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» LymeNet Flash » Questions and Discussion » General Support » Upset

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Author Topic: Upset
mariana
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After I saw the neuro I went to see the LLMD.
Apparently we have to wait for the MRI for some type of diagnosis,maybe,who knows. Meanwhile I am not being treated at all. No Antibiotics ,supplements.
I still don't have the blood test results after 10 days. I am worried about the multiple myeloma test but both drs.offices don't seem to care. I called and even went there in person . They printed the test and said they would call with results and here I am waiting. I wish they would show some compassion,I'm sure they understand people are anxiously and nervously waiting for the results.I saw a little triangle next to one of the tests which is probably my Vit.D
I don't think I have myeloma (but it would be nice to be sure). I think this is my neuros imagination.
Sorry about this post.I'm just upset .

Posts: 54 | From catskills NY | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
nonna05
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It's so hard to wait. With the illness we do it a lot.

Maybe some supplements while you wait?/
by the way hope you're OK were you are.
It's hard for me cause I don't know which days I'll start before 6 pm and everybody is done with their day.
I don't know when my next function time will be or how good/strong.

DUMB SKETES [shake] [loco]

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Robin123
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[QUOTE]Originally posted by mariana:
[QB] After I saw the neuro I went to see the LLMD.
Apparently we have to wait for the MRI for some type of diagnosis,maybe,who knows. Meanwhile I am not being treated at all. No Antibiotics ,supplements.

I still don't have the blood test results after 10 days. I am worried about the multiple myeloma test but both drs.offices don't seem to care. I called and even went there in person .

They printed the test and said they would call with results and here I am waiting. I wish they would show some compassion,

I'm sure they understand people are anxiously and nervously waiting for the results.I saw a little triangle next to one of the tests which is probably my Vit.D

I don't think I have myeloma (but it would be nice to be sure). I think this is my neuros imagination.
Sorry about this post.I'm just upset .

..................................................

Breaking this up for easier reading for many here.

I guess just stay on top of the plan, like when they will have results for you - hopefully you will start to treat soon.

If you need any info about that, you can use the search function at the top of the page to type in any word or phrase and archived threads will come up that you can read, like about how others have treated, etc.

Posts: 13116 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
mariana
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by the way hope you're OK were you are.

Do you mean because of Sandy? Yes .we are fine thanks.We got it worse with Irene.
I took supplements for a month -Tox ease and BB-CC (something like that).LLMD gave them to me.
I am taking vit D but that's because it came out very low in test in April.

Posts: 54 | From catskills NY | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
Lymetoo
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Doesn't sound like an LLMD who is on top of things.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
   

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