Guest guest Posted June 29, 2009 Report Share Posted June 29, 2009 Welcome Debbi!!!!SharonThis email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Subject: New memberTo: MSersLife Date: Sunday, June 28, 2009, 5:52 PMI have a lady in the breast cancer group that also has MS. Her name is Debbi and I gave her the info to join the group. Hugsnne------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2009 Report Share Posted June 29, 2009 Welcome Debbi!!!!SharonThis email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Subject: New memberTo: MSersLife Date: Sunday, June 28, 2009, 5:52 PMI have a lady in the breast cancer group that also has MS. Her name is Debbi and I gave her the info to join the group. Hugsnne------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2009 Report Share Posted June 29, 2009 Welcome to the group Debbi! Jolie > Welcome Debbi!!!! > > Sharon > This email is a natural hand made product. The slight variations in spelling > and grammar enhance its individual character and beauty and in no way are to > be considered flaws or defects. > > > > > > Subject: New member > To: MSersLife > Date: Sunday, June 28, 2009, 5:52 PM > > I have a lady in the breast cancer group that also has MS. Her name is Debbi > and I gave her the info to join the group. > Hugs > nne > > > > ------------------------------------ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2009 Report Share Posted June 29, 2009 Welcome to the group Debbi! Jolie > Welcome Debbi!!!! > > Sharon > This email is a natural hand made product. The slight variations in spelling > and grammar enhance its individual character and beauty and in no way are to > be considered flaws or defects. > > > > > > Subject: New member > To: MSersLife > Date: Sunday, June 28, 2009, 5:52 PM > > I have a lady in the breast cancer group that also has MS. Her name is Debbi > and I gave her the info to join the group. > Hugs > nne > > > > ------------------------------------ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2009 Report Share Posted June 29, 2009 Welcome to the group Debbi! Jolie > Welcome Debbi!!!! > > Sharon > This email is a natural hand made product. The slight variations in spelling > and grammar enhance its individual character and beauty and in no way are to > be considered flaws or defects. > > > > > > Subject: New member > To: MSersLife > Date: Sunday, June 28, 2009, 5:52 PM > > I have a lady in the breast cancer group that also has MS. Her name is Debbi > and I gave her the info to join the group. > Hugs > nne > > > > ------------------------------------ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 8, 2010 Report Share Posted March 8, 2010 Welcome back! When I am stressed by some other disease I find it hard to keep my sugars on an even keel. so I guess your husband can just try to stay with the best diet, etc. until his shingles are over with. Stress like that can make your sugars go the way they are with him. Dean new member | BlankHi friends, My name is Nan and I have been on this list a couple of years ago. I have macular degeneration. | My husband Del has diabetes and has had it for twenty years. He also has a bad heart and has a defibrular. Also he now has shingles. | I wanted to rejoin this list because I thought I could get some help with helping Del at this difficult time. Because of the pain he has with shingles his sugar goes way up and then way down. | His eyesight is getting worse also. | Del is 75 and I am 70. | any advice and information would be appreciated. | Nan | Exercise daily, Walk with the Lord | | | | Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 8, 2010 Report Share Posted March 8, 2010 Welcome back! When I am stressed by some other disease I find it hard to keep my sugars on an even keel. so I guess your husband can just try to stay with the best diet, etc. until his shingles are over with. Stress like that can make your sugars go the way they are with him. Dean new member | BlankHi friends, My name is Nan and I have been on this list a couple of years ago. I have macular degeneration. | My husband Del has diabetes and has had it for twenty years. He also has a bad heart and has a defibrular. Also he now has shingles. | I wanted to rejoin this list because I thought I could get some help with helping Del at this difficult time. Because of the pain he has with shingles his sugar goes way up and then way down. | His eyesight is getting worse also. | Del is 75 and I am 70. | any advice and information would be appreciated. | Nan | Exercise daily, Walk with the Lord | | | | Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 8, 2010 Report Share Posted March 8, 2010 Hi Nan, good to have you here. sugar When you can't put your prayers into words , God hears your heart. ~Be Blessed, Sugar new member BlankHi friends, My name is Nan and I have been on this list a couple of years ago. I have macular degeneration. My husband Del has diabetes and has had it for twenty