Which advice would you give to someone who has just been diagnosed with Multiple Systems Atrophy?

See some advice from people with experience in Multiple Systems Atrophy to people who have just been diagnosed with Multiple Systems Atrophy



First of all, I want to express my empathy for your recent diagnosis of Multiple Systems Atrophy (MSA). Receiving a diagnosis of a chronic and progressive condition can be overwhelming and bring about a range of emotions. It is important to remember that you are not alone in this journey, and there are resources and support available to help you navigate through the challenges ahead.



Educate yourself about Multiple Systems Atrophy: Understanding your condition is crucial in managing it effectively. Take the time to learn about MSA, its symptoms, progression, and available treatment options. Knowledge empowers you to make informed decisions about your health and enables you to communicate effectively with your healthcare team.



Build a strong support network: Surround yourself with a supportive network of family, friends, and healthcare professionals who can provide emotional support, guidance, and assistance when needed. Consider joining support groups or online communities where you can connect with others who are also living with MSA. Sharing experiences and advice with individuals who understand your challenges can be immensely helpful.



Establish open communication with your healthcare team: Your healthcare team will play a vital role in managing your MSA. Establishing open and honest communication with them is essential. Ask questions, seek clarification, and actively participate in your treatment plan. Ensure that you have a clear understanding of your medications, potential side effects, and any lifestyle modifications that may be necessary.



Focus on symptom management: MSA symptoms can vary from person to person, and managing them effectively is crucial in maintaining your quality of life. Work closely with your healthcare team to develop a personalized symptom management plan. This may involve a combination of medications, physical therapy, occupational therapy, speech therapy, and other interventions tailored to your specific needs.



Adopt a healthy lifestyle: While there is no cure for MSA, adopting a healthy lifestyle can help improve your overall well-being. Engage in regular exercise as tolerated, eat a balanced diet, and prioritize sufficient sleep. Avoid smoking and excessive alcohol consumption, as they can worsen symptoms and have negative effects on your health.



Manage your emotional well-being: A chronic illness diagnosis can take a toll on your emotional well-being. It is important to prioritize self-care and seek support when needed. Consider engaging in activities that bring you joy, practicing relaxation techniques such as meditation or deep breathing exercises, and exploring therapy or counseling options to help you cope with the emotional challenges that may arise.



Plan for the future: MSA is a progressive condition, and it is important to plan for the future while focusing on the present. Consider discussing advanced care planning, including your healthcare preferences, with your loved ones and healthcare team. Having these conversations early on can ensure that your wishes are respected and provide peace of mind for both you and your family.



Stay informed about research and clinical trials: Medical research is continually advancing, and staying informed about the latest developments in MSA research can be beneficial. Discuss with your healthcare team if there are any clinical trials or research studies that you may be eligible to participate in. Participation in research can contribute to the advancement of knowledge and potentially provide access to new treatments or interventions.



Take it one day at a time: Living with a chronic illness can be challenging, but it is important to remember to take it one day at a time. Celebrate small victories, be kind to yourself, and seek support when needed. Remember that you are not defined by your diagnosis, and with the right support and management strategies, it is possible to live a fulfilling life despite the challenges posed by MSA.


by Diseasemaps

Be helpful to your caregiver; let them help you however they want to or can. Be cheerful and laugh; it makes their day.

7/9/17 by Mary 1000

The best advice is to reach out for support and information. Don't feel that you are completely alone, there are resources available and people who understand. Connecting with other families who are dealing with the disease will be your best source for support. Connections can be made through this disease map and also through the various Multiple System Atrophy advocacy organizations around the world. Here is one MSA discussion group open to anyone around the world: groups.yahoo.com/group/shydrager

7/11/17 by Pam Bower 2952

Try to do the thing you always dreamed of now.

1/4/18 by Jan 1500

It is just a word to describe what the doctor thinks is happening to you. Do not be afraid. At the same time, this is a disease that can move rapidly. A lift chair and full electric bed can help you stand. Walkers and wheelchairs can help keep you safe and conserve your energy. Get familiar with what your insurance will cover. I found many helpful items on Amazon simply by looking at the items other people bought. We used grab poles, a scooter, an electric wheelchair, a manual transfer device, and today a hoyer lift. All did the same thing, made the impossible possible. Our neurologist gave us some wonderful advice. He said to decide then how we defined quality of life. For us, this meant no feeding tube, no pacemaker, no tracheotomy and no ventilator. We may change our minds, but that is because we do not believe anything is written in stone.

3/23/18 by pastorbobbie@gmail.com 3020
Translated from spanish Improve translation

That should keep The inner Peace, because the road is not simple

5/10/17 by Lorena. Translated

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