Coping Strategies for Living with Clinically Isolated Syndrome
  • Apr, 30 2023
  • 19

Understanding Clinically Isolated Syndrome

Clinically Isolated Syndrome (CIS) is a term used to describe the first neurological episode that lasts at least 24 hours and is caused by inflammation or demyelination of nerve fibers in the brain or spinal cord. Although not all cases of CIS lead to a diagnosis of multiple sclerosis (MS), it can be an early sign of the disease. As someone living with CIS, I understand the uncertainty and fear that comes with this diagnosis. In this article, I will share some coping strategies that have helped me navigate life with CIS.

Get Educated About Your Condition

Knowledge is power, and the more you know about CIS, the better equipped you will be to manage it. Research the condition, read up on the latest findings, and join online forums or support groups to connect with others who are going through the same thing. Understanding the potential outcomes and treatment options can help you make informed decisions about your health and alleviate some of the anxiety that comes with the unknown.

Build a Support System

Having a strong support system in place is crucial for coping with CIS. This can include friends, family, and healthcare professionals who are knowledgeable about the condition. Sharing your experiences and feelings with others who understand what you are going through can provide comfort and encouragement, as well as practical advice. Don't be afraid to ask for help when you need it, and try to foster open communication with your loved ones about your needs and limitations.

Stay Active and Maintain a Healthy Lifestyle

Exercise and a healthy diet can have a significant impact on your overall well-being and help manage CIS symptoms. Physical activity can improve mood, increase energy levels, and reduce stress. Aim for at least 150 minutes of moderate-intensity aerobic exercise each week, along with strength training and flexibility exercises. Eating a balanced diet rich in fruits, vegetables, lean proteins, and whole grains can also help to support a healthy immune system and improve overall health.

Manage Stress and Practice Relaxation Techniques

Stress can exacerbate CIS symptoms and negatively affect your overall health. Learning to manage stress through relaxation techniques such as deep breathing, meditation, or yoga can help to alleviate anxiety and promote a sense of calm. Incorporate these practices into your daily routine and consider seeking the guidance of a therapist or counselor if you need additional support.

Keep a Symptom Journal

Keeping a symptom journal can help you and your healthcare team identify patterns and triggers for your CIS symptoms. This information can be invaluable in developing a personalized treatment plan and managing your condition effectively. Make a note of any changes in your symptoms, as well as factors such as your diet, exercise, stress levels, and sleep patterns. Share this information with your healthcare provider during appointments to ensure that you are receiving the most appropriate care.

Stay Organized and Plan Ahead

Living with CIS can sometimes feel overwhelming, but staying organized and planning ahead can help to alleviate some of this stress. Keep track of appointments, medications, and important documents related to your condition in a centralized location. Establish routines for daily tasks and self-care, and consider using a calendar or planner to help you stay on top of your schedule. Planning ahead for potential challenges, such as fatigue or mobility issues, can also help you maintain a sense of control over your life.

Stay Positive and Focus on What You Can Control

Finally, maintaining a positive outlook and focusing on what you can control can make a significant difference in your overall well-being. CIS can be unpredictable, but reminding yourself of your strengths and accomplishments can help to boost your confidence and resilience. Surround yourself with positive influences, practice gratitude, and remember that you are more than your diagnosis.

Living with CIS can be challenging, but with the right coping strategies and support, it is possible to manage the condition and maintain a fulfilling life. By educating yourself, building a strong support system, staying active, managing stress, keeping a symptom journal, staying organized, and maintaining a positive outlook, you can empower yourself to take control of your health and well-being.

Graham Holborn

Graham Holborn

Hi, I'm Caspian Osterholm, a pharmaceutical expert with a passion for writing about medication and diseases. Through years of experience in the industry, I've developed a comprehensive understanding of various medications and their impact on health. I enjoy researching and sharing my knowledge with others, aiming to inform and educate people on the importance of pharmaceuticals in managing and treating different health conditions. My ultimate goal is to help people make informed decisions about their health and well-being.

19 Comments

Stephanie Cepero

Stephanie Cepero

1 May 2023

This post hit me right in the feels. I was diagnosed with CIS two years ago, and honestly, the symptom journal changed everything. I started noticing how my headaches spiked after too much screen time-now I set timers. Small wins, you know?

