Could you or someone answer a question about weight gain. My family is following Freddd's protocol and we are gaining weight. We can tell it's edema but 7,000 mcg of Solgar folate every 3 hours is not reducing the weight or edema? We were taking Acetyl Carnitine (which worked better for us) but had to stop due to anxiety and increased heart rate. We are taking 5 mg of magnesium per lb. and all the correct brands/cofactors including B complex that doesn't exceed the levels in B1 B2 and B3 plus taking the other 3 deadlock quartet.
What could be causing this or are we missing something? We've been on the protocol for 6 months.
Thanks
Could you or someone answer a question about weight gain. My family is following Freddd's protocol and we are gaining weight. We can tell it's edema but 7,000 mcg of Solgar folate every 3 hours is not reducing the weight or edema? We were taking Acetyl Carnitine (which worked better for us) but had to stop due to anxiety and increased heart rate. We are taking 5 mg of magnesium per lb. and all the correct brands/cofactors including B complex that doesn't exceed the levels in B1 B2 and B3 plus taking the other 3 deadlock quartet.
What could be causing this or are we missing something? We've been on the protocol for 6 months.
Thanks
@lenaFreddd, I think I was on page 100 before and somehow missed your posts. I'm interested to see that for you, and in at least some research, methylB12 and methylfolate are the big players in digestive issues. I'll be interested to see if my own gut issues straighten out over time. If I'm "healing backwards", it would make sense that the gut issues might be up front for me, because I've only had serious problems for the last year or so.
Lena, my own gut got better on this protocol, but only after something like 6 weeks to 2 months of constant nausea in with other bad crashiness. I didn't even have anything as severe as Freddd's disgestive problems, and yours sound severe to me as well; I originally started out with a cast-iron gut. Now my gut has healed some, I'm amazed at how much more present I am and I'm wondering too if this wasn't part of my lessening brain fog. I hadn't realized how much energy it takes to be nauseated all the time, and how it kind of puts a cloud of wooziness between you and your daily activities.
Hello Nikki7,This morning I upped my adenocobalamin by 1mg at most and have been on 300mcg l carnitine fumerate for a few days...I feel super swollen...this may be nerves but also edema? My clothes aren't fitting now! Anyone have issues with water weight? How do you regulate it? I'm also more emotional than usual. I've been taking more potassium to try and help. Anything else I should do?
Thanks a ton Johnmac , for posting a detail recipe, makes lot of meaning, i will try this and update all in 2-3 weeks.
Thanks a ton @Johnmac , followed the titration, it works perfect and smooth . im dosing hourly 1 drop, it just got me out of a crash.
now i got a hang of managing the dose between anxiety and depression. got energy to think and work too
Have been on the protocol for a few weeks.
Most of my adult life I have suffered from fatigue. After some huge stress in my life in 2001 and then surgery my entire body seemed to collapse further the following were/are my symptoms following these events:
- lose balance when walking
- burning mouth and eyes
- fatigue
- couldn't stand on one foot in the Tai chi exercises I use to do
- sensitivity to light
- post nasal drip (thick mucous) and allergies
- dizziness
- mcs
- complete blunting of emotion (flat affect)
- inability to think deliberately
- sore throat
- ringing ears
- bad memory
- in recent years buzzing and tingling of the nervous system
- irritable bowels
- hands seemed to have pink dots
- shaky personality
- low libido
- dead look in eyes
- shortness breath
- the feeling of having lost my soul so to speak
- also nerve damage from nasal surgery where the sneezing nerve was impacted.
- stiff neck buzzing back of head
The upshot of this I lost my family in 2009, my house, my well paying job and eventually was even living in a tent for a bit. Constant ridicule from a family of hard workers/achievers doesn't help. In recent years I have had the opportunity for a couple of beautiful relationships with women I completely adored but once again CFS set in and a general level of pain derailed things not to mention my loss of personality that I used to have. My thoughts started to become increasingly dark especially the non ability to feel any normal emotion coupled with the total inability to cry - this to me is akin to losing ones essential humanity. Living a life with no emotion and just a wired and tired tingly existence - hellish. Constantly living in fear as even with a basic job now often I can feel huge crashes coming on and there is no stability of when one is going to feel normal it is total carnage. Everyone on here has lived through this type of stuff.
