Community News - Macmillan Online Community

Deaf Awareness Week 2021

This week (3 rd -9 th May) marks Deaf Awareness Week 2021, a week where we raise awareness of deafness and the Deaf community as well as the support available for deaf/Deaf people. You may wonder why I have written the word deaf with a lower-case d, as well as with an upper- case D. This is because we want to reach out to anyone affected by hearing loss, whether they are part of the Deaf community and identify as a Deaf person (Deaf), or not (deaf). The word deaf can be used to describe someone who is severely hard of hearing. With a capital D however, it is a term that is used to describe someone who is part of the Deaf community and culturally Deaf. What is the Deaf community? The Deaf community is a community of people who identify as Deaf and who share their culture and sense of identity…

Former Member
May is sun awareness month - let's talk about the sun, sunburn and skin cancer

We often refer to the sun when talking about happy times. Saying that sunny days make us feel good or telling someone you hope the sun shines for them. Comments about enjoying the sun might not always be appropriate, especially for people affected by skin cancer. We should be mindful of this when we're talking to others. We should also remember that sun awareness is a really important issue for us all. Sun exposure can put you at risk of sunburn, or skin damage. Ultraviolet (UV) light from the sun is the main cause of most skin cancers. UV light damages the DNA (genetic material) in our skin cells and can cause skin cancer. In this Community News blog, we'll feature conversations from our skin cancer and melanoma forums. You'd be very welcome to join in if you have your own tips or questions…

Steph - Macmillan
Notice: improvements release postponed

This morning, Wednesday 5 th May, we had planned to move forward with our first batch of improvements to the Community. As many of you may have noticed, the site was down for longer than we had expected. Unfortunately, we ran into some problems when we released the changes into the site. We did not want to introduce any issues into the Community, and therefore we made the decision to roll back the improvements. We are really sorry for any inconvenience the downtime may have caused, and we’d like to thank you for your continued patience. We’re working really hard to get this fixed, so we can release these improvements as soon as possible. If anyone has any questions or concerns, please do not hesitate to get in touch with us by commenting below or by emailing us on community@macmillan…

Ellen - Macmillan
Improvements are coming

On Wednesday 5 th May, we will be introducing the first of our improvements to the Community. In our previous blog, ‘Look out for improvements’ , we announced that we would be making some key improvements to the site. We are continually grateful for all of the feedback that you send to us, the Community team, as this is what has helped us to work on the things that matter the most to our members. We’ve got three releases coming to the Community over the coming months. Each of these releases will bring improvements to the site – some small fixes and some larger developments. On Wednesday 5 th May, we’ll be introducing the first of these three. EDIT: We've been informed that there will now be some downtime needed to release these improvements. The Community will be down for half an hour…

Ellen - Macmillan
Being bodies - Sophie, body confidence and her double mastectomy

Our new series “Being bodies” aims to explore our relationships with our bodies, from head to toe and everything in between. We recently featured Sophi e ’s story, where she talked about her experience being diagnosed with the BRCA2 gene mutation at 24 years old. Today, she’s here to talk about how having a double mastectomy changed how she felt about her body, for the better. A bit about me... I’m Sophie, 28 years old, queer and a BRCA2 gene carrier. Many of my family members have been affected by breast cancer. At 24, I decided to get genetically tested for the gene after my dad was diagnosed with prostate cancer. After that test came back positive for BRCA2, I decided to have a preventative double mastectomy with reconstruction. I have always had a positive relationship with my body…

Eliza - Macmillan
Planned Online Community Maintenance - Thursday 28th of April, 4am onwards

Hi everyone, Due to some planned maintenance, the Online Community will enter a read-only mode for 4-8 hours, beginning this Thursday at 4:00am . It may last until midday but has been planned at this time to provide minimal disruption to our members. This means that you will not be able to log in, post or reply on the Online Community during this time. You will still be able to read posts and blogs on the site. If you feel you need some support while the Online Community is unavailable, please remember our Support Line is here for you. Our teams are available 8am-8pm, 7 days a week by phone on freephone 0808 808 00 00 and also by email or on webchat . Thank you for your patience and support as Macmillan continues to update and improve our online services. If you have any questions,…

