Multiple Sclerosis Health Coaching Home Study Course

29 Jan, 2010  MS Health Coaching

110 Comments so far »

1. Mrs Teresa Williams said

   am January 29 2010 @ 4:19 am

   I would like to say that even though I dont have such bad Multiple Sclerosis as some other people, I do have secondry progresive MS, and I get dreadful pains in both my legs, and I am worried how bad I am going to get, I know there is no an answer which no-one can give me, I am 49 years old and was diagnosed about 9 years ago, but they said that I probably had it for 10 years previous, which means I was about 30 when I first started with MS. The medication I am on, I was told I could put on some weight, which I have ( to my distaste!!)I am worried as I just dont know what is going to happen to me. The medication which I am on for the pain isLyrica 300 mg, however this will probably be changed yet again as it doesnt affect the pain as well as it did in the begining when I first started with this one approx a year ago and I am due to see my ms nurse next week when it will probably be changed, any ideas on what to ask for? I was also told by someone that going in a compression chamber ( which divers use) can help ms???

2. Karyn Sullivan said

   am January 29 2010 @ 5:05 am

   It would be a God send to finally have something that would relieve all of these uncomfotable symptoms. I do believe that there is something. I think it is about time to end this suffering.

3. Rolande Roy said

   am January 29 2010 @ 5:07 am

   Hi my name is Rolande
   I have MS since 1996 but have felt symptoms at the age of 15. I saw the webinar but was not able to participate due the time zone. Depending on the day and time for the home study course will be held I would be very interested in participating in this.
   Thanks for your great information.

4. Lorna McGann said

   am January 29 2010 @ 5:43 am

   Have been managing RRMS for more than 20yrs & know quiet a bit about stating in remission. Always interested in knowing more.
   Because our finances are tight, cost would be an issue. Are you charging for this info?

5. Lorna McGann said

   am January 29 2010 @ 5:53 am

   Tried leaving a comment, did not accept.

6. arminda audette said

   am January 29 2010 @ 7:33 am

   I thought Dr. Cartwright’s video was very informative and especially beneficial to newly dxd. I wish I had followed his protocol years ago and possibly I would be walking and not in this wheelchair for over 5 years.

   I missed the coaching sessions but am interested in the videos.

   Thanks.

7. michele garneau said

   am January 29 2010 @ 7:39 am

   looking for information at all times . diagnoised with m.s. in 2005.

8. Eunice Nafziger said

   am January 29 2010 @ 7:40 am

   I have not walked in 10 yrs, thanks for hope!

   Any exercises to improve dexterity

9. Patricia (Nova Scotia, Canada) said

   am January 29 2010 @ 8:26 am

   That is great, after reading the first part of the email, I was so excited but then at the end you said that you might only have 50 copys available. I will try to be in the first 50 but what if we are not in the first 50 people to get it, are we gone be able to get all this informations somewhere else at another time. I think these informations are the KEY ON GETTINS BETTER but if there is only 50 available, the 12000 other people wont know what to do.

   Hopefully you will be able to make more than 50.
   Sincerely.
   Patricia

10. Stacy said

    am January 29 2010 @ 8:35 am

    Thank you so much for deciding to release this information in a home study course. It is very helpful to me to be able to study this information on my own schedule as I have two daughters, ages 9 and 5, that need my undivided attention when they are home from school. This way I can study this information when it is convenient for me and continue to make the proper changes to my lifestyle to rid myself of this horrible disease! I so want to be there for my family and I am determined to get rid of these symptoms so that I can be!

    I will be first in line for your course!

    Thanks again –

11. Deidre Brown said

    am January 29 2010 @ 8:45 am

    I really would like to say thank you for what you are doing because I want to be normal again,I am to old to be useing the restroom on myself,I cant control the bladder or bowels when I have to go I have to go among other things thats going on,so again I thank you.

12. Gilles Lafrance said

    am January 29 2010 @ 9:05 am

    Dr. Cartwright seem to be somebody who know and want to help peoples like me who got MS. The probleme for me was to follow him in the webinar the sound was no good maybe it because I live in Canada near Ottawa. Thank Sue Ellen for your help, I receive your book “No more MS”. Here in Ottawa we start a petition for Dr. Zamboni we want the medical research take his discovery serious and be able to do some CCSVI to see if it true. They should put moneys on some positive research the medication that we inject every days don’t cure and cost lot of moneys I will be not able to take anymore.

13. Hussein Saber said

    am January 29 2010 @ 9:20 am

    I have not read any replies from you for dealing with severe leg stifness due to MS. Currently my wife have great difficulties in mobility, and we would appreciate any comment regarding this symptom. Thank you.

14. cecilia E. SASSE said

    am January 29 2010 @ 9:43 am

    I AM 70 YEARS OLD, AND HAVE HAD MULTIPLE SCLEROSIS FOR 38 YEARS. WHEEL-CHAIR 25-30 YEARS. HELP! I WANT TO GET THE TMJ SPLINT, WHICH IS A CURE FOR M.S., BUT DON’T HAVE THE MONEY–$18,OOO.00. HOW CAN YOU HELP ME?

15. Ka Yan Ho said

    am January 29 2010 @ 9:44 am

    Got my MS when I was 17,18. Went on the study and is stable now with Tysabri. Take Tysabri every other month now.

    Ka Yan Ho

16. Gilles said

    am January 29 2010 @ 10:14 am

    I was not able to follow the webinar because the sound was not good but i’m interest on CD’S Thank

17. Barb Rickard said

    am January 29 2010 @ 10:18 am

    I missed the webnar(?) but was very pleased to get notification of its existence. My computer skills are very limited but I will try my best to read the e mails i have received from Sue Ellen Dickinson.

    I would like to be among the 50 who will receive the latest info.

    Thank-you.

18. debbie said

    am January 29 2010 @ 10:36 am

    iam so thankful for Dr. Cartwright for helping in getting all the vital information out to people about this monster disease!!..iam 36 and have had ms for 10yrs now when i first got diagnosed i really wasnt bad compared to what iam like now ..i have 3children ages 10 11 13 and it is incredably difficult to be there for them the way i want …iam very interested in the home course and i would love to be one of the 50 for if it is going to require money for it i wont be able to learn more what to do since i dont have the money …i have tried alot of different ways that just might help me but then i realize my system is too sesitive so im at the end of my rope now ..somethings have to work and help me out there and from what i have heard from Dr.Cartwright he does have the answer!!!..im very hopeful here ..thank you for all that you guys have done and offered to all of us suffering from ms..

19. Elwin Jensen said

    am January 29 2010 @ 11:08 am

    I am 56 years old was just diagnosed with MS 4 months ago they think I have had MS ever since my first episide with optic neuritus in 1984 and have had episodes of numbness and dizzyness over the years looking into this program with alot of hope to be rid of these problems.

