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I'd like to ask what your calcium/magnesium product has in it.
Most combinations, have magnesium oxide, and that we know now is not well absorbed and is lost in the stool. In fact it is a well known and commonly used laxative. Vitamin D however will improve absorption of calcium (and magnesium) in the GI tract. Some cardiologists suggest only using a maximum dose of calcium of 600mg a day to avoid hypercalcemia and plaque formation in the arteries. Get you actual B12 results in numbers. B12 should be at 400pg/ml at least, but lower results are still called "normal" because the labs are not updating their ranges. So you could be "normal" and in fact actually be low. Different countries use different reporting concentrations so if yours is not pg/ml, then post it here and I will look up the conversion for it. |
If you list your most bothersome symptoms, that might be helpful.
[I was told by one Dr i have RSI] About the RSI possibility - What kind of work or activities have you done now & in the past? desk work, repetitive, past whiplash, sports , music? Useful sticky - TOS & RSIs - http://neurotalk.psychcentral.com/thread84.html |
Long one!
JoMar what were you diagnosed with in the end? Was it RSI or are you saying it was a misdiagnosis?
Me? I have been writing and on a laptop 5 days a week for 10 years! Lots of high pressure, fast typing too. *administrative edit per guidelines* So I think I will now have to retype my symptoms - here goes!
So! Sorry for the LAUNDRY LIST everyone! But I had to get it all out there. Now. My blood test came back with Vitamin D3 at 6 ng/ml and D2 at 2.4ng/ml. That's low! The more reading I did on the net, the more I realised at least some of these symptoms may be attributable? I took a booster of D at Docs recommendation. Honestly - after 1 month I feel like myself again. Literally everything on that list has improved. The depression and mental fog lifted week by week. The crazy constant butterfly muscle spasms have reduced significantly - still there but i would say 75% reduction. The hand and internal 'vibration' i could feel and noone could see has stopped altogether. The finger sideways waggle remains - but lessened. Not sure if thats cause i have been doing massages and acupuncture for tendonitis in right arm? or Vit D? Dont know if its muscoskeletal issue or neuro. I do know I constantly have burning pain when i type - in my righthand, particular to my ring finger and pinky. also my right hand is always cold! my fingertips especially. But anyway, I bought some cheap imitation converses. I went for a walk before my VIT D treatment. I was already super weak but determined not to stay depressed. On my walk I felt tingling pretty much everywhere, but mostly in right leg. Then i just had to sit. I dont know if i imagined it but my right leg felt 'lazy when i walked. but seeing myself in the reflection i looked totally normal when walking. my leg just felt - too light or something. like i couldnt feel my foot land as well as i had before? maybe bad circulation? anyway . walked home alright just felt weird. also tripped on concrete slightly - though these shoes are a little 'floppy' big and not well made. when i walked with my nikes and after vit d treatment - i consciously focused on my walk and had no trips or strange weak feelings. i am hyper aware of one hip being higher though, and was once told to wear a special insole on my right foot. wondering if now i am paying the price of not doing that! anyway now i can sit up and type. I can wake up at a normal time (10am). I am not constantly spasming - i am not brain foggy and depressed. I remain slightly anxious - but thats because my Dr gave me 'the face' when i explained my symptoms. He first thought essential tremor, now he wants to rule out MS. mind you, there has been no follow up assessment from him. he just saw me at my worst. Im not convinced he is a 'good' or even slightly 'thorough' dr. Another Dr said RSI and anxiety. But still to go to neuro. But she took the time to assess my muscles and see if their was wastage or anything, and compressed nerves in wrist to see if it tingled etc. My acupuncturist - chinese dr said i have tendonitis badly on right side and some liver expel issues plus generally stressed and 'sad'. haha. yay! My neuro is late feb - *administrative edit per language filter guidelines* Just got married and started my life. I keep being paranoid about any little symptom now. keep staring at my outstretched hands to assess a slight tremor. I test my memory worrying about alzheimers. I keep youtubing sideways finger waggles and MS. I dont know why im so convinced I have MS. I hope I dont. I guess i want to prepare myself if it is? Magnesium and Vit B seems to have helped me a lot too. The magnesium I take is normally H&B 500mg. As I was told with my D that low, i was surely super deficient in Mg too. Now due to budget (not working right now), im on Boots Mag & Calcium combo. It does have mag oxide! its 800 calcium and 375 mag. I honestly only bought this one due to money issues and an interim solution. i know for sure the H&b brand is better and i also 'feel' i need more MG over calcium. it somehow balances my muscles. Ever since stopping the old brand, my little fasculations and muscle butterfly twitches are back. Only slightly, but it was an interesting observation. My vit B12 was 467ng/L. Serum folate was 9 ug/L I was concerned that my Red Blood Count was 4.83 (10*12/L). that's the high range for this report. Also my Red Blood Cell Distribution Width was 14.3% which is the high range for this report also. What does that mean exactly? Nurses, anyone? Corrected serum calcium 2.16mmol/L - lower than normal range. If anyone has any inklings - let me know! Otherwise I will say - vitamin D made me feel SANE again. Thank God. I felt so miserable and not myself. I am convinced Magnesium helped a bucket load. And maybe I'm the type that needs a higher B12 baseline. ANYWAY! Sorry for the ramble appreciate any thoughts and hope I can help people on here too with my experience and ideas :) :grouphug: LondonLady |
Is this your magnesium product?