Started the FP recently and the first 3 weeks was on fire for the first time in my life I had meaningful sustained energy. I started it because i had a b12 jab 2 years ago and it was like being on speed (well to be honest havent done drugs but I did some tasks with ease) but subsequent jabs failed to have the same effect. I read freddd talking about this. I now understand why i have always felt like life was impossible. The first 3 weeks on FP I would wake jumping out of bed with energy something I hadn't had since being a young child. Normally I feel more devastated waking up than the night before. Sometimes now I even have feeling in my legs like i am reconnecting to my body and not just bad electrical buzzing/tingling. Brightening of the mind a beautiful thing. My sneezing nerve seems to be carrying more sensation helping me sneeze better and I get some pleasant tinglings afterward. I don't think I will ever regain that feeling of my soul like I had before 2001 but I do think I can have a life very well worth living on the protocol assuming the energy gains are stable enough. Hopefully I can start to cry soon.
However the past week and a bit there have been days with crashes again. Anyhow fear has been setting in as I didn't want to lose what I was starting to have - it would be like losing my entire existence I told the big bloke upstairs I have come to the end of my tether and will not accept anymore false hopes. I will start experimenting with smaller doses of LCF as I was popping an entire Drs Best 855mg or not taking it at all. At first i seemed to be successful with a haphazard approach but now i am guessing i must have some precision with my dosages. Fingers crossed going forward and thanks to @Freddd for the heart and soul he has put in. Reading his story I get the sense of a genuine man of steel to have not given up.
@suraj,
I din't find any need to titrate TMG, not the slightest. It smoothed out the LCAR, solid energy without the edgy feeling. I know there have been a variety of reactions to TMG, so I don't know. It is methylation side operations, not the ATP that you appear to be more sensitive to as you are starting very low.
I did the SAM-e first, then the TMG which I think is a better order to see the effects.
For the SAM-e. I don't know. I didn't try it until after I had methylation well started and then it gave just a little additional improvement for a 400mg dose.
I know nothing about lithium.
I've never felt a need to take amino acids. I eat meat and beans and eggs, high quality protein.
Glad it's working @suraj. My experience is pretty much identical to yours (& exactly what Fred said would happen.)
@Johnmac @Freddd now that, its 4+ months into FP, i had throttled up to B12 (20mg) + folate (23mg) in the first 4-6 weeks ( & it was a honeymoon period), but had crashed since then for various reasons like ( no LCF or too high dose of LCF or abruptly added SAM-e).
now that im doing good, titrating LCF with precision, would you like to worn me of any pit falls ahead, or should i see only positive days ahead.
just too scared of crashes and awful startup.
I'm flattered that you asked Fred & me in the same breath. But he's the expert round here: I flail in his wake.
The FP has basically been great for me.
LCF can be a right MTHFR, and I don't mean methylenetetrahydrofolate reductase (NAD(P)H. Like you, I am sensitive to LCF - way more than you, I think, as I can't take it at all - I gather because the dosages in capsules are too big. On Fred's advice I had to switch to liquid carnitine, which I can titrate up slowly from tiny dosages. (Now on 4 mg after several months.)
My most recent augmentations have been:
* Switching from sublingual to transdermal, via the world famous @ahmo method (patent pending): grind the B12 & folate pills up, mix them with oil, and bandage them against your body. (She uses wristbands; I use elastoplasts. More sophisticated operators use commercial oils: tho folate oils are hard to come by, & the Australian guy who makes B12 oils isn't even sure they could work.) That took me from 65% functioning to 75%, & allowed me to cut doses by 1/3. I.e. lower dosage, higher effect.
* Upping my B2 from 10mg to 40mg. That has kicked me from 75% functioning to about 90%, at least for the week since I began it.
I don't know what's going on with the B2; but my experiment suggests, to me at least, that transdermal methy-folate works, & that transdermal methylfolate, methyl B12 & adenosyl B12 achieves more penetration than the other methods.
Good luck...