Sorry About That
Answering a couple other questions not in the video:
As for ongoing support after you have received the MS Health Coaching Home Study Course, in addition to the VIP webinar for the new class members, we will be posting follow up information on important topics here on the blog.
We will also be holding bonus webinars to go over other hot topics.
As for going through the material, you will receive all of the CDs, etc. at one time. You can go through them at your leisure. It is probably best to go through one CD per week so that you can really absorb the material, read through it, and make the necessary changes in your life.
If you sit down and watch and read everything in a day, you WILL be overwhelmed and not know where to start.
It is best to take it slowly…one step at a time…and not try to consume too much information too quickly.
The good thing is that you can always go back and listen to and read all the info again whenever and as many times as you like…just to make sure you are doing all the right things.
Instructions on what to do to on Thursday will be sent out tomorrow (Wednesday).
Hope this helps!
Diana said
am February 2 2010 @ 7:05 am
Hi Scott
Thank you for the clarifiction. I have a couple concerns not addressed in your presentation. In addition to the cost of the program, there will be the fees associated with the cost of supplements. I have priced them and found they can vary significantly but the cost is easily reaching $200/month in my area. Then the cost of the groceries. This is not the season to be purchasing fresh fruit and vegetables as the winter cost in the northern climates is 3-4 times the price when they are in season.
I understand that it can take up to 2 years to see full effects of relief from the symptoms. If I took the 6 week course, do I get personal supporft during that time. What do I do for the reamaining 98 weeks. I believe it personal dedication and commintment to be able to stick to the program and that is why so many of us fail. What support is being offered for the balance of the time during recovery. This is vital or old habits will come back. I can’t tell you how many healthy things I bought in way of food, exercise equipment or memberships to exercise programs but if you do not fulfil that obligation, it is money out the window. I need on going support.
You offer is 6 audio presentations which is duplicted to 6 video presentations and then duplicated again to 6 printed transcripts. Would it not of been a cheaper alternative just to offer one source of the information and not 3. Are these designed to be listened to all at once or one a week for 6 weeks. If all at once, that is a lot of information to grasp and then implement.
I am still struggling with the funding but at least now I now the base cost and can go from there.
katie said
am February 2 2010 @ 8:11 am
How will we be contacted to purchase this kit
Stacy said
am February 2 2010 @ 9:03 am
Thank you so much for clearing up all the questions we have had about your Home Study course. I have been following all of your webinars and blogs and have implemented your suggestions from the supplements to going Gluten Free (it was difficult at first, but once I began to see improvement, it’s totally worth it). I know that with your full program I will get my life back. Thank you again for all you are doing. My husband and daughters thank you too!
June Stephenson said
am February 2 2010 @ 10:46 am
This sounds terrific. However, I do not have the finances to be able to take advantage of the course, unfortunately. I have lost my income and home due to the MS, so money is extremely tight, so I am trying to do whatever I can. So from what I can glean I am trying to change my eating habits. I can’t afford to purchase all the supplements, but do take fish oils and the like. So I know I wont get anywhere near the benefits, but I am hoping it is something I can at least do to help myself.
The course seems very reasonable and if I can ever afford it, I am sure it would be a great advantage, however, I am sure there are thousands like me who are unintentionally condemned to scrape together ideas to make life at least bearable.
The people I meet when I receive MS treatment, all have varying degrees of difficulty – not particularly associated with the MS, but as a result of it. We are together for about three hours during the treatment, and I often discuss your plan and any ideas that are put forward, also the MS Nurses themselves are interested, so the idea to be able to spread the message and help more people improve their lives and have the chance to hope once more, is what keeps me going.
I just hope that what I achieve in my little way from the scraps of information I have collated, and what extras I can afford to buy, that I can show others that there is some improvement and inspire them to take it further.
Sue Ellen and your blog have at least given me hope, when I felt that I had little to look forward to. Thank you.
Mark Hoeksema said
am February 2 2010 @ 11:01 am
I still do not know the cost of the Home Study Course. Can anybody help me with this information Please.
Liezl Lötter said
am February 2 2010 @ 11:16 am
Thank you very much for clearing this up. Just one more question: Will you still be helping the people that could not buy the Course due to the fact that there is only 50 available? I truely hope so, cause this is the best and most helpfull info I received since being diagnosed.
deb said
am February 2 2010 @ 11:33 am
when is dr. cartwright going to answer the question on where to obtain Catalase. He said he would check with his supplier and no-one has received a response.
Lynda Phippen said
am February 2 2010 @ 11:46 am
Can I get a paperless version of the essentials?! Of course I would pay a reduced price!
Thanks,
Lynda
Denise Morrison said
am February 2 2010 @ 11:54 am
It would have been nice if the free gift were available in candada, I can not afford the course myself, though I am interested in it, I also already share information on MS that I have learned with others that I know that have MS.