20. Katherine Angileri-Suergiu said

    am January 29 2010 @ 11:30 am

    If I don’t get all the videos and cds that’s fine let 50 people who are sicker get them. I think it would be helpful to post some of the diet. Perhaps a sample weekly diet or somethng like that. Give us something to go on until you can get more cds/dvds set up. Hopefully cost won’t be too prohibitive will they? Some of us are on disability.

21. Norma J Borchert said

    am January 29 2010 @ 11:33 am

    I would like to know what the replacement for calcium supplements was. and what was wrong with calcium?

22. william baldridge said

    am January 29 2010 @ 11:38 am

    the new pill for somebody with ms that might help me to walk again could you tell me when the fda is going to approved it thanks very much

23. Joanne Walcer said

    am January 29 2010 @ 11:39 am

    I of course would like to be one of the first 50, but I will wait until you will be able to get more out.The info that I got already was helpful, so it will be nice when you are able to release a bit more . FOREVER THANKFUL Joanne Walcer Saskatchewan Canada!!!!!!!!!!!!!!!!

24. Kimberly said

    am January 29 2010 @ 11:54 am

    Does anyone have experience with the Rife Beam Ray machine?

25. David Lanni said

    am January 29 2010 @ 11:56 am

    Help Sinking fast what do u know about the Venus drainage procedure.

26. Amy K Breault said

    am January 29 2010 @ 11:59 am

    I am 26 and was diagnosed with MS when I was 16. I have tried alot of different things and I am currently receiving chemo. I’m not really sure if it is helping yet. I would like to have more information on your home study course. Thanks Amy

27. Staci Cannon said

    am January 29 2010 @ 12:04 pm

    Was diagnosed with MS in 2004, but have suffered undiagnosed for much longer. I am interested in fighting this wretched disease aggressively. I will not let it consume my life. I am so happy to learn about the information that you provide.

28. Evelyn Blasi said

    am January 29 2010 @ 12:11 pm

    I’ve had MS for 16 yrs and have been dealing with it all naturally. Thanks for the webinar. I started that diet you suggested 8 days ago and have had much more energy. I am so excited, and when I am just longing for a bagel and butter I think of how much better I feel now, and grab an apple instead. Looking forward along with God’s help to better walking , balance and hand movement. Looking forward to learning more of your suggestions. Thank you so much.

29. C. Moir said

    am January 29 2010 @ 12:17 pm

    Hi! Was interested in your site after listening the webinar on MS. Thank you so much for offering it free of charge. I would really like to sign up for the course; however, like so many others, I need to know the cost. Looking forward to receiving this information.

30. Anna said

    am January 29 2010 @ 12:24 pm

    Your webnar sight has attracted alot of attention as it gives people hope. I have only just been diagnosed but like others know I have had MS for well over 13 years. I have read the posts from people who have suffered for years and lost a part of themselves in this fight agains MS. Your are offering people something to grab hold of, to fight and gain back what has been taken from them. If there is anyway you can, please find a way to share your homestudy report to the thousands of people who believe in you and believe with your help they can come back from the darkness to the light.

31. Karen Williamson said

    am January 29 2010 @ 12:25 pm

    Hi

    Please can you let us all know how much the home study course will cost and if there will be more than 50 available in due course?

    Many thanks

32. Lillian Coomer said

    am January 29 2010 @ 12:26 pm

    I have had m.s. for 12 years and the dr. told me a couple months ago
    that looking at my mri it was in 2nd progression i am not on any injection for it .
    I did do Avonex for 7 yr. and i felt it made me worse , but i kept telling my dr. i was getting worse and he would say you dont know what kind of shape i would be in if i wasnt on it . I went to another Dr. and he told me to stop the Avonex , i did and i got feeling better but not well. my balance is really bad , my hands tingle and my walk is not good. i would like to be in the 50 to get the cd. Thank you

33. Andrea said

    am January 29 2010 @ 12:27 pm

    What is the cost going to be and only 50 will be a hard choice you will be able to get the info. It is always about the money and I realize that the materials are not free but we all do not have extra with this economy and I have 7 children.

34. Bridget W said

    am January 29 2010 @ 12:31 pm

    Sue Ellen was kind enough to get me a copy of her book and I also listened to Dr Cartwright’s seminar. Does Dr. C know anything about serrapeptase for MS?

35. Judith Norris said

    am January 29 2010 @ 12:36 pm

    My MS symptoms and difficulties seem very insignificant when i read all the other comments.

    God bless you all. I pray His divine spirit to rest on you and help you to cope with your symptoms. He has been gracious to me for over 50 years.

    Read my E-Book (website above) to see how I lived successfully over 50 years, diagnosed 1958 at 17.

    God, Exercise, Classical Music and Life Purpose of Teaching Music are the four components that have helped me.

36. Judith Norris said

    am January 29 2010 @ 12:39 pm

    Sorry about the duplicate submission, just a bit of editing that was noticed. JG

37. Joanne Walcer said

    am January 29 2010 @ 12:42 pm

    I should tell you that I am taking SOMALIFE,that is amino acids also vitmans,omega3 mand superX. In 2003 I first had some symptoms( balance problems, double vision,fatigue,dizziness).I had an MRI,but the neurologist never really said if it was MS,but he put me on Copaxine, I also didn’t like being a pin cushion.In Dec 03 my sister sent me a bottle of SOMALIFE.I was hesident to take it because my neuroligist say not to take any natural supplements. So after being poked for a will I asked my family doc about taking the amino acids I also told her that the copaxine had 4 amino acids in it but they were made chemically and the somalife were made of 8 amino acids that were made of soya bean that were grown in Manitoba then sent to China to be colpact ,after being colpact they have no soya left in the tablet,then they are sent back to Canada where they were packed in veg caps,my doc said that she seen no problem with taking them ,but I must say that she was not the one that told me to stop taking the copaxine I made that decission on my own , I was symontom free until now.

38. Rick Best said

    am January 29 2010 @ 12:55 pm

    I know in my heart that you all are so on the mark with your information.Reading all of these comments is really bringing my situation into focus,thank you, thank you, thank you!

39. Christina said

    am January 29 2010 @ 1:05 pm

    I listened to the Fireside Chat, it was very interesting. I didn’t think I would be able to change my way of eating as well as I have. I need more details and I feel the Home Study Course will be of immense help. I cant tell how well it is working for me because I got a bad cold in the mean time.I do seem to have more energy and not as much pain. I am looking forward to finding out more and being able to finally do something to help myself feel like myself again.

