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#1 | ||
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Member
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Are any of you dependent for BM help. I am, I never go without help, I am taking magnesium 900 mg now which helps. I just don't want to be at the point where I can't go at all without help and now I am here and it is terrible. Just wondering if I am the only one.
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"Thanks for this!" says: | Dejibo (08-16-2011), dmplaura (08-16-2011), DVORA65 (08-16-2011), Motors Mommy (09-11-2011), SallyC (08-16-2011) |
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#2 | ||
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n/a
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you are not alone. My docs are aware of this and they say while its not ideal there are worse diseases to have and worse drugs to be dependent on. It is an unfortunate reality (sad face)
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#3 | |||
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Senior Member
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You are not alone. There are plenty of us with all sorts of medicines and foods we use to help.
I use Miralax as needed. Magnesium did not work for me. Yogurt - activia for me - seems to help, apricots, prunes, canned pears are all in my diet due to recommendations here. If misery loves company, you have plenty of people that are totally in the same predicament. ![]() |
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"Thanks for this!" says: |
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#4 | |||
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Elder
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I am a slow lane girl. its not that I dont go almost everyday, its that when I do go, its hard, and pellet like or dry, really dry and hard to pass. I need help to move things along.
You are in good company.
__________________
RRMS 3/26/07 . Betaseron 5/18/07 . Elevated LFTs Beta DC 7/07 Copaxone 8/7/07 . . |
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"Thanks for this!" says: |
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#5 | |||
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Grand Magnate
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hi pooch,
i'm not at the end of the line yet. i've tried a couple of things that work for me. 1. i've taken metamucil 1 heaping kitchen teaspoon every nite. if it's too much pull back. and 2. now i take 200mg (2 pills) of docusate sodium. it's the generic for colace which is very expensive. the generic is much cheaper. you can get a huge bottle at walgreens. but, start small. also make sure you take in at least 8 cups of water each day. hydration helps. good luck.
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Judy trying to be New Skinny Butt ______________________ You are a child of the universe, no less than the trees and the stars; you have a right to be here. And whether or not it is clear to you, no doubt the universe is unfolding as it should. -------------------------------------- "DESIDERATA" by Max Ehrmann |
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"Thanks for this!" says: |
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#6 | ||
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Member
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well, I hate that ya'll have this problem, but I'm glad you know what I'm talking about, I was wondering if anyone else went through this. Thanks for the advise.
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"Thanks for this!" says: |
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#7 | ||
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Member
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I was thrilled when I realized that Magnesium helped....but I didn't realize that doctors consider it drug to be dependent on. I don't think my doc knows I even take it!!
__________________
Dx: RRMS Jan 2010; LDN: March 2010-Dec 2010; Aug 2012-Nov 2012 Tysabri: Feb 2011-March 2011 reaction Gilenya: August 2011 reaction Copaxone: October 2011 reaction Tecfidera: May 2013 reaction |
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"Thanks for this!" says: | dmplaura (08-19-2011), Motors Mommy (09-11-2011) |
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#8 | |||
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Magnate
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If your GPs are like ours.... they'll fluff off discussions about a lot of vitamins/supplements/alternative treatments. Sometimes founded, most times not. The only my GP actually backs me on is Vitamin D, but she knows I'll take what I find works for me, so she leaves me be.
__________________
2004 to present - Trigeminal Neuralgia 2007 to present - Burning Mouth Syndrome March 2008 - Multiple Sclerosis DX 05/2008 - Relapse 05/2008 to 02/2009 - Copaxone 10/2011 - Relapse - Optic Neuritis developed 9/2012 - Relapse - Balance issues 1 sided 8/2012 - Erythema Nodosum - diagnosed 10/2012, reaction to Topiramate (Topamax) April 7/14 - Raynaud's Syndrome DX |
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"Thanks for this!" says: | Motors Mommy (09-11-2011) |
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