Denise
Denise Morrison said
am February 2 2010 @ 11:55 am
oops – missspelled Canada
Debbie said
am February 2 2010 @ 12:18 pm
i dont get this free gift thing that was to be told on here…has anyone heard of trager therapy for ms ?…it is suppose to give help with the pain from the muscles being so tight ..iam going to give it a try ..it works with the mind as well as the body ..it involves light touches and movements different than a regular massage which is to much for me as the nerves take over in my legs and do whatever …i thought i would tell people about it cause if it can help someone along with Dr.Cartwrights suggestions then that is very good.. i hope this just might assist someone with ms along with the home study course…i wonder how much it is going to be for the study course and iam also wondering about the support offered through this as well…it is amazing how alone you can feel from having this ms even when there are people around you…
Evelyn said
am February 2 2010 @ 12:20 pm
I agree that perhaps you should let us choose which media we want, Cd, DVD or paper. I prefer reading. Others might prefer another media. Then we would not have to pay for everything. thanks for ALL you are doing. I am so excited and encouraged by your life. I loved your book, it totally inspired me. Thanks for the good dr too for his work on MS and giving us free help on the webinars. how kind.
Debbie said
am February 2 2010 @ 12:25 pm
i understand the free gift now…sorry i acted before i listened …sorry
Mark Hoeksema said
am February 2 2010 @ 12:45 pm
I am hoping the Home Study Course Will do what Scott said it would. I thank Scott and Sue Ellen for everything that they filled me in with. I know that it is still up to me to kick this M.S.in the tail.
Debbie said
am February 2 2010 @ 12:53 pm
i hope this is the right area for me to write this regarding the 2 free give away contest for the home study course.
my current condition is not good ..i have had ms for 10yrs now and i was a hairdresser for 11 yrs but had to stop as i just wasnt able to keep up with the salons damand and i wasnt able to be dependable …i havent worked in 7 yrs now and it would be so great to get back to work but this time i dont want to go back to hairdrssing..the ms has gotten extremely bad in the last 2yrs it is progressing very fast and iam so close to being in a wheelchair now!..iam very scared of this !..i spend my days alone in bed or the tv as well as evenings unless my kids need me to take them somewhere for there activities…i still do drive but most days i honestly shouldnt but there is no one else to do it..my kids are 11 10 13 ..i dont have them full time cause of my ablility to care for them from the ms and this breaks my heart !!..i want my life back so badly..i am on disability only for income…i dont have family to help and friends have there own things going on ..if i was able to get this course i would use it faithfully and do it for myself and my children..it is so hard knowing what a better mother you could be if it werent for this ms …i can see it in my daughters eyes how badly this affects her and it tears me up inside …i love helping others and i defenatly would spread the word of all that helps in fighting back ones health from ms..one of my dreams is to go to the ms society here in my town and talk to who ever will listen and assist those who want it in regaining there life and health..if something works for me then iam a great sales person persay in spreading the helpful information …no one should ever have to live with ms in my opinion!!..i just need a helping hand for me to be able to get me better then i can give my helping hand to others ..there is no doubt that i want this more than anything and i will help whoever i can who wants help …i would love to start something as well like a website to get the info out but sue ellen has already done that and iam not one to step on anyones toes..i would find a way like maybe start a ms group or something .. i do have 3 great reasons to get myself better and do what i know iam capable of doing for me and others …please give me this chance to have my life back so not only me can benefit … i thank you for taking the time in reading this and i will be happy with whatever you decide…take care all
Jill said
am February 2 2010 @ 1:11 pm
I listened to your “I’m sorry” video several times which I found to be very helpful and explanatory of the cost of the course. I also went on to the website mymsyoga.com and can’t thank you enough for providing this website as I have been searching for the last two weeks for an exercise program to help me stretch so I am able to maybe, possibly regain some of my mobility. I ordered the DVD and watched all the videos on the site and am very pleased with the content and the program.
I too am financially strapped as my husband hasn’t worked in about three months and I receive Social Security disability which just about allows us to survive. But I agree with many of the bloggers that discourse looks to be very beneficial and I am going to try and find a way to sign up for it.
This is also my blog entry to submit for the “free home course.” I was diagnosed with primary progressive MS in July 2006. I had been having balance issues, backache, benign vertigo, vision problems, etc. for about 11 months (after I had a severe kidney infection with kidney stones blocking my urethra in August 2005). I first had a brain MRI, which showed a lesion on my Paratial cortex close to my motor controls (which affect in my right side) and then I had a spinal tap which actually confirmed the diagnosis. Looking at my symptoms, I was informed by neurologist I would probably be wheelchair-bound within the year. Well, I am not a quitter and as the saying goes “I have MS and MS does not have me.” I have fallen a lot over the last 3 1/2 years, have a motorized wheelchair which I use about every other day, I used a walker to get around in the house and two canes for assistance when I go outside. Due to the fact it is winter and we had about 7 feet of snow last week, I haven’t been outside in about 2 to 3 weeks.
