Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×

HectorConvector

Advanced Members
  • Posts

    101
  • Joined

  • Last visited

Recent Profile Visitors

The recent visitors block is disabled and is not being shown to other users.

HectorConvector's Achievements

  1. The pain preceded the weight training, but it was very slight until I started weight training. The weight training exacerbated it, but MASSIVELY. Basically took it out of control and to the point of heavy medication. At first I thought it was my higher calorie diet causing the pain to be worse but turns out it wasnt that.
  2. Latest update. So after even more time I've become more sure about what the cause of the symptoms mentioned throughout this thread actually are. Nerve pain in feet/lower legs: caused by exercise, particularly weight bearing. Repeat experiments with weight training have now proven this, and I got rid of my weights set and stopped going to the gym...
  3. Hi, Yeah I also cook my own meals which are typically simple with meat & veg. I don't eat rye or barley and make sure they're not in anything I buy if I buy anything processed. Not eating beans or rice atm either, though I never had problems with rice, beans, not sure. Bear in mind, I live in the UK, not sure how different it is here, but legally...
  4. From what I've researched, I doubt a spinal fluid leak is the cause. The headaches (more of an ice pick stabbing pain behind the eyes and in the forehead) has been now resolved - it was a direct consequence of nuts (mostly cashew nuts) and a lot of eggs in my diet. I was eating more high protein/unsaturated fat foods to reduce my carb intake thinking...
  5. I'm just reviving this thread to update with *factual* information. Not assumptions, or anything vague but known facts. 1). results of an MRI scan show a herniated disc in the lower spine area. However, the letter from the doctor says they don't believe this explains the symptoms. However, the symptoms were very severe and violent when I did weight training...
  6. Finally, I'm very grateful for the advice and suggestions from members of the forum regarding my neurological symptoms, and I'll suggest some of the tests mentioned to my neurologist. I'm now going to leave this in the hands of the clinicians doing their evaluations. I am now unfollowing this thread. Thanks everyone.
  7. While I'm still on duloxetine and taking lots of thiamine (400+mg) and vit C (1,000mg+) the symptoms are generally consistent with no clear change in any direction, so I'll wait and see how the clinical evaluation goes, and at some point in the future when I really know something I can start a new thread and link to this one once I know some information.
  8. Well lots of people have suggested things from their own experience, which I have considered (though not necessarily acted on yet, and I'm not one to jump to conclusions, as you have insinuated) and you describe it as a "clusterfuck", I would say it's let me discover a number of tests to recommend to my neurologist, so I can eliminate things during the clinical...
  9. The reality is, this being a public forum, I'm getting a lot of different people coming in reading my descriptions of my symptoms and therefore a lot of suggestions, which while helpful, puts me in a position where it's quite overwhelming, and not easy for me to know what to do next. So I've been hesitant to make any meaningful changes to my current diet...
  10. I'm not trying to do an elimination diet, I've been following the initial advice of Wheatwacked in keeping a dairy of food and concentrating on getting the minimum RDA of all the vitamins/minerals I wasn't getting before. I'm not sure what you mean. I've simply described the way different foods make my pain respond, and haven't tried keto or said...
  11. Thanks for the info, agree with most of this, except I'm pretty sure I'm not getting any gluten, as I make all my food myself, and none of my utensils have ever had gluten in contact with them as I've been on a gluten free diet for more than 10 years and moved house/flat and have different utensils since then. Also, my nerve pain didn't actually start until...
  12. Peanuts never used to be an issue, but maybe I'm starting to develop an intolerance to them? It's all a mystery. My doctor is supposed to have referred me to a dietitian but heard nothing yet. Yes I have a food diary since November 2021.
  13. You quoted AAARTIST not me, I don't personally drink any juices, only water. Anyway an update, I replaced the cheese with a peanut butter sandwich to get the same calories (400). Not good results. My nerve pain turned more into intense stabbing burning pains in the feet, and I am getting lots of wind/bloating etc.... which I didn't have before. This...
  14. Not been tested for Lyme Disease. Can add it to my list of things to get checked. Don't recall having any initial signs of being infected. I don't eat anything with MSG or much L-glutamine that I know of.
  15. The pain is generally limited to hands and feet. Pain feels like short, sharp but intense stabs, or slightly longer, repeated burning sensations in the feet and it happens in random parts of my feet in different nerves. Sometimes it feels like something is crushing my feet for a few minutes. It can be in a toe, or the heel, top of foot, ankle. These "attacks...
×
×
  • Create New...