Socializing tips for Peristeen® Plus users
Whether it’s a meal out with a partner, going on vacation or just visiting friends, we believe nothing should stop you from going out and having a good time. Read on to learn some helpful tips to make sure your next social activity is a success and get some practical advice from Peristeen users.
Consider building your support network
Having a trusted friend or relative who is aware of your situation can help. If you would like someone to accompany you on your first few trips, be sure they are aware of your medical needs. Before deciding to share your situation with others, consider reflecting on the following questions:
- Why do I want to share my situation?
- Who do I want to tell?
- When do I want to tell them?
- Do I want anyone with me when I tell them?
It can also help to prepare in advance by writing down what you want to say, and trying to anticipate some of the questions you might be asked.
Build your confidence by setting small goals initially
Start relatively close to home and only stay out for a short period of time. Then ease into things like using a public restroom for the first time or visiting a relative for several hours. It can be helpful to start with a relative or friend who already knows about your situation.
Prepare before going out
Consider using your Peristeen Plus system before you go out, and wear dark colors if you’re worried about leakage. Bring extra clothing, wipes and bag, and identify the nearest restroom at your destination.
Pack accordingly for longer trips
Going away for longer than a day or two is possible with the Peristeen Plus system, but preparation is key. We have developed a travel fact sheet with tips and advice that can help.
Remember you are not alone
Meeting others in your situation can help. You can learn from their experience and also gain reassurance from knowing others who have succeeded with Peristeen Plus and are able to participate in the social activities they love. Consider searching for patient organizations in your area through social media or reach out to local patient support or community organizations.
Bob, spinal cord injury, US, “I always plan my irrigations around my social schedule. It helps because then I know I have a 48-hour window where I don't have to worry about my bowel.”*
Becky, spinal cord injury, US, “There’s a lot more than the four walls of your home. You’ve got to push yourself, don’t give up. Baby steps are OK. Going to the mall is one thing, going to Mexico to scuba dive is another thing.”*
Sarah, spina bifida, US, “You don't need to tell everyone about your bowel issues but it's a good idea to have a small support network of people who can be there for you.”*
*Coloplast has compensated these users to share their product experiences. Each person's situation is unique so your experience may not be the same. Talk to your healthcare provider about whether this product is right for you.
Information from Coloplast Care is for educational purposes only. It is not intended to substitute for professional medical advice and should not be interpreted to contain treatment recommendations. You should rely on the healthcare professional who knows your individual history for personal medical advice and diagnosis.