In utilizing this home course study program provided by the Cartrights, it is my hopes up that I will be on the road to wellness, be able to walk again, and crusade in getting the message out there that although MS is a debilitating disease, faith in wellness can prevail. I live in a county in Northern California (Siskiyou County) which has no MS support groups and one would have to travel an hour south or an hour and a half north to attend any support group meetings. Whether I regain all my mobility or not, it is my intention to start a MS support group in Siskiyou County by the end of the summer as I have run into 3 to 4 people who live nearby who have MS and really no support, like me. I am determined to beat MS and show/tell others how they can too.
I am extremely excited that I came across Sue Ellen’s website over the past month as I am ready to embark on a better life-with or without MS.
Mary W said
am February 2 2010 @ 1:16 pm
To the Cartwrights: You are sounding very grandiose in your last apology, and your cost for the home study course is still extremely expensive for those of us on SS disibility!
Rachel Savala said
am February 2 2010 @ 1:30 pm
I AM EXHAUSTED. I NEED SOMETHING NOW.
Bridget W said
am February 2 2010 @ 1:39 pm
I have been on DMD for 15 years and none have helped. I just got divorced and my SS disibility does not kick in until April of 2010 so I have literally no money, what with rent, bills and all.
I will tell everyone I know and spread my knowledge about the course to people who may not even care. I WILL walk and ride for MS, which I have not been able to do before, all the while talking about this course. I have written to newspapers before re: MS issues and will again, this time about you! I am barely walking now but have stated with Sue Ellen’s detox programs and food changes and WILL see a difference soon I KNOW, that is how much I believe in you all. I will praise your names to all forever, and tell my Neuro where he can go!! He actually told me to eat a big bowl of ice cream every night. I will leave info in my neuro’s office about you and how they too can get their lives back. I will volunteer for any MS event in my area to spread the knowledge I’ve learned from you, you guys are the best.
Thank you.
Jeanenne Wright said
am February 2 2010 @ 2:05 pm
Hello,
I am a mother of 4. My first marriage I had 3 children and was a classroom mother for all 3 ,and did everything with them. In 1992 I was s diagnosed with Multiple Sclerosis and my husband then left for another woman leaving me and my 3 kids on the streets. With Gods help and a local organization I got a place to stay and food for my kids.
It’s been a long road but now I’m remarried and have an 8 [almost nine year old, he makes sure that I add that part.] This time around it is so very different being a mom and wife. I want to be able to walk around the block with my son and my husband, and be able to go in Walmart with them.
I have tried everything including bee venom therapy and everything I can find. My husband and I have researched natural remedies for Multiple Sclerosis . We have decided the medicines they prescribe help symptoms only and leave all the side effects with the drugs.
I would so love to take your course but do not have the money and I feel my life sipping away. Please, I beg you to consider me in this opportunity to take your course.
All 3 of my adult kids walk in the MS walk every year. I would do everything in my power to get the word out when your program works for me.
May God Bless you in advance,
Jeanenne Wright
Patty T. said
am February 2 2010 @ 2:49 pm
Hello, this is my registration for the free home study course. I have enjoyed listening to the webinars, could not get video. I am 58 years old and have had MS since the early l990’s. However, I know in my heart I had it long before that time. I have been wheelchair bound for several years, and I have an implanted Baclofen pump to help with spasticity. My husband is legally blind, and we also care for my 88 year old Mom who has suffered several mini-strokes. In addition, my daughter also has MS. If I were graced to be the recipient of the gift of this course I know in my heart it would benefit all aspects of my life. Not only for myself, personally, but for my family. I would be able to apply the knowledge to help my daughter’s fight her disease as well as being able to better care for my mom and help my husband. My being stronger and healthier would enable me to help make life better for others. I would share with other MS sufferers what I learned which would give them hope and confidence.
Thanks very much.
Samantha Kennedy said
am February 2 2010 @ 3:11 pm
Hello, my name is Samantha Kennedy, age 32. I am a mother of 3 boys and a wife to my wonderful husband of 15 years. I was diagnosed in 2004 after I was knocked down while working with some of our livestock on our farm. My right leg from the knee down started to go numb and I thought maybe I had pinched a nerve when I fell. I saw my chiropractor but with no luck. I then, after 2 months of no improvement, went to my doctor who ordered an MRI from the waist down. It came back clear so he consulted a neurologist who suggested an upper MRI of the spine and brain. It came back showing lesions in both areas and I was diagnosed with RRMS. This actually was a huge relief because I had started fearing that maybe I had a brain tumor. As long as it’s not terminal I felt that I could deal with it.
I very slowly progressed and in February of 2007 I lost my ability to walk and ordered a wheelchair. I’m a very positive, happy person but the day the chair arrived was devastating. I put on a happy face because I didn’t want my family to know how much it upset me. I’ve continued to slowly progress to where I still have no balance, my hands are numb and stiff, my legs are numb, I have lost sight off and on in my left eye which is rough because I’ve been blind in my right eye since I was a child and I deal with incontinence and constipation.
