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Greg’s MDS

It’s a little bit odd to have a website and blog about a disease, I suppose, especially if you have the disease. But I’ve found, when members of my extended family are diagnosed with something - particularly something you might not hear about every day - that it can be hard to find out exactly what they have, what they are doing about it, and how well that’s working. So this is my attempt to get the straight scoop about my MDS out to the folks I care about. You can read The Basics. Just because I’m putti...

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Greg’s MDS | greghankins.com Reviews
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It’s a little bit odd to have a website and blog about a disease, I suppose, especially if you have the disease. But I’ve found, when members of my extended family are diagnosed with something - particularly something you might not hear about every day - that it can be hard to find out exactly what they have, what they are doing about it, and how well that’s working. So this is my attempt to get the straight scoop about my MDS out to the folks I care about. You can read The Basics. Just because I’m putti...
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Greg’s MDS | greghankins.com Reviews

https://greghankins.com

It’s a little bit odd to have a website and blog about a disease, I suppose, especially if you have the disease. But I’ve found, when members of my extended family are diagnosed with something - particularly something you might not hear about every day - that it can be hard to find out exactly what they have, what they are doing about it, and how well that’s working. So this is my attempt to get the straight scoop about my MDS out to the folks I care about. You can read The Basics. Just because I’m putti...

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Greg’s MDS

http://www.greghankins.com/gregsmds/The_basics.html

MDS is short for Myelodysplastic Syndrome. Like a lot of medical terms, this one is needlessly complicated. Myelo means bone marrow and dysplastic means messed up. Here’s a guided tour.

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Greg’s MDS

It’s a little bit odd to have a website and blog about a disease, I suppose, especially if you have the disease. But I’ve found, when members of my extended family are diagnosed with something - particularly something you might not hear about every day - that it can be hard to find out exactly what they have, what they are doing about it, and how well that’s working. So this is my attempt to get the straight scoop about my MDS out to the folks I care about. You can read The Basics. Just because I’m putti...

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