Welcome to This Is MS!

     Modules
· Home
· Content
· Downloads
· Encyclopedia
· FAQ
· Feedback
· Forums
· Journal
· Private Messages
· Recommend Us
· Search
· Site_Map
· Stories Archive
· Submit News
· Surveys
· Top 10
· Topics
· Web Links
· Your Account

     Google
Google
Web
This is MS
These ads help pay for the upkeep of our site. They are automatically served by Google and are not affiliated with This is MS.

     Languages
Select Interface Language:


     Who's Online
There are currently, 54 guest(s) and 12 member(s) that are online.

You are Anonymous user. You can register for free by clicking here

     Next Step

From the creators of This is MS comes Experience Project

EP is a community where members connect through shared life experiences-- like MS--and so much more. You are not defined by any one thing, so be your true self and find others just like you at Experience Project.

Get started by sharing your Multiple Sclerosis story.


     Donations

To remain unbiased, This is MS does not accept corporate sponsorships.

Therefore, we must rely on our users to help support us. Please donate to our upkeep if you have the means. Thank you!


ThisIsMS.com :: View topic - Headaches
 Forum FAQForum FAQ   SearchSearch   UsergroupsUsergroups   ProfileProfile   Log in to check your private messagesLog in to check your private messages   Log inLog in 


Headaches
Goto page Previous  1, 2, 3
 
Post new topic   Reply to topic    ThisIsMS.com Forum Index -> General Discussion
View previous topic :: View next topic  
Author Message
Nenu
Family Elder


Joined: Apr 21, 2008
Posts: 217
Location: New Brunswick, Canada

PostPosted: Tue May 13, 2008 10:46 pm    Post subject: Reply with quote

Sigh, well after a short sleep, everything seems to have come back. What's up with this? Sad Head's feeling full again, burning mouth back, etc. I can literally feel my nerves in my face on the right side twitching. Migraine possibly? I don't know what this is anymore. It may just be the MS, but I can't really tell. Looks like steroids in my immediate future.

Oh yeah, and my Copaxone injection sight from yesterday formed a nice bump. Doh!
_________________
Dx RRMS March 5, 2008.
Back to top
View user's profile Send private message
jimmylegs
Family Elder


Joined: Mar 12, 2006
Posts: 2006

PostPosted: Wed May 14, 2008 8:07 am    Post subject: Reply with quote

ugh lame! i'm casting around for other ideas.

does anyone know off the top of their heads if high folic acid doses can drive b12 excretion, in spite of supplementation? or is it just that folate can "mask a b12 deficiency"

all i can come up with is a hint... in vervet monkeys no less...

http://www.ingentaconnect.com/content/rsm/lab/1993/00000027/00000001/art00008
"The B12 levels for all the groups ranged between 866 and 5867 pg/ml and showed an inverse relationship with the FA measurements."
Back to top
View user's profile Send private message
DIM
Family Elder


Joined: Feb 29, 2008
Posts: 220
Location: GREECE

PostPosted: Wed May 14, 2008 1:48 pm    Post subject: Reply with quote

If you look at every B-complex it has large quantities of other B vitamins but almost the standard folic acid dose, do you know why?
It causes stiffness and other MS problems in high doses and works against B12 as you say.
Choline help it's absorption as does with every other B vitamin but better to take standard or slightly higher dose rather have problems, always IMHO!
Back to top
View user's profile Send private message Visit poster's website
Nenu
Family Elder


Joined: Apr 21, 2008
Posts: 217
Location: New Brunswick, Canada

PostPosted: Wed May 14, 2008 6:30 pm    Post subject: Reply with quote

I do take my B12 with folic acid separately from my other B's. Sublingual tablets.
_________________
Dx RRMS March 5, 2008.
Back to top
View user's profile Send private message
jimmylegs
Family Elder


