It has been a while since I last blogged, mostly because life has gone on, and we are busy living it.
Also, I couldn't get access to my own blog, thanks to rapidly changing technology and to some European Union rules. I'm not sure how this is going to work out, but I'm going to attempt to show pictures from our recent trip to Cozumel, Belize and Honduras, as soon as I figure out how to get my pictures posted!
It's amazing how much has changed on the Internet since Ted's diagnosis, almost 12.5 years ago. Coming soon.. photos from our trip and advice and details about traveling with a disabled person who doesn't meet the stereotypes of what a disabled person should look like.
Also, I couldn't get access to my own blog, thanks to rapidly changing technology and to some European Union rules. I'm not sure how this is going to work out, but I'm going to attempt to show pictures from our recent trip to Cozumel, Belize and Honduras, as soon as I figure out how to get my pictures posted!
It's amazing how much has changed on the Internet since Ted's diagnosis, almost 12.5 years ago. Coming soon.. photos from our trip and advice and details about traveling with a disabled person who doesn't meet the stereotypes of what a disabled person should look like.
Hello, I am 68 years old-female. I was diagnosed in July 2019 Tumor was aspirated(It was not deep)August 2nd I am going thru 30 radiation treatments Mon-Fri and TMZ every day. I will be done Oct. 2nd -then one month off for good behavior. In Nov. I will have some sort of arrays on my head from NovoCure Optune. and a weekly BIG dose of TMZ
ReplyDeleteI am so happy to see there are long term survivors . It give me lots of hope.. I live in he Upper Peninsula of MI. I was so lucky to have a great neurosurgeon in Duluth Mn.100 miles away and wonderful Cancer Center in Ashland, Wi.40 miles away..I am more than 1/2 thru treatment , doing well and blood work is good Keep posting!!My email xiaxia@sbcglobal.net