40. mary morton said

    am January 29 2010 @ 1:06 pm

    I have had MS for 3 years now and I still do not know what to eat and what vitamins to take and my biggest problem is my balance or lack of it, I used to work out every day but right now I can’t, are there some small exercises I could do on my own, I worked 30 years of my life but now social security is ms is not disabling so I don’t have hardly any income coming in so please help

41. Jill said

    am January 29 2010 @ 1:07 pm

    I too am interested in home study course and was wondering about cost?? I was diagnosed with PPMS in 2006 , with all my symptoms appearing after severe kidney infection in Aug 2005. I do not walk much anymore (legs don’t want to work), can’t write as right hand is affectedand, am extremely interested in any exercise suggestions as well as any alternative therapies as I tried steroids (did not work), 1 round of chemo (will never do that again!) and my dr. says i am not candidate for any of the drug therapies (ok, well ????)

42. Wendy Johnson said

    am January 29 2010 @ 1:08 pm

    Thank you for all of your help. I hope to be one of the fifty.

43. Grace Wiltshire said

    am January 29 2010 @ 1:22 pm

    I am very interested in the Home Study Course, hoping I am one of the 50. I am not sure if my comment gets through, because I never see it or a response on the info sheet.

44. Wendy Hawthorne said

    am January 29 2010 @ 1:33 pm

    I must take this home study course. I have had MS for 26 years or so and the last two years has brought numbness and stiffness. I have tried various supplements to try to fend off those symptoms – tumeric, NerveFix, magnesium, D-3, fish oil and nothing seems to help. I will not take the MS CRAB drugs, as I call them, because they are poison. I do take LDN.

45. Barbara B said

    am January 29 2010 @ 1:36 pm

    I don’t think I can get the webinars with webtv. I can’t get video but can sometimes get audio. I have had MS for about 10 or more yrs. I believe because back in 2,000 I had to have help walking outside but was later diagnosed in about 2004 or 05. I am taking Copaxone shots.I guess its suppose to slow the MS down but there are some really bad days. I want to be able to learn all I can of what will help and it seems like Dr. Cartwright knows how to get rid of it. I just cannot afford some of these things because I like many others are on a small fixed income. I am 64 yrs. old.PLEASE HELP US!!!!

    Thanks for listening to us.

    Barbara B.

46. Susan Paskert said

    am January 29 2010 @ 1:36 pm

    I would be very interested, but cost is a big issue for me as well. Save me, please!

47. Lisa Kohn said

    am January 29 2010 @ 1:37 pm

    I have had MS for over 25 years. I was RR for 12-16 years until a car accident. I have such back heat, I can’t drive my car sometimes. And I am always in panic mode. I can’t calm down. They have me on anti-depressant Effexor 112.5, and klonopin .5 2-3 times a day. Copaxone (after 6 mo. on Tysabri)–(the BK virus not the JC (PML) virus was detected in my spinal fluid. Therefore the switch. I am 2nd progressive by now. Without my antidepressant I can’t walk. My cognitive is way off.I’ve put on 70 lbs. I am in a rut, and I do not have how much is Dr. Cartright’s video? Does he Talk about Low Dose Naltrexone? Thank you for letting me speak. I don’t have much money, I am short saling my house. I feel like I have no purpose. Divine or otherwise. God Bless Everyone, may you heal, may we find our passion in spite of this MS Diagnosis.

48. Jose Navarro said

    am January 29 2010 @ 1:38 pm

    BOY OH, BOY I CAN’T WAIT FOR THE HOME STUDY COARSE! SET ONE ASIDE FOR ME TOO…JUST SAY IT’S A GO AHEAD, I’LL BE SURE TO GET ONE:-). P.S. YOU GUY’S ROCK!!!

49. Lisa Kohn said

    am January 29 2010 @ 1:41 pm

    Just one addition: I was on BetaSeron for 12 years when it first came out. That was positive for me, except I got bipolar from it. It does work though for anyone who is newly diag.–I have to find a way to get my weight off. And I suppose I have to change my life style. HOW??? HELP???? I don’t mean to sound like a child. I’m 51..and scared that’s all. (That’s enough!)

50. Helen Moonin said

    am January 29 2010 @ 2:10 pm

    I am on SSDI so if it is expensive, i am out. I do take vitamins, I would like to be able to walk with a cane instead of a walker.

51. Joel R. Alexander said

    am January 29 2010 @ 2:15 pm

    I am 57 years old and has had M.S. since I was 45. It has been getting worse the last few years I don,t exspect to walk much longer.

52. Val Rechenmacher,Saskatchewan-Canada said

    am January 29 2010 @ 2:28 pm

    I live in the province that has the highest ratio of MS per capital.
    I was diagnosed in the summer of 2007,(at the age of 50) and spent 1.5 years on disability insurance. During this time -I went through the grieving process ( although I did not realize it,at the time, until I started to improve,and returned to work).
    I too did lots of research,and most of what Sue Allen describes,I have done.
    A friend saw how I was struggling,and passed my name on to someone whom had received help ,using the essential glyconutrient sugars .I will not mention the company name,other than to say they are in 16 different countries, and have patents on several of their products.
    I would be wiling to share this with anyone who wishes.

    Long story short-I was able to return my walking cane after 4 months ,and return back to work in the education field.
    I am looking forward to see results of the blocked artery studies.
    I am also grateful for this site, and for the work that Sue Allen, and the Cartrights are doing,to educate people about M S

53. adrian said

    am January 29 2010 @ 2:33 pm

    I am writing this on behalf of my son Adrian. He has primary progress MSand has all the awful symtoms.he desperately needs pain relief,nothing helps. We exist on benefits and need to know the cost of this course which sounds as if there is some hope for those who are suffering greatly with this terrible condition. thankyou

54. Mark Hoeksema said

    am January 29 2010 @ 2:52 pm

    I would like to know the cost of this Home Study Course and how soon it will be available. I am on my third medecine now and I am tired of switching with no inprovement. “You Can’t Keep A Good Man Down” but getting some assistance with my M.S.would be helpful.

55. GABRIEL CORREA ESCOBAR said

    am January 29 2010 @ 3:05 pm

    mi diagnostico fue en el 2000, ya es tiempo de comenzar una dieta y ejercicios para mejorar la calidad de vida, no solamente con el rebif, gracias Dr por entregar su tiempo investigando como se puede llevar una mejor vida con este problema que se llama MS
    Gabriel -Cali-Colombia

56. Ruth Sorenson said

    am January 29 2010 @ 3:06 pm

    Thank you so much for the information that has been provided so far. I really look forward to the Home Study course, and I hope you will find a way to make it available for all of us. I started following the GFDF immediately after listening to the Fireside Chat, and I stopped taking calcium and iron (I have been anemic.) In less than a week I had a measurable difference in strength at my physical therapy sessions. I am really excited and hopeful for the future after seeing improvement so quickly.

