’m so glad you found your way HERE to vent. I'm really grateful for this space too. It's such a huge relief to be able to share the real and sometimes hinky details with people who get it and don't recoil in horror or embarrassment.”
Community member, Anal cancer forum

“I want to thank everyone that helped me… It was just so helpful with everyone's comments. It is great to know you are not alone - and the fact others had the same problem enabled me to realise I was not being stupid, so it immediately took away the embarrassment bit of the problem”
Community member, Head and neck cancer forum

“This is a great group for support. You can ask any question without any embarrassment as it will have been asked before.”
Community member, Anal cancer forum

Having a place like the Community can help reduce the feeling of embarrassment as there probably isn’t a topic of conversation we haven’t seen before and it’s also a safe and anonymous space for you to talk openly. Having support from family and friends is great but it may not always be comfortable to talk to them about the signs and side effects of cancer.

"Please all new people and even people who pop in and out, ask us anything. We have been through it all. Nothing can shock or embarrass us. We have walked that mile in your shoes and one of us will have had whatever it is you going through so please, however embarrassed or reticent you feel… just ask!"
Community member, Anal cancer forum

“I have a stigmatised cancer-cervical- and although I obviously talk about it within the community I don’t do so elsewhere. I did tell a couple of friends at my initial diagnosis, and yes, got the judgment, so I keep quiet now-I don’t need to be judged for something that I was unlucky to get.

Having a cancer which is tied up with sex is very difficult. I don’t want to keep quiet as I have plenty to say, but I still haven’t found my voice outside of here to correct all of the inaccuracies I see and hear about this cancer, because although it’s so linked to sex and intimate parts of the body.”
Community member, Cancer chat forum

“I’m out the other side now, though I still have the occasional caught short moment. It doesn’t bother me in the least anymore, whereas before the thought of having an accident or showing my bits to radiologists or wearing some Tena lady pants or sitting on my bed mats or discussing anything bottomley, would have made me keel over with embarrassment… It’s so fantastic to have others on here in the same boat. I think it has helped me more than I can ever say. Immense thanks to all the people on here and to all those who are years past their treatment and are on here every day helping others. Thank you!!!!!”
Community member, Anal cancer forum

How to overcome embarrassment

Talking about intimate parts of your body, poo and other bodily functions with anyone can feel embarrassing, and often an uncomfortable topic of conversation. This embarrassment may lead to missed cancer screening appointments and not wanting to access cancer treatment or ask for help. Although we are told medical professionals and your healthcare team have seen it all before, it’s natural to not want to talk about things that make you feel self-conscious or awkward. You are not alone if you feel this way.

“I’m told not to worry as nobody knows what’s happening to you but I do know and it’s the embarrassment and humiliation that gets me. It’s just relentless isn’t it?”
Community member, Bowel (colon and rectal) cancer forum

Going to your appointments with prepared questions is often what members of the Community find useful. We see this being said in our discussion threads often and it is a good tip to try if you feel awkward talking to your healthcare team about your concerns. 

“I would start by making a list of questions and then either telephone your oncology nurse or oncologist’s secretary and ask your questions. If you have an appointment soon, then ask your questions then. My team are extremely helpful and take the time to answer all my questions and believe me there are many.”
Community member, Vaginal cancer forum

“With regards to what questions to ask, I have found it useful to make notes on the kinds of things that I want to ask when I think of them. Then I make a list before my appointment so that I don't forget any of them. I guess questions are different for different people, but for me, I wanted to know how often my check ups would be and who I should contact if I had any concerns- eg any new symptoms.... I think the thing to remember is that there's no such thing as a silly question. If you would like to know the answer then its an important question.  
Community member, Vulva cancer forum

Further support and information resources

Alongside talking to members in our Community groups, there’s lots of information and resources available to help you with coping with your emotions. The Macmillan website has some useful information about cancer and your emotions, with further support guidance about signs, symptoms and cancer treatment options. 

Found this blog helpful? Why not read the following:

There's lots of support to be had by connecting with others who share a similar experience. Why not share what is worrying you by posting in our Community groups. There's no judgment here and remember, the Community is an embarrassment free zone. 

Anonymous
  • I think I must be a bit weird. I don’t stop talking about my bowel cancer experience to anyone who wants to know! I’ve been very pleasantly surprised by how many people are interested, and pleased that my friends and colleagues still ask me questions. Having recently been diagnosed with liver cancer I’m sharing what little information I can. I didn’t have any symptoms and looked very healthy, so people find it confusing. Keep up the great work.

  • I would love to be able to talk face to face with someone about my breast cancer and vin 3.  Unfortunately my husband finds it very difficult, so we only have brief chats about how I feel.  I have spoken to family and friends but none of them want to chat about it.  

