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New Message on Pituitary Chat

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From: Marcia
Message 2 in Discussion


Hello Helen. I'm sorry to hear you are having so many problems! Helen, I have 
some of the same levels that you do. I cannot stand heat! I keep the thermostat 
at about 68. If it rises above 69, I am sweating!  In the summertime, the air 
conditioning is running constantly!  And I will probably never wear a warm 
sweater again. One difference for me, is that I take Levoxyl. I do not have any 
side effects, and it works great! Without it, I'd be sleeping during meetings, 
and falling asleep at the wheel!


 


My advice, is to always have a fan available, and ask your family members to 
wear sweaters if they are cold. It is much easier to put clothes on, that to 
take them off! And, take walks on cool days. Exercise really makes me feel 
better.


 


Helen, how is it that you were diagnosed with lyme disease? And, what do you 
know about a connection between Lyme and Pituitary disorders?



Sincerely,

Marcia





-----Original Message-----

From: VibrantHelen <[EMAIL PROTECTED]>

To: Pituitary Chat <[email protected]>

Sent: Sun, 25 Nov 2007 9:23 pm

Subject: pituitary insufficiancy?? I'm NEW!! Help!!






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New Message on Pituitary Chat

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From: VibrantHelen
Message 1 in Discussion

Hi All, SO glad I found this group. I have chronic late stage lyme disease and 
other tickborne diseases. One is babesiosis which causes sweats and fever. I 
developed those symptoms some months after my total hysterectomy (BIG mistake). 
O was an OR RN before I got really ill. The babesiosis has been treated very 
aggressively but it can be chronic. The main symptom that is driving me crazy 
is 
profuse sweating esp face etc. At ti1mes I have a low grade fever but the 
sweating is out of control. I can't even mop half my kitchen floor in a cool 
room or I sweat to death and need to sit or lay to cool off. Now everybody 
thinks it's from an endocrine disorder. My estrogen is almost nonexistent and 
my 
TSH is extremely low even being on 90 of armour thyroid. This has been going on 
over 5 years. I am losing my mind. I was very ill for over 4 years after I 
relapsed after my surgery and not until they discovered this strain of 
babesiosis did I even begin to improve at all--I was bedridden. I used to see a 
great endocrinologist but she came to my lyme doctors office every 2 months 
from 
Kansas because so many late stage lyme patients have problems with pituitary. 
So 
I didn't find another endo until Sept who uses human growth hormone which I too 
desperately need and was on with the other endo. I do not like this endo who I 
looked for so long because she uses human growth hormone. She is abrupt and 
hardly looked at me. She put me on levoxyl--125mcg and estratest 1mg. I've been 
on a week and feel no different and she can't see me until early Feb. WAY too 
long. I need to have my levels checked much sooner than that. OK, my TSH is 
0.175 and the range is0.350--5.500. My estogen is <7 and the range is 19--528. 
I'm so down because I cannot stand sweating all the time. ANY advice--help or 
please e-mail me of anybody knows a good endo who "gets" pituitary problems in 
Phila, NY. I love in West Windsor NJ in between Trenton and Princeton. 
Thankyou! 
Helen

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