Join Date: May 2006
Location: Alexandria, VA
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Originally Posted by chasmyn
It's likely. when will we get our own subforum???
|It's likely. when will we get our own subforum???|
Originally Posted by krissi
Poking my head in to say that would be too cool. We do a lot of gut healing stuff in this family but I haven't posted in this thread before because it is way too hard to follow any discussion that is all combined into one reaaaally long thread!
But while I'm here, I'd love to hear any success stories for getting rid of yeast once and for all. DD has been on SCD for closing in on six months and gets no grains of any kind but we still had a super nasty yeast flareup earlier this week. I have to keep her on antifungals constantly to control it and that is probably not good for her liver. She has such a restricted diet as is. I suspect we'll have to take the plunge and start limiting fruit more, but then she'd be on a diet of only meat and veggies and she really loves fruit. I've already had to cut pretty much everything else she really liked out and I hate that. She is allergic to nuts and beans and eggs so pretty much all SCD-legal foods except meat, fruits, and veggies are not an option.
Originally Posted by babygrant
i think i may need to do the SCD. TMI allert ahead. lately i've been having pains in my belly and feels like i need to go to the washroom really bad. well i try and go and the only thing that comes out is this clear goopy stuff that looks like egg whites. its coming from my bum. any ideas?
|I have done so much reading on this topic and still have not found
more than 2 sources that agree on any one "cause". Here's a read
that I can across during my hunt for truth in healing my daughter,
and all that it speaks of is exactly what we experienced. We tried
it ALL...except for (at that time) the fermented foods to feed good
flora. We did take probiotics but NOTHING worked until we started
eating kefir and kim chi. She can now eat anything with
no "symptoms"...this includes the occassional birthday party garbage
she eats. And since we've been eating the WP way she's only had 2
headaches and NO other symptoms...that's within 8 months, before
she'd get about 4 to 6 in a month and every symptom you can think
of...headaches, smelly feet, blisters in her mouth, dark circles
under the eyes, ezcema, constipation, caught infections
easily..colds/flu/pneumonia and on and on and on.....
Anywho here's the link to read
|Unfortunately fruits are very high in sugar even if it's legal. This feeds the yeast. My DD has very mild yeast issues but she gets a bad diaper rash if I give her more than one little bit of fruit a day. You could just try keeping low sugar fruis like berries and avocadoes. Avocados make great dessert.
Have you tried coconuts? Coconut milk, oil etc. You can make coconut milk jello with stevia. Definitely cut out juices. I know stevia is illegal but it's still the best sweetener if you can't do honey.
Sorry to say I haven't been able to get rid of yeast on SCD so I'm doing the yahoo group candida diet, which would be hard for kids without eggs.
Have you tried buckwheat? I know it's a complex carb and illegal. However, its gluten free and not really a grain... If you prepare it a la Nourishing Traditions, soaking it in yogurt or water and whey/lemon juice, and then make pancakes or something. This candida diet doesn't recommend it per se but it's the best option if you must cheat.
Are you giving her enzymes?
Originally Posted by krissi
Maybe researching fermented veggies a little more might be good too. She loves cabbage salad and maybe some kind of fermented cabbage would be a hit.
Originally Posted by firefaery
subbing. Just got through a couple of days with an infant pooping mucous and spitting up mucous so thick I had to remove it from his mouth. It started the day I tried clarified butter. Ugh. It may be a bug, but that would be a very strong coincidence.
Originally Posted by JaneS
Success story on yeast from someone I know IRL:
Originally Posted by Kundalini-Mama
Sigh. Good news and terrible news.
Well on the good news front, I started my older DS on reuteri for his loose poops. The results are phenomonal!! He is a normal boy after all. I plan to keep both of us on the diet for a long time, is there any problem w/that nutritionally speaking?
And the awful news.
It looks like my 21m old has a rare genetic disorder, MPS. We are very lucky though because it seems that he is on the very mild end of the spectrum. I'm thinking Schiele's or mild Hunter's. I'm going back and forth btw the two. His urine was sent out on Thursday to the U of Alabama to the top guy in the field to get more answers. We are seeing the geneticist on Wednesday, and the ENT on Thursday (to remove his adenoids and put ear tubes in). We are hoping to get this diagnosed ASAP so that he can start the enzyme therapy (once a week for life or until a cure).
On a side note, my lil' guy is much MUCH healthier than other MPS kids his age. I am attributing this 100% to his non-vax, non-crap (only SCD), and no antibiotic ever history. Because of all this, I know he is going to be okay.
Onwards to another journey.
Originally Posted by Pattyla
Ok Jane, I'm now more confused than ever. : I want what that says to be true but I don't trust it. I feel terrible when I eat anything off this diet. Horrible stomach pains. I just don't know what to do anymore. :
Originally Posted by txgal
New here, hope someone can help. I posted this above, but someone suggested posting here too.
Dh was just diagnosed with Diverticulitis via a lower abdominal CT Scan. The doc says there is about 6 in. of intestines that are affected. He wants to do a colonoscopy in Oct., but told Dh that surgery is the only way to help him. We know enough to know that this may not be the case so wanted to try some dietary/supplement changes between now and the colonoscopy to try and improve things naturally. Any advice? Also other than not enough fiber what else causes diverticulitis? Dh eats more fiber than anyone I know, in fact we think the attack was brought on by eating too much. TIA
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