Which advice would you give to someone who has just been diagnosed with Scleromyxedema?

See some advice from people with experience in Scleromyxedema to people who have just been diagnosed with Scleromyxedema


Scleromyxedema is a rare skin disorder characterized by the deposition of mucin in the skin, leading to thickening and hardening of the affected areas. Being diagnosed with this condition can be overwhelming and may raise many questions and concerns. While it is important to consult with your healthcare provider for personalized advice, here are some general recommendations to consider:



1. Educate yourself: Take the time to learn about scleromyxedema, its symptoms, causes, and available treatment options. Understanding your condition will empower you to make informed decisions and actively participate in your healthcare.



2. Build a healthcare team: Seek out medical professionals who specialize in scleromyxedema or related conditions. This may include dermatologists, rheumatologists, and other specialists who can provide comprehensive care and guidance tailored to your specific needs.



3. Follow your treatment plan: Work closely with your healthcare team to develop a personalized treatment plan. This may involve a combination of medications, physical therapy, and lifestyle modifications. Adhering to your treatment plan is crucial for managing symptoms and slowing down the progression of the disease.



4. Manage symptoms: Scleromyxedema can cause various symptoms, such as skin thickening, joint stiffness, and muscle weakness. Discuss with your healthcare provider strategies to alleviate these symptoms, which may include topical creams, pain management techniques, and exercises to improve mobility.



5. Prioritize self-care: Taking care of your overall well-being is essential. Ensure you get enough rest, eat a balanced diet, and engage in regular physical activity within your capabilities. Additionally, managing stress levels through relaxation techniques or seeking support from friends, family, or support groups can positively impact your quality of life.



6. Monitor your skin: Regularly examine your skin for any changes or new symptoms. Report any concerns to your healthcare provider promptly. Early detection and intervention can help prevent complications and ensure timely adjustments to your treatment plan.



7. Seek emotional support: Dealing with a chronic condition like scleromyxedema can be emotionally challenging. Reach out to loved ones for support, and consider joining support groups or seeking counseling services. Connecting with others who share similar experiences can provide valuable emotional support and practical advice.



8. Stay informed about research: Stay updated on the latest advancements in scleromyxedema research and treatment options. This knowledge can help you have meaningful discussions with your healthcare team and explore potential new therapies or clinical trials that may be available.



9. Be proactive: Take an active role in managing your condition. Keep track of your symptoms, treatment progress, and any questions or concerns you may have. Prepare for your medical appointments by writing down your questions in advance and discussing them with your healthcare provider.



10. Stay positive: While living with scleromyxedema may present challenges, maintaining a positive mindset can make a significant difference in your overall well-being. Surround yourself with a supportive network, engage in activities you enjoy, and celebrate small victories along your journey.



Remember, this advice is not a substitute for professional medical guidance. Always consult with your healthcare provider for personalized advice and treatment options.


by Diseasemaps

If you have been diagnose with the disease you need to know that IVIG is the best known treatment but the health services at some stage will try one or more drugs to see if that works because IVIG is expensive. Some have said it costs $3,000-$4000 per session . So depending on which country you live in the treatment will vary. In the US they are heavily biased towards drugs as the insurance companies sometimes wont cover IVIG.

1/18/19 by Rob 2750

Because it is such a rare condition, it is a lonely disease. I find the Facebook Scleromyxedema group invaluable and would be lost without the friends I have made there.

1/26/19 by Kay 2500

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