I have researched natural avenues to healing and am very interested in this because I know it works. With 3 growing boys it is sometimes difficult to stay on a good diet so I struggle with it. I am studying to be a Natural Health Consultant and would love to help other people with MS in their fight to better their lives. I love helping and love seeing people that see results by making nutritional changes. I know this course will be a tool to help me do that. I am hoping to be able to go work at my Neuros office and talk to other people with MS about natural healing.
I would love to have this course and be able to get back on my feet and let my youngest son, who was 2 when I went in the wheelchair, see his mom walk and be able to have me come on his field trips at school and play with him like I did his older brothers. I would love to be able to ride a horse again and dance with my husband again and play hide and seek with my children again. If not then I will still be happy and live my life to the absolute fullest I can.
Sincerely,
Samantha Kennedy
Kay Mifsud said
am February 2 2010 @ 3:36 pm
I went to order the free dvd on yoga for ms but it is for United States only.I am in Australia.
Thankyou for everything you are doing
Melinda Nace said
am February 2 2010 @ 3:40 pm
Dear Scott, Dr. Cartwright and Sue Ellen,
I am unable to afford the MS Coaching Materials. I do not have the income. As much as I would love to participate I can’t manufacture the money. Therefore, I am requesting that you consider me for one of the FREE materials.
I have had MS since I was 19 and was only diagnosed in 2005. I have three Undergraduate Degrees and a Masters Degree. I speak two languages fluently and need to brush up on the other two for three weeks before I am fluent again in them also. I am American but my last job was working for the Federal Government only speaking Spanish. As a child I was raised in Mexico City. Anyway, it took the Federal Government only 28 days to decide they didn’t need me anymore and put me on Permanent Disability.
I do not have any support from my family, neither financial nor moral support. I am grateful for my friends and God. I am divorced and have no other income.
I GAVE YOU GREAT MARKETING TIPS FOR YOUR PRODUCT, in my prior blog: NMSS (The National MS Society), MSAA (The MS Association of America), MSF (MS Foundation – they publish MS Focus). If you haven’t already contacted them may I humbly suggest you do so?
I thank you for letting me listen to your MS Webinar. I am trying to follow the diet info you gave me. I got a lot out of it and am looking forward to the MS Coaching.
When a product helps me I believe in telling everyone I run into about it. It has always been my nature to help others:
• I met someone with MS, Cathy Downie, and she taught us yoga. I believed in what she did so much that I was even in her video ‘Yoga for MS’. We did not ask for any royalties. I helped with marketing, spreading the word about the video, by calling doctors offices and talking to them about the video. When I went to coffee houses, doctor’s offices, gyms, and seminars: I tell everyone I meet how this yoga can help them.
• I went to the MS Walk and boasted at a table and gave out flyers as to how good this video was.
• I also help people who have MS. I e-mail and/or call them, from Alaska to New York, from Paris to Mexico. I teach them what I have learned about yoga from Cathy. There are millions of us with this horrible disease and if I can make a difference with even one of them I will. I believe everything happens for a reason and nothing happens accidentally, everything is gifted providentially.
• I could even translate your MS Coaching Materials and Webinar’s.
• I think you are limiting your scope of the market you should address. I believe this diet and way of life might also help head, spinal injury people as well as cancer patients. Help market to other’s that don’t have MS.
• I visit rest home and give communion to the sick. I sit and show them how to help themselves with the yoga Cathy taught me.
• I WOULD DO NO LESS FOR YOU!
Please consider me for one of the free materials for the coaching. I think I have proven myself previously as well as presently. I think I would be a great candidate to help spread the word about your products. I think it would be a win win situation.
Again, I do not have the money to purchase the program but would love to have it. Even if you don’t choose me, I wish you the best and thank you from the bottom of my heart for the good information that you have already given me in the Webinar.
God Bless you,
Melinda Nace
Janet Passman said
am February 2 2010 @ 3:45 pm
Lately I have lost my balance and have fallen several times.
Mike said
am February 2 2010 @ 4:01 pm
I was very interested in following up about the Yoga DVD on http://www.mymsyoga.com and ordering it. Unfortunately, I live in the UK and this DVD is only available to people in the USA.
Deb Christman said
am February 2 2010 @ 4:19 pm
Have you ever suggested any support web sites such as PLM (PatientsLikeMe)? I stumbled upon it while searching on alternative therapies for myself. It has been a real eye opener for me because it is open to anyone with MS, their caregivers, even their Dr., if they agree to it. My Naturopath really likes the tracking info that can be printed out for my visits with him. They are good for me too with keeping track of everything. The forum is great for asking questions, complaining when you need to just whine about it, and most of all, you’ll get lots of support. They even have mentors that you can ask questions privately if you are more comfortable with that. I have gotten help with recipe sites for bread that doesn’t crumble and has a decent taste. I was given a suggested site by another PLM’er and it is good. No gluten, no eggs, no sugar, no yeast, you may ask what’s left, a pretty good, easy to make, tasty, substitute for bread. I keep the sucessful ones in a binder so that I can share them, and I have with the local Nature Food store owner. My Dr. actually switched from his medical training to a Naturopath because the first and foremost therapy is to “do no harm”.