Tom C - Macmillan
Cancer & me 35 years on - Vol 11 Good news, bad news

We are back today with the next instalment of Willo’s blog series ‘Cancer & me 35 years on’. Willo is a member of our Community who was diagnosed with Anal cancer in 1986 while living in Zambia and has been sharing her experience of life post diagnosis, as well as her amazing artwork, in her blog series with us since last summer. So far Willo has covered her experience of moving back to England for treatment, her Brachytherapy and Abdominoperineal Resection and the amazing friends and family that helped her through. In today’s blog we pick back up with Willo as she prepares to start a university course in Graphic design at Liverpool Poly. Sketch by Willo - Wigan to Euston 'Once more I heard him snort – “see your solicitor – write to your MP – don’t give up!” I did just that and got…

Former Member
National pet month

April is National Pet month and we want to take a moment to talk about the support given . F or those who have furry, smooth, big or small animals in y our lives , you know how much they can affect your we l lbeing. In our Animals are family too forum , we see how much a nimals mean to you and how they have provided support in different ways. “While I was having my radiotherapy and chemotherapy in March/April 2019, Chynna would always come on my knee every day while I was waiting for the hospital transport to collect me. It was almost as if she knew what I was going through.” - blackstuff “About 6 weeks before I was diagnosed with cervical cancer my dog would not leave my side, he's normally quite clingy but I noticed he was exceptionally clingy just would not leave me, I am about to…

Former Member
Hair Loss - Information and Guidance

Image: Landscape of Yorkshire moors with dark clouds sitting over a valley on a spring day. On the Community team we often ask for your input or feedback, we want to make sure we’re listening to our members. In a recent newsletter we asked for you to get in touch with the topics you would like to see us write about. In today’s Community News Blog, we’re talking about a topic you asked for - hair loss. We know from many of our members’ comments that hair loss can be difficult to deal with, both physically and emotionally. "The hair loss was something I was absolutely dreading and absolutely heartbroken about." Fifitrix , Breast cancer forum "Main one for me is hairloss Hair loss was awful but I've learned to accept myself with short hair now. Take each day at a time." , Breast cancer…

Tom C - Macmillan
Community guidelines update – sharing medical pictures

Please note that this blog is no longer up-to-date. To see the most recent review of the Community guidelines, please see our more recent blog here . We have some important information to share here on the Online Community. We have decided to trial updating part of the Community guidelines around medical images. Our Community guidelines are what everyone agrees to when they join the Online Community. They’re in place to ensure that everyone is safe while using the site. Previously, our guidelines asked that members not to upload any photos of body parts or medical documents, as this often leads other members to try and diagnose, or offer medical advice. We’ve seen from feedback and conversations on the site, that seeing images of people’s medical journeys can be an important source of…

Eliza - Macmillan
Cancer & me 35 years on - Vol 10 'A Chance encounter'

We are back today with a further instalment of Willo's blog series 'Cancer & me 35 years on.' Willo is a member of our Community who was diagnosed with Anal cancer in 1986 while living in Zambia and has been sharing her experience of life post diagnosis, as well as her amazing artwork, in her blog series with us. So far Willo has covered her experience of moving back to England for treatment, her Brachytherapy and Abdominoperineal Resection and the amazing friends and family that helped her through. In today’s blog we pick back up with Willo on the day of her interview for a course in Fine art at a university in Liverpool. Throughout her series Willo has written about all aspects of her life after diagnosis, helping us to remember that life after cancer and moving forwards from treatment…

Former Member
Let's talk about treatment: sinus cancer and surgery.

Dan (pictured above), known on the site as Defiantlydisfigured, was diagnosed with squamous cell carcinoma in the ethmoid sinus in 2012, which is a very rare type of cancer. He underwent surgery, radiotherapy and chemotherapy. Dan found support from sharing his story online in blog posts and on social media, and he continues to raise awareness for facial cancers. I was 34 and told that I had a large tumour growing inside my head and it was not long before it would invade the space where apparently my brain was. In order to make sure I had a chance to live, they would have to take out my eye to make sure they got it all. Well as shitty as it sounds, it was an easy decision: "whatever it takes,” I said. The wheels moved swiftly after that and before I knew it, I was nervously twiddling…

Steph - Macmillan

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