years. He also has a bad heart and has a defibrular. Also he now has shingles. I wanted to rejoin this list because I thought I could get some help with helping Del at this difficult time. Because of the pain he has with shingles his sugar goes way up and then way down. His eyesight is getting worse also. Del is 75 and I am 70. any advice and information would be appreciated. Nan Exercise daily, Walk with the Lord Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 8, 2010 Report Share Posted March 8, 2010 Hi Nan, good to have you here. sugar When you can't put your prayers into words , God hears your heart. ~Be Blessed, Sugar new member BlankHi friends, My name is Nan and I have been on this list a couple of years ago. I have macular degeneration. My husband Del has diabetes and has had it for twenty years. He also has a bad heart and has a defibrular. Also he now has shingles. I wanted to rejoin this list because I thought I could get some help with helping Del at this difficult time. Because of the pain he has with shingles his sugar goes way up and then way down. His eyesight is getting worse also. Del is 75 and I am 70. any advice and information would be appreciated. Nan Exercise daily, Walk with the Lord Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 8, 2010 Report Share Posted March 8, 2010 Hi again, Nan, Your husband has multiple overlapping conditions (the heart issues and the shingles), and his blood sugars may well be influenced by both stress (mental and physical) and biological factors due to his medical problems. We don't know if he is type 1 (on insulin) or type 2 (on oral medications). If he is on insulin, perhaps he can take some additional quick acting insulin like Humalog. Is he (are you) checking his blood sugars at least somewhat regularly? Dave Visit: http://www.bardtalk.com and find answers to commonly asked questions concerning BARD. Join the online discussion list, and discover many other resources to help make your digital talking book experience more enjoyable! new member BlankHi friends, My name is Nan and I have been on this list a couple of years ago. I have macular degeneration. My husband Del has diabetes and has had it for twenty years. He also has a bad heart and has a defibrular. Also he now has shingles. I wanted to rejoin this list because I thought I could get some help with helping Del at this difficult time. Because of the pain he has with shingles his sugar goes way up and then way down. His eyesight is getting worse also. Del is 75 and I am 70. any advice and information would be appreciated. Nan Exercise daily, Walk with the Lord Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 8, 2010 Report Share Posted March 8, 2010 Hi again, Nan, Your husband has multiple overlapping conditions (the heart issues and the shingles), and his blood sugars may well be influenced by both stress (mental and physical) and biological factors due to his medical problems. We don't know if he is type 1 (on insulin) or type 2 (on oral medications). If he is on insulin, perhaps he can take some additional quick acting insulin like Humalog. Is he (are you) checking his blood sugars at least somewhat regularly? Dave Visit: http://www.bardtalk.com and find answers to commonly asked questions concerning BARD. Join the online discussion list, and discover many other resources to help make your digital talking book experience more enjoyable! new member BlankHi friends, My name is Nan and I have been on this list a couple of years ago. I have macular degeneration. My husband Del has diabetes and has had it for twenty years. He also has a bad heart and has a defibrular. Also he now has shingles. I wanted to rejoin this list because I thought I could get some help with helping Del at this difficult time. Because of the pain he has with shingles his sugar goes way up and then way down. His eyesight is getting worse also. Del is 75 and I am 70. any advice and information would be appreciated. Nan Exercise daily, Walk with the Lord Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 9, 2010 Report Share Posted March 9, 2010 Hi Dave, Del has type 2 and and takes 25 units of insulin every evening with his meal. I know our daughter who is a nurse tells him to take the insulin after he eats. Del takes his sugar reading every day and more when he is feeling really bad. And he tries to take it several different times of the day. He now has to have tests for blood in his urine. Saw the doctor today. he feels a little overwhelmed with everything that is happening to him. Nan new member > > > > BlankHi friends, My name is Nan and I have been on this list a couple of > years ago. I have macular degeneration. > My husband Del has diabetes and has had it for twenty years. He also has > a bad heart and has a defibrular. Also he now has shingles. > I wanted to rejoin this list because I thought I could get some help with > helping Del at this difficult time. Because of the pain he has with > shingles