Christine Walters said
am February 2 2010 @ 4:20 pm
You might want to know that the free Yoga DVD is available only in the U.S.
AMELICA FODOR said
am February 2 2010 @ 4:25 pm
For all of you out there who you were abandoned in the time of suffering and when you needed help I want to tell you that GOD is not forgetting you even though maybe you think He did.There is a promise from GOD that if we are gonna sick HIM from all our heart HE will be there to help us.Do you believe this?I do.Some people think that this life is everythink and they don’t realize how short it is.Some of us are suffering because we did not sick HIM and some others because HE wants to test our faith and that is because HE loves us in both situtions.Sometimes GOD uses other people to help us from what I know and DR. CARTWRIGHT can be one of them . I do believe in what he recomend us to do and to take.I know that can take some time to restore our health and this depend of everybody condition too and we have to do our part too.I was part of the six weeks seminar and I try to follow what DR. CARTWRIGHT told us to do.I don’t have catalase and DHEA yet but some changes with my balance I can see.ALL of you out there are diferent so the results can be diferent,Some needs more time to recover than others that doesn’t mean that we don’t have to continuu.GOD bless you all and give you strengh to fight against this mysterious disease and don’t forget that GOD IS IN CONTROL.
Ursula said
am February 2 2010 @ 4:41 pm
Hi my name is Ursula from Ireland
I was diagnosed with MS in 1996 after vision problems and pins and neddles in my arms. Since then I have had several attacks including
stroke like symtoms – numbness down right side and dragging leg to walk,
most of other attacks were nevre pains – I was told my MS is sensory.
I am in alot of pain at times and its gets me down so times wondering where it all will end. I wish to register for home study course. I think all of comments are so reassuring for people with MS. Its good
to hear there is hope for us and not to give up. I am currently on alot of Medication Rebif 44mg 3 times a week, 4 x 25mg Amnitripyline at night and 100mg Zydol 3 times a day for pain. I have being taking this mediation now since 1998. I would love to have healthier alternative as my pain is not getting any better and I feel no relief from this pain most days. I would love to try your home study course and really do believe that this could be the answer.
Thank you so much for all of your information and I will follow your guide for as long as it take,
Many Many Thanks to you all.
Ursula -
Rick Best said
am February 2 2010 @ 4:52 pm
This is a small price to pay for what I can already tell is 100% honest intentioned program to help ms suferers…thank you!
Doris Dorado said
am February 2 2010 @ 5:40 pm
I was very happy to hear all the good news about the Home Study Course. Unfortunately it is still unaffordable for me. As I mentioned before I’m on Disability and my husband’s job is not doing very well. My income is practically keeping us going. I hope that maybe you can find a way to lower the cost or as another person mentioned just send us copies of the essential products that have to be used, I don’t something, but please try. I am very grateful for all that you are all doing.
Thanks a million,
Doris
Suzi Reed said
am February 2 2010 @ 7:26 pm
Has anyone else taken the colostem products? I have read of amazing results from MS patients after taking these.
I am about to commence taking this and will definitely report back on this blog.
Keep smiling everyone
Suzi
Wendy Hawthorne said
am February 2 2010 @ 7:36 pm
I have lived with MS for the last 26 years, but the last two or three years have brought an onslaught of numbness and tingling – a combination of MS or perhaps low-back injuries from two auto accidents. I tried the route of betaseron in the mid-1990s, but took myself off that “poison” and knew I could not suffer the lingering side effects. The only prescription drug I used now is Low-Dose Naltrexone.
I have used vitamins and supplements to combat MS since the mid-1980s, based on my own research and advice from two or three complimentary doctors and I also have “payed it forward” since then by discussing the role of vitamins and supplements with others that I have encountered with MS DXes. Two or three people stopped their prescription MS drugs in the past and tried some of the vitamins and supplements I suggested, such as fish oil, Vitamin D-3 and magnesium. I have had doctors tell me to “keep doing what I am doing,” but they also state they do not know what I am doing. I always tell them, but they do not want to “hear” because it is not drugs dispensed from the pharmacy.
My goal in taking this course is to eliminate the numbness and tingling that lingers and decrease the low back pain.
As being considered for one of the free copies, I will share the information with my friends with MS – five of them, and also with people I meet in the future. It is essential to help people steer clear of the poisonous drugs that most neurologists and conventional doctors promote, because of the damage those drugs do to the body and the lingering side effects. I will continue to pay it forward to show MSers how to live a healthy lifestyle without the unneeded prescription drugs.
Thanks
Wendy
Debbie said
am February 2 2010 @ 7:58 pm
i went to the website to order the free dvd exercise yoga and it is only in the states and i live in canada so that really sucks…i wonder if there is still a way i could get it..any suggestions?…thanks
Norma J Borchert said
am February 2 2010 @ 9:10 pm
I have a problem with DHEA being recommended, because I already have hair loss, and it has been found that DHEA and another hormone collect together accumlating in the scalp and starves the hair follicles from nutrients.
