Becoming a member is open to anyone who is 16 years and over. You can join in your own right, or perhaps you are a parent, family member, or a friend. You can also join if you are a health professional, or hospital representative, in fact anyone who wishes to support the work of the Charity.
As a member you will receive:
- National Newsletter
- Membership/Can’t Wait Card
- Information Sheets and Booklets relating to your condition/illness
- A vote at our National Conference and AGM
For more details on how to become a member, click here
Sometimes the best way to learn more about the benefits of something is to hear what other people had to say about it. Here is a selection of feedback we received from members:
An email from someone who had been recently diagnosed:

A parent who joined on behalf of their son:
"I joined your charity soon after our son was diagnosed and was so pleased to receive such useful information given in a non-alarmist way. My husband and I attended a number of your annual meetings when they took place in London. We were impressed with your organisation, the content and the wide variety of speakers. We would therefore like to take this opportunity of thanking you for all the invaluable support and information you have given all of us over the years."
Someone not renewing their membership following surgery:
"During the time of being a member of NACC it's been invaluable"
A parent who took out membership following her son's diagnosis:
"I need the Newsletters even if I felt really sad, because it helped me understand his illness."
A lady who was on benefits and unable to pay for her membership:
"I am thrilled you were able to help me and am very grateful for your prompt response and great kindness at this time where not much seems to be good."
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