When I took sublingual, I took B12 + folate AM, midday, and folate alone PM. Now, using transdermal, I take B12 + folate AM, folate only PM.
Hi ahmo,
I am brand new to this forum and have had no forum experience for 10 years due to vision loss/sensitivity to computer screens from uveitis. It's difficult, but after surgery I can finally see well enough to look at the screen minimally, but don't know what I'm doing, so please excuse! I have gotten the most help from your posts, so hope you don't mind that I'm starting here. (I could not find the Write Something box on your profile page. If this post goes to the wrong place, maybe someone could tell me how to send you a post?)
History: Asthma since childhood, then triggering of CFS, fibromyalgia, and multiple chemical sensitivities after series of multiple accidents, injuries, and surgeries in the 80's. Got much better from nontraditional allergy shots from England called EPD but the FDA disallowed them into US in the mid-90's, and the new US version called LDA (formulated by my long-time environmental/allergy MD) never worked for me (mid-2000's). Meanwhile a protocol of high dose folic acid in conjunction with these shots caused a severe B12 deficiency that led to body-wide neuro damage.
Took daily injections of MB12 to try to stop the rapidly spreading neuro damage that could develop into subacute combined degeneration. The eye problems made it hard, but in 2004 I joined my only other forum called BrainTalk, and the member who helped me the most was a very intelligent, informed man named Fred! After rereading some old posts I am certain it was Freddd! Methylation never came up, but with Fred's help I got on sublinguals and some of the other items in his current protocol (no Methylfolate, but he may not have known about MF back then).
The obvious severe neuro damage got better, so I stupidly stopped taking MB12 several years later because of side effects, and I had to focus on dealing with worsening eye disease. Also intense fluctuating hormones from peri-menopause made it hard to know what was causing my symptoms. Then after dropping to under 90 lbs, I found out 3 years ago that I had high levels of arsenic from brown rice, one of the only foods I could tolerate with my IBS. Had to wait to start EDTA chelation IV's until I could gain some weight and get stronger.
Started EDTA very slowly April 2015 at half dose, but every time we did it too often or increased dose too fast, I felt like I was getting brain damage, tho IBS and some other symptoms improved. Finally stopped in Aug 2015 after total of 8 IV's when several people told me to try glutathione to heal my detox pathways before more chelation. After 3 weeks on low doses of S-acetyl glutathione, I couldn't handle the detox, so stopped it. However thankfully a google search on acetyl glutathione led me to Rich and this forum, which led me to Freddd's Protocol!
I started FP slowly 3 weeks ago, but was looking at older posts at first, so it took awhile to do it right. At first I mostly used the guide called Active B12 Therapy and Methylation FAQ (An Index to 'B-12 the Hidden Story'), until your posts eventually led me to your Guide to FP. Start up was a little rough, but not as bad as many other people. AdB12 has caused most side effects (tight chest, increased asthma, too speedy/hot) even starting at 1/4 of Country Life 3,000 mcg (waiting for Anabol order).
I had problems with it 10 years ago too. Trying 1,500 mcg twice a week for now, but can tolerate it only if I take it late at night when really tired! Otherwise I get unbearably speedy if I already have decent energy. Will try crumb of Anabol with MB12 when it arrives. The first time I added MF, I felt like something turned on. Several recurring muscle/joint pains came on at once, even a very old low back pain, but not nearly to the original intensity, and they all passed quickly.
When I increase MB12 and/or MF (not sure which one yet) too quickly, I feel some of those pains slightly coming on again, especially in my lower legs. Never experienced any muscle cramping or other noticeable low potassium symptoms. I have been taking a little potassium citrate anyway, and also eat wild salmon regularly that is high in potassium. I have a 10 MEQ potassium chloride RX on hand just in case.
I have had soft stools/borderline diarrhea daily, but that started before FP, and recurs due to IBS, but not usually for this long without some normal BM's in between, so could be from FP too. Angular chellitis flared up, but is now healing after 1 week on MF. I have a little more fatigue now (except for when I feel too speedy from AdB12, B-Complex, or LCF, which us even worse than the fatigue), but that's getting less intense and passing more quickly. Sometimes I feel really out of it and can't think straight, but other times my brain is working a lot better and my memory has definitely improved.
Currently taking: 1/2 Enzymatic Therapy 1 mg MB12 3x/day (1.5 mg total daily), 1/2 Country Life AdB12 2x/week until Anabol comes in next week (both dissolved 45+ min),1/2 Solgar 400 mcg MF 3x/day, (600 mcg total daily + 100 mcg MF in 1/4 Pure Encap B-Complex (still too strong for me, looking for alternative), 1/8 LCF (might try Acetyl but somewhat tolerating 1/8 LCF for now).
I hope you don't mind that I have several FP questions:
1. Is MF absorbed better with or without food? In the Protocol and Start up section of the Active B12 therapy and methylation FAQ, Freddd says "Methylfolate appears to be absorbed better without food but with food works ok." However in sheclimber's My Understanding of FP, in section 3c it says "Methylfolate is absorbed better with food, but is ok without." So complete opposite. Due to my eye issues, I can't scour the forums as much as I would like to see what updates or changes have come out since the latest revision of these guides, and they are both invaluable.
2. Do I take MF 30-60 minutes prior to MB12 as per your Guide to FP? There was conflicting information in sheclimber's guide at the end of Step 3 under Some Thoughts on MeB12 Timing and Dose. "Freddd: The MeB12 has to come before the methylfolate to protect your neurology.
So swallow the folate and putting the ENZY in your mouth at the same time will work well on both counts."
3. If taking the Anabol AdB12 crumb with each MB12 doesn't work for me, how much of the tablet (or estimated mcg) should I take per week to be in proportion to taking 1.5mg to 2 mg of MB12 per day?
4. It says that the Acetyl L-Carmitine works better for 10% of people. Do you have any idea what criteria applies to that 10%, like do have to have some special type of gene mutation? I was thinking of trying it, because I have a lot of brain issues, and I don't love the LCF. While I normally have some fatigue upon excessive exertion, I bounce back quicker than I used to, and my energy is fairly good at certain times of the day. Of course I would love to have energy like a normal person, but I have to take the AdB12 and LCF in minute amounts and/or late at night when I'm so tired they don't get me so revved up.
5. I keep reading about donut hole folate deficiency, but I don't really understand it. Can you explain a little?
Thanks so much for taking the time to read my post, and I really hope to hear from you soon! I also hope to connect with Freddd at some point, although it looks like he hasn't posted recently. Aloha!