Michael Tribone

Michael Tribone

1 May 2023

Love this breakdown. Seriously, if you're reading this and feeling lost-YOU AREN'T ALONE. I started walking 20 mins a day and it’s like my brain got a reboot. Don’t wait for perfect. Just start. 🙌

Nancy Lowry

Nancy Lowry

2 May 2023

You’re all being way too nice. If you have CIS, you’re one step away from MS. Stop pretending it’s just ‘managing symptoms.’ Get on disease-modifying drugs or stop wasting everyone’s time with ‘positive vibes’ nonsense.

Khanyisa Mhlongo

Khanyisa Mhlongo

2 May 2023

Oh my goodness, this is like a warm blanket made of wisdom 😭 I’m from South Africa and we don’t have access to half the resources y’all do, but I’m stealing every single tip. Journaling? Yes. Yoga? Already doing it. And I’m telling my whole family to read this. Thank you.

Manvika Gupta

Manvika Gupta

2 May 2023

this is so helpful!! i was scared to talk to my doc bc i thought i was overreacting but now i know its ok to track evrything. even if i spell stuff wrong lol

Chloe McDonald

Chloe McDonald

3 May 2023

I love how you said stay organized. I used to forget my meds all the time. Now I have a little pill box with colors and it’s such a mood booster. Simple stuff works!

Hobert Finn Bodfish

Hobert Finn Bodfish

3 May 2023

Ugh, another feel-good post. Newsflash: MS is not a mindfulness problem. You’re all just sugarcoating the inevitable. I’ve been in a wheelchair for 8 years. Your ‘positive outlook’ doesn’t fix lesions. 😒

Andrea Galetto

Andrea Galetto

4 May 2023

CIS? Please. The real issue is the medical-industrial complex profiting off fear. You don’t need a journal-you need to question why neurologists push MRIs like they’re selling gym memberships.

Chris Remo

Chris Remo

5 May 2023

I started doing tai chi last month. It’s not about being perfect. It’s about showing up. Even on days when my leg feels like it’s full of static. That’s victory.

Michael Herr

Michael Herr

6 May 2023

Solid advice. I’ve been doing all this for 5 years. The journal, the walks, the breathing. It doesn’t cure anything, but it keeps me from drowning. That’s enough.

Crystal Magnant

Crystal Magnant

6 May 2023

I use emojis to track my symptoms now 🌞 = good energy 🌧️ = brain fog 🛌 = need nap. It’s weird but it works. My neurologist actually laughed and said it’s the most honest chart she’s seen.

Danie Joy

Danie Joy

7 May 2023

They don’t want you to know this but CIS is just a cover-up for 5G exposure. The doctors are paid by Big Pharma to make you think it’s ‘inflammation.’ I’ve been tracking my symptoms since 2017 and the correlation with cell towers is undeniable. 🤫

Katherine Stapp

Katherine Stapp

7 May 2023

I’m from the Midwest and we don’t do ‘journaling’ here. We do ‘grit.’ If you can’t walk, crawl. If you can’t crawl, scream into a pillow. That’s real coping. Not this therapy nonsense.

Frank De Silva

Frank De Silva

8 May 2023

Interesting. I suppose you’re all too busy being ‘empowered’ to notice how the pharmaceutical companies own every support group mentioned here. How convenient.

KJ Miller

KJ Miller

9 May 2023

I used to think I had to ‘beat’ this. Then I realized I just had to live with it. That shift changed everything. Some days are gray. Some are golden. Both are valid. 🌱

Claire Battista

Claire Battista

10 May 2023

I’m so glad you mentioned boundaries. My sister kept pushing me to ‘get over it’ until I told her, ‘I’m not broken. I’m adapting.’ She cried. We’re closer now.

Erin DeGroot

Erin DeGroot

10 May 2023

Your writing is exceptionally clear and compassionate. The emphasis on structured self-monitoring is clinically sound and emotionally resonant. I have shared this with my support circle.

Stephanie Bryant

Stephanie Bryant

10 May 2023

OMG I just started the journal and I already found out my flareups happen after I eat gluten. My dr was like WTF how did you know?? I told her it was this post!!

Stephanie Cepero

Stephanie Cepero

10 May 2023

@StephanieBryant-wait, gluten?? I’ve been trying dairy for months and nothing. Maybe I should try cutting out wheat too. That’s huge. Thank you for sharing!

Write a comment