LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Alternative to Diamox

 - UBBFriend: Email this page to someone!    
Author Topic: Alternative to Diamox
AP
LymeNet Contributor
Member # 8430

Icon 1 posted      Profile for AP   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Anyone know of one? I was just on Diamox and Potassium Cl, but had a bad reaction to it. I have to wait the weekend before I get a new RX. I was kind of enjying life without headaches.

--------------------
Sometimes when I say �Oh, I�m fine� I want someone to look me in the eyes & say �tell the truth�

Myspace: http://tinyurl.com/5p64ed

Posts: 644 | From WA | Registered: Dec 2005  |  IP: Logged | Report this post to a Moderator
pab
Frequent Contributor (1K+ posts)
Member # 904

Icon 1 posted      Profile for pab     Send New Private Message       Edit/Delete Post   Reply With Quote 
Have you tried Topamax?

--------------------
Peggy

~ ~ Hope is a powerful medicine. ~ ~

Posts: 2775 | From MN | Registered: Apr 2001  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
a beta blocker perhaps?

or CoQ10

or MY favorite....Mangosteen juice

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

Posts: 96223 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
AP
LymeNet Contributor
Member # 8430

Icon 1 posted      Profile for AP   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Diamox has been the first thing prescribed since I just only started meeting with an LLMD, who is also making me take CoQ10, Alpha Lipoic Acid, B-Complex (Stress Tabs), Probiotics (I use Jarro-Dophilus since it was reccomended)...
He also has me on Klonopin and Neurontin for sleep and Cymbalta to help me cope a bit better.

The Diamox was working to kill the headaches, but my reaction to it was't a desirable one. Just looking for something else out there.

--------------------
Sometimes when I say �Oh, I�m fine� I want someone to look me in the eyes & say �tell the truth�

Myspace: http://tinyurl.com/5p64ed

Posts: 644 | From WA | Registered: Dec 2005  |  IP: Logged | Report this post to a Moderator
mjo
LymeNet Contributor
Member # 7876

Icon 11 posted      Profile for mjo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Don't you have to supplement magnesium when you take Diamox? Asked one LLMD about the drug and he said, "You're already very low in magnesium. If I gave you Diamox you'd have to have IV mag which would be fine if you lived here but you're too far away for us to co-ordinate the drip for you." Sounded like he wouldn't want me monitored by a hospital far away. Is this right? Would like to hear more on diamox from others. Thanks.
Posts: 422 | From Luck home | Registered: Sep 2005  |  IP: Logged | Report this post to a Moderator
AP
LymeNet Contributor
Member # 8430

Icon 1 posted      Profile for AP   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by mjo:
Don't you have to supplement magnesium when you take Diamox? Asked one LLMD about the drug and he said, "You're already very low in magnesium. If I gave you Diamox you'd have to have IV mag which would be fine if you lived here but you're too far away for us to co-ordinate the drip for you." Sounded like he wouldn't want me monitored by a hospital far away. Is this right? Would like to hear more on diamox from others. Thanks.

I hadn't heard that. I'm just counting down 'til Monday when I can try something new.

--------------------
Sometimes when I say �Oh, I�m fine� I want someone to look me in the eyes & say �tell the truth�

Myspace: http://tinyurl.com/5p64ed

Posts: 644 | From WA | Registered: Dec 2005  |  IP: Logged | Report this post to a Moderator
trueblue
Frequent Contributor (1K+ posts)
Member # 7348

Icon 1 posted      Profile for trueblue     Send New Private Message       Edit/Delete Post   Reply With Quote 
AP ~
What was your reaction to the Diamox? I tried it once about 10 years ago to find out it was a sulfonomide. Um... I'm allergic to sulfa drugs and had lovely red itchie hives.

If that's what happened...

I'd like to suggest not trying Topamax. Which I just tried last week. The sulfa in it is a different form and the pharmacy said I might be able to tolerate it. Well, at least I didn't get the giant hives... just really itchy.


I'm just mentioning this in case you are sulfa allergic.


I hope monday comes fast.

--------------------
more light, more love
more truth and more innovation

Posts: 3783 | From somewhere other than here | Registered: May 2005  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.