Guest guest Posted June 26, 2007 Report Share Posted June 26, 2007 Hi, Cactusabby! Welcome to the group! D. > > Hi all, > > Please welcome cactusabby. I hope to see an intro. soon from our new member. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2012 Report Share Posted March 26, 2012 Hi KimSounds like she might have 'MS' but I'd start changing her ideas on diet before she gets trly freaked out if the diagnosis IS 'MS'. Diet is (in my opinion one of the trigger factors). There are so many things besides the drugs she can do for herself.I'd get her Candida situation checked - many of us have had it throughout our lives without knowing it and it really doesn't help matters....especially if it's systemic. A fantastic thing to look into is LDN (Low Dose Naltrexone). It truly is a help and is something which has really helped people manage the funny feelings and pain too. Once she knows her Candida situation, (LDN doesn't give as many benefits when Candida is in the mix) I'm sure she'll find many benefits come with it. There are many others who can give you more info about it here though.I'd head along to get her scanned for CCSVI (Chronic CerebroSpinal Venous Insufficiency) - the procedure has helped so many and is something which I'm VERY passionate about. (I'll send you the info I've been sending out for the past 4 years which will explain a lot more and will help her get her head around it)Changing her diet is something she sounds to be needing to do too. Whilst it might've been a bit of a shock for you and therefore seen as a bad thing, having the reaction to the chocolate cake is a brilliant thing! It's a sign post of what is going on at the root of all this! I recommend the BBD (Best Bet Diet). You'll find further info at www.msrc.co.uk and www.direct-ms.org nd here she'll find a diet which cuts the things which might be causing her trouble by the sounds of things. Getting an ELISA test done will show as well as these tests can, what foods she reacts badly to and shouldn't be touching. She won't be happy to hear that she'll need to cut dairy out of the picture and whilst chocolate is one of her faves, she'll need to lower her sugar intake anyway. The BBD allows small pieces of dark chocolate only. You'll work it out - she's a lucky girl to have a Mum who is so supportive! :)An 'MS' diagnosis is not 'THE END' though - life does go on and the diagnosis is a chance for her to reshape her life to a truly healthy shape.We're all here to help and will provide as many answers as we can for every question you throw our way! ;)I hope this has helped (even if only a little). 'What we do in life, echoes through eternity.' MARCUS AURELIUS (121 - 180 A.D.) To: mscured From: atlanteanproductions@... Date: Mon, 26 Mar 2012 08:25:17 -0500 Subject: new member ---------- Forwarded message ---------- Date: Sun, Mar 25, 2012 at 11:16 PM Subject: Re: Yahoo! Groups: Welcome to mscured. Visit today! To: mscured Moderator <mscured-owner > My daughter is a 26yr old Social Worker in Cleveland Oh. Last fall she started complaining about dizziness and then got tingeling in her hands and was very tired and run down. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 2, 2012 Report Share Posted May 2, 2012 Look into CCSVI treatment (which I have had with most symptoms disappearing) along with many alternative ways of dealing with ms. Look in the archives here then one of us will be happy to answer any queries.Don't get talked into DMDs (disease modifying drugs).Good luckJanet To: mscured From: atlanteanproductions@... Date: Wed, 2 May 2012 13:49:59 -0500 Subject: new member ---------- Forwarded message ---------- Date: Wed, May 2, 2012 at 1:18 PM Subject: Re: Yahoo! Groups: Welcome to mscured. Visit today! To: mscured Moderator <mscured-owner > hi, i'm debby, & i live in southern texas (near corpus christi). i was diagnosed by my chiropractor in 2000; it then took a little over a year for the medical doctors to diagnose rr/ms. i was on copaxone for about a year, but have not taken any meds since then, almost ten years now. problems & symptoms have been tolerable until the last couple of months, and i'm now trying to get set up with a new neuro, as i've moved almost 300 miles from the last one i saw! i am very interested in alternative methods, even if i do ultimately go back on 'standard' ms therapies. i look forward to the opportunity to learn from the group's experience!! thanks & nice to meet y'all! debby ------------------------------ Quote Link to comment Share on other sites More sharing options...
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