Posts
- What works for me: lifestyle changes
- What works for me: CBD oil usage
- My thoughts about vagus nerve stimulation
- What I learned about epilepsy surgery
- What I wish I knew about treatments
- My thoughts on experimental therapies
- My experience with ketogenic diet therapy
- My journey with seizure diaries
- My experience with natural supplements
- My experience with medication side effects
- How I tackled treatment anxiety
- How I use mindfulness for seizure management
- How I discovered alternative epilepsy treatments
- How I find support during treatment
- How I handle medication adherence challenges
- How I adjusted to new medications
- What works for me in managing epilepsy research
- What epilepsy research means to me
- What I learned from epilepsy research conferences
- My thoughts about new therapies in research
- My take on the latest research findings
- My reflections on recent epilepsy studies
- My personal insights on drug efficacy research
- My journey through epilepsy research advancements
- How I navigated epilepsy research publications
- My experience advocating for epilepsy research
- How I track my progress in research
- My experience with clinical trial participation
- What I learned from my first seizure
- What works for me during an aura
- How I interpret epilepsy research studies
- How I found reliable epilepsy research sources
- How I engage with epilepsy research communities
- My strategies for managing triggers
- My experience with epilepsy in relationships
- My journey through an epilepsy diagnosis
- My journey to acceptance with epilepsy
- My thoughts on medication challenges
- My experience facing stigma and misconceptions
- How I practice self-care amidst challenges
- How I found support in unexpected places
- How I educate others about epilepsy
- How I communicate my needs
- How I cope with seizures daily
- How I balance work and epilepsy
- What helps me with sleep issues
- How I advocate for myself
- My thoughts on coping mechanisms
- What safety measures work for me
- What works for me during seizures
- My thoughts about living with epilepsy
- My strategies for managing stress
- My experience with lifestyle changes
- My journey to understanding triggers
- My experience with epilepsy medication adjustments
- My experience navigating disability benefits
- How I stay active with epilepsy
- How I keep track of my seizures
- How I find support from others
- How I educate my family about epilepsy
- What Works for Me in Court
- How I cope with my epilepsy flare-ups
- How I communicate my needs
- My Journey with Workplace Accommodations
- What I Learned from Legal Advocacy
- My Story on Accessing Health Services
- My Thoughts on Legal Protections
- What I Discovered About Consent Forms
- My Experience with Employment Law
- How I Managed Legal Documentation
- My Experience Challenging Discrimination Claims
- My Journey to Understanding Care Rights
- How I Navigated the Disability Benefits Process
- How I Asserted My Educational Rights
- How I Advocated for My Rights
- How I Found Legal Support Resources
- How I Handled Prescription Issues
- What works for me in sharing my story
- My story leading workshops for others
- My thoughts on youth epilepsy initiatives
- What works for me in community advocacy
- What I've learned from group discussions
- My thoughts on connecting with other families
- My journey with peer support networks
- My experience with online epilepsy communities
- My experience attending epilepsy community events
- How I manage stigma within my group
- My experience volunteering at epilepsy camps
- How I formed my local epilepsy support group
- How I engage with first responders in my area
- How I found friendship through epilepsy groups
- How I contribute to local epilepsy charities
- How I advocate for epilepsy awareness in my community
- What works for me in communication
- What works for me in stress relief
- My efforts in raising funds for research
- How I educate others about epilepsy
- My journey with caregiver support groups
- What I learned from organizing events
- My experience in finding respite care
- My experience with creative awareness projects
- My experience navigating healthcare systems
- How I celebrate small victories
- How I handle social isolation
- My thoughts on managing resentment
- My reflections on awareness month activities
- How I engaged my local community
- My journey to share my epilepsy story
- My experience advocating for seizure education
- What works for me in spreading awareness
- How I balance self-care and caregiving
- My experience with epilepsy-first aid training
- My thoughts on community support for epilepsy
- How I connected with other advocates
- My personal approach to destigmatizing epilepsy
- How I started my epilepsy awareness campaign
- What I do to educate peers
- How I learned to ask for help
- How I cope with caregiver fatigue
- My approach to sharing lived experiences
- How I inspired others to advocate
- My thoughts on journaling my experiences
- What works for me during seizures
- How I utilize art for awareness
- How I used social media for advocacy