Hello young lady, you are truly an inspiration to me. I was just recently diagnosed with MS . I found Dr Wahls and have never looked back. Its only been about about 2 months on the diet and im loving the results already. Good on you young lady ! Im very proud of you. Canada loves you ❤ 🇨🇦
Great story!! You have inspired me! I was just diagnosed with PPMS. I just purchased the Wahls protocol book! A must buy for anyone with a autoimmune deficiency! I pray that God continue to heal you!
I am also diagnosed with an autoimmune illness name CIDP. It started when I was 20 and now I’m 25. It was just mild in the beginning but it started to grow slowly in my body. Those weaknesses in my legs and then hands. There’s no one in my family whose diagnosed with autoimmune disease so the reason is unknown. And it’s really hard cause nobody knows how it feels. The mental health is hard to deal with. Sometimes it’s hard you know, your mind starts thinking lots of things about yourself and where you’ll be in the future. Sometimes I want to cry out so loud but I stay silence. I’ve visited so many hospitals but the diagnosis was unknown until 2 years ago my illness was similar to CIDP. I’m on medication and physiotherapy. It’s still hard for me to walk alone or get up from the floor without help of 2 people or climb the stairs. And the grip in my hands are weak. Yet I’m still not loosing any hope. I’m staying strong and one day I’ll beat this illness. Having this illness I came to know how valuable is life and how important is your health. When I’ll beat this disease I’ll be the happiest person to be alive.
You turely such an inspiration to me and all ms warriors, there’s always hope no matter what and the important thing we just have to believe in ourselves and how our bodies can heal If we give it the right nutrients that it needs.. you’re a queen and your words are powerful, keep it up 👍🏻 we all in this together!
Thanks for your reply. I have successfully managed my ms for two years .. I eat greens, fats from nuts and seeds , turmeric, garlic, ginger, broccoli and super healthy food . I still have lesions on my brain but I am symptom free 😊.
Thank you for your story. I can’t wait to get started and hope that I can report back to you how I’ve been healed. Keep doing what you’re doing you’re an inspiration
OMG! I didn't expect you to be so young! You Brave girl! I am honored to fight this #MonSter side by side with you! Awesome video! I subbed! See you down the road kid! Keep fighting. #aMSm #anotherMSmonday
Thank you for sharing your story. I've been watching a lot of Dr. Wahls videos recently as I have an Uveitis (severe eye inflammation) and they are running some tests to see if an AI issue caused it. I think this way of eating is good for everyone in general.
I know this is an older video but I had a few questions. Aside from the Wahls Protocol, are you on any disease modifying therapies (dmt). You also mentioned that you take vitamins and supplements, can you name the primary ones that you take. I’m very keen and heard the benefits on Vitamin D, can you name others. Thank you for the advice and stay strong.
Thank you for your story! Are you on meds currently? Also, have you seen any improvements or changes in your spinal/brain MRI's? (Lesions, demylination)
I am 1 mon into the Wahls protocol. For those who are following this lifestyle/diet how long before you noticed a difference in how you felt? I have been dealing with numbness and tingling down both arms and left leg. Also burning/cooling sensation across my shoulders. Fatigue, aches and skin sensitivity (even the lightest touch on my skin is painful).
I have a similar early story to yours. When I was diagnosed in my early 20s I refused treatment and changed my lifestyle (quit smoking, non more alcohol, diet and exercise). I have been relapse free and feeling great for 8 years, until MS struck again... Unfortunately MS is not caused by what we eat (wouldn't that be wonderful?), but our lifestyle can definitely influence our level of inflammation which is what makes us feel bad and what makes this disease worse. I know the story and work of doc Whals and is right to point out that when she was diagnosed the treatment options were very few and undoubtedly not very effective. Doctor Whals said in an interview a couple of years ago that she is now not against disease modifying therapies anymore. I don't want to convince you to start a therapy, I know it won't work because I was exactly like you. Definitely medicines alone don't work, if one keeps smoking or eating very badly, but in the same way only lifestyle changes won't work either, at least not in the long run. I don't think your story is outrageous, I think it's human nature to avoid a life of medication with side effects. Hoping you'll keep staying strong and healthy!