Joined: Mar 12, 2006
Posts: 2006

PostPosted: Wed May 14, 2008 7:50 pm    Post subject: Reply with quote

dim i don't know why it's usually the same from complex to complex, but i do know that when i switched from my usual b-complex to prairie naturals with 1mg folic acid (significantly more than the previous brand), i started to get symptoms and my lab test showed my folic acid was way out the top of the normal range.


where do you see the problems with stiffness etc listed, DIM? the only problem i had was itching and i have not found reference to that anywhere yet. i have not been able to establish confirmed toxic effects - all the sites i can find say that the "risk of masking b12 deficiency" is about it.

i'm still confused about how folic and b12 might bounce off each other...
again, i'm pretty much stretching for ideas but the first time i looked at nenu's regimen, the 1000+ folic per day did ring a warning bell. i don't know if it's possible for that dose to be interfering with nenu's b12 absorption..?? plus there are parts of the complex missing in the compound... another possible malabsorption suspect...

and then, how could one possibly test for a related b12 deficiency, if the folate supplementation is masking its possible existence?

anyway it was just searching "burning mouth deficiency" in google and seeing all the b12 hits come up that made me start to think about the high folic and potential impacts again...
Back to top
View user's profile Send private message
Nenu
Family Elder


Joined: Apr 21, 2008
Posts: 217
Location: New Brunswick, Canada

PostPosted: Wed May 14, 2008 8:47 pm    Post subject: Reply with quote

Ok put this into dumb dumb terms for me. Do you think I may not be absorbing the b12 tablets I take separately from the compound? And if so why? (I'm really bad at understanding all of this, and due to the pain they put me on oxycodone temporarily until I begin the steroids and get that going in my system tomorrow, so my head's not all here!).
_________________
Dx RRMS March 5, 2008.
Back to top
View user's profile Send private message
jimmylegs
Family Elder


Joined: Mar 12, 2006
Posts: 2006

PostPosted: Thu May 15, 2008 7:53 am    Post subject: Reply with quote

hi nenu

hey don't apologize, we're all here tryin to figure things out! Smile

basically, yes, i think in general you could be having some problems with absorbing your b-vitamins both in the compound and in the sublinguals.

you may want to consider adding the missing B3, B5, and B6, and backing off on the B9 for a while. the imbalance could be affecting your body's ability to fully utilize the b vitamins that it does get now.

i've had my own issues with an out-of-balance b-complex regimen so now it throws up warning flags for me. if they occur together in food, we should supplement them in a complete complex too!

here's a bit of explanation:

Quote:
The vitamin B complex consists of 12 related water-soluble substances. Eight are considered essential vitamins because they need to be included in the diet. Four are not essential because the body can synthesize them. Although these vitamins are chemically distinct, they are grouped together because they are found with one another in the same foods. Since they are water-soluble, most are not stored for any length of time, and must be replenished daily. The eight vitamins have both names and corresponding numbers. They are:

* B1 (thiamin)
* B2 (riboflavin)
* B3 (niacin)
* B5 (pantothenic acid)
* B6 (pyridoxine)
* B7 (biotin)
* B9 (folic acid)
* B12 (cobalamin)

Biotin is not always included among B complex supplements. The numbers that appear to have been skipped were found to be duplicate substances or non-vitamins. The four unnumbered components of the B complex that can be synthesized by the body are choline, inositol, PABA, and lipoic acid.

As a group, the B vitamins have a broad range of functions, including the maintenance of myelin, which is the covering of nerve cells. A breakdown of myelin can cause a large and devastating variety of neurologic symptoms.


hope that helps?
JL
Back to top
View user's profile Send private message
Nenu
Family Elder


Joined: Apr 21, 2008
Posts: 217
Location: New Brunswick, Canada

PostPosted: Thu May 15, 2008 9:29 am    Post subject: Reply with quote

That does help! Thank you very much Smile

First round of steroids today went very well!

