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Old 03-14-2005, 12:34 PM   #1
raleigh86
Senior Member
(female)
 
Join Date: Apr 2004
Location: USA
Posts: 135
It's a bad time...

I don't know if I'm feeling sorry for myself, or if I really am having a rough time. I've felt ill for 1 year, in lyme treatment for 5 months, I realize many of you are in the same boat, or worse. My worst symptoms, pre diagnosis, are behind me, the all the others are still here. The last 2 months taking Levaquin along with either minocycline or septra, plus adding flagyl, have been nightmarish. I've had to rearrange my meds schedule due to a 2 week cold and cough and changed flagyl so I wouldn't be taking it while away for a few days. As it is, I'm only on meds 3 days a week because of white blood count. Pain in joints and all over came with levaquin. My PA had me stop meds for 1 week. I started again last Wed. and pain came back. Some pain had never left in the week I was off med. My shoulders, arms and elbows hurt so much, especially in bed, I can't roll over and pull up blankets. I haven't found anything that helps with this pain. I am currently taking lodine, but haven't had much relief. I do go to Jemsek on Friday. In a way I'm looking forward to it, in case they can change meds not to make me feel so ill. I now dread the drive, as the driving time and appt. take the whole day. I am just in a dreadful mood, restless, fatigued, no motivation, mostly mental issues. Minocyn or combo with levaquin has made me itch dreadfully. Also, I read post about doubting lyme test. I feel I have lyme, but some symptoms are same as thyroid. I did develop thyroid nodules the same time I was diagnosed with lyme. According to endo, I do not have thyroid disease because of thyroid test results. I am on synthroid to shrink nodules. I had thyroid ultrasound last week to see if nodules have shrunk. I will go for more blood work and visit endo in the next 2 weeks. I am on low dose of synthroid, but will increase after my endo visit. I worry that some of my symptoms are thyroid related and not lyme and wonder if I will have proper thyroid treatment to resolve these symptoms. The endo or lyme PA cannot say for sure what symptoms belong with which ailment.

I changed my flagyl schedule so I am not taking it the same 3 days as other meds. As it is, I get chest pressure taking it, but it is magnified when taking it with levaquin. Will it hurt not taking flagyl the same days as other meds? I am taking the correct amount of meds in a week, just not at the same time.

Thanks for letting me vent. Not too many people care to hear this saga, again.

Raleigh86
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Old 03-14-2005, 12:39 PM   #2
sagedreamer
Junior Member
(female)
 
Join Date: Feb 2005
Location: new jersey
Posts: 42
Re: It's a bad time...

Raleigh :: i cannot answer any of your questions, as i am new to the lyme nightmare. But i do hope you get relief


be well::
carole
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Old 03-14-2005, 08:00 PM   #3
ncgirl88
Senior Veteran
(female)
 
Join Date: Aug 2004
Posts: 1,490
Re: It's a bad time...

Hi Raleigh86 -

I hear you loud and clear. The amount of cloudiness and trying to sort it all out sometimes drives me absolutely to my breaking point. I really think Minocycline for me makes me depressed. I have less of the depression on flagyl.

Anyway, I wished we could just have tea. It so helps to be in the presence of others who have been there or are going through it now.

Take care my friend. I wished I was a doctor and could help you but alas I am not. But know I am thinking about you and wishing you healing energy.

-ncgirl88
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Old 03-14-2005, 08:54 PM   #4
outinthe_woods
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(female)
 
Join Date: Jan 2005
Location: connecticut
Posts: 661
Re: It's a bad time...

NCgirl: Having a cup of tea with everyone sounds SO wonderful at this point. Even if we don't solve anything, the spirit of being together with the only people who really understand what you're going through would be great!
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Old 03-14-2005, 09:16 PM   #5
fotomom
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Join Date: Nov 2004
Location: Calif
Posts: 437
Re: It's a bad time...

(((((hugs)))))
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