High Blood Pressure

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mother natures child
Regular Member


Date Joined Oct 2009
Total Posts : 231
   Posted 10/14/2009 6:02 PM (GMT -6)   
 Does anyone else with Lyme have high blood pressure? Mine is skull !!!

alone&scared
Regular Member


Date Joined Sep 2009
Total Posts : 177
   Posted 10/14/2009 6:06 PM (GMT -6)   
I actually have extremely low blood pressure with it. Like 90/70. A lot of the time they can't even get a correct reading and guess at it. Comforting, hun?lol.
But, we all react differently to this horrible disease:(

mother natures child
Regular Member


Date Joined Oct 2009
Total Posts : 231
   Posted 10/14/2009 6:20 PM (GMT -6)   
Ill give you some of my high if you will give me some low and we will both be normal. Now just have to find somebody skinny!

CajunGrl
Veteran Member


Date Joined Mar 2009
Total Posts : 4717
   Posted 10/14/2009 7:25 PM (GMT -6)   
Hi there Mother Natures Child,

Welcome to the forum!

I've been having slightly high BP for a few years now. Usually it's around 130/90. How high is yours? Are you on BP medicine?
**You never know how STRONG you are....until being STRONG is the ONLY choice you have**

Co-Moderator Lyme Disease Forum


mother natures child
Regular Member


Date Joined Oct 2009
Total Posts : 231
   Posted 10/15/2009 1:49 PM (GMT -6)   
 I am on 5 BP meds and when I stand up it goes to 195/125. Its positional. Makes me feel dizzy. Feel better lieing down confused

CajunGrl
Veteran Member


Date Joined Mar 2009
Total Posts : 4717
   Posted 10/15/2009 2:54 PM (GMT -6)   
Yikes hun. I hope that gets better for you. Did you do a tilt table test?
**You never know how STRONG you are....until being STRONG is the ONLY choice you have**

Co-Moderator Lyme Disease Forum


mother natures child
Regular Member


Date Joined Oct 2009
Total Posts : 231
   Posted 10/15/2009 7:31 PM (GMT -6)   
 No but I have decided to see a LLMD.  Its a big move for me since I swore off Doctors.

CajunGrl
Veteran Member


Date Joined Mar 2009
Total Posts : 4717
   Posted 10/15/2009 8:05 PM (GMT -6)   
That's good. I know what you mean about swearing off doctors. I did the same thing back in 2007. I had had enough of going from doctor to doctor and having bruises up and down my arms from giving blood. The good thing about LLMD's though that separate them from regular doctors is that they listen and they understand. I find that they are more compassionate too. I came to realize that "I" am paying them and it is my choice to find a doctor that "I" am comfortable with. Don't settle is all I'm saying.
**You never know how STRONG you are....until being STRONG is the ONLY choice you have**

Co-Moderator Lyme Disease Forum


mother natures child
Regular Member


Date Joined Oct 2009
Total Posts : 231
   Posted 10/16/2009 10:51 AM (GMT -6)   
When Doctors cant diagnois correctly, rather then admit their own failure, they blame the patient. Completely offended with being labeled as crazy.

JELAINEP
Veteran Member


Date Joined Sep 2007
Total Posts : 2017
   Posted 10/16/2009 11:30 AM (GMT -6)   
Mine went through the roof as of yesterday. Now, I'm also on Zestril....

Lyme disease, still sucking after all these years.
Never doubt that a small group of thoughtful, committed citizens can change the world. Indeed, it's the only thing that ever has.  - Margaret Meade
10/01- Igenex and CDC LD positive Rx's: Wellbutrin 300, Paxil 60, Xanax 5, Acidophilus, Flagyl, Hydrocodone, Glutiathione injections, Vitamin B compound, Invanz IV, LD theme song: http://www.youtube.com/watch?v=MgHioCC3yCo&feature=related
 

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