![hero_emotional-wellbeing](/more-than-scleroderma/sites/default/files/2022-06/hero_emotional-wellbeing.jpg)
Emotional wellbeing
Caring for someone with scleroderma is different for everyone. Although there is no right or wrong way to feel, here you can find ways that may help you cope.
2 min read
Your relationship dynamic with the person you care for may change. Whether they are your husband, wife, grandparent, child, friend or neighbour, what you can give and receive from one another may alter. It may not be easy at first, but be open and honest with each other.
![facts-4-0-8in10](/more-than-scleroderma/sites/default/files/2022-06/facts-4-0-8in10.jpg)
people say that caregiving strengthens their relationships.1
Caring for someone with scleroderma can also be stressful at times—and that’s understandable.1,2
- Someone you love is experiencing pain, discomfort or distress.
- Illnesses like scleroderma are often unpredictable.3 You will have to look out for any new symptoms or problems.
- If you take on extra responsibilities, your day-to-day life may have to adapt. This will put strain on your personal relationships and finances.
However, there are practical ways that may help you to manage your own stress and wellbeing. These simple changes don’t take much time but may make a big difference to how you feel.
![story-alex-video](/more-than-scleroderma/sites/default/files/2022-06/story-alex-video_1.jpg)
Reflection
![hero-diet-and-exercise](/more-than-scleroderma/sites/default/files/2022-06/hero-diet-and-exercise.jpg)
Diet and exercise
You may also like to read:
![hero-understanding-scleroderma](/more-than-scleroderma/sites/default/files/2022-06/hero-understanding-scleroderma.jpg)
Understanding scleroderma
![hero-specialist_team](/more-than-scleroderma/sites/default/files/2022-06/hero-specialist_team.jpg)
Specialist team
![hero-i_have_scleroderma](/more-than-scleroderma/sites/default/files/2022-06/hero-i_have_scleroderma_0.jpg)
Monitoring scleroderma
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AP-NORC. Long-Term Care in America: Expectations and Reality. The Associated Press-NORC Center for Public Affairs Research, 2014.
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Schultz R and Sherwood P. Physical and mental health effects of family caregiving. Am J Nurs 2008 September;108(9 Suppl):23–7.
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Nakayama A, et al. Patients’ perspectives and experiences living with systemic sclerosis: A systematic review and thematic synthesis of qualitative studies. J Rheumatol 2016;43:1363–75.
![quote-maria-3](/more-than-scleroderma/sites/default/files/2022-06/quote-maria-3.jpg)
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"I see my daughter trying to deal with the problems that I have, and she finds the balance to help me and then to study. She's doing very well and I'm very proud of her."
– Maria