I've posted a couple of messages in another group, but I'd like to introduce myself properly here.
I'm a 36 year old male diagnosed 2 years ago with RRMS. When I was initially diagnosed, I ended up spending a week in hospital as I was not in a good way and they wanted to keep me in for observation. MRIs showed significant scarring both in brain and spinal area, with one large scar right in the middle of the brain. Another scan 6 months later showed more scarring. At this point I did some research and found the Paleo movement and Terry Wahls's ideas. The diets seemed to make physiological sense to my mind, and I proceeded to give up a lot of foods. I think at this point, I just don't think my body was being given what it needed - I started feeling a lot better as I lost weight, then I slowly started feeling worse again. Plodding along for another year, I ended up eating a criminal amount of kale, broccoli, cauliflower etc all raw with hands and feet getting colder and colder.
Next I bumped into an old friend who has become a personal trainer. He had suffered a couple of health issues and had found a couple of guys (Rob Turner and Matt Stone) that helped him out of the hole. I started training with him while he looked at my diet and suggested a few supplements: ALA, Magnesium chelates, Zinc, good multivitamin, methylation support etc. He told me to quit the tinned fish and raw veg, which I did. I didn't feel a lot better or stronger after that, and we discussed that I may just not be eating enough. So up went the sweet potato, rice and coconut oil. Since then I have got much much stronger, however I still get random tingles.
I looked up the guys that helped my PT and saw they were all in the Ray Peat camp. I read a few things by Ray Peat, Danny Roddy, Matt Stone, Andrew Kim and they seem to research independent of large corporations. Since then I have increased my salt, fruit and gelatine. This helped my cold hands slightly but they're still not great.
My hands have had minor numbness for the whole two years, this is not improving. I have urgency, but I'm not sure if that's to do with my broken metabolism or the MS. I have improved in some ways since diagnosis and have probably had a couple of minor relapses, but since I feel randomly tingly I can't tell for sure.
The next things I need to do in no order are:
Improve sleep - not good ATM
Reduce cortisol/adrenaline - not good ATM
Have some comprehensive bloods done
Have my DNA tested and analysed
Look into progesterone
Methylate my muscle meats
Figure out whether dairy is OK or not!
Would anyone be able to suggest what bloods I need to get done? I potentially need to go private here in the UK as GPs seem unwilling to test thing that are not on their checklist.
What DNA test by 23andme is the right one and who would be able to analyse the results?
My Routine is as follows:
Morning, wake have a smoothie with berry, sometimes cinnamon, coconut milk, orange juice, with acetyl-l-carnitine, taurine, creatine, collagen powder (great lakes), sometimes undentured rice protein, sometimes a little salt
Supplements: Poliquin Mutlivitamin, zinc glycinate, calcium citrate, R-lipoic acid, Thorne B vitamins, 5000iu D3
Morning snack
Well cooked kale with tumeric and omega-3 eggs
Lunch
Large bowl of salad, 300g mixed seafood, fruit, berries
Snack
Fruit
Dinner
Meat + usually starchy veg/rice + greens, gelatine + orange juice
Supplements:
Multivitamin, magnesium, R-lipoic acid, probiotic
Bed:
Magnesium, sometimes valerian
Thanks
