Rare Disease Day 2018 - Information about rare cancers

5 minute read time.

February 28th is Rare Disease Day. It aims to raise awareness about rare diseases, including rare cancers, and the impact they can have on people’s lives. About one in five people with cancer in the UK (20%) have a rare cancer.

In this blog, editor Sadie takes a look at what rare cancers are and the extra challenges having a rare cancer can bring. We will also suggest ways of coping with these challenges if you are affected by a rare cancer. And finally, we will let you know where to get further information and support.

What is rare cancer?
A rare cancer is a cancer that fewer than 6 in 100,000 people in the UK are diagnosed with each year.

The diagram below shows the proportion of common, less common, rare and very rare cancers diagnosed in the UK:

This is a pie chart. It shows that 20% of cancers are rare and very rare. 53% of all cancers are called common cancers, such as breast, prostate, lung and bowel. 27% of cancers are called 'less common cancers' which includes cancers like bladder and melanoma.

There are 198 different types of rare cancer. You may have heard of some of them, such as thyroid cancer, acute lymphoblastic leukaemia (ALL) and mouth cancer. But there are many very rare cancers most people will not be familiar with. We have information about many rare cancers – this A–Z list has links to the different types.

Diagnosing and treating rare cancer
Having a rare cancer can mean extra challenges during diagnosis and treatment. The cancer may take longer to diagnose. This could be because:

  • the symptoms mimic other more common conditions
  • the symptoms are unusual and less well known by doctors
  • the cancer develops in a person ‘not expected’ to get cancer, such as a young adult or teenager
  • extra tests are needed to diagnose the cancer
  • the person with cancer needs to be referred to more than one specialist before the specific type can be diagnosed.

This is a quote from Harriet. She says ‘I was diagnosed with a rare type of non-Hodgkin lymphoma when I was 39. Because the disease is rare and usually affects older people, it took several months to get diagnosed.’

Finding the best treatment for a rare cancer may involve travelling to a specialist centre some distance from home. The treatment may be planned by an MDT (multi-disciplinary team) at the specialist centre and given in a hospital closer to home. Or the treatment may be highly specialised and given in the specialist centre.

If you are having treatment for a rare cancer in more than one hospital, you may want to keep a record of your treatment and appointments to help you to keep track. Our Macmillan Organiser can help with this. 

Some people with rare cancer are invited to take part in a cancer research trial (clinical trial). This means they may be offered a new treatment that might not otherwise be available.

Coping with rare cancer
Two issues people with a rare cancer may face are uncertainty and isolation. There is often less information available about rare cancers, so it can be harder for doctors to answer your questions or predict what may happen. You may also need to travel a long distance for treatment, and you may feel your family and friends don’t understand what you are coping with.

Some things that may help are:

  • talking about your feelings to someone you trust and feel comfortable with
  • talking to your cancer team or GP
  • calling the Macmillan Support Line on 0808 808 00 00
  • writing your feelings down or writing a blog about your experiences
  • making contact with others through an online cancer community, such as Macmillan's Online Community.

This is a quote from Waheed, saying ‘I found the Macmillan Online Community, where I could talk to other people going through similar experiences. I wasn’t expecting to find that. It was really helpful.’

Further information and support
Your cancer team at the hospital will know the details of your situation and are in the best position to give you information and support.

Patient organisations may also be able to offer helpful information. They may know about new treatments, research trials and leading specialists in the UK.

The Macmillan website has information about many types of rare cancer. Here are some other websites you may find helpful:

  • Orphanet provides information on rare conditions, including cancers.
  • Cancer52 is an alliance of patient organisations for less common cancers in the UK.
  • Rareconnect provides a space where people affected by rare diseases can connect with each other, share experiences and find helpful information and resources.

If you can’t find the information you are looking for, speak to your healthcare team or call our cancer support specialists free on 0808 808 00 00.

To see what else Macmillan's cancer information team has been blogging about, please visit our blog home page! You can subscribe to receive our blogs by email or RSS too.

We're with you every step of the way

The Macmillan team is here to help. Our cancer support specialists can answer your questions, offer support, or simply listen if you need a chat. Call us free on 0808 808 00 00.

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Keep in touch Follow Macmillan’s cancer information team on Twitter @mac_cancerinfo

Anonymous
  • FormerMember
    FormerMember

    Hi Nan62

    I’m sorry to hear that your mum is not doing so well. If you have any questions about her symptoms or changes to her health, please do speak to her healthcare team who know her medical history and can give you advice.

    We have information about looking after someone with cancer which you may find helpful. You can order this here. We also have information about managing symptoms – including fatigue – on our website here.

    If you want to talk to someone about your situation, you can call our support line on 0808 808 00 00 (Monday to Friday, 9am to 8pm) where you can speak to a cancer information nurse specialist. I hope this is helpful.

    All the best, Liza

  • FormerMember
    FormerMember

    Ah yes - Rare Diseases.... Does anyone know how to get a rare disease added to the recognised lists of rare diseases? In other words, how do people with diseases that haven't so far gained recognition in those lists get just that one step nearer to feeling that at least someone has noticed their problem? Who knows, maybe then it might follow that there is seen even the faintest glimmer that somebody or other might start caring about it. 

    What I am talking about? In my/our case, I am talking about late-onset post radiotherapy nerve damage - my own particular one-in-a-million  'Brucie Bonus' going by the snappy title Radiation-Induced Lumbosacral Plexopathy. If you want the story, you can find it here: www.rarediseaseday.org/.../p>

    But, enough of me and my treatment inheritance. As far as I can see, there's not even a catch-all of radiation nerve damage in all its various forms in the 'Rare Disease' lists. It is a ludicrous situation, and it's not helping anyone.

  • FormerMember
    FormerMember

    In addition to RILP's point there's nothing here about Radiation induced plexopathy here at all! I know it is rare, but as one out of 1000 patients who received more than 25 sessions of radiotherapy gets plexus nerve damage we are definitely not the only ones.

    I myself had breast cancer in 2007 and received thirty three sessions of radiation therapy in my right breast and shoulder area for breast cancer. In 2009 the first symptoms of failure of my nerves en muscles started showing, I lost feeling in my fingertips and started to have problems with the muscle coordination in my hand. Now, 7 years later, my arm is practically fully disabled and in a brace.

    So, yes, rare enough. But gladly I'm still here. But this post-cancer problem does need more attention.

  • FormerMember
    FormerMember

    I too have RILP as mentioned above ..I was treated for uterine cancer in 2001... the first side effect that appeared very quickly was lymphoedema and then the bowel issues started ... 2010 I stated to notice pins and needles in my feet .. 2012 tests at the doctors showed nothing sinister but I was starting to notice weakness going upstairs.. long story short on February 27th 2015 I stood for the last time...since then I have been living as a paraplygic not even able to weight bear. All this due to radiation for cancer treatment. The part that makes me angry and sad is the lack of recognition by the cancer community for this late stage side effect that s very real.. I also added my story to the rare diseases day and I started a blog to be able to share with others my experience

  • FormerMember
    FormerMember

    Sorry ..this is the correct link to my story above <a href="lifeinawheelchairblog.wordpress.com/.../a> thanks