his sugar goes way up and then way down. > His eyesight is getting worse also. > Del is 75 and I am 70. > any advice and information would be appreciated. > Nan > Exercise daily, Walk with the Lord > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 9, 2010 Report Share Posted March 9, 2010 Hi Dave, Del has type 2 and and takes 25 units of insulin every evening with his meal. I know our daughter who is a nurse tells him to take the insulin after he eats. Del takes his sugar reading every day and more when he is feeling really bad. And he tries to take it several different times of the day. He now has to have tests for blood in his urine. Saw the doctor today. he feels a little overwhelmed with everything that is happening to him. Nan new member > > > > BlankHi friends, My name is Nan and I have been on this list a couple of > years ago. I have macular degeneration. > My husband Del has diabetes and has had it for twenty years. He also has > a bad heart and has a defibrular. Also he now has shingles. > I wanted to rejoin this list because I thought I could get some help with > helping Del at this difficult time. Because of the pain he has with > shingles his sugar goes way up and then way down. > His eyesight is getting worse also. > Del is 75 and I am 70. > any advice and information would be appreciated. > Nan > Exercise daily, Walk with the Lord > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 9, 2010 Report Share Posted March 9, 2010 Hi Dean, Thank you for the welcome. It seems that everyone is telling me the same thing. I guess the important thing is to take his sugar several times a day and eat accordingly. Nan new member > > > | BlankHi friends, My name is Nan and I have been on this list a couple > of > years ago. I have macular degeneration. > | My husband Del has diabetes and has had it for twenty years. He also has > a > bad heart and has a defibrular. Also he now has shingles. > | I wanted to rejoin this list because I thought I could get some help > with > helping Del at this difficult time. Because of the pain he has with > shingles > his sugar goes way up and then way down. > | His eyesight is getting worse also. > | Del is 75 and I am 70. > | any advice and information would be appreciated. > | Nan > | Exercise daily, Walk with the Lord > | > | > | > | Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 9, 2010 Report Share Posted March 9, 2010 Hi Dean, Thank you for the welcome. It seems that everyone is telling me the same thing. I guess the important thing is to take his sugar several times a day and eat accordingly. Nan new member > > > | BlankHi friends, My name is Nan and I have been on this list a couple > of > years ago. I have macular degeneration. > | My husband Del has diabetes and has had it for twenty years. He also has > a > bad heart and has a defibrular. Also he now has shingles. > | I wanted to rejoin this list because I thought I could get some help > with > helping Del at this difficult time. Because of the pain he has with > shingles > his sugar goes way up and then way down. > | His eyesight is getting worse also. > | Del is 75 and I am 70. > | any advice and information would be appreciated. > | Nan > | Exercise daily, Walk with the Lord > | > | > | > | Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 1, 2011 Report Share Posted November 1, 2011 -Hello and welcome The links provided in this last post are a good place to start but I think it's *CRITICAL* at this early stage of an MS diagnosis especially PPMS that you are particularly focused on ruling out any other possibilities.  In the beginning stages of identifying and treating MS I think many of us are and were sucked into depending a great deal on the direction and recommendations of a neurologist.  As we all know MS is very particular to each person and no one treatment method should be expected to work the same for you as it did for others whether it's conventional, alternative, holistic or whatever the case. I'll say from personal experience that I was misdiagnosed with RRMS 5 yrs ago.  I don't know if my RRMS is not MS at all or if it's MS induced by my *Lyme Disease* going untreated for so long,  I say two things with a strong sense of certainty.  I don't have RRMS.  If anything MS related it's SPMS that was induced by untreated  Lyme Disease and Conventional meds DID NOT work for me.  I think that last bit can be echoed by every member in here.  I implore you to urge your husband to follow-up ANY previous testing with an IgeneX Lyme Disease test ASAP.  Tread very lightly in trusting a Neurologist.  Unfortunately your inexperience with MS is a green light for any nuro, MD, etc to pool you into a particular diagnosis and therapy choice based on symptoms, MRI imaging or Spinal Tap reports.  LYME DISEASE MIMIKS MS  & ALL MS MARKERS.  I personally think that PPMS or SPMS is very easily a lasting or Chronic Lyme infection.  You need to be sure and treat the right thing.  