Another Note: Your story gave me pause. .. Now that I think about it., I realized something. I'm thinking to myself: .. She's mentioning the way the problem comes back and hits you like a ton of bricks, the moment One experiences a stressful low point in life. Hmm..., that reminds me of the way I almost always end up getting sick with a cold, flu, or that same cold sore I got back in 2004 from some girl I once dated. It comes back every spring, and right on schedule. For this reason, this tells me.., is telling me, that this disease is very much and somehow connected to the Family of Viruses That Typically Cause Epstein Barr, Herpes Simplex Viruses, and the like. Wahl's Protocol seems to have some degree of efficacy, as it works to make the body stronger, so as to keep those very viruses from going from [Dormant] to [Active]. Hmmm.... Thanks for posting. My Best, MDM JD Candidate. \\//
Hey!! I was also just 15 Years old when multiple sclerosis diagnosed and everyone was making me feel scared by telling it's so dangerous disease. After every 3 months i was getting one eye blind. Some people says me to not go school stay home you can't study and everyone was making me feel that I'm not of any work but i never feel like a loser. I fight with multiple sclerosis with help of doctors. Now I'm 18 years old and feeling like a normal person how i was before 4 years. My story is same as yours..
Hello young lady, you are truly an inspiration to me. I was just recently diagnosed with MS . I found Dr Wahls and have never looked back. Its only been about about 2 months on the diet and im loving the results already. Good on you young lady ! Im very proud of you. Canada loves you ❤ 🇨🇦
God bless you ❤️
I was diagnosed and happened on wahl's and have regained my life. Thank you for your story🙏
Praise God!!!
Great story!! You have inspired me! I was just diagnosed with PPMS. I just purchased the Wahls protocol book! A must buy for anyone with a autoimmune deficiency! I pray that God continue to heal you!
I was able to cure my Hashimoto's the same way. It' s great that you're spreading the word :)
I am also diagnosed with an autoimmune illness name CIDP. It started when I was 20 and now I’m 25. It was just mild in the beginning but it started to grow slowly in my body. Those weaknesses in my legs and then hands. There’s no one in my family whose diagnosed with autoimmune disease so the reason is unknown. And it’s really hard cause nobody knows how it feels. The mental health is hard to deal with. Sometimes it’s hard you know, your mind starts thinking lots of things about yourself and where you’ll be in the future. Sometimes I want to cry out so loud but I stay silence. I’ve visited so many hospitals but the diagnosis was unknown until 2 years ago my illness was similar to CIDP. I’m on medication and physiotherapy. It’s still hard for me to walk alone or get up from the floor without help of 2 people or climb the stairs. And the grip in my hands are weak. Yet I’m still not loosing any hope. I’m staying strong and one day I’ll beat this illness. Having this illness I came to know how valuable is life and how important is your health. When I’ll beat this disease I’ll be the happiest person to be alive.
Amazing testimony! I also believe that the Wahls Protocol is the blueprint to optimal health.
Crystal Robinson thank you 🙏 & I truly think so too!
This is an outstanding video and testimony!
Wishing you continued success and remission on your health journey.
Thank you for sharing.
A very brave, courageous and optimistic girl.....
Bow to ur sunshine!!!!
You will definitely succeed coz u r a real hero.
Greetings from India 🇮🇳 😀 ❤
Best wishes. Proud of you and your willingness to express everything on here for others.
You turely such an inspiration to me and all ms warriors, there’s always hope no matter what and the important thing we just have to believe in ourselves and how our bodies can heal If we give it the right nutrients that it needs.. you’re a queen and your words are powerful, keep it up 👍🏻 we all in this together!
Thank you for telling this , recently diagnosed with MS. It's a tough life for us but won't give up.
Its life long not fatal. Exercise is the key
Thanks for your reply. I have successfully managed my ms for two years .. I eat greens, fats from nuts and seeds , turmeric, garlic, ginger, broccoli and super healthy food . I still have lesions on my brain but I am symptom free 😊.
Thank you for your story. I can’t wait to get started and hope that I can report back to you how I’ve been healed. Keep doing what you’re doing you’re an inspiration
OMG! I didn't expect you to be so young! You Brave girl! I am honored to fight this #MonSter side by side with you! Awesome video! I subbed! See you down the road kid! Keep fighting. #aMSm #anotherMSmonday
Truly a Success Story!
Gen Z Money Mind thank you 🙏
A queen, you are such an inspiraton!
That's so sweet! Thank you!
Melody you are so strong! I am so proud of you for sharing your story 💛 what an inspiration
Gee Graciano thank you GiGi! ❤️ That truly means a lot!! 🥺
Thank you for sharing your story
Thank you for sharing your story. I've been watching a lot of Dr. Wahls videos recently as I have an Uveitis (severe eye inflammation) and they are running some tests to see if an AI issue caused it. I think this way of eating is good for everyone in general.
Thank you
I know this is an older video but I had a few questions. Aside from the Wahls Protocol, are you on any disease modifying therapies (dmt). You also mentioned that you take vitamins and supplements, can you name the primary