[Image: a split picture. One side is a photo of a Black man wearing glasses in a hospital bed with oxygen tubing under his nose. The other side is a sign that reads: “My name is Michael Hunter. I was diagnosed with leukemia in June 2013 & was told on June 11, 2014 that I only have a few months left to live if I can’t find a donor. Please help me with my biological family or a donor match! I was born in Columbus, OH 3/1/1985 at Doctor’s North Hospital and given the name Christopher Brown. Please share”.]
"My name is Michael Hunter. I was diagnosed with leukemia in June 2013 & was told on June 11, 2014 that I only have a few months left to live if I can’t find a donor. Please help me with my biological family or a donor match! I was born in Columbus, OH 3/1/1985 at Doctor’s North Hospital and given the name Christopher Brown. Please share"
Michael is a friend, I’m asking that you all take the time to share this. He desperately needs a bone marrow donor and there is very limited number of African American donors. Without a donor Michael is going to die.
Michael was adopted and does not know his birth family. We know he has a half brother but have no information about him.
He does not specifically need an African American Donor but because of all of the things that factor into finding a match (blood type, dna tissue etc.) , someone of similar descent is more likely to be a closer match.
If anyone knows anything about Michael’s birth family or if you would like to see if you are a match, please privately message me. I can put you in touch with him and his caregivers directly!
We hope through spreading awareness we can either find his birth family whom he does not know or find a donor match. Michael lives in the Cincinnati, OH area. Please dont just like this or scroll past. Please share this! You could save his life!
BOOST. Its so hard for Black people to find donors.
Today’s picture for invisible illness is a personal one. This is one of about 30 notes that my friend has received since using her handicapped placard. I’m going to say this to you, have you ever seen someone get out of a car parked in a handicapped space and said to yourself “they look too young or they don’t look disabled.” I’m going to go with yes you have, because we all have at one time. I can’t remember doing it, but before I understood the difficulties of invisible illness when I was younger I probably did. Let me ask you this though, when you had that thought was it because you knew with 100% certainty that they weren’t handicapped or did you assume that because of their age and/or not seeing a cane, walker or wheelchair? All I’m asking is that we stop and think when we someone need a mobility aid, park in a handicapped space or say they are disabled that we remember this “DISABILITY HAS NOTHING TO DO WITH AGE OR APPEARNACE.” #spoonie #invisibleillness #disability #chronicillness #rheumatoidarthritis #lupus #fibromyalgia #myofascialpainsyndrome
If nothing else, this post needs to be seen around the internet more. This harassment is not okay and no one should have to deal with it on top of having an invisible illness. This is just another form of anonymous bullying to add to the internet bullying these TROLLS are capable of.
If you are healthy, please reblog.
If you are sick, please reblog.
If you have a disability, please reblog.
If you have an invisible illness, please reblog.
If you know someone with a disability, please reblog.
If you are a human being, please reblog.
Let’s spread the word and help those of us that may not look like it.
Ignorance isn’t bliss, ignorance is ignorance.
Books: check ‘em out.
Look. Do you want to understand what it’s like in my head? Do you? WELL HERE YOU GO, I PUT TOGETHER A PROTOTYPE
(from this ad that’s been in my head for 22 years)