migraine brain fog

Join the Conversation on
migraine brain fog
518 people
0 stories
20 posts
  • Explore Our Newsletters
  • What's New in migraine brain fog
    All
    Stories
    Posts
    Videos
    Latest
    Trending
    Post

    Canes & Brains

    I was looking everywhere for my cane one afternoon. Couldn't figure out where the heck I put the thing. My partner comes home and goes to get a water from the fridge and there it is, hanging up on the shelf, literally just chillin.
    #Cane #funny #BrainFog #ChemoBrain #Humor #Laugh #gallowshumor #MigraineBrainFog

    1 reaction 1 comment
    Post

    Toothpaste Follies

    Today I went to get my blood drawn. I take off my hoodie and feel something tubular and squishy in the pocket. So I reach in and what do I find? When I burshed my teeth I put the toothpaste in my pocket afterwords because THAT is where the toothpaste goes, my friend!🤣😂🤪
    #BrainFog #FibroFog #MigraineBrainFog #funny #Humor #lol #CheerMeOn #whoops

    10 reactions
    Post
    See full photo

    Chronic Migraine awareness

    Today I am featured as blogger on Chronic Migraine Awareness website. Please go support them as we try to raise awareness about these poorly understood and researched conditions.
    chronicmigraineawareness.com/2023/03/07/mitas-story

    #chronicmigraine #ChronicMigraineSyndrome #ChronicVestibularMigraine #Migraine #MigraineBrainFog #MigraineWithAura #VestibularMigraine #migraineawareness #ChronicPain #Pain #ChronicIlless #Raiseawareness #ChronicMigraines #ChronicHeadaches #OccipitalNeuralgia #Dysautonomia #Fibromyalgia #ChronicFatigue #Spoonie #SpoonieProblems #spoonielife #Support #resilience #creativecopes

    1 reaction
    Post
    See full photo

    Concussion, Migraines, major Balance issues, Parkinson’s, tremors, Neuropathy, shoulder/neck pain, back pain, brain fog, poor memory, and no appetite.

    (PART ONE) Please send me prayers, good vibes, healing energy and keep me in your thoughts. It would really be appreciated. It is very hard for me to ask for help…but bedrudgundly I have been parking in handicap parking spaces and recently began using a walker. To be honest I’ve had to! I had four falls at the end of December and I am constantly catching myself from falling over and having to regain my balance and re-direct myself. It is very challenging in my apartment where I have no support and very often find myself leaning against walls and always being very conscious to make slow turns part by part like a clock, and get up from a sitting position very carefully the special way I was taught.

    Just this past February I was diagnosed with Parkinson’s with Essential Tremors and balance problems, and had to stop a med I took before bed for over 10 years that may have been causing it and then without it I didn’t get a good night’s sleep for over a month and woke up 3-4 times every night.

    Two and a half months ago I had a bad fall at my mom’s, scared her half to death and injured my neck and shoulder. I had just started PT for that when I had another big fall … hard, and my head snapped back as I hit the ground. Later that week I was diagnosed with a concussion and I have seen 5 doctors and had about 10 appointments so far since then and been to a concussion clinic. Then I saw another Neurologist and he confirmed what another said…that my symptoms from my concussion likely will last up to 6 months!!! Thankfully it’s already been 6 weeks but there is 4.5 months ahead. But he was optimistic about the progression I’ve had and said I am on the Path to Recovery! But it sure is a rocky path!

    Other symptoms I have had are really bad brain fog and memory issues which have left me having to stop and take a long break to find the right words or even remember where I am in a conversation, and having to look up the spelling or meaning of simple words. These two things are very scary and embarrassing…(please continue to Part Two below)

    #MentalHealth #Depression #Anxiety #ChronicPain #ChronicIllness #Disability #Selflove #Selfcare #Concussion #balance #ParkinsonsDisease #EssentialTremor #PTSD #COVID19 #Migraine #MigraineBrainFog #Memory #HIVAIDS #longtermsurvivor #BipolarDisorder #Bipolar2Disorder #Bipolar1Disorder #BipolarDepression #ADHD #TheMighty #MightyMinute #MightyMoment #MightyTogether #DistractMe #IfYouFeelHopeless #Hope #relief #Love #PeripheralNeuropathy

    51 reactions 12 comments
    Post

    New member for the migraine community

    Hi everyone. I get daily migraines and look forward to being part of this community #Migraine #MigraineBrainFog #ChronicMigraines

    4 comments
    Post

    Migraine hangover

    I hate the post migraine hangover when I'm in such a fog I can't function.
    I had plans with a friend to have a picnic with our toddlers today and I don't know if I can manage.

    Then my anxiety takes over and I feel like a crap mom. My baby deserves a mom who can function to do all the fun things. 🥺 #Migraine #MigraineBrainFog #Anxiety

    1 reaction 8 comments
    Post

    the brain fog... #Migraine #MigraineBrainFog

    I fail to accommodate to the two opposite paradigms of 'the show must go on, life goes on' and 'taking notion of my body and letting it rest'. I cannot help but regularly feel bad for the fact that my migraine condition comes with fatigue and brain fog, lack of concentration, too regularly. I have learned that making it to the pain part of a migraine multiplies the possibility of having a rough postdrome during which I cannot function for about a full day because my brain feels raw and bruise like it just received a beating.

    I am free of this postdrome problem for a while now, and for this while now I have stagnated in life, did not pick up my university courses nor did I whole-heartedly change my paths in life towards something new instead.

    Just me sitting here taking notes of my migraine situation and wondering what I can (or should or want to) start in life now. I feel perfectly overwhelmed without having a migraine attack ;)

    (like...will they come back if I finally make my move on the chest board of life?)

    Post

    Any recommendations for menstral migraines? #Migraine #Migraine associated vertigo #MigraineBrainFog #ChronicMigraines #Endometriosis

    Since developing chronic pelvic pain with a possible endometriosis diagnosis (still waiting on surgery to confirm) I have been having chronic migraines. It seems to be cyclical and starts just before menstration and will last up to 2 weeks. The luteal phase doesn’t seem to bring on the migraines as much but I always have a headache no matter what time of the month. I’m currently taking amitriptyline for prevention and sumatriptan as an abortive. I’ve started a progesterone birth control pill to see if that helps but it’s too soon to tell. I also take magnesium oxide, omega 3, melatonin, B complex vitamins, and vitamin D. Over the counter pain meds do absolutely nothing. These migraines have made it so I can no longer work, get my degree, or enjoy life. If you have any suggestions or recommendations I’d greatly appreciate it!

    15 comments