With the exception of having Lyme Disease these remarks are all my opinion. Best Wishes, Mike Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 1, 2011 Report Share Posted November 1, 2011 hello and wel The links provided in this last post are a good place to start but I think it's *CRITICAL* at this early stage of an MS diagnosis especially PPMS that you are particularly focused on ruling out any other possibilities.  In the beginning stages of identifying and treating MS I think many of us are sucked into depending a great deal on the direction and recommendations of a neurologist.  As we all know MS is very particular to each person and no one treatment method should be expected to work the same for you as it did for others whether it's conventional, alternative, holistic or whatever the case. I'll say from personal experience that I was misdiagnosed with RRMS 5 yrs ago.  I don't know if my RRMS is not MS at all or if it was induced by my *Lyme Disease* going untreated for so long,  I say two things with a strong sense of certainty.  I don't have RRMS.  If anything MS related it's SPMS that was induced by untreated  Lyme Disease and Conventional meds DID NOT work for me.  I think that last bit can be echoed by every member in here.  I implore you to urge your husband to follow-up ANY previous testing with an IgeneX Lyme Disease test ASAP.  Tread very lightly in trusting a Neurologist.  Unfortunately your inexperience with MS is a green light for any nuro, MD, etc to pool you into a particular diagnosis and therapy choice based on symptoms and MRI imaging or Spinal Tap reports.  LYME DISEASE MIMIKS MS  & MS MARKERS.  I personally think that PPMS or SPMS is very easily a lasting or Chronic Lyme infection.  You need to be sure and treat the right thing.  Best Wishes, Mike Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2012 Report Share Posted March 27, 2012 Hi ZoeHave you changed your diet at all?I felt better after I went onto the BBD (Best Bet Diet). If you don't know much about it, go to www.msrc.co.uk or www.direct-ms.orgIt has helped me hugely Supplements are a good start and you've done well by the sounds of things.Fatigue left the building for me when I got onto D3 at a 'high' dose - I'm at 5000IU these days an i's working well.I also take B Complex and B12 to kick the tiredness. LDN is something you should look at too - Low Dose Naltrexone. It's something which has helped me beyond masure to kick the pain I had been experiencing each night. LDN's results can be hampered by any Candida you may have in your system - I know hat's what has stopped it doing all it can do for me.....I still have those issues as I believe it is systemic in me. I hope I haven't given you a bunch of info that you already know as you're a longtime member 'What we do in life, echoes through eternity.' MARCUS AURELIUS (121 - 180 A.D.) To: mscured From: zoehealthy@... Date: Mon, 26 Mar 2012 18:43:36 -0700 Subject: RE: new member Hi. I'd like to chime in here because I am not a new member but right now I feel like one. I have tried so many things. For a while I felt like I was staying stable --for about 3 or 4 years -- but now the last year I definitely feel a decline in a number of areas. I am not interested in CCSVI for myself personally but I am really interested in trying to figure out what are the most important supplements. How does one know which supplements they need. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2012 Report Share Posted March 27, 2012 Kim, Unidentified bright objects seen on MRIs are often called " lesions " . These pages explain " lesions " in layman's terms. http://www.medhelp.org/health_pages/Multiple-Sclerosis/MS-Information-and-Resour\ ces-Index/show/22?cid=36 There is a section on Testing --- MRI's. How MRIs Show Lesions in MS Lesions vs. Symptoms And another section for Ruling Out the Diseases that Look Like MS MS Mimics And a third section farther down the page called What We Know about Lesions Lesions! Lesions Lesions! Spinal Cord Lesions Lesions - Can They Disappear? A Hypothetical Case Overview KC > > > > ---------- Forwarded message ---------- > > From: Kim McMahon <kimmcdarr@> > > 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. Went to family Dr when she also started having > > headaches. She sent her to get MRI and it came back with a few white spots. > > We then went to neurologist who wasnt impressed with the MRI. (I am still > > not sure what that meant)we went back in 3 months got another MRI. She > > still has all the symptoms, he says he is " Concerned " about the white spots > > , but come back in 6 months and he wont commit to a diagnosis > > We are curious about several things and the connection, or not? Before all > > these symptoms showed up she had several out breaks of cold sores, and we > > have heard about maybe a connection, she was also very sick before all this > > with a strep and run down. As a baby she had thrush, I have read of some > > connection with