alfreda89: 3 foot concrete Medieval style gargoyle with author's hand resting on its head. (Oxblood Lilies)
alfreda89 ([personal profile] alfreda89) wrote2005-12-06 03:36 pm
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Amy Tan says this better than I can right now

http://www.amytan.net/LymeDisease.aspx

I found this reassuring, by the way. I didn't know her hallucinations were triggered by the steroids. I've been dealing with frozen shoulder, and was afraid I'd need steroids--but one injection is not like taking oral steroids, even if I need one. So, back to the exercises...

[identity profile] incandragon.livejournal.com 2005-12-07 12:33 am (UTC)(link)
Yow. I'm proud of her and her husband for getting through it. It's good that Lyme now has a "celebrity" voice.

[identity profile] alfreda89.livejournal.com 2005-12-07 07:26 am (UTC)(link)
They're calling themselves the Lyme Literati. Ginger jokes that I'm starting up the local Literati. (Too true--I know way too many writers with Lyme/CFIDS/Fibro...)

[identity profile] silona.livejournal.com 2005-12-08 04:21 am (UTC)(link)
it is strange at this point.

how many and how effected.

very frustating.

hugs

ps i'm have a meeting of my editors on the 12th at 8pm interested?

[identity profile] alfreda89.livejournal.com 2005-12-14 06:54 am (UTC)(link)
Hi, there--

I didn't get this in time. I was in Oklahoma until about 8 that night! How did it go? Are things starting to move?

I would be happy to help, but am aware that I am easily distracted and hyper-focused at the same time. So not sure where my best contribution will be. Rumor has it I go to 2x a week for shots next week. Hope it's an improvement--hands unhappy.

Making cinnamon walnuts is probably one place of contribution... ;^)