Thank goodness for painkillers in moderation. I don't think I'd have made it through the night last night without the help. It was a considerably bad night for pain, but they helped.
_________________
Dx RRMS March 5, 2008.
Back to top
View user's profile Send private message
jimmylegs
Family Elder


Joined: Mar 12, 2006
Posts: 2006

PostPosted: Thu May 15, 2008 10:03 am    Post subject: Reply with quote

good!
glad to hear you're having a better day today nenu Very Happy
Back to top
View user's profile Send private message
Nenu
Family Elder


Joined: Apr 21, 2008
Posts: 217
Location: New Brunswick, Canada

PostPosted: Thu May 15, 2008 10:37 am    Post subject: Reply with quote

Yeah, just got a call from the neurologist's office to go see him tomorrow after my next dose of steroids. My neurologist is out currently, so I'm going to see this man instead. I'm sure it's just to get prescribed the oral dose of steroids following the IV doses, but we'll see.
_________________
Dx RRMS March 5, 2008.
Back to top
View user's profile Send private message
dg980
Getting to Know You...


Joined: May 11, 2008
Posts: 13

PostPosted: Thu May 15, 2008 8:43 pm    Post subject: headaches Reply with quote

I had lots of headaches in the early years but do not get them anymore. I had ms for 10 years and had problems with acne and the only treatment that worked was acutane. The acne is back after years of remission and the dermo put me on solodyn which is extended release mino. I think this stuff is more powerful than the twice a day approach. Did that, did not work. The wierd thing is.......one week into the treatment, I was put on bylofen for muscle pain. I had never had this before and I think it is related to the mino.
Back to top
View user's profile Send private message
Nenu
Family Elder


Joined: Apr 21, 2008
Posts: 217
Location: New Brunswick, Canada

PostPosted: Thu May 15, 2008 9:19 pm    Post subject: Re: headaches Reply with quote

dg980 wrote:
I had lots of headaches in the early years but do not get them anymore. I had ms for 10 years and had problems with acne and the only treatment that worked was acutane. The acne is back after years of remission and the dermo put me on solodyn which is extended release mino. I think this stuff is more powerful than the twice a day approach. Did that, did not work. The wierd thing is.......one week into the treatment, I was put on bylofen for muscle pain. I had never had this before and I think it is related to the mino.


Interesting... well, my acne issue is an 'out of sight' one (location wise), so I'd rather just be diligent with washing/polysporin if it gets crazy than pumping myself with an antibiotic which I feel contributed to my recent relapse.

Btw... feeling SO much better since the steroid treatment today. Went on a walk and could smell the earth and other nice scents I had not in the last few weeks. Smile Plus the oxycodone is helping immensely with the pain aspect (the last time I was prescribed this stuff I found it didn't touch my facial pain, but maybe because it's being combined with steroid treatment it's the key to it's success).
_________________
Dx RRMS March 5, 2008.
Back to top
View user's profile Send private message
Display posts from previous:   
Post new topic   Reply to topic    ThisIsMS.com Forum Index -> General Discussion All times are GMT - 6 Hours
Goto page Previous  1, 2, 3
Page 3 of 3

 
Jump to:  
You cannot post new topics in this forum
You cannot reply to topics in this forum
You cannot edit your posts in this forum
You cannot delete your posts in this forum
You cannot vote in polls in this forum





We encourage you to also visit our Multiple Sclerosis story and support community on Experience Project. Experience Project is a vast and powerful community where people connect anonymously through life experiences. It's made by the same people who built This is MS, on the premise that no one life experience-- like having MS-- defines a person. It now covers over 2 million life stories. Find and share yours!

Experience Project: I have Multiple Sclerosis


Anonymous Confessions | Free Dream Interpretations | Ask Any Question
Site Map

This site does not offer medical advice. All treatment decisions should always be made with the full consent of your physician.


All logos and trademarks in this site are property of their respective owners. The comments are property of their posters, quoted articles are © referenced source, all the rest © 2002-8 by thisisMS.com.
PHP-Nuke Copyright © 2005 by Francisco Burzi. This is free software, and you may redistribute it under the GPL. PHP-Nuke comes with absolutely no warranty, for details, see the license.
Page Generation: 0.12 Seconds