Feeling like you’re part of a community that understands what you might be going through can make a huge difference to how you are able to cope with head and neck cancer; for patients and caregivers alike.
Sharing the stresses and strains of the bad days can help lift the pressure and allow you just to let it all out when it gets too much. And, passing on the triumph and happiness of your good days might just perk up another patient or caregiver and give them the strength to keep going.
Many people are not aware of the sacrifices and stresses that those looking after the patients encounter. These aren’t the trained healthcare professionals that are paid to care; but the caregivers who are there 24/7 and are often overlooked and forgotten. Some might not even consider themselves caregivers and won’t ask for help and support.
Mucosa Matters is a community for patients suffering from oral mucositis and dry mouth, along with their caregivers and aims to provide a supportive setting where tips, advice and information can be shared.
You might be a patient who suffers from dry mouth, or be in the throes of chemo or radiotherapy and be struggling with oral mucositis. Or, you might be a caregiver and have first-hand experience of what it’s like to care for someone with oral mucositis or dry mouth.
If this resonates with you, then we want to hear from you and give you the platform to share your story, tips and experience, in the hope that it helps others along the way.
Click here for the patient and caregiver form which is a quick and easy way of passing on your top tips and advice, and to tell your patient/caregiver story to be shared with others on Mucosa Matters. There is an option to make this anonymous if you’d prefer.
If you would like more information, please visit the website, or visit the Mucosa Matters social media pages by clicking on the icons below.
Instagram: https://www.instagram.com/mucosamatters/
Facebook: https://www.facebook.com/mucosamatters/