advertisement
Reply
 
Thread Tools Display Modes
Old 05-05-2010, 08:56 PM #1
katikat katikat is offline
New Member
 
Join Date: May 2010
Location: Sunny Florida
Posts: 4
10 yr Member
katikat katikat is offline
New Member
 
Join Date: May 2010
Location: Sunny Florida
Posts: 4
10 yr Member
Heart Back from the doctor

Well, so continues the search to see what is causing the neuropathy. The neuro looked into all the meds I am taking and told me to go of zocor for a month as it can make neuropathy worse. I go back in 4 weeks. If there is no improbement he is sending me to the Mayo Clinic. I asked him if it could be small fiber neuropathy and that is a possibility.

I was interested to learn on this forum that low B12 can also cause problems and that metformin can interfer with it. I take avadamet, so maybe that is causing some problems. My goal is to get off that as soon as possible.

I have lived with this neuropathy for so long that I wonder if they will ever find out what is causing it. And if they find out, will there be anything that will help. I know Lyrica helps a little, but it is still spreading. Oh well, things could be a whole lot worse. All I can do is become better informed about what I can do about it myself.

Thanks to all that have posted and left tidbits of knowledge for us new to the site to learn from. Your successes give me hope. It is good to know we are not alone. I guess neuropathy is more widespread than I thought.

Well, getting late. Thanks again.
Elizabeth
katikat is offline   Reply With QuoteReply With Quote

advertisement
Old 05-05-2010, 09:46 PM #2
george75 george75 is offline
Junior Member
 
Join Date: Jul 2007
Location: orlando,fl.
Posts: 70
15 yr Member
george75 george75 is offline
Junior Member
 
Join Date: Jul 2007
Location: orlando,fl.
Posts: 70
15 yr Member
Default zocor caused my neuropathy

it used to say it on the box years ago. I took zocor in 1999 and in 3 months i had PN and i still have it. It use to say it could cause PN> Now it says nerve damage.

email me if you want too.

George
george75 is offline   Reply With QuoteReply With Quote
Old 05-06-2010, 09:22 AM #3
mrsD's Avatar
mrsD mrsD is offline
Wisest Elder Ever
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
mrsD mrsD is offline
Wisest Elder Ever
mrsD's Avatar
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
Lightbulb

Four weeks off? Not going to do much for PN improvement.

One way this happens is that the statin drug blocks the pathway to making cholesterol in the liver. That pathway also makes CoQ-10 which is a nutrient all our cells use to help the mitochondria (energy producing portion).

In order to help recover from any statin damage, taking high dose high absorbable (enhanced and expensive) Co-Q 10 is necessary. Did he advise you to do that? I betcha he didn't.

Now if you are on a statin for a LONG time some of the damage may not be repairable. We just don't know just how much mitochondria can be damaged before they die. I think Acetyl Carnitine also helps with drug/toxin damage, so you may think about that too.

About 40% of patients on metformin, develop lowered B12 levels. This is easier to fix, and less expensive. That you can do yourself. See my B12 thread for more details:
http://neurotalk.psychcentral.com/thread85103.html

There are other causes of long term progressive PN.
Hereditary causes (no treatments available)
Gluten intolerance from diet... see my new thread here:
http://neurotalk.psychcentral.com/thread121516.html

If you continue to eat something (or take a drug) that is bothering you, the PN remains and increases.
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei

************************************

.
Weezie looking at petunias 8.25.2017


****************************
These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
mrsD is offline   Reply With QuoteReply With Quote
Old 05-08-2010, 08:50 AM #4
pabb pabb is offline
Member
 
Join Date: Sep 2006
Posts: 779
15 yr Member
pabb pabb is offline
Member
 
Join Date: Sep 2006
Posts: 779
15 yr Member
Default

Quote:
Originally Posted by mrsD View Post
Four weeks off? Not going to do much for PN improvement.

One way this happens is that the statin drug blocks the pathway to making cholesterol in the liver. That pathway also makes CoQ-10 which is a nutrient all our cells use to help the mitochondria (energy producing portion).

In order to help recover from any statin damage, taking high dose high absorbable (enhanced and expensive) Co-Q 10 is necessary. Did he advise you to do that? I betcha he didn't.

Now if you are on a statin for a LONG time some of the damage may not be repairable. We just don't know just how much mitochondria can be damaged before they die. I think Acetyl Carnitine also helps with drug/toxin damage, so you may think about that too.

About 40% of patients on metformin, develop lowered B12 levels. This is easier to fix, and less expensive. That you can do yourself. See my B12 thread for more details:
http://neurotalk.psychcentral.com/thread85103.html

There are other causes of long term progressive PN.
Hereditary causes (no treatments available)
Gluten intolerance from diet... see my new thread here:
http://neurotalk.psychcentral.com/thread121516.html

If you continue to eat something (or take a drug) that is bothering you, the PN remains and increases.
yup, cant keep doing the same things and expect a different result....
pabb is offline   Reply With QuoteReply With Quote
Old 05-08-2010, 09:23 AM #5
nide44's Avatar
nide44 nide44 is offline
Senior Member
 
Join Date: Aug 2006
Location: Chesapeake Bay, Land O' Pleasant Livin'
Posts: 1,660
15 yr Member
nide44 nide44 is offline
Senior Member
nide44's Avatar
 
Join Date: Aug 2006
Location: Chesapeake Bay, Land O' Pleasant Livin'
Posts: 1,660
15 yr Member
Default

Quote:
Originally Posted by katikat View Post
............. Oh well, things could be a whole lot worse. All I can do is become better informed about what I can do about it myself.

Thanks to all that have posted and left tidbits of knowledge for us new to the site to learn from. Your successes give me hope. It is good to know we are not alone. I guess neuropathy is more widespread than I thought.
Elizabeth,
You have hit the proverbial nail on the head.
This is the clue to getting a grip on what you can do for yourself.
You have to be your own advocate, as most of the docs
won't have as much info as you will have.
Also, having a doc that will work with you and your research, is a great help. Strive for that type of relationship.
__________________
Bob B
nide44 is offline   Reply With QuoteReply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
Upset, back from doctor. nanapickle Reflex Sympathetic Dystrophy (RSD and CRPS) 11 03-13-2010 09:54 PM
Doctor Fred is now MY DOCTOR!!!! MelodyL Peripheral Neuropathy 3 03-01-2007 01:29 PM
Just came back from my doctor MelodyL Peripheral Neuropathy 10 12-18-2006 06:32 PM


All times are GMT -5. The time now is 12:57 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.