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About Tehuti
I am an amateur writer of novels, serials, and novellas. Most of my work is in the genres of fantasy, mythology, drama, occult, GLBT, and erotica.
As I'm not seeking publication, I offer my work online for free reading. I'm not seeking stylistic critique so much as feedback from people who just like reading what I write. I love hearing what people think of my characters, plots, themes, etc., so if you have any comments or advice on those, feel free to share. I'm not hugely popular and often go many months without hearing from readers so I enjoy all the comments I get!
My interests are Ojibwa mythology, Mackinac Island, Egyptian mythology, Jungian symbolism and dream interpretation, ritual crime, fantasy writing, and various other things you can find in my personal bio, available just to the right. Please click to learn more about me and what I'm looking for in terms of readers and potential friends.
Feel free to hit me up if you're interested in any of these things, and enjoy my writing!
Tar! :) |
 Content Rating Notice: Recommended for Readers 18 Years and Older Only |
Untitled Tentative Blog-Type Thing Entry #678746, added on 12-04-09 @ 10:32 pm EST
Entry Access Restriction: None.
Suprisingly, Medicaid covered both medications, Elmiron (the non-generic) and "Atarax" (a generic, hydroxyzine, which is actually an antihistamine/anti-anxiety/sedative).
I was honestly kind of hoping it wouldn't cover the Elmiron since "hair loss" is a possible common side effect. If my hair starts falling out there is no way I am continuing this crap. Plus it says to take it three times a day, well before or after eating, and with a full cup of water. No way in frigging hell am I taking it with a full cup of water three times a day which is three cups (24oz) of water. I can drink only 24oz of tea in an entire day, plus a little water, and that only after 4PM, without my bladder starting to go haywire with all the urine, and even then it still acts up, so no thank you, I'll have to do with just a swallow. Stupid-ass medications for a disorder I probably don't even have. Stupid-ass doctor who can't even listen to plain English.
I guess I'm to start taking them tomorrow, the generic one at bedtime as it's a sedative, and see if they at least make my bladder less twingy while I wait three months to see the doctor and tell him AGAIN that the problem is still there. While this disorder could explain my oversensitivity, it doesn't explain my output, and I read that "pain" is a symptom described by 100% of people with interstitial cystitis. I have no pain. Just extreme discomfort, which, IMO, is just as bad as pain so to me personally yes, is pain, but I'm fairly certain it doesn't count as pain to doctors, so no, I do not have bladder pain. I've told them this repeatedly. So I haven't any idea how he made this diagnosis aside from the fact that I happen to go to the bathroom a lot, BECAUSE I HAVE TO FRIGGING PEE A LOT.
I'm tired of this and have to pee so tar.
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This page last updated 11/11/09. Still under construction so may change at any time.
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