As summer temperatures rise, many of us find ourselves reaching for fans, water bottles, and shade. But for people living with Parkinson’s, the heat can bring more than just discomfort—it can trigger or worsen skin and sweating problems, which are already common symptoms of the condition.

If you’re caring for someone with Parkinson’s, you may notice changes in how their body handles temperature. They may sweat excessively, barely sweat at all, or experience skin that’s overly dry, oily, or itchy. Understanding why this happens—and what you can do to help—can make a big difference to their comfort and wellbeing.

Why Does Parkinson’s Affect Skin and Sweating?

Parkinson’s can interfere with the autonomic nervous system—the system that controls things like sweating, temperature regulation, and skin oil production. This means people with Parkinson’s may:

·         Sweat too much (especially on the upper body, hands, or feet)

·         Sweat very little, even in the heat

·         Experience oily, flaky, or itchy skin (especially around the nose, scalp, or eyebrows)

Some medications used to manage Parkinson’s can also contribute to these issues. That’s why it’s important to monitor symptoms and communicate any changes to your loved one’s healthcare team.

Practical Tips to Manage Sweating and Skin Problems in Summer

Here are some simple, supportive ways you can help your loved one stay cool, comfortable, and confident this summer:

1. Stay Hydrated

Encourage regular fluid intake—water is best—to help regulate body temperature and prevent dehydration. Keep a cool drink nearby at all times.

2. Choose Breathable Clothing

Natural fabrics like cotton or linen can help wick away sweat and allow skin to breathe. Avoid tight, synthetic clothing where possible.

3. Manage Overheating

Use fans, cooling sprays, or a damp washcloth to bring the temperature down. Try to stay indoors during the hottest parts of the day, or seek out shaded outdoor areas.

4. Gentle Skin Care

Use mild, fragrance-free moisturisers or creams for dry skin. For oily or flaky areas, products designed for sensitive skin can help restore balance without irritation.

5. Keep a Sweat Diary

If sweating patterns change suddenly or become distressing, it can be helpful to keep a simple diary to share with a GP or Parkinson’s nurse.

6. Talk to Professionals

Never be afraid to ask questions. If sweating is disrupting sleep or daily life—or if skin issues become sore or infected—it’s worth discussing with a healthcare provider. Sometimes, adjustments to medication or new products can help.

You’re Not Alone

Supporting someone with Parkinson’s is a journey—and no two journeys are the same. But you don’t have to navigate the ups and downs on your own. If you’re feeling unsure, frustrated or just need to talk, the We Talk Care community is here to listen.

Join our friendly carer community for practical advice, emotional support, and a space where you’re always understood.