    I do not suffer as much as so many of you, but I do cope with many symptoms of MS. I was diagnosed in Nov. 08, but have had weakness, spasms, and difficulty walking for several years. I have numbness and tingling in my hands and lack of strength and control in my hands.

57. joe ulsamer said

    am January 29 2010 @ 3:28 pm

    Could you please add my email address to your information so that I can keep getting all the helpful information.
    Thank you

58. Heather Foreman, Werribee Vic. Australia said

    am January 29 2010 @ 3:47 pm

    What a wonderful man you are, I am trying to change my husbands diet, but it is hard work getting him to change things I think he is giving up.

59. DAVE FAGAN said

    am January 29 2010 @ 3:48 pm

    HI I AM 51 AND HAVE HAD MS FOR 5-6 YRS.I AM TAKING COPAXONE FOR ABOUT 1 YR AND IT SEEMS LIKE IT HELPS ALIITLE.I AMS TAKING ALOT OF VITAMIN D AND EATING VERY HEAALTHY.I USED TO BE VERY ACTIVE IN SPORTS ETC..ALL I WOULD LOVLE IS ABLE TO WALK WITHOUT A WALKER AND GET QUALITY OF LIFE BACK..I KNOW IT CAN BE DONE BECAUSE I KNOW 3 WOMAN THAT HAVE BEEN TAKING AVONEX FOR 6-7 YRS AND ALL 3 STOP TAKING THE DRUGS AND ARE WALKING….COULD YOU CALL IT A MIRACLE I DONT KNOW…ALL I WOULD LIKE IS SOME ADVISE TO GET BETTER,,,THANKS

60. Rhenia Carter said

    am January 29 2010 @ 4:17 pm

    I am interested in the home study course. Will the participants in the 6 week MS Health Coaching webinars have to pay all over again to have access to the home study course?

61. Evelyn Perez said

    am January 29 2010 @ 4:26 pm

    Please let me know about the study course of Dr.Cartwright. Please help I need that my brother be normal again.

62. Delaine Patterson said

    am January 29 2010 @ 4:32 pm

    I was diagnosed with RRMS in 2001. Have tried several different “synthetic” drugs but keep going back to by naturalpath for an extensive array of herbs and vitamins which I take on a daily basis. They always work the best I have found and I will never stop taking tham again. (When I ceased taking them after about six months, because I felt SOOO godd, the MS would come back to haunt me with fresh symptoms. Although I take a variety of herbs, and alot of minerals every day(some three times a day) I wil never stop agaom. somce tje o, overall impreovment to so good)
    My diet has also changed dramatically and is another thing that one should be aware of.
    I hope everyone out there can achieve the improvement that I have hrough the use of Natural medicines.

63. anitarpiccola said

    am January 29 2010 @ 5:21 pm

    I would like to know more about glconutrient sugars why do these
    effect MS. Thankyou Godbless Anita piccola

64. Mary said

    am January 29 2010 @ 5:40 pm

    I did your 6 week course and it was awesome. Lots of great info and I did start the vitamins and they are working. I would like to have a copy of this home course as there is so much info that you give that it would be great to be able to look back at it. Just wondering if there will be a cost to it?
    Thanks again!

65. Darlene said

    am January 29 2010 @ 5:41 pm

    I was diagnosed with M.S 23 yrs ago with symptoms for about 10 yrs before that,. I have raised 2 kids and continue to work full time.Recently I am proud to say that I have become a Grandmother for the first time. Unfortunately my dexterity is so bad I’m afraid to carry my granddaughter ‘ along with that I have such extreme leg spasm I sleep very little because of that and my leg muscles are so stiff that that walking is painful and very “guarded” .I have a very extensive shoe collection and am very sad that I can no long wear any other kind of shoes but sneakers. So all in all my top two complaints are I want to walk so no one stares at me and I miss my shoes and being able to have some fashion in my life I can’t wait to watch your videos maybe they’ll help in someway

66. Louise Harris said

    am January 29 2010 @ 5:43 pm

    Thankyou for deciding to share your ‘Baby’ with us.
    The Joy your ‘Baby’ will bring to our lives is incalculable.
    Thankyou!!!
    Kindest Regards
    Louise

67. Teresa Buhs said

    am January 29 2010 @ 5:53 pm

    I was diagnosed with MS in 2003. (They said I had had it for 10-12 years.) When I was diagnosed, I was walking with a cane with great difficulty. I took Copaxone for 3 months. I fell 5 times, so I quit taking Copaxone. By that time, I could no longer walk with a cane and was forced to use a small scooter to get around-even in the house. Insurance would not pay for my scooter because they said it was recreatiional! I use mu total gym and a healthrider to try and keep up my muscle strength in my legs. When I was diagnosed, they said I had lesions in my brain and down my spine, but they were all inactive.
    I’ve been taking supplements for years-B-100s, flush-free niacin, D3, magnesium and either fish oil or cod liver oil. Any diet or supplement tips would be appreciated. I tried to get on the webinar, but the address given to me by Dr. Cartwright did not work. I ordered both of Sue Ellen’s books (CD copy and written copy). I never did get the written copy.

68. Doris Dorado said

    am January 29 2010 @ 5:56 pm

    I’m so anxious and excited about all the comments that have been posted. They are all so familiar.
    I’m 58 years old and was diagnosed in 1986 at 35. I was able to work for 10 years with no one knowing I had MS even though I was in the hospital twice with ACTH IV and also Steroids. I finally had to go on disability because my fatigue and my symptoms were worsening. I was on Betaseron, Avonex and Rebif but they were helping and had a lot of Steroids IV. I also had Stem Cells implant in Argentina but continue to have some decline. I need to use a cane for my balance and have no endurance standing up or walking. Presently I’m only doing a vitamin protocol taking injections of B1, B12 and Liver plus many other oral vitamins including calcium and magnesium but not seeing any improvement.
    I’ve been on both Webinars that Dr. Cartwright has given. I had also purchased Sue Ellen’s book which I read a number of times. Money is very short these days but I hope to be able to get the Home Study Course. I need help with this horrible disese. I hope I can get it from you
    Dr. Cartwright and Sue Ellen.

69. Bridget W said

    am January 29 2010 @ 6:39 pm

    I would like the home study course also but being unemployed and recently divorced I have no money to spend, please make it available for all of us living with this monster. God Bless everyone, you’re always in my prayers.

