Finally got dr permission for IV magnesium. I don’t absorb it any other way so I am extremely deficient in it and ill. Can provide materials.
Problem is that I can’t find anyone to come out here in suburbia for less than $600 (check cost of wellness clinics in Melbourne. Expensive or don’t do at all. )
If you are a #nurse#phlebotomist#hcw or have any experience running a drip, please reply/DM. I don’t care if you learned it DIY as long as you know what you’re doing.
This treatment changes my life from bedridden to 60% of normal in a few months! That’s mildly ill in comparison.
It helps every symptom I have.
Hospitals only give it for preeclampsia. Hospital in the Home is the same. Private nurse services same.
It’s so basically going through proper channels doesn’t help.
It’s not illegal to have someone qualified come out and do it as long as doc has signed off on it which is why wellness clinics can do it. But medical system won’t. I know it doesn’t make sense but it’s Australia 2024. If you don’t have formal qualifications we can figure it out.
I’ve even asked the government for help. Nothing.
Was informed even private insurance wouldn’t help with this (I don’t have it ofc but this is an example of how hard and stupid this is.)
P-l-e-a-s-e post to other platforms. I have no team to help promote me I barely have any energy for basics . I have no energy to advertise. If you can help an team also let me know.
Please give me some quality of life.
I’m in #Melbourne#Australia.
If you’re willing to drive a distance will compensate for petrol and pay what you think is fair for your time.
TLDR: Need nurse or any qualified healthcare worker to come to my place to give magnesium IV.
Even consider unqualified if you know what you’re doing.
For the first time, people with hidden conditions such as #fibromyalgia, ME and #autism will be eligible for disability benefits after Malta adopts World Health Organisation functionality assessment
Def not your fucking token Negro, so fuck off.
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:transgender_flag_black: It/Its | He / Him
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Disabled w/ chronic pain, mad & emotionally unstable at times.
Early 30's. I'm Moo. :cowroll:
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profile pic desc: a frame from the Mamushi music video a silhouette of Megan in front of a large red moon, one of her arms outstretched behind her
header desc: Megan Thee Stallion along with her dancers standing in front of the progress pride flag
2 months later [everyone in the world has monkey pox and we r in lockdown]
me: NO WE ARE NOT DOING THIS SHIT HOME SCHOOL
people who hate school: yay
world health organization: TIME TO WORK
those who know: 💀
random 8 yr old: skirby fucked a dog
those who follow: I'm voting for Kamala
those who pretend to know: Nothing ever happens
those who know: 💀
𝐅𝐮𝐥𝐥 𝐌𝐞𝐠𝐚 𝐅𝐨𝐥𝐝𝐞𝐫 𝐂𝐡𝐞𝐜𝐤 𝐌𝐲 𝐁𝐢𝐨
me at the tik tok rizz party: ENGLISH OR SPANISH
mah bois: frozen
hawk tuah caseoh: moves CAN I GET A HOYAAAA?
me: SUSSY AYOO
those who know:💀
(5 likes for part 2)
𝐅𝐮𝐥𝐥 𝐌𝐞𝐠𝐚 𝐅𝐨𝐥𝐝𝐞𝐫 𝐂𝐡𝐞𝐜𝐤 𝐌𝐲 𝐁𝐢𝐨
"How to be an Effective Advocate for a Disabled Patient: #Disabled patients are rightfully terrified of being hospitalized. We are stripped of our agency & control in a hospital environment. Having an effective advocate can vastly improve the experience"
“When you are hospitalized - you give up your agency. You are put in the control of doctors & nurses who may have limited understanding of your condition. What & when you eat, when you take your medications (and what medications you’re given)…it’s all out of your control”
“Which brings us to the need to have an advocate. If you have the luxury of choosing your advocate (many of us do not) you want to pick someone who is knowledgeable about your conditions, readily available and calm and cool under pressure.”
“Have a detailed care plan & advanced directive they can follow which CLEARLY states your wishes should you be incapacitated or unconscious & unable to make decisions for yourself. Make sure your advocate keeps copies of these documents in a safe place & brings them to the hospital”