  • Hi Jools63,

    Thank you for commenting, it’s great to hear that you want to share your personal experiences with people, I’d like to take a moment to thank you for doing so here on the Community. I’m sure there are lots of people who find it comforting to read your posts and to know they are not alone.

    I hope you’ll continue to find lots of support here on the Community and if you need additional support, please don’t hesitate to get in touch with the Macmillan Support Line on 0808 808 00 00 from 8am to 8pm 7 days a week.

    Best wishes, 

    Megan
    Macmillan's Online Community team

  • Hi Pariscat,

    It’s Megan here from Macmillan’s Online Community team, I’d firstly like to wish you a warm welcome to the site, I hope you’ll find it to be a comforting source of support.

    We see everyday how helpful it can be to speak to others with a similar cancer experience and access peer support when you need it. To start talking with others who are in a similar situation, you may find joining the Breast cancer forum a good place to start.

    Our Community groups are safe and supportive places for you to chat with others, ask questions and offer support back. I’m sure once you share what’s brought you to join the Community, others will be close by to offer some support.

    Once you’re a member of a group by clicking the grey ‘click to join’ button, you’ll then be able to start a discussion by clicking the ‘+new’ or ‘+’  to share what’s brought you to the site. I’ve added an image below to help explain.

    Breast cancer forum page with red circle around the +new button

    If you prefer face to face support, you may wish to contact the Macmillan Support Line as our specialist teams can look at the options available to you. The specialist teams are there to help every day from 8am to 8pm.

    To get in touch, you can call freephone 0808 808 00 00 from 8am to 8pm, 7 days a week. There’s also an option to send an email or use live webchat during the opening hours.

    I hope the above makes sense and if you have any further questions, please don’t hesitate to reply here in private messages or send an email to community@macmillan.org.uk. We’re here to help you use the Community and find the support you’re looking for.

    Best wishes, 

    Megan
    Macmillan's Online Community team

  • You folks have been through so much more than me, that I'm a little embarrassed to share my embarrassment.  It seems rather insignificant in comparison. Still, I find it overwhelming at times, almost sick with anxiety.  I'm on active surveillance for prostate cancer.  An area of suspicion showed up on my MRI  in my last check up.  As a result I had another templated biopsy, in addition to needle samples focusing on the area in question.  This started a month of hell.  The evening after the biopsy, I went into acute urinary retention (AUR) and had a catheter inserted in A&E.  The whole episode was incredibly painful and lacking of dignity and hugely embarrassing; lying there naked from the waist down, with a doctor and nurse hovering over me, touching me, the curtain from the cubicle not quite closed tight...horrible.  I've been catheterised before, but this was so painful.  Anyway, I was admitted the next day for IV antibiotics and pain control.  I was released three days later without the catheter (thank god) and went into AUR 4 days later, this time with Prostatitis.  Back to hospital, catheterised again - the hospital is not a place for privacy.  I always felt terribly exposed and my body wasn't responding weirdly.  I was released, heavy-duty oral antibiotics and pretty sick from the infection, with a fever and the meds upsetting my plumbing.  About three days later, I felt better for the first time in ages. It was really hot out and I was wearing shorts.  I had a flip-flow valve in my catheter, so I could walk around without a leg bag.  I thought I would walk to the high street, a small Tesco there, so I could buy a few things and cook dinner for me and my wife.  It was brilliant.  No one knew I had cancer.  No one knew I was catheterised.  I was just like everyone else, popping into Tesco to pick up a few things. On the way home, just a 10 minute walk, a young women with her dog was walking towards me. When she was a couple of steps away, she looked up and gave me a toothy smile, which was really nice. Just as I was about to pass her, I help the flip-flow valve drop off the catheter.  I instinctively reach down and caught it...looking down, I saw that the whole front of shorts were wet through.  I hadn't noticed until the valve dropped.  I'm not sure if she saw it, I think she did.  The embarrassment was overpowering.  I had been so up.  And dropped so low.  I went inside and...well...cried. It took me a long time before I could leave the house again.  Things got worse from there for a bit.  I ended up with a urinary tract infection, another trip to A&E, another embarrassing examination in a crowded area with so little privacy.  I feel so utterly embarrassed with it all.  I know I shouldn't.  I can't seem to get over it.  MacMillan has been fantastic.  They have been helping me with counselling.  I'm getting better.  And best of all, the area of suspicion turned out to be benign.  I still have cancer, of course, but at least no new lesions. There are so many people worse off than me, I feel like such a baby.  I'm hoping I'll get used to the intrusion into my privacy.  It's very hard.