Migraines are not just painful; they can also be very unpredictable. For Laura McKee, who has over 15 migraines each month, this unpredictability affects her mental health. The constant worry about whether her day will be manageable or overwhelming often leaves her feeling emotionally exhausted.
Despite these challenges, Laura has discovered ways to handle the instability of living with chronic pain. Today, she shares the strategies that help her cope and feel more in control.
Chronic migraine interferes with every aspect of my life - work, family, and relationships. I hate missing out on social activities, so I would overcommit and then have to cancel. But I've lived with this condition for over 10 years. Over that time, I've sought a lot of support and developed coping strategies for dealing with the unknown every day.
Living with chronic migraine has made the world a lesser-known place for me. Not knowing how I'll feel from one day to the next has led to fear about the future. In turn, this fear has affected how I view the world and my role in it.
At the beginning of my journey with this illness, I didn't receive the support I needed from my medical team. I was left feeling overlooked and alone, especially since I was unable to work. Many of my friendships were tested from the very beginning, so the friends who stood by me were precious.
Later, I was diagnosed with another chronic condition - idiopathic intracranial hypertension (IIH). IIH symptoms feel like migraine but even more severe. Both leave me with constant head and neck pain, sensory disturbances, severe fatigue, and brain fog.
Living with unpredictable chronic conditions severely affected my mental health. I felt like I was in a permanent state of anxiety and despair.
I was so ill that I became confined to my bed. The lack of specialist support and treatment options led me to catastrophize my situation. I was more isolated, which led to depression and a vicious cycle of physical and mental pain. My relationships with my husband and children became strained.
Thankfully, my primary care physician was supportive of my mental health. Over time, I started taking better care of myself. I worked through my dark thoughts with a counselor and learned to put self-care as my main priority for the first time in my life.
Through self-care, I began to understand how chronic migraine impacts my daily life. This awareness led me to create long-term plans for managing my condition. By focusing on both my current and future needs, I developed stronger coping strategies, including:
At the top of my priority list was understanding how much rest I needed and listening to my body. I learned to assess my needs on an hourly basis and develop a routine to balance my energy levels.
Using a journal has been key in helping me do this. I keep a symptom and pain diary to arm myself with knowledge of what support I require from my medical team. I can spot patterns and balance my activity time and rest.
Since my understanding has improved, I've set self-care goals that accommodate my fluctuating health. I've gradually reintroduced exercise, a needs-based diet, and social activities into my daily life.
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Alongside planning, I reflect on the positives I find every day. Practicing gratitude improves my mental health and capacity to cope with migraine. Having this more mindful approach has led to a better quality of life.
I've had to accept how much effort is needed to manage the constant pain and sensory symptoms that are part of living with chronic migraine. Just when I think I've sorted it, it can fluctuate again, so understanding grows with experience.
Living with chronic pain brings constant change. When that’s combined with my urge to stay in control, the pressure to cope can feel overwhelming. For example, after a medication change or surgery, it takes time for both me and my caregivers to adjust to a new routine. To handle these shifts, we rely on clear communication and a flexible mindset.
Improving the coping strategies that I've built for living with chronic migraine is essential as I navigate the world. When treatment changes feel overwhelming, I make it a point to seek support from my medical team, pay attention to my body, and practice mindfulness and self-care.
As I engage in more exercise and socializing, I must be mindful of striking a balance between activity and rest. Increasing these activities is great for my mental health, so I set my goals around this.
Accepting and communicating my physical and emotional needs during change is crucial. I'm clear about what practical support I need during a migraine attack. This, in turn, helps stabilize my mental health.
To develop coping strategies, we must accept that chronic migraine isn't "fixable." Constantly searching for migraine cures and niche triggers can lead to excessive research and information overload, which may cause anxiety.
Anxiety may make it harder to seek support and manage chronic migraine. While feeling anxious doesn’t outright cause unpredictability with migraine attacks, it can heighten our sensitivity to changes and make it feel harder to cope. It often leads us to overanalyze or try to find patterns in something that may simply be random.
I've also learned about the intolerance of uncertainty (IU), which refers to how well someone can handle the unknown. People with chronic pain and high IU are often more affected by pain because of fear and negative thinking.
"Individuals who find uncertainty intolerable may be particularly threatened by the experience of having a [long-term physical health condition] and fearful of its implications, and thus engage in behaviors and cognitions aimed at controlling, reducing, and/or avoiding uncertainty."
~ The role of uncertainty intolerance in adjusting to long-term physical health conditions: A systematic review 01
This can hinder our ability to build the mental strength needed to cope with long-term conditions like migraines. Attempting to control the situation may lead to poor self-management. IU lowers our quality of life, but taking steps, such as CBT, can help us better handle the uncertainty of migraines.
“High levels of IU are associated with increasing efforts to regain control of the uncontrollable situation, which can result in dysfunctional coping strategies.”
~ Acceptance of Mobile Health Apps for Disease Management Among People With Multiple Sclerosis: Web-Based Survey Study 02
Accepting that you need support is the first step to building mental resilience against chronic migraine.
Next, you need to identify the barriers that prevent you from getting that support. Once you recognize the barriers, it is much easier to find ways around them.
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I've spent time understanding my pain, the unpredictability of my symptoms, and how they impact my mental health. I've worked hard to identify self-help strategies that support my treatment plan.
The key to coping with chronic pain's unpredictability is trust. We can only build trust through clear communication. This includes trust between me and my caregivers, so they know when to assist me, and trust in myself to understand and respond to my own needs.
Gibson B, Rosser BA, Schneider J, Forshaw MJ. 2023. The role of uncertainty intolerance in adjusting to long-term physical health conditions: A systematic review. https://pmc.ncbi.nlm.nih.gov/articles/PMC10237456/. Last accessed June 26, 2025.
Apolinário-Hagen J, Menzel M, Hennemann S, Salewski C. 2018. Acceptance of Mobile Health Apps for Disease Management Among People With Multiple Sclerosis: Web-Based Survey Study.https://pmc.ncbi.nlm.nih.gov/articles/PMC6334710/#abstract1. Last accessed June 26, 2025.
The information presented is solely for educational purposes, not as specific advice for the evaluation, management, or treatment of any condition.
The individual(s) who have written and created the content and whose images appear in this article have been paid by Teva Pharmaceuticals for their contributions. This content represents the opinions of the contributor and does not necessarily reflect those of Teva Pharmaceuticals. Similarly, Teva Pharmaceuticals does not review, control, influence, or endorse any content related to the contributor's websites or social media networks. This content is intended for informational and educational purposes and should not be considered medical advice or recommendations. Consult a qualified medical professional for diagnosis and before beginning or changing any treatment regimen.
NPS-ALL-NP-01583 AUGUST 2025