Ferial Tonekaboni said
am February 2 2010 @ 10:31 pm
diagnosed with ms 20 years ago am getting worse every day hope by getting home study course be able to find my path toward health. I am having unbalanced gait need to hold on to someone while walking also have very weak visioin, hopefully will find this path. As soon as I reach my goal, I will go to my Country and will go to ms society and give them all the knowlege and information that I have gained from you and will help them to get rid of this monster disease. In Iran so many young people are suffering from ms I will give them all the information that I am gaing from you. God bless you all
thank you so much for every thing
FERIAL
Jeanette Dixon said
am February 2 2010 @ 10:37 pm
The program sounds awesome. Is there any possibility that you can have a payment plan, so MSers like myself who is on ssi can afford it
Thanks
Jeanette.
Judy Brewster said
am February 2 2010 @ 10:55 pm
Too expensive for me. And the ‘free’ yoga course is unavaiable in Australia.
I dont know what to do anymore. Is this it ?
Arthur said
am February 2 2010 @ 11:40 pm
I really hope this works I’m buying it!
Arthur said
am February 2 2010 @ 11:56 pm
How do you buy it? Is there a link or something? I’m not the sharpest knife I’m the drawer, am imissimg somethng? Help please!
diana said
am February 3 2010 @ 5:14 am
I would like to be considered a candidate to “Pay it forward”. At the risk of being too lengthy, I feel I should give a bit of history. I divorced from my husband when my children were both under the age of 2. I thought I could dedicate my time to educating and bringing them up then worry about myself. This all took a turn when they were 12 and 13 and I awoke one morning unable to move or see. I was hospitalized and told I had MS and might not ever walk again. Two weeks later I was discharged and started immediately on the clinical trials for interferon. I did the injections for 3 years not knowing if I had the real drug or not. I did improve and was able to go back to work. My biggest fear was no job, no benefits. (I discontinued the use of Rebif last year after being on it for 15 years because of severe reactions when they changed the product to the new formula and am not currently taking anything) I was able to function well for another 10 years. Other than walking cautiously nobody saw the down side. I sheltered myself because I did not want anyone to see me. If they didn’t see it, maybe the MS didn’t exist. How wrong I was. I continued to try and do things on my own and after breaking my leg, ankle and finger in separate occasions as well as having 5 hernia operations in 8 years, I learned I needed help. Gradually I had to forfeit various projects and ask for help to cut the grass, clean the house, collect my mail, get groceries. Basic things people take for granted. Who would think a swifter is a lethal weapon but it can knock me on the floor in one swoop when I loose my balance. Bruised and battered in a heartbeat. Just getting up and going to work was an Olympic event. I had to give up my house because of the stairs and relocated to what I considered my final residence. I became a hermit and did not attend any social events because it was too taxing to go anywhere. All my energy was spent on work and trying to maintain the house on my own. My idea of finding someone went out the window when I was diagnosed. The thought of this scared anyone away. I was alone and lonely
Over the last year I have been on a downward slide and am not adjusting well to it. My daughter got married and after raising her for 29 years I was so proud of her. I could not walk her down the aisle. It humiliated me to be propped up from like a manikin waiting for her to arrive. She indicted that I was not smiling in any of the photos. I wasn’t. I was in pain and did not like what I had become. But then I only had myself to blame. With living alone I ate for comfort. What was wrong with eating chocolate bars for a meal? I had enough other anxieties, so why not enjoy it. I was a dashboard diner. Grab that burger on the way home and no dishes to do and no mess to clean up. It worked for me. But then I was failing miserably and started to research the internet for a miracle cure. This when I came across Dr. Cartwright’s program and realized I was putting myself over the edge. I went to health food stores and talked to them about supplements and they were interested in following my progress. I called the local MS society and although they could not endorse or promote the program, they were interested if I wanted to do a private presentation about my person experiences. Perhaps if they could witness someone progress through the phases they would be interested in purchasing the program and follow though with me. I could reach out and help not only MS patients, but those with other auto immune processes. I think this is my calling. I was trying to figure out what I could do with my time when I retire because I have made myself a shut in and needed to find a purpose. I know this is it. Not only will I be getting to become productive again, I can educate others.
Before I close, I want to share a recent experience I just had that also enlightened me to help others. It was pouring rain out and I was walking across a parking lot. Out of nowhere this young man approached me and positioned his umbrella over me. A total stranger in a different city. I was using my cane and thanked him but asked him to go on because he was being compromised and I was going to take the path of least resistance and if that meant trudging through puddles, I was going to and did not want to take him there. He ignored my request and continued on through the puddles in his fancy shoe and suit until we reached the building. I do not know if there was more waterworks coming from the sky or my eyes by the time we arrived. I was so dismayed that someone would do that for someone he did not know. His mother obviously brought him up right. Before I could turn around to thank him, he was gone. This made me realize that there is those out there that need help and there are ones who are willing to help. After having that courtesy extended to me, I want to reach out and help as many as I can to realize that the symptoms can be defeated.
