Surviving As Mom

Life after Healing from Sjögren's Syndrome

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  • In Limbo

    In Limbo

    I seem to be stuck in some kind of sick limbo. I think I’m starting to come out of a months long flare. I say “I think” because I have been very inconsistent overall. One day I can feel good enough to be productive at home or even go out to the store. Another day…

    Meredith Gallie

    January 8, 2021
    life
    autoimmune disease, bedridden, chronic fatigue, chronic illness, chronic pain, disabled, dysautonomia, flare, housebound, in limbo, invisible illness, pots, sjogrens, sjogrens syndrome, spoonie
  • The All Too Familiar Sjogren’s Flare

    The All Too Familiar Sjogren’s Flare

    For me, a flare comes in many shapes and sizes. It is constantly evolving and always keeps me on my toes. I wake up each morning wondering what symptoms today will bring. My symptoms in general vary greatly. An autoimmune disease such as Sjogren’s Syndrome comes with many varying symptoms. Some come and go. Some…

    Meredith Gallie

    December 29, 2020
    life
    anxiety, autoimmune, brain fog, chronic fatigue, chronic illness, chronic pain, depression, diary, disability, disabled, flare, housebound, invisible illness, mental health, sjogrens, sjogrens syndrome, spoonie
  • Imprisoned Again

    Imprisoned Again

    As I’ve mentioned in previous blog posts, I am mostly homebound. I say mostly because its not quite 100%. I’d feel like I was being dramatic by claiming I am fully homebound. This is because on rare occasions I do actually leave the house. Usually its only for doctor appointments or when I absolutely MUST…

    Meredith Gallie

    December 29, 2020
    life
    anxiety, bedridden, chronic fatigue, chronic illness, chronic illness warrior, chronic pain, chronically sick, depression, disabled, dysautonomia, fibromyalgia, homebound, housebound, invisible illness, isolation, loneliness, mental health, prison, sick, sjogrens, sjogrens syndrome, spoonie
  • Chronic Illness Doesn’t Rest for Christmas

    Chronic Illness Doesn’t Rest for Christmas

    Yesterday was Christmas day. We all woke up at 6am and had a great time opening presents and just being together as a family. The kids had a great time and I enjoyed seeing their happiness. It also happened to be a terrible day for me. My body was fighting me very hard. I woke…

    Meredith Gallie

    December 26, 2020
    life
    anxiety, christmas, chronic fatigue, chronic illness, chronic illness mom, chronic pain, depression, diary, disabled, dysautonomia, flare, housebound, ibs, invisible illness, sick, sjogrens, sjogrens syndrome, spoonie
  • Foggy…

    Foggy…

    I’m very scattered today. Having trouble concentrating. I have a million tasks running through my head… things on my To-do list, but I can’t seem to get my act together to make it happen. I’ve walked in various rooms with intentions of doing something, then aborted mission and went back to my safe place on…

    Meredith Gallie

    December 21, 2020
    life
    anxiety, autism, autoimmune, blog, blogger, brain fog, chronic fatigue, chronic illness, chronic illness mom, chronic pain, covid, depression, diary, homebound, housebound, invisible illness, isolation, mental health, momlife, quarantine, school, sjogrens, sjogrens syndrome, social, spoonie
  • It’s ok to be Unproductive Sometimes

    It’s ok to be Unproductive Sometimes

    I changed my clothes today after about a week. I’m still wearing sweats and no bra, but I feel like I look a little cuter; a little more stylish. Maybe I don’t, but I feel like I do so I’ll just go with it. I really do get tired of always looking like a slob.…

    Meredith Gallie

    December 18, 2020
    life
    boymom, chronic fatigue, chronic illness, chronic illness mom, chronic illness warrior, chronic pain, disabled, friday, housebound, invisible illness, mom of 4, momlife, sjogrens, sjogrens syndrome, snow, spoonie, spoonie mom
  • Snow Day!

    Snow Day!

    Yesterday was our first big snow of the season. We had a Nor’Easter which gave us about 7 inches of fresh, fluffy snow. I love the snow but only when I don’t have anywhere to go. This is also the first snow in our new house. The landscape is absolutely gorgeous! We have such a…

    Meredith Gallie

    December 18, 2020
    life
    autoimmune disease, chronic fatigue, chronic illness, chronic illness mom, chronic illness warrior, chronic pain, diary, disabled, family, family fun, flare, happiness, homebound, hope, invisible illness, mom, my story, sjogrens, sjogrens syndrome, snow, snow day, spoonie, the mighty, unchargeable
  • Learning How to Save Myself…

    Learning How to Save Myself…

    I wanted to write this blog to share something that has truly helped me during my darkest times. I was drowning in pain, depression, hopelessness, and despair and I needed to find a way to save myself. This is how I’m doing it. Its true that when you are sick, tired, and in pain nearly…

    Meredith Gallie

    December 16, 2020
    life
    advice, anxiety, buddhism, chronic fatigue, chronic illness, chronic illness warrior, chronic pain, coping, diary, disability, disabled, hope, hopeless, housebound, how to, invisible illness, meditation, mental health, mindfulness, my story, peace, positivity, prayer, religion, save myself, sjogrens, sjogrens syndrome, spiritual, spoonie, suffering, unchargeable
  • My Not-So-Invisible Illness

    My Not-So-Invisible Illness

    I’ve always referred to my chronic health problems as my “invisible illness”. In a lot of ways it is invisible. In general, I appear to be a normal, healthy 39 year old mother of 4. This is especially true for the rare times that I feel good. However, over the last few years as my…

    Meredith Gallie

    December 15, 2020
    life
    acceptance, anxiety, autoimmune, brave, cane, chronic fatigue, chronic illness, chronic illness warrior, chronic pain, depression, disability, disabled, disease, ecv, hair loss, handicap, housebound, invisible illness, life, mobility aid, my story, scooter, sick, sjogrens, sjogrens syndrome, skinny, social anxiety, spoonie, ugly, unchargeable, weight loss
  • Leveling Up in the Disability Game

    Leveling Up in the Disability Game

    Like many people who suffer from a chronic illness, I require the use of mobility aids. I had a very hard time admitting this to myself. I was admitting defeat. I couldn’t function like everyone else anymore. I had to accept a new term to describe myself; DISABLED. It hurt! I couldn’t accept it. I…

    Meredith Gallie

    December 15, 2020
    life
    anxiety, autoimmune disease, brave, cane, chronic fatigue, chronic illness, chronic illness warrior, chronic pain, depression, diary, disabled, ecv, handicap, invisible illness, life, mobility aid, mom, my story, scooter, shame, sjogens, sjogrens syndrome, spoonie, surviving as mom, unchargeable, wheelchair
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