MS?Then I have read maybe some connection with Chocolate, > > guess what she loves? The other day was kind of a good day and we went to > > lunch had choc cake and half hr later she had weakness , numbing hands and > > increased headache. > > we are now going for a second opinion, but i fear the worst. She is very > > interested in NOT taking medicine so we are exploring all options, vit D > > magnesium, raw food, CoQ10 and anything > > thanks for listening > > Kim > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2012 Report Share Posted March 28, 2012 I just saw an allergist as I felt I was have a reaction to a medication. She told me that 10 people could be tested for food allergens and 1/2 would come back allergic to something. Out of those 5- 4 of them would be wrong. I personally think its more of a go on your gut feeling. Cut out a food and see if you improve. I feel better when I don't eat dairy or wheat. I feel very much in pain when I have gluten. So for me I may test positive I may test negative for gluten intolerance why risk it though. I know how it makes me feel. Take care Donna in VA " Stress is the confusion created when one's mind overrides the body's basic desire to choke the living daylights out of some jerk who desperately deserves it. " --Unknown >________________________________ > >To: mscured >Sent: Monday, March 26, 2012 9:43 PM >Subject: RE: new member > > > > > >Hi. I'd like to chime in here because I am not a new member but right now I feel like one. I have tried so many things. For a while I felt like I was staying stable --for about 3 or 4 years -- but now the last year I definitely feel a decline in a number of areas. I am not interested in CCSVI for myself personally but I am really interested in trying to figure out what are the most important supplements. How does one know which supplements they need. I do take Vitamin D3 and my Vitamin D tests come back pretty good at about 60 where the normal range is 30-100. I have been interested in possibly meeting with a chelation specialist and getting tested for mercury poisoning because I was overvaccinated in the past. However, I read so many scary stories about herx reactions from chelation that it does scare me and a few times I took a small dose of oral DMSA and I felt much more cognitively confused for the next few days each time. Regarding the ELISA, I have >now had it done five times over the past 6 years. Last year, just to see what would happen, I had the blood drawn at the same time and sent to two different labs--one blood speciment to Cambridge and the other specimen to York. Well sorry to have to say this but even though it was the same blood draw the ELISA results from each lab was extremely different, with only a little bit of overlap. To me that pretty much washed away the validity of the ELISA testing, because, again, this was taken from the same blood draw at the same exact time (no eating in between, etc) and sent to two reputable labs with extremely different results. I gave up on ELISA testing after that. However, I do notice I feel much better when avoiding gluten, dairy, and eggs. Lately I am having a lot of trouble falling alseep at night. I am very wired at night. I was diagnosed with hypothyroidism 3 years ago and I take Naturethroid and my thyroid numbers always come back normal now, >but I don't feel normal. My brain fog and fatigue are the biggest problems, followed by paresthesias of the limbs and also my vision has been deteriorating. I am scared. I feel like I don't know what road to take. I made an appointment with an extremely expnsive holistic MD but then I heard he was not too good, so I canceled. I just feel right now like I don't have a plan, and I really need a plan--a plan at least gives me hope. Thank you if anyone can comment on what I should do. I fear that it is like the traditional view of MS that tries to tell us we will go downhill in most cases and I used to not believe that, but now I feel, at least for me, it is happening like that. Thank you for any suggestions. > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 11, 2012 Report Share Posted June 11, 2012 Hi Jen, Like you I have been digging and pushing mountains aside to find what causes this and how to rectify it. I believe you are right, drugs are not the answer, or at least not for me. Anti-inflammatory diet, detox,detox detox, and targeted supplementation are working for me. I also fully completed my dental revision 8 months ago. I do fall down occassionally when I forget to pay attention, but that is getting better too.   