United we stand
diana
Karyn Sullivan said
am February 3 2010 @ 6:12 am
How do you get this as I am extremely interested.
Jeanne K. said
am February 3 2010 @ 6:50 am
How do I blog. Is this blogging? I would like to tell my story and tell how I may be of help to others with MS but I have never blogged before and am wondering where do I go.
Jeanne ;}
Gail S said
am February 3 2010 @ 8:17 am
I am listening about the cost of the program. Unfortunately, the price inhibits me from participating. I guess getting healed from this monster is impossible for people on a limited income like me. HELP!
June Higgins said
am February 3 2010 @ 9:23 am
I was a registered nurse prior to being diagnosed, and was put on total disability. Once I recover I am going to volunteer at my local junior high and high school to teach children who are handicapped about math skills and also overcoming obstacles. I will also become the advocate in my area for MS. My neuroligist has asked me to do this because of my medical background, but as of now, my gait is unsteady and fatique, as well as speech are a problem. There are currently no support groups in my area, and he has asked me to remedy the situation. I feel that I could help others to recovery. A support group is so important for people who have had no relief with traditional medicine. Word of mouth goes a long way when people are looking for a cure. I believe that this program will be the cure and can help so many people. I can’t wait to talk about this program. I have so much hope.
Arthur said
am February 3 2010 @ 10:21 am
How do I buy this?
Jane Schmitz said
am February 3 2010 @ 10:41 am
Thank you Dr. Cartwright for your information. I’m 52 and pro’bly had MS since high school. Formally diagnosed in 1992, married and God willing raised four boys with my husband. I have experienced many of the MS symptoms through the years, taken the ABC shots, prescribed drugs, physical therapy and am now on a mission to find answers with natural means and supplements. I presently use a cane, have difficulty with balance, eye blurriness, stiffness, cognitive issues, etc, etc. I’ve had MRI’s done and purple dye added for lesion enhancement. BIG MISTAKE! Purple dye known as gadolinium is a poison and promotes MS problems. My walking/balance got worse. Cognitive issues manifested, eye blurriness and my hair continues to fall out. I’m going to try EDTA (chelation) treatments to gradually remove the gadolinium and other metals out of my body. ie. Aluminum, cadmi, lead and mercury.
I’m very interested in your course study and learning correct ways to eat and supplements to use on a daily basis. Thank you for your interest in multiple sclerosis. A collection of ideas and studies from your vast experience and work is much better than trying to do this alone. Pay it forward everyone! God bless!
Arthur said
am February 3 2010 @ 11:31 am
Is there a moderator of this blog? I’ve noticed that no one has answered any of the questions posed on here. like…….How do you buy the program. I’m desperate to change my situation.
Gilles said
am February 3 2010 @ 11:48 am
I have to ignore the cd from msyoga because I live in Canada. I don’t want to cry because I can do that by myself. The only think I can say is two years ago I got all one side paralyse the only answer i got from my doctor,”you have to make a choice from this medications and I will see you later how it work for you,I’m steel waiting. Here we have a web “Ms liberation.ca”it is interesting to follow but nothing like you. The way I can help is to talk about you and how I and you can help them Sue and Dr.Carwright’s program and if I have good result from you it will be a pleasure to write it and get back to work. Thank
Patricia Webb said
am February 3 2010 @ 12:01 pm
HELP FOR FINDING SUPPLEMENTS AT REASONABLE PRICES.
I have been buying at a local health food store but find that SWANSON HEALTH PRODUCTS carries all the same products and brands cheaper and shipping is often FREE. You can call them @ 1-800-824-4491 or find them on the web at this address:
http://www.swansonvitamins.com/
My customer number is 013250477, if you mention that I gave you this information, they will give me a coupon to help me afford my products, too. Just type in name of supplements; i.e.; Catalase
All the products that contain catalase will be brought up for your consideration. They also have really good special offers and sales!
Just my effort to help out my brothers and sisters (MS challenged and financially strapped) searching for better health. BETTER HEALTH IN 2010!
Clár - Ireland said
am February 3 2010 @ 1:00 pm
Looking forward to tomorrow – Thursday & release day … – Life is on the UP & UP. Thanks to all behind this mega movement.
Please, can we get access to the MS exercise DVD this side of the Atlantic – Europe that is – & for me Ireland.
… Clár … Irish lass
Linda said
am February 3 2010 @ 1:39 pm
Why only 50 for the MS Study course. What about the ones who miss out, dont they count? We’re all needing help.
Linda
Josie Pottinger said
am February 3 2010 @ 1:41 pm
The work in this area sounds excellent and as someone who has lived with MS for years I really hope that individuals are able to gain strength mentally and physically. It is really hard to come to terms with how I now feel. I used to be able to do so much,both in the workplace and at home and now it is so frustrating and difficult to recognise the person I have now become. I would love to feel more in control and less dependant and in a position where I can set up a talking clinic at my local hospital to be a pair of ears and also share my own path in how to deal with MS. I wish everyone well and hope that you are all able to derive benefits from this course.
