TheBostonChannel is looking for people who have been battling MRSA in their families for an interview for an upcoming story - email rhondamann@hearst.com if you would like to be included.
Boston, Massachusetts, MRSA Affected By MRSA in or Around Boston?
August 22nd, 2006 · 5 Comments
Boston, Massachusetts, MRSA Tags: Massachusetts · MRSA
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5 responses so far ↓
RJS // Aug 22, 2006 at 7:31 am
Hey, I live near Boston, but I haven’t been affected, so I guess I don’t count. :p
Christina // Aug 22, 2006 at 7:33 am
LOL And consider yourself lucky.
Megan Day // Nov 19, 2006 at 10:23 pm
I have CA-MRSA, which I aquired from an ex-boyfriend, who I believe aquired it through athletics- specifically by climbing in an indoor climbing facility. I was misdiagnosed through 6 infections which lead to serious complications, including a serious and highly resistant infection in both kidneys. The infection required hospitalization for 6 days, and a PICC line to recieve antibiotics. At this point I was still being misdiagnosed. It wasn’t until recieving another infection on my ear that my mother and I did extensive research and suspected I had CA-MRSA. I insisted on a culture of the ear infection, and it was determined I had CA-MRSA.
Hopfully it is not too late to use this story somehow.
Megan
alysia // Dec 1, 2006 at 10:24 pm
I’m a mother of 2 sets of twins 6&7 yrs old we all have mrsa we want to get “intouch” with the right Doctor we live in the LA area we all have Kidney Infections the twins arent in public school because all to sick If someone can PLEASE HELP US we would gladly appreciated it my email is my4babys@outgun.com
Tammy // Oct 12, 2007 at 7:59 am
: Hi. Just wantted to say How great this site is. I was dx with MRSA last week and I have learned more about it on line then with my own Doc And would like to learn more. So if anyone would like to share info with me that would be great. I need as much info as I can get (well I think we all need as much as we can get). Plus I all so have Crohns disease and a blood clot disease call factor 5( Think I am falling apart:) Like I said i am new to this disease so any and all info would be great so please if you would like to talk e-mail me Or I.m me . And again I think sites like this are great. With out them many well at least me would be lost. Doctors look at me like I have 10 head give me med witch are CLINDAMYCIN,CIPROFLOXACIN and a ointment called MUPIROCIN. does this sound rigth to anyone? Please if it does not let me know And the doc tells me tells me the boilel i have looks like someone stabed me (Thanks doc : ). so that tells you how much help he is . So THANK YOU all for the help you have given me PLEASE e-mail me @ blubee66@yahoo.com OR BlueeBee66@aol.com Have a good Day
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