Chilly Truth: Scleroderma & Cold Temps Don't Mix!
June is not just the start of winter, it's also the month we ask for your support through our SNUGGLE UP campaign, raising funds for World Scleroderma Day!
Find out why people living with scleroderma need to take extra precautions in the cold and how they can stay warm and safe! 👇
▶️Raynaud's phenomenon is a common symptom of scleroderma, causing blood vessels to constrict in response to cold temperatures, leading to discoloured fingers and toes (white, blue, or purple).
▶️Scleroderma can cause blood vessels to narrow, reducing blood flow to extremities, making them more susceptible to cold temperatures.
▶️Cold temperatures can exacerbate joint pain and stiffness, which are common symptoms of scleroderma.
▶️Cold-induced vasospasm can lead to digital ulcers, painful sores on fingers and toes.
▶️Cold air can trigger respiratory problems, such as bronchospasm or asthma-like symptoms, in people with scleroderma-related lung disease.
So, to manage cold temperatures throughout our winter months, people living with scleroderma need to dress warmly, use gloves and hand warmers, and some take medications to dilate blood vessels. We need to SNUGGLE UP!
One of the ways Scleroderma Australia celebrates World Scleroderma Day on 29 June is by encouraging people to hold a Snuggle Up event. This can help raise awareness for our cause and raise funds to support those who are living with this condition and to help find a cure.
You can hold a Snuggle Up event that involves you keeping warm this June.
You could:
🧣 Hold a slumber party in your favourite PJs, either in real life or online
🧣 Organise a film night and gather friends at your place or online
🧣 Host an afternoon tea wearing your favourite gloves and scarves,
🧣 Arrange a casual clothes day at work.
Learn more here:
👉https://lnkd.in/gwXa_h2J
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#SclerodermaAwareness #ChronicIllness #StayWarm #SnuggleUp #Scleroderma #WorldSclerodermaDay2024 #WSD2024 #DonateNow #AutoImmune #SclerodermaNurses #SclerodermaResearch
#SclerodermaCommunity #SytemicSclerosis #ChronicIllness
Disability and Human Rights Professional
1yAlways so exciting to see the amazing work you’re doing Amanda!