Soy, canola, corn, gluten, msg, gmo foods, and heavy metals are the primary enemies. Coconut oil(research lauric acid) is your friend, as is cilantro, parsley, squash, lemons, fresh young coconuts, and aloe vera. All fresh and of course organic. Lots to learn. Research pertussis toxin and aloe vera as a moderator of MS in mice. Research orotic acid and the remyelination of axonal ganglia in rats and you won't wonder why I use magnesium orotate as my chioce of magnesium supplement. Research the apoptic death of neurons due to the hardening of their mitochondria and glutamate transfer defect and you will never touch msg or any other excitotoxin. Don't forget that cream and burtter are ok in moderate amounts,(for me), but milk contains butyrophilin which causes our immune system to attack myelin. P.S. 4 weeks since I have used even one cane or crutch. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 19, 2012 Report Share Posted June 19, 2012 Have you been tested for Lyme Disease through IgeneX?  Your initial symptoms looked very similar to mine.  I went 6 yrs thinking I had MS only to find out last August that I actually have Lyme Disease.  Now I'm not saying I don't have the classic symptoms of MS (which are all mimicked by Lyme BTW).  I believe my MS was induced by Lyme if it is MS at all.  Fact is chronic Lyme is extremely difficult to recover from.  If it is Lyme in your case it would be a great idea to find it out and begin therapy.  I highly recommend Igenex labs, Good Luck.......... Mike  Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 19, 2012 Report Share Posted June 19, 2012 I 2nd MM's comments entirely, 100%. Randy > > > > Have you been tested for Lyme Disease through IgeneX? Â Your initial symptoms looked very similar to mine. Â I went 6 yrs thinking I had MS only to find out last August that I actually have Lyme Disease. Â Now I'm not saying I don't have the classic symptoms of MS (which are all mimicked by Lyme BTW). Â I believe my MS was induced by Lyme if it is MS at all. Â Fact is chronic Lyme is extremely difficult to recover from. Â If it is Lyme in your case it would be a great idea to find it out and begin therapy. > Â I highly recommend Igenex labs, Good Luck.......... > Mike Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 21, 2012 Report Share Posted June 21, 2012 Can you send more information please. Email harj_sweet@... ------------------------------ >Hi , > >I would be interested to learn more about " the science " you've found on the subject. > >Please tell. > >Cheers, > >Pinda > > > >> >> Hello folks, >> >> I suffer from and am disabled by a mitochondrial disorder that shares many of the symptoms of MS. There is much research that links MS to mitochondrial dysfunction such as here: >> >> http://www.ncbi.nlm.nih.gov/pubmed/19607913 >> >> I have recently tried a very simple therapy that has made a huge difference in my life and, as the following study from Stanford suggests, could make as much of a difference in yours: >> >> http://www.ctsaip.org/create-pdf.cfm?id=5893 >> >> The therapy: >> 5 mg of benadryl every 4 hours during the day. That's it, costs about $4.00 per month! >> >> I started this therapy due to revalations in a thread in a mito yahoo group I moderate and have since ferreted out the info on how and why this works and exactly what low doses of certain antihistimines are doing. A hint: it is similar to LDN in function, but considerably more wide spectrum >> >> IF anyone is interested I will post on what prompted me to try this (the revelations) and on all the science I've found on the subject (what, how, why). >> >> Folks this is being hidden, as it turns out this could be benificial in MANY diseases, AND it doesn't require a prescription, AND it's cheap. >> >> >> >> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 21, 2012 Report Share Posted June 21, 2012 OK I need to rest my hands so I'll post tomorrow, probably too late for you Brits tomorrow...sorry > >> > >> Hello folks, > >> > >> I suffer from and am disabled by a mitochondrial disorder that shares many of the symptoms of MS. There is much research that links MS to mitochondrial dysfunction such as here: > >> > >> http://www.ncbi.nlm.nih.gov/pubmed/19607913 > >> > >> I have recently tried a very simple therapy that has made a huge difference in my life and, as the following study from Stanford suggests, could make as much of a difference in yours: > >> > >> http://www.ctsaip.org/create-pdf.cfm?id=5893 > >> > >> The therapy: > >> 5 mg of benadryl every 4 hours during the day. That's it, costs about $4.00 per month! > >> > >> I started this therapy due to revalations in a thread in a mito yahoo group I moderate and have since ferreted out the info on how and why this works and exactly what low doses of certain antihistimines are doing. A hint: it is similar to LDN in function, but considerably more wide spectrum > >> > >> IF anyone is interested I will post on what prompted me to try this (the revelations) and on all the science I've found on the subject (what, how, why). > >> > >> Folks this is being hidden, as it turns out this could be benificial in MANY diseases, AND it doesn't require a prescription, AND it's cheap. > >> > >> > >> > >> > > > > > Quote Link to comment Share on other sites More sharing options...
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