70. Ann Byrne said

    am January 29 2010 @ 6:54 pm

    Sorry I didn’t leave any comments. My 33 yr old son has MS and is seeking to get off of Avonex. He has done a colon cleanse and is taking multiple vitamins. Jon is seeking to be fully restored. His left side is affected and his left leg has a mind of its own sometimes. He holds his right arm out for balance and uses a cane. He exercises regular, but didn’t the first 18 months of having MS due to circumstances beyond his control. He is otherwise healthy. What does this “coaching plan” cost. I read the other comments. So, now it’s your turn. Money would be a hinderance. He is on diability.

71. yoya mack said

    am January 29 2010 @ 7:59 pm

    Hi I have read most of the comments, and I all so agree. I would like my life back too. I was told the day before Thanksgiving I was in the secondary progression and the Avonex is not doing any good, so I stopped taking it. I have chosen to trust God and His will to be done. I read about the home course, truly interested, just like the question what must I do to be saved, how can I obtain this study? What will it cost, prayerfully I can be in the fifty. It was not an accident I read this,so what is the next step?

72. Sybil Windham said

    am January 29 2010 @ 8:26 pm

    I thank God for all the comments made by other individuals diagnosed with this dis-ease. I am interested in information from Val Rechenmacher of Saskatchewan-Canada and also the name of the herbs Delaine Patterson is taking.

    Can someone share an exercise program? I started exercising at Fitness USA and oh boy was I surprised when I could barely walk after being on the bike for 20 minutes.

    I share the same comments as the other individuals. I would love the home study course but my funds are limited as well.

73. Teresa R.N. said

    am January 29 2010 @ 8:30 pm

    Dx with M.Ss. 29 yrs. My neaurologist is Dr. Roy L Swank MDPhD professor emeritus Oregon Health Sciences Univ. Portland, OR. He has done 50 yrs of research. I can say that as he died last year at age 99. He found our plasma was abnormal, we cannot handle fat. We need to cook with oil, no butter, no crisco. Easy, there are conversion charts. My family has taken on healthy eating since I was diagnosed age 27 and had become an RN age 24. I appreciate Drs. information. It compliments Dr. Swanks & my regime. I was told to rest everyday i.e. lay down for half hour mid day or an hour. I did even as an RN doing ‘floor nursing’ at a hospital or as supervisor at the hospital. Lay down mid day. Blood to the brain is seems to me. I also received fresh frozen plasma infusions whenever I was very fatigued/exhausted. I am a single mom and my neuro said the preganancy would be fine, it is in the raising of the children you will have difficulty. I hope moms can teach their children to nap. It is a way of life. I am 56, still play the organ, have fine motor movement play with both hands, and my feet on the foot pedals. Stress whether good stress or bad stress, is my enemy. I eat 15 gms of fat per day cooking only with oil that remainsliquid in the regrigerator. I also add, black olives or avacado to daily diet and bring the oil up for the linolic and linoleic acid for nerve health. We are on the right track! As an RN and having family taking the drugs or doing diet, I find diet in my experience is the most helpful. The drugs are not helping. Bless all of you. We are in this together. I also hope for an affordable cost on the information about the diet and from Dr. Cartwright. Maybe we could download readable stuff on our computers? Thank you so much.
    I am, Teresa age 56, WASHINGTON, single mom of 26 yr old., and an R.N. for 33 years. I still work very parttime doing Private duty nursing in the home. Dx: MS 29 yrs ago when age 27.

74. Teresa R.N. said

    am January 29 2010 @ 8:33 pm

    I just remembered that cannibas is legal and helps MS pain. It can be eaten, put into capsules, smoked. I have worked for a pain clinic all over the Pacific Northwest. We are going to make it! Rest eat right and do not over do!! I did and have!!!

75. Laxmi said

    am January 29 2010 @ 8:55 pm

    I was diagonised 20mths back with MS, doctor did mention that I had it prior. Though diagonised by this deadful disease 4 yrs after I delivered my child, did feel that something about my body was not right since pregnancy. Have a 6yr old, would like to be for her as every mother would want to for their children. The uncertainity scares me every minute and day, especially when thinking of my family.
    After listening to Sue and Dr Cartwright, I have some hope and would not like to loose it. I sincerely, like everyone here, pray to be one of the 50 so that i can work to not let my conditions progress and be for my family and friends.
    Thanks
    Laxmi

76. Mary Allard said

    am January 29 2010 @ 9:32 pm

    Would like to get the study course.

77. Liliane said

    am January 29 2010 @ 10:05 pm

    My wife was diagnosed with MS in the 80″s but she had her first attack one year after we were married at 21 and went into remission until at 37 she had to quit teaching. We have 4 children and she is now 57 and presently in hospital for almost a month recuperating from her second attack in 10months.She in unable to walk but had beem using a walker for the past 5 years. She has been on Betaseron and in now on Rebif but the neurologist thinks her body is producing antibodies preventing the Rebif from working.I don”t know who to believe anymore. WE are seriouly considering this Liberation Treatment since this might be her last shot at staying in our home but it not readily available and costly with little support from her neurologist. Any suggestions to help the lady I have shared 40 years of my life? Again we would appreciate a copy of your study course.

78. David Wise said

    am January 29 2010 @ 10:30 pm

    I’ve been strictly following Ann Boroch’s MS diet for 7 months and it’s helped me a lot. I went on vacation for a week recently and tried to be careful eating out at restaurants. Fortunately you can’t always avoid certain hidden ingredients and I’ve suffered a slight relapse. I’m gradually getting back to normal again.

79. parmjit said

    am January 29 2010 @ 10:48 pm

    my daughter has ms for last 6 years she is 26 years old she just got her mri done and they are worse than they were 6 years ago right noe she cant walk she on wheelchair when doctors say that wheelshair is your option she is in shock she is in bad depresson i think there is always hope now ican see there is hope please say when are cd and tapes are coming out please help my daughter

80. Judy Brewster said

    am January 29 2010 @ 11:05 pm

    Im from Australia and was diagnosed 17 years ago. Have now been unable to walk for 3 yrs now. I cannot stop my hands from shaking, takes me a long time to type letters. Shocking, since I used to be a typist . I also had taken Betaferon then Avonex.

81. Marina Minko said

    am January 29 2010 @ 11:15 pm

    Would really like the homestudy course,hope it’s an affordable cost as on disability. I am greatful for the information so far, have stopped all calcium supplements , dairy foods & gluten containing foods, i do feel i have a bit more energy, since doing so.

    It’s so good to read all the comments, I can relate to most of them, especially the extremely painful cramps / spasms in both legs at night, every night, so my nights are sleepless – broken blocks of sleep at best. It would be good to know what can bring some relief, the drugs don’t work & give many undesirable side effects. i am a vegetarian & have always preferred the natural approach to illness, i take magnesium powder, vit D3, multi B complex especially with higher dose of B12. i try to excercise in fresh air(even on balcony) in my wheelchair & ’sit to stand’ exercises, aquats & rises all holding onto guard rail, every morning.

