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Hi, my name is Irishdollhnm8. I'm here because
Hi, my name is Irishdollhnm8. I'm here because
This tip is one of the most helpful ones I've learned on my healing journey. I hope it's helpful for you today.
#ADHD #AnorexiaNervosa #Anxiety #AutismSpectrumDisorder #Addiction #MentalHealth #BorderlinePersonalityDisorder #BipolarDisorder #BackPain #IrritableBowelSyndromeIBS #ChronicFatigueSyndrome #CeliacDisease #Cancers #Depression #Epilepsy #EatingDisorders #EhlersDanlosSyndrome #Endometriosis #Fibromyalgia #Lupus #LymeDisease #MajorDepressiveDisorder #Mania #PTSD #PanicAttacks #PanicDisorder
#RestlessLegsSyndrome #Schizophrenia #Selfcare #Selfharm #SocialAnxietyDisorder #TouretteSyndrome #Trauma #SuicidalThoughts
Hi, my name is Kathy. I'm here because I live with and fight daily, Lyme and late stage Babesia(a confection to Lyme disease.) And because of that,I'm always open to learning more from others,that might be in the same boat,to learn and also help where I can.
Living with Lyme disease can be unpredictable, frustrating, and exhausting. Symptoms can range from chronic fatigue and pain to rashes, neurological and cognitive challenges, mental health struggles, arthritis, heart palpitations, and much more. Because many symptoms are invisible or fluctuate over time, the realities of living with Lyme disease are often misunderstood.
What do you wish others understood better about living with Lyme disease? What has been the most challenging part of your experience? What resources, treatments, or coping strategies have been the most helpful? Where do you feel you need more support right now?
#LymeDisease #ChronicIllness #MentalHealth #CheckInWithMe #ChronicPain #ChronicFatigue #Arthritis #Anxiety #Depression
Hi! My name is Emilie Delaye, and I’m one of the cofounders of Nova — a brand creating premium stylish piccline covers using unused luxury textiles.
This mission is deeply personal to me because I myself had both a piccline and a port, and I know firsthand how difficult it can be to feel confident and comfortable during a medical journey.
We’re currently casting individuals in New York City who currently have a piccline or have had one before for an upcoming campaign shoot taking place May 27–29.
Our mission is centered around confidence, representation, and creating medical wear that feels more personal and empowering.
No modeling experience is needed at all — we’re simply looking for real people and real stories.
If this sounds like someone in your community (or yourself), we’d love to connect. Please DM us or email emiliejd@udel.edu for more details 💌
Thank you so much for your support!
#PiccLine #medicaldevice #ChronicIllness #ChronicPain #Cancer #Diabetes #LymeDisease #CysticFibrosis
Hi, my name is deannadawn78. I'm here because I was diagnosed with Lyme disease and a couple co-infections about 10 years ago. Haven’t been able to keep up with it since insurance doesn’t cover anything!! And EVERYTHING is so dang expensive!! At this point I’m not living I am just surviving!! Any tips, advice etc I would be grateful. Thank you.
#MightyTogether #Anxiety #Depression #Migraine #lyme#co-infections
Here it goes y’all. I have been feeling so defeated and down lately. My husband switched our insurance with his work from their hmo to a crazy hmn (I have never heard of this type) and no one is covered. I lost the ability to see my complex care internal medicine doctor who took care of *everything* for me.
So in an attempt to find resources to help all of my laundry list of illnesses, I started with a rheumatologist who supposedly helps my mixed connective tissue disease according to Dr. Google.
Spoiler, he did not and basically told me I need to find a functional medicine doctor who prescribes traditional medicines and takes my insurance, a neurologist, a endocrinologist and a new primary care doctor “to start”, his words not mine. Also I have to continue with the new heart doctor who also is referring me to a dysautonomia specialist because it is above his comfort level of treatment he said. He can try but he’d feel better sending me down town. I can no longer drive fyi.
All of this with my new crazy insurance who does not cover even a box of tissues for these stress tears that they’re causing. My husband promised he’d help try and coordinate all of these new crazy doctors I need but this was nearly two weeks ago and nothing has happened. I’ve been trying to dig and dig for a functional medicine doctor who treats whole body and not “gut health” only type things or box o’ vitamins. It’s just so gimmicky. #Depression #Fibromyalgia #Dysautonomia #AutoimmuneThyroidDisease #MentalHealth #LymeDisease #Anxiety #MixedConnectiveTissueDiseaseMCTD
Hi, my name is hlord84. I'm here because I have been looking for peers to connect with. I have been diagnosed with so many things and cannot leave the house most days. I live with my husband and dogs but feel so alone after having been an extremely active, social person in my before life. My therapist suggested I search for support groups and I found this app. I hope to meet some wonderful people and make some connections that can help me feel not so alone out here.
#MightyTogether #Anxiety #Depression #PTSD #Migraine #Fibromyalgia #LymeDisease
Hi, my name is Dylan Rothbein. I'm here because I'm always looking for support and I care about community and disability. I'm currently a rabbinical student and a musician and filmmaker. I have been and activist and disability studies scholar for 10 years. I have a BA in history and an MBA in music business.
#MightyTogether #BipolarDisorder #Migraine #LymeDisease #CerebralPalsy #EhlersDanlosSyndrome #Epilepsy #PTSD #Dyslexia #Blindness
Hi, my name is Rawya.
#MightyTogether #Grief #ADHD #Anxiety #Depression #LymeDisease