Comments on green words growing: If wishes were fishes

Hi Kim, thanks for stopping by and for your kind w...

2009-11-18T08:27:13.549+10:00

Hi Kim, thanks for stopping by and for your kind words. I'm sorry to hear about your daughter, 6 years without a diagnosis is a long time - especially at that tender age - but I'm so glad she got one in the end. I have heard of a couple of people being diagnosed with EDS after a previous CFS diagnosis. Interesting!

My daughter, Veronica became ill when she was 14 a...

2009-11-14T20:13:17.333+10:00

My daughter, Veronica became ill when she was 14 and I know very well how you were feeling when you wrote this post. Veronica,(somedaywewillsleep.com) was diagnosed with Ehlers Danlos syndrome when she was 20, which is commonly misdiagnosed as CFS. It has been a long journey and I empathise with you.

Thanks so much, Jennie. Cinderkeys, I totally agr...

2009-08-26T11:46:15.294+10:00

Thanks so much, Jennie.

Cinderkeys, I totally agree with you about the research, it's one of my hobby horses!

Rachel M and Amanda, thanks for the finger and toe crossing, you can take a break and uncross them now.

Thank you for that great blog link, Priscilla - what an amazing story!

Oh, do keep us updated. I had a doctor like that ...

2009-08-21T22:42:13.761+10:00

Oh, do keep us updated. I had a doctor like that for a time. So difficult, but also rather useful.

Here's another sick-chick blogger who recently got an unexpected, totally different diagnosis:

http://acomiclifeindeed.wordpress.com/2009/07/17/that-new-diagnosis-announcement/

Interesting...I too will have some digits crossed ...

2009-08-20T20:20:22.815+10:00

Interesting...I too will have some digits crossed for you. Good luck!

I'm so sorry that you had to go through such a hor...

2009-08-20T03:34:33.177+10:00

I'm so sorry that you had to go through such a horrible interrogation.

I'm hoping it will bring you hopeful news with effective treatment. I'm keeping my fingers and toes crossed for you.

There needs to be so much more good research on ME...

2009-08-20T03:10:53.569+10:00

There needs to be so much more good research on ME, not just to help the people who have it, but others who get misdiagnosed with it. Good luck!

Thinking of you, friend.

2009-08-20T02:55:34.322+10:00

Thinking of you, friend.