    I am interested in the information about essential glyconutrient sugars from Val Rechenmcher Saskatchuen-Canada & the herbs Delaine Patterson is taking. Please let me now somehow.

    God bless you all in your quest for freedom from MS symptoms. I believe that a healthy diet & my faith in God keep me going, i refuse to mentally give in to MS, i remain very hope ful.

82. Vivienne said

    am January 30 2010 @ 12:09 am

    Have had MS over 20 years. Have found natural treatments best, as drugs seem to make me worse. Massage and Foot Reflexology ( especially good for numbness & strange sensations etc) , and lately manipulative physiotherapy are very helpful to cope with leg stiffness. Chinese Sunrider Food Herbs helped greatly with fatigue. I found out soon after diagnosis that milk products made the MS worse so I avoid them. I also take various supplements. Was interested to hear about the need to avoid calcium as I felt with no dairy one would need to replace the calcium so have taken calcium supplements for years !! I have not used a gluten free diet, so maybe this is something to try. Balance is a problem so I walk with a cane at present. The study course sounds interesting, so long as the cost is not prohibitive. Here in Australia so many natural therapies are beyond the reach of folk on pensions as they are not covered by the government like the drug therapies prescribed by doctors. Keep up the good work. More of your written work on the computer would be great. Thankyou.

83. Trevor Parsons said

    am January 30 2010 @ 3:12 am

    My sister was diagnosed at age 16, after a few years of awkwardness in movement. She lived in a wheelchair for almost 25 years but died of pneumonia. She never had any drugs, only personal care. I wonder, after reading all the varied comments , if it could be better to drop the drugs altogether. People seem to have very different feelings about their usefulness, so maybe spending nothing on drugs would help to allow spending on better quality organic foods to be increased. Not all extra vitamins are helpful, especially if taken in excess quantities, so do your research.

    And with exercise, remember that even well people suffer after taking it, if they are out of practice, so be gentle with yourself when you start, and take a couple of weeks to build up the time spent on it. And then be really consistent: three sessions a week are needed to stay right. You don’t need a gym, as yoga type exercises can be done just as well at home, saving even more money.

84. Trevor Parsons said

    am January 30 2010 @ 3:20 am

    P.S. I am astonished to read so little comment about the place of cannabis in pain relief for MS. Just because many Governments fear the association of cannabis with drug-takers doesn’t mean that ill people have to bear pain for many years, as well as their physical disability. Time and again the blog refers to uncontrolled pain in MS sufferers. It is high time to protest loudly and often about this cruel neglect of ill people’s welfare.

85. Mary said

    am January 30 2010 @ 7:33 am

    My boyfriend has the progressive MS, and is almost in a wheelchair. I believe this would be an excellent program for him. He doesn’t work, and I spend most of my time taking care of him, so neither one of us currently works and outside job. Will this be available with a MEDICAL CARD? We’re broke, but he needs the badly. How much is this program going to cost?
    Thanks.

86. Jan Embree said

    am January 30 2010 @ 7:36 am

    My husband has MS. He is not taking any prescription medication. We do not like the side effects for the supposed benefit that they give. Craig is drinking carrott juice and taking Ambrotose from Manatech each day. We would love to know better supplements to take and what to eat and what not to eat. Craig is a beef lover — he cut back for several months and saw no change in his health, so really didn’t see the point. He as relapsing remiting. Has lost mosdt of the sight in his left eye, and gets tired easy. Other than that, he’s pretty good. My husband is a minister and doesn’t make very much money. The town we are currently living in is smaller and very bad economically. I work as an aide at the Middle School and plan to return to school this summer to get my teaching degree (about 2 1/2 years left). We have two children 20 & 19 years old, both in college. We really don’t have money to spend on trial stuff. I am all about the natural cures and am interested in what you have to offer. I am so against those crazy shots that have a list a mile long of side effects, cost a fortune, and don’t “promise” anything. In fact, I see the people who are on the therapy and they seem to be in worse condition than Craig.

87. Ursula said

    am January 30 2010 @ 7:48 am

    If it’s too expensive, I won’t be able to afford the course. I rely on disability which in UK is an insult to someone who paid into the system for her entire working life. I am 55, diagnosed at 43, walked until 2003 and felt quite good until beginning of 2007. I was unable to take any of the drugs prescribed, such as Rebif, Copaxone because they affected my liver so badly. I do watch my diet, have always been intolerant of milk products. I eat wheat products very occasionally and buy myself gluten free pastas and make my own bread. I use a bit of yeast in my bread and a little honey to sweeten. I buy Saint Dalfour Fruit spread’s for toast which is a real luxury. These mimic a jam but they are sweetened with grape juice concentrate. I eat lots of fruit and vegetables. Occasional grass fed beef, minced to make bolognese sauce. Free range chicken and local fresh water fish – sea fish is too toxic.

88. Terry bedney said

    am January 30 2010 @ 8:03 am

    I have had ms for a long time – got married ,had children,and slowly getting worse. 3 years ago I stopped all med’s and I’m going all natural,
    some thing are better – but it’s a fighting battle – I can only hope and pray

89. Anna said

    am January 30 2010 @ 8:12 am

    Thanks everyone, you have all helped me with your comments on how the different drugs have effected you over the years, I am not on any drugs but have my first appointment next month at a ms clinic.
    Since the last webnar, I have totally followed the diet recommended, no wheat, dairy, red meat etc. Even though it has only been about a week or so I have noticed a change, my husband as well. I have more energy and my moods are better, its a start. I no this diet will be for life but I also know combined with the other information it will give back quality of life.

90. Joanne Walcer said

    am January 30 2010 @ 9:56 am

    I was wondering if anyone else had the same experience as myself ? When my eyesite would become blurry I would bring my chin to my chest and for some reason my eyesite clears for awhile. PLEASE RESPOND IF THIS HAS HAPPENED TO YOU THANK YOU

