Se vuoi ridere sei nel posto giusto😎 If u wanna laugh u r in the right place😎
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@mel.dgf
♿️ disabled cosplayer ♿️ 💞🦓Chronic illness awareness🦓💞 @💫Bridget🌙 Bridget's Gofundme-https://gofund.me/6303fb0ff 💙
Mel🩵 is a TikTok creator in the United States with 18K followers and 459.4K likes. Their videos average 2K views, an engagement rate of 3.8%. Most-used hashtags: #disabledcosplayer, #wheelchairuser and #ehlersdanlossyndrome.
https://linktr.ee/Mel.dgfEstimated rate per sponsored post: $90 to $450, based on roughly $5 to $25 per 1,000 followers. This is an estimate from audience size, not reported income.
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@💫Bridget🌙 @MySaltyFace @Phantom Please take a moment out of your day to read this if you are able to. My best friend Bridget is currently dying from a long list of serious medical conditions with some of the main ones being hEDS, smas, mals, nutcracker syndrome, and Severe me/cfs. This year has been one of the worst ones she’s had to go through yet. Battling with severe malnutrition, becoming homeless, having sepsis twice, and being severely medically neglected all throughout this. We’re reaching out for help now as a final act of desperation. Bridget is a full time wheelchair user with a feeding tube and a Hickman line. However she has not been able to tolerate feeds for some time now. She is currently bedridden and relies completely on her caretaker Cody for everything. On top of this she is homeless and no longer has an income of her own. Despite everything she has tried her smas and nutcracker syndrome has gotten worse and she is looking into going on tpn and potentially having surgery to fix it. However traveling to have these surgeries done is expensive. Especially for someone who already doesn’t have an income. Her husband Josh and her caretaker Cody would be traveling with her and most hospitals do not allow guests to stay overnight meaning they would likely to have stay in a hotel during the recovery from the surgery. Ways you can help -Donate to her gofundme which is linked and both of our bios -Supporting her content -Helping spread awareness for severe me/cfs, -Helping spread awareness for vascular compression syndromes like smas, mals, and nutcracker syndrome -Purchase comfort items or medical necessities from her Amazon wishlist -Offering friendship, and support to her, her husband, her caregiver, and her friends Links Gofundme New/updated: https://www.gofundme.com/f/donate-to-give-bridget-a-chance-at-life/cl/o?attribution_id=sl:22b27dfc-f465-40ce-9be0-3d83cc61ad05&lang=en_US&ts=1788309439&utm_campaign=man_sharesheet_dash&utm_content=amp30-treatment-6&utm_medium=customer&utm_source=copy_link Original gofundme: https://gofund.me/6303fb0ff Bridgets linktree https://linktr.ee/Dummygummygurl Bridget’s wish list https://www.amazon.com/hz/wishlist/ls/35YSBBE0DPFIS?ref_=wl_share
@💫Bridget🌙 @MySaltyFace @Phantom Hello! We are hoping this post will reach someone who has had a kidney auto transplant to help with nutcracker syndrome or smas or both. We’re desperately looking for more information for my friend Bridget who is currently dying from these conditions. She’s been looking into going to Cleveland clinic to have this surgery done. But we have no idea what to expect from it. If you yourself have had this surgery or you know someone who has please don’t hesitate to reach out. We’re scared that we’re running out of time to save Bridget. Any information about this will help. Want to reach out but aren’t sure who to reach out to? Because of everything Bridget is going through right now she may not be able to respond right away or respond on her own. it is best to reach out to her caregiver Cody, her husband Josh, or me with any information you have. #nutcrackersyndrome#smas#ehlersdanlossyndrome#kidneyautotransplant#mals
Hi guys! I know it’s been awhile. I haven’t been very active on this account or really any of my other accounts over the past year. To be honest I don’t really plan to be more active on any of my accounts than I am now. I feel at peace with where I am right now. I still enjoy cosplaying and still do cosplay. I just don’t have the desire to post it half of the time. I’ve also found new hobbies that bring me a lot of joy like crochet, jewelry making, and painting. I had my health take a huge downward spiral this year and have ended up using my wheelchair basically full time. Shortly after this I got my new wheelchair and it has been amazing so far. I got to trial some different power assist options and ultimately decided on the empulse m90. However it is not currently compatible with the brand of chair I have so I decided to wait until it’s compatible instead of going with another option. I’ll still post sometimes but it will no longer be active or on an actual schedule like it used to be. Mainly just whenever I actually want to post. I felt so pressured in the past to keep up an active posting schedule because whenever I didnt my views went down. It would make me spiral both physically and mentally and put a lot of stress on me. Thank you all for being so kind to me, and thank you to everyone who has stayed for this long. It truly means so much to me.💞 #disabledcosplayer#mikantsumikicosplay#mikantsumiki#danganronpacosplay#danganronpa
Mel🩵 (@mel.dgf) has 18K TikTok followers as of 2026-10-11.
Se vuoi ridere sei nel posto giusto😎 If u wanna laugh u r in the right place😎
orca enthusiast meg thee stallion fan i post on youtube on saturdays (for the most part)
Your next discovery is waiting on TikTok.
Picnic At The Cemetery
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