We all live with an acceptable amount of pain since we have no choice.
What do you rate your every day pain?
If someone swapped bodies with you, what would THEY rate that pain?
We all live with an acceptable amount of pain since we have no choice.
What do you rate your every day pain?
If someone swapped bodies with you, what would THEY rate that pain?
I am so sorry this sounds horrible. No one should have to go through this.
If you don’t mind me asking, are the tumors cancerous or just growths?
I don’t mind. One of my life’s missions is to make more people aware of this rare genetic disorder.
The tissue is like a fibrous benign tumor. My body can no longer produce bone marrow since I hit puberty. Though there’s about a 1 in 6000 chance of this becoming malignant cancer
Thankfully I can’t pass it down, as it’s a random mutation that happened in the womb.
For the most part there are two kinds the poly version and the mono version. Mono has this issue just in one bone or in the knee, but just one spot. Mono is super rare, but the poly (the multi bone version I got) is even rarer. You can have McCune-Albright and not have bone issues, but bone issues usually come with McCune-Albright
The McCune-Albright is the worst part to get though, IMO. I can get on disability and get all the pain meds that I want until the day I die with the bone portion of the disease. Yeah, it sucks to suffer in agony the rest of my life, but at least I have a life.
McCune-Albright causes your endocrine system to randomly go hyper, hypo, or parts just shut off for no reason
That means my type 1 and 2 diabetes almost kills me once a year no matter how well I take care of it, my testosterone was a 7 before treatment (about 700-ish is normal), my Thyroid is all befuddled. Then it suddenly fixes itself, and then it does the opposite.
All in all, it’s a hard condition to live with. There is maybe 10k-15k worldwide with the mono version, and only a handful with the poly version like myself. And I know about 50 of them, which may be a significant chunk of English speakers with the disease
Really, the only way that I got lucky was I’m not really badly disfigured. I look almost normal. It’s just my insides that are severely disfigured.
You got dealt a very heavy hand. I’m glad you’re still here kicking it with us. I can only imagine how hard that is. At least the cancer risk is pretty low but everything else sounds not fun at all.
Since this is so rare have they done studies on you to learn more about it?
There’s a ‘community-driven nonprofit’ that all of us put together and run called The FD/MAS Alliance
We all raise any money that we can and funnel it into genetic research to find a cure for this monstrously life altering condition.
Being able to pool our money like that and apply for grants allows us to hire doctors and labs to look for a cure. Fingers crossed with CRiSPR!