91. Clár Ní Mhadoige - Clar Ni Mhadoige said

    am January 30 2010 @ 9:59 am

    Clár – Irish Girl – 46 yrs old.
    Diagnosed Oct.’86 at 22yrs old – was at undergraduate Phys Ed college training to be a Phys Ed teacher – managed with difficulty to complete & graduate in ’87. Since then have taught in 3 countries but over time the ability to teach pe declined. Currently, am teaching other subjects in a secondary school. As Phys Ed person, I abhored the idea of putting toxic chemicals into my body especially since the establishment … i.e. the Doctors disgrard my questions / queries regarding the importance of DIET. – what MORONS … I continued from ’86 following my own diets / supplements & was able to continue exercising – cycling until 2001 & swimming until last year – Fatigue / leg weakness means that currently even Yoga & Tai Chi is too much for me.
    I always think that the worst part has been the uncertainty … & the false hope that MS throws at you … one week you could be feeling fairly OK & the next you could be wretched … this has changed to one day good / next bad … to one morning good / the afternoon wretched … & can get to one hour good / the next hourS wretched AND not knowing why really. Continurally taking diaries of what you eat / took / did can become exhausting & you really cannot tell / work out that by doing X you get Y result. So what to do … I followed the route of TOTAL avoidance of the NORMAL medical route for 18 years as I had been GETTING BY – still & still am in full time employment … until I had disimproved so much I finally went back to a neurologist in Jan ’04 & had my first MRI (it had’nt been around here (Ireland) back in 1986) – it confirmed … Yes … you have MS. But I wasn’t happy to try any of the suggested drugs – so I continued with my own healthy eating & exercising when I could routine. Had another visit with a neurolgist & DID try some spasm realaxing drugs he perscribed BUT that had me bedridden & unable to eat…. after just half a tablet!!! So that was scraped – I was back walking & able to eat within the week.
    And so YES … I DO WANT TO BE CONSIDERED FOR THE HOME STUDY COURSE … & PLEASE WHEN WILL THERE BE MORE THAN 50 AVAILABLE FOR ALL SUFFERS … & WHAT will the COST BE please – we really are good people – we deserve to have our lives back – I SO WANT to be able to do more – Half of my current life is gone … I want the next 40 years to be good ones & MS FREE.
    ….
    And for those who have it … more extra points from me … I really dislike the following MS linked facts:
    **Not being able to exercise – legs too weak.
    **Having to ‘Stand up straight’ – before taking a step, or I might fall over.
    **Having to ALWAYS wear trainers – as my feet hurt in normal shoes – they (the feet) seemed to have expanded over time so at the moment I cannot tolerate nice shoes, mind you my poor balance would also discount.
    **Not wearing nice clothes … as they would look wretched with trainers.
    **Not bothering to buy new clothes – what’s the point.
    **Having to always have a spare change of clothes (bottom half) … in case of accidents.
    **Having to alter the under bedclothes / place towels on sheets at night … in case of accidents.
    **Having to plan when to eat / drink – ALWAYS knowing that a toilet is within 20/30 steps if I do. (I know all the bathrooms in Ireland!!!)
    **Putting on weight … cos I can’t exercise.
    **Counting the number of steps it takes to get to a point – to help keep my focus on my walking & telling my legs / feet to lift…move so I do get there!!!.
    **Not being able to go for a walk on the beach.
    **Having to cancel or NOT MAKING plans to go somewhere as I can’t guarantee to be there.
    **Stoping going OUT – I always loved that … felt half normal when I was out when I could see a favourite artist / show / film.
    **I stop now as I waffled on enough … STAY STRONG & POSITIVE – cry & release if needed – I do & it helps. XX- Clar- XX
    But I’m sure there are many other instances you could all mention – my thoughts are with you … BUT DO REMEMBER … the class is ALWAYS HALF FULL & not half empty
    … Clár – the realistic optimist – who KNOWS she will get better – my body can do it – I just have to make the right choices & do the right things.
    So ROCK ON …Dr. Rudy Cartwright & Sue Ellen Dickson– THANKS so much for your work.

92. Cindy Iabone said

    am January 30 2010 @ 10:18 am

    Thank you so much for presenting these wonderful and knowledgeable webinars. I also did not know what to totally avoid in my diet. I knew milk was an issue for me, so I eliminated it from my diet, but did not even think about cheese and yogurt. Thanks to Dr. Cartwright, I also stopped taking my calcium supplements. I’ll be going to the health food store and pick up the additional supplements you suggested, along with the fruits and vegies I should be consuming. I’ve also switched to purchasing only organic and natural products. I’ve had issues with using regular detergent and cleaning products like Tide, Downey, Joy, and even bath and facial cleaning products.

    I have question though, I love artichoke hearts and avocados (practically consume daily), are these okay or should I avoid these as well?

    Thanks again for sharing this information.

    Sue Ellen, I been detoxing for a month now, and I couldn’t believe how great I felt even after a week of detoxing. I knew it was working when I tasted metals in my mouth for a few days at the beginning of the detox. Now I have more energy and feel a whole lot better. Now I’ll follow Dr. Cartwright’s advice and hopefully soon I’ll be as good as new!!! YEAH!!!

93. Liezl Lötter said

    am January 30 2010 @ 12:44 pm

    Hi, my name is Liezl, 35 years old and I’m living in Kuruman, Northen Cape, SOUTH AFRICA.I have a wonderful husband and an adorable 2 year old daughter. Been diagnosed with RRMS in 2008, but as many others I’ve had it for about 10 years.
    It feels like here in South Africa we are cut out of what is happening in the rest of the world! I am trying to do everything I can to improve myself as our medical aids mst have 4 relapses documented by a neuro before they even consider you for treatment!
    Your webinar was VERY interesting and did answer much of my questions – which our doctors can’t. Thank you so much for your time!!!!!! It really gave me hope, but the fact that only 50 copies of yout Home Health Course will be available is not good news!!!
    I realize that there is alot of people that’s worse off than me, but I really would like to make my life easier for my little girl and husband.
    Surpose I would have to calculate our time difference before hand and stay glued to the computer. ha-ha-ha
    Thank you to Sue Ellen for her ebook! Thank you Dr. C and Scott for the information on stress-I now know where everything went wrong. But I still need some info as to how to reverse it! I believe that with your guidance and Sue Ellen’s and Noël Batten’s ebook’s I WILL recover.
    Thank you so much.
    God bless you all.

94. Denise Scott said

    am January 30 2010 @ 12:57 pm

    I agree with Trevor’s blog about cannabis. One hit off a joint relieves my pain far more than the gabapentin pills I’ve been prescribed. But the PA Senate will not sign the House bill to approve the use of medical marijuana. They say they will not approve a bill that will turn sick people into “junkies”. But isn’t that what we are by taking the pharmaceutical companies meds. The drug companies are probably lobbying against the bills passage, to ensure they will continue to make big profits.

95. Paul said

    am January 30 2010 @ 3:01 pm

    Am 68 & have PPMS – was diagnosed in 1985 but in retospect have had it since a teenager. Currently using CBT (Cognitive Behaviour Therapy)and it does help me to deal with the heat pain. Previously was unable to get much sleep and became suicidal/heavily depressed. CBT does help your body overcome the pain.

    Interestingly, a neighbour who is diabetic has the heat pain issue in her legs also.