It is magnesium oxide.... it is useless except for laxative actions. It is not absorbed into the body to help with anything else. You need a chelated form like citrate, glycinate, malate, chloride, etc. http://www.hollandandbarrett.com/sho...250mg-60005830 Boots brand also is magnesium oxide.... useless. http://www.international.boots.com/e...lets-_1139816/ |
Quote:
Possibly an expert chiro that also does the c1 c2 adjustment (upper cervical/atlas axis) might be of help with. www.upcspine.com *you may have trigger points so a skilled DC that does PT type modalities or a very skilled PT should be able to address those. A good friend can do much also if they read up about Triggerpoints and look at the info links as they go.. http://neurotalk.psychcentral.com/thread125577.html Most MDs , neuros etc, do not really study TOS/soft tissue conditions much.. Perhaps a physiatrist or DO that is more studied in the whole body mechanics might be helpful. *I would search out a few really knowledgeable DC & PTs and meet with, get an evaluation to see if you think they really know about it. But you have to learn a lot first so you can tell if they are knowledgeable or not.. so your time & money isn't wasted. Poor PT can make it worse. If you haven't had any MRI /x rays to check spine that would be a step, to rule in/out any spinal causes. My dx was a mix of chronic RSI with some myofascial symptoms.. |
mrsD you are a lifesaver :) thank you SO much for looking out for me and educating me!
Being that I am in the UK, and actually have access to amazon - would you recommend any brands in particular? Also any doses? The links you posted are spot on - except I had a 500 Mag from HB. Many Many thanks to you again. Jo*mar - WOW! I was tenative to re-check my post for replies as this MS fear is real. Though funnily enough I woke up with a crook neck today - can hardly turn it! I have a deep suspicion you are right. I need to get to a soft tissue specialist for sure. In the past, I had so much relief from chiro - I wonder if being a big breasted woman plays a role in my posture? Despite having ballet training in the past - and above aberage awareness of posture and its importance,years at a desk has surely affected me! Thank you so much for your time bolding my symptoms and reading them all. Its so comforting discussing these things and I really can't thank you enough!! By the way - I did have a xray and no abnormalities found on neck. I guess that doesnt rule out soft tissue issues though. Just comments that all vertabraes in normal alignment and spaces maintained between. How long do you think it took until your RSI improved? And what symptoms dd you have? Very Best - you guys are great!! :grouphug: |
This is one example that is a quality magnesium product:
http://www.amazon.co.uk/Doctors-Best...nesium+tablets This link is to Amazon UK. Doctor's Best products are high quality and labeled clearly as to what is contained in them. Many of us on the Neuropathy forum here use them. If you see a combination product where magnesium oxide is listed along with some other types, assume the majority is oxide (as that is inexpensive and allows for smaller sized tablets/capsules.) Avoid those products if you need your magnesium to be other than a laxative. Here is our link to our magnesium post here: http://neurotalk.psychcentral.com/thread1138.html It is a long post, but if you read a bit here and there you'll find some interesting information that is helpful. |
So when I get constipated next time, I know what to take ;):D
Thanks again - you've really helped me out. You know, my mum always talks about good quality vitamins. It's so true. I'll check those links out! |
I had too many symptoms to list, there is a thread with many members symptoms listed on TOS forum, a search for " top TOS symptoms" or "TOS symptoms list" should find it.
http://neurotalk.psychcentral.com/search.php I quit my assembly job long ago, but improved with good treatment/therapy & a lot of self care in 2.5 yrs.. delays due to work comp issues/red tape made it take longer than if I didn’t have to deal with that process. Also my dr not knowing much about chronic RSI/TOS and the fact I didn't have high pain , only a lot of symptoms /discomfort that moved around.. I did a lot of searching, reading online and library books, nutrition, self care.. Main point is I got the best help from a multi modality chiropractor and a PT guy that taught PT at local university. |
Hi again Everyone!
How are you all doing? Well I thought I'd update. Today I felt great. I had been on the computer for most of the day doing some writing and marketing, taking little breaks for relief in my hand hand and forearm. When I took a hot bath tonight, I noticed that I got a little shakey in my hands. Now I'm aware that's typically a MS symptom, so I'm hopeful there might also be another reason? I wasn't super tired or dizzy, just my hands were slightly shakey. Stopped after I got out and cooled off. What else, since I took my VIT D Booster and now am on 10,000IU a day, my muscle spasms continue to be much better. Muuuch better. No painful cramps anywhere. Though I have random, sporadic, butterfly-like painless spasms through my body. Very light, don't last long. can be anywhere from a calf, to stomach, to arm, to butt. I have a feel i better get that good Magnesium soon! Anyway, getting closed to my neuro appointment. Kind ofscared to find out IF there is anything wrong! I still feel like 90% than before I took my Vit D treatment tho. I guess what worries me is knowing that they are now using Vit D to treat MS ...so could it be that the reason my symptoms are better, is because I'm treating it? I should stop freaking out. I dont know why I gravitate to MS. the other day ,with tiny spasms everywhere, I thought I had ALS ... oh the mind. sigh! hug xo :grouphug: |
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