Theresa Norton said
am February 3 2010 @ 1:58 pm
Feb 3 2010 In the early to middle stages .
Theresa Norton said
am February 3 2010 @ 2:00 pm
Hi would like to hear treatments re helping with M S Theresa .
MARIA said
am February 3 2010 @ 3:10 pm
MS HEALTH COACHING HOME STUDY COARSE PACK IT IS A GREAT IDEA ,IT IS BETTER FOR ME BEING ON A WHEELCHAIR I CAN LISTEN OR READ WHEN I FEEL BETTER , I AGREE WITH THE PRICE $397 , I HOPE I FIND SOME USEFUL INFORMATION FOR MY PRIMARY CHRONIC PROGRESSIVE MS. I WOULD LIKE TO LET PATRICIA WEBB KNOWS I WILL HELP HER WITH COUPONS BECAUSE I BUY SUPPLEMENTS FROM DR. SWANSON. ALSO I CAN PAY EXTRA 20-30dol’s
FOR PEOPLE WHO CAN NOT AFFORD IT AND MAYBE OTHER PEOPLE CAN DO THIS.
SCOTT ,I REALLY LIKE THE WAY YOU TALK TODAY ,VERY NICE OF YOU TRYING TO HELP
GOD BLESS YOU AND YOUR FATHER ! MARIA
FROM CALIFORNIA
sharon levering-mccoll said
am February 3 2010 @ 8:02 pm
I realy can not believe so many people are living life fighting for some kind of relief. I know when I get that one good day, I roll with it, even though I know I’ll pay for it later, I have to do it for my sanity. When you have triple the bad days compared to mildly good, It is a form of medicine and you antisapate your next dose. I just can not believe so many of us are left to deal wiyh MS with our eyes shut because we are complicated cases. I am only 40yrs old and would love to be able to walk my dogs!More inportantly walk to the bathroom in morning or at night without falling on my face or going before i get there. I am willing to try anything it just seems the harder I fight the more it fighta me back. My family even abandoned me, they are unwilling to except my diagnosis or think that i am looking for self pitty when all I pray for is peace not just for MS patients.,but for everyone still waiting for an answer. Just if you do not have it do NOT JUDGE THOSE OF US THAT DO> INSTEAD BE GRATEFUL AND HELP IF YOU CAN(CARRY BAGS< THANK YOU !!!! KEEP SMILING EVEN THOUGH THAT MIGHT HURT AT LEAST IT LET"S YOU KNOW YOUR STILL ALIVE AMEN!!!!!
Bridget W said
am February 3 2010 @ 9:24 pm
In addition to what I wrote yesterday, my family wants to put me in an assisted living community, and I just can’t do that, I’m only 44 and I want to live again, please consider me for one of the two free study courses, please!
marguerite said
am February 4 2010 @ 12:36 am
As I sit hear reading everyone’s posts my legs are in pain and my eyesight is blurry. I am 58 years old and was diagnosed in 1973. When I was 14 years old my mother died at age 38 from a severe case of ms so I knew the signs. When I felt tingling in my hands and arms I went to see a neurologist and after a very painful spinal tap experience I was told I had ms. Over the years I’ve taken the ABC drugs and steroids. When I lost my fulfilling job and health insurance four years ago I started LDN and suggested supplements. Nevertheless, I find myself confined to my house, spending most of my time in my recliner, battling spasms, nerve pain, incontinence, tremors, poor eyesight. I am currently on disability and live with my husband who suffers from heart disease. When he feels well enough he will push me around in my wheelchair. I am so excited to hear about Dr. Cartwright’s program. I feel it will be the solution to giving me my life back. At my age, there is so much more living I want to do. I cannot envision spending the rest of my life sitting in this recliner. I would like to go back to work, walk to the store and along the beach, travel, ride my bike, snow ski again. I would like to be able to take take of my husband the way he should be taken care of. If being blessed with given Dr. Cartwright’s program for free, I would spread the word to every outlet I can conceive of (doctor’s offices, ms groups, ms online groups, etc.). Thank you Dr. Cartwright and Scott for the opportunity to know of your incredible program.
Mark Hoeksema said
am February 4 2010 @ 6:58 am
It is sad that there is not a monthly charge similar to the Home Shopping Network (HSN)for the Home Study Progam. If this was set up I think so many people including myself could afford the Home Study Program. If I am fortunate to get one of the free programs this morning, I would be willing to share it with somebody else that needs the M.S. help.
Scott please consider the payment plan again. It can work. It would be a win-win solution for everyone.
Brunhilde Rundell said
am February 5 2010 @ 3:10 am
If anyone reads that far, check this out:
http://www.msrc.co.uk which is the UK website of the multiple sclerosis resource centre. you find diet advice, medication etc and a downloadable info pack on LDN. Does not cost you anything.
http://www.susiecornell.com is another website worth investigating. Susie has ms herself and written a manual for ms sufferers. worth while reading! it is £4.99 (!!!!) and downloadable.
I have tried it, I have ms, too, and these websites gave me a lot.