96. BRENDA BLAKE said

    am January 30 2010 @ 4:46 pm

    I’m very interested in the study course. I had my first symptom, double vision, in my early thirtes. I got well and didn’t have another symptom until 2004; then it was mis-diagnosed. So in 2008 my balance kept getting worse. I am an above the knee amputee, so the prosthesis was the suspect.Finally after many tests, it was diagnosed MS. I was sympton free for 19 years.
    I take Copaxon and have had some relief. I need the walker; the cane is not enough support anymore.what is the cost of the course?

97. Debbie Wilson said

    am January 30 2010 @ 8:40 pm

    I am looking forward to your Home Study! As a person with MS it is great to know you guys are able and willing to share your knowledge! Thanks – DEbbie Wilson

98. valerie pare said

    am January 31 2010 @ 12:51 am

    Did I already register for this program? I am very overwhelmed and this is the type of problem I was having at work. I couldn’t remember what I did or didn’t do. I’m an RN-newly diagnosed and on short term disability.
    Thank you,
    Valerie

99. Lorraine said

    am January 31 2010 @ 6:26 am

    Thank you to you all – it is fantastic what you are doing. I was diagnosed with PPMS in December 2008. I didn’t like being told that there was nothing I could do -here isn’t even anything that I can be given! I started looking on the web for success stories and came across Sue Ellen’s story/book. I’ve got the book – a truely interesting read; both inspirational and very positive. I also have The Secret. I do believe in the Laws of Attraction and I know, from Sue Ellen’s book, that ultimately there will be a happy outcome. Despite my normally positive attitude, it can be a real struggle – not helped by the fact that I am also going through The Change. So when I have “mood swings” and tears – is it MS? Is it the Change? Or, am I just being miserable and feeling sorry for myself? I am following a very healthy diet – no diary, no CHOCOLATE and only cheat by having candy (a packet every night) and a small glass of wine. My skin, hair and nails are amazingly heathly and I no longer get pain in my legs. I do pilates – basic – every week, which has given back my stability – although I still can’t wear even a low heal on my shoes, but I am still struggling with weakness and exhaustion. I take supplements as per a nutritionalist and Dr Cartwright’s suggestions. Is it a matter of keep doing what I’m doing and I will recover? Or is their something else I should do?

    Many many thanks, for everything you are doing.

    Wishing us all good health -

    Lorraine
    England

100. Linda Beechey said

     am January 31 2010 @ 10:51 am

     Diagnosed RR in 1992 commuted and worked City of London 10 years then symptoms became troublesome. Real problems Fatigue, balance and walking now due to shortened muscles in right leg, doing all I can to stretch muscle hence aid walking. Have cut out dairy, wheat, yeast, sugar, have Dr Swank’s diet book. Would love some help as noone seems able to advise on how I can improve the MS. Now SP as no relapse for 5 yrs so in a downward spiral, need more help now and think the course would be so good for me to improve.
     Thank you and god bless you all
     Linda

101. Diana said

     am January 31 2010 @ 11:59 am

     Have you considered releasing your information to local MS Chapters so they can offer guidance through their support gourps. I think the more people it gets out to, the better we can become. I accept it is not 100% and requires a lot of time from each candidate. Everyone will not show improvement. I have failed miserably this past year after being on Rebif for 15 years had to give it up. The odds of being one of your 50 people is like winning a lottery. I am desperate to relieve any sympton and having this waved in my face and told it is only being 3 out of every 1000 people currently interested is enough to put 997 people in a depressed state. I am sure you could recruit several coaches in local areas to promote your teachings and still be able to collect revenue. We are suffering enough now and don’t need another disappointment ealizing it weill be months before you offer this again. A month makes a world of difference when you cannot do something today you could do yesterday. Six weeks from now is likely to bring on 42 things I could not do yesterday and put me in a condition that his program will not effect.
     Thinking of you all in my situation
     Diana

102. Betty said

     am February 2 2010 @ 12:59 pm

     This sounds too good to be true! I’ve had MS for 20 years….symptoms were an annoyance but I got over them mostly….I have the remitting type of MS…well, the last few years, especially now, my balance/walking is awful, need some one’s arm when I go from car to where I’m going. I work 1 day a week, that’s good, gets me out, husband helps alot and has been unemployed for over a year.

103. Jamie Bailey said

     am February 2 2010 @ 4:51 pm

     What is the free gift??? There is no mention of what and how to obtain the gift. I think this is a bunch of ****8

104. Ron said

     am February 2 2010 @ 8:45 pm

     I think it would be very sad if you only let 50 people have the MS health coach .All of us are sick and need help..Please sign me up for the program

105. Ferial Tonekaboni said

     am February 3 2010 @ 2:56 pm

     please allow me to sign up for ms health couch program. do not leave me out if I am not one of the 50 people who are first in line. God have send to you for rescue. Bless you
     sincerely yours Ferial

106. Michelle Terry said

     am February 3 2010 @ 9:25 pm

     What an obsticle course – just to get a straight answer(s) – the usual: Cost/payment options, time involved, material to receive, how to sign up/purchase. I guess the loss of 20+ IQ points really adversley affects my ability to mnauver thru websites; coupled with short term memory leaves me unsure I can accomplish his.

107. Michelle Terry said

     am February 3 2010 @ 9:32 pm

     I can’t believe I hit “send” before I actually got to the main point; I would like to purchase the course; in addition sign me up for the health coach, please confirm this. I will check again later tonight and first thing tomorrow (Thursday 2/4/10).

108. Ana Esaclante said

     am February 4 2010 @ 3:12 pm

     Would like to order the health coaching home study course as soon as it is available.

109. Peggy Joiner said

     am March 3 2010 @ 7:24 pm

     Dr. Cartwright, Scott, and Sue Ellen,

     Thank you for your commitment and dedication to sharing your knowledge with those of us with MS!! I don’t think I was one of the first 50 but did receive my kit. Thank you for your hard work and time spent in getting more copies put together!! I was, also, not able to get on your webinars.

     Along with the lady from Canada, I, too, am a product of the Manna… glyconutritionals and they have helped me. However, I have been paralyzed from the waist down from onset of my MS and for almost 40 years now, so, I figure that whatever I can learn about and do to help myself, is a move in the right direction…

     I have always believed in the power of the body, given the right fuel, to take care of itself and maintain its balance. I see that I am not alone in this, and yet the medical community continues to try and force harmful drugs on us!

     Before I really get on my soapbox, love and prayers to you all,

     Wishing you nothing but the best,

     Peggy

110. Verity Howson said

     am April 16 2010 @ 2:01 am

     Hi

     I have has MS for 6 years now and in the past year I have started having more symptoms. I would be very grateful for any advice and help with getting back to my old self.

     Thank you
     Verity

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