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#1 | |||
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Wisest Elder Ever
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http://www.swankmsdiet.org/About%20The%20Diet
Does anyone here follow the Swank Diet? Or any dietary program which helps their symptoms? If so, what program do you follow? If not a specific program what changes have you made to your diet that seem to help with your MS symptoms? It's expensive to eat all organic. But it's also expensive to be on a DMD. What, if any, eating and/or vitamin program or regimin do you follow that seems to help?
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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. |
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"Thanks for this!" says: | dmplaura (01-13-2011) |
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#2 | |||
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I've been doing a cross between the Swank/American Heart Assoc. recommended diet for 4 years. Both are low fat but Swank doesn't allow chocolate and is more specific about limiting certain foods. I don't know if it works but my cholesterol is low, my heart is good, and I have energy so I'll stick with it.
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"In retrospect it becomes clear that hindsight is definitely overrated!" ~ Alfred E. Newman |
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#3 | |||
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Elder
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I am very close to the "makers diet" which stresses eating clean. no boxed or canned anything. ALL our food is made from scratch, from organic or local sources and is a nice diet. It took some getting used to. My DD has celiac and we were gluten free here for a long time, this was long before it was popular, and you had to figure it all out on your won.
I am very happy with my diet and notice quickly when I have strayed from it. No high fructose corn syrup, no MSG, no preservatives... I do have an emergency pantry incase of God knows what that would make me worry, because its all canned, and preserved, but that is what is going to last in an emergency. Its hard to cook from fresh and scratch if we cant get out of the house. I have noticed I feel better when on it, and I feel bad when I cheat. Splenda gives me an instant mind blowing headache. I just dont see how folks can eat that stuff. Ick!
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RRMS 3/26/07 . Betaseron 5/18/07 . Elevated LFTs Beta DC 7/07 Copaxone 8/7/07 . . |
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#4 | |||
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Wisest Elder Ever
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Splenda gives me a headache, too. I can only imagine what it's doing to my insides to produce such pain.
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__________________
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. |
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"Thanks for this!" says: | Dejibo (01-13-2011) |
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#5 | |||
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In Remembrance
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NO CHOCOLATE!!!!
![]() ![]() ![]() All artificial sweetners give me a headache and they can also add to your depression. ![]()
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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#6 | |||
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Elder
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I have heard so many with MS say that ALL artificial sweetners give them a headache or migraine. When I was preggers in 1983 the MD told me then STAY AWAY! we have no idea what effect it can or will have on a developing fetus. That got me to thinking more closely about what I was shoving in my pie hole while I was making a baby. I rarely had a diet anything cause I was super skinny then but it made me switch gears and think before I ate.
Years later I know within 5 minutes of eating something with splenda or aspertame or equal. My brain feels like its boiling. I am dizzy, and nervous and really feel ill. I had a close friend tell me that she used to feel that way but it passed after sticking with her diet soda. She really wanted to lose weight. MS was hard enough skinny, let alone plump she said. I was shocked to hear that even tho something made her quite sick she kept eating it and ignored what her body was telling her.
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RRMS 3/26/07 . Betaseron 5/18/07 . Elevated LFTs Beta DC 7/07 Copaxone 8/7/07 . . |
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#7 | |||
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Magnate
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I eat a no red meat, low Saturated and Trans fat diet (if I see Trans on the label, I don't buy). I took these aspects from the Swank MS diet.
I try to eat a balanced diet, Swank was entirely too restrictive for my tastes starting out (I've been eating this way 2-2.5 years now). I found foods I like that avoid red meat and the fats mentioned, avoid eating away from home (no fast foods). I'm certainly no angel with my foods, I don't eat organic, I eat some processed stuff (I work a full time job... I wish I could eat everything fresh out of the ground, just not possible for me with my schedule). I'm not on DMDs, Ty, nadda. Just 2 pain medications. I will say up front my MS is low on the EDSS (sensory symptoms) and I've had 2 relapses (one was ongoing a long time, the second about 2-3 months after the first one and the round of IVSM/prednisone). Then I changed my diet a couple months after relapse 2 and the rest is history. Remission! ![]()
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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: |
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#8 | |||
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Member
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I am one of the not-so-lucky Crohn's patients who can not eat fiber, foods with residue (no whole grains) . . . meaning I fare best on processed foods! I hate it, but no matter what I do, I can't change it. Before Crohn's I was >75% vegetarian, at over 50% raw foods, and loved fiber! Now I can't even look sideways at whole wheat bread, Shredded Wheat cereal, or raw celery and carrots. Arg-g-g-g-g-h!
So when it comes to nutrition for my neuro issues/MS/TM, I am unable to eat so many of the things that I know would be good for me. What I can do is balance meat/fish/poultry with steamed veggies (limited to those that are not blockage-producing), peeled fruits (no more biting into a juicy apple or pear -- I have to peel them first) and find new and exciting ways to prepare the same-old same-old week after week. I mean, who else has problems with the blueberries in their yogurt, or can't eat lettuce? Bleah! I hate these diseases!
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We live in a rainbow of chaos. ~Paul Cezanne . |
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#9 | ||
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Member
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Hey Lefthanded, you asked who can't eat blueberries or lettuce? Me. Because I have Porphyria. It has nothing to do with roughage in my case. It has to do with the chemicals in those foods. Lettuce and all cruciferous veggies are high in sulfur. I am not sure what
blueberry's problems are, maybe sulfur. I can eat other berries, especially blackberries. I have been on the Swank diet for over a generation, so long I forget what was the start date--I know it was within weeks of dx of MS. The only main modification is that I often eat two eggs for breakfast. Swank allowed only two a week. I have always gotten on well with eggs, even when I was pregnant and could eat only eggs and oranges during the fourth month. Right now I am feeling that healthy people should eat more fat, i.e., more than the organic canola and olive oils that I eat--a health site recommends organic butter, but of course that is not on Swank. Swank felt we had autoimmune reactions to fat, which attack myelin. He was one of my physicians, a wonderful man. Because I have porphyria I also cannot tolerate Aspartame and Sweeta. I knew that long before dx. |
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#10 | |||
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Elder
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Quote:
I used to be a clean eater when I was a kid, and then I moved off the rez, and ta da! the world was full of instant food. I went hog wild. When my DD developed really bad celiac, we had to really reconsider what we put in our pie holes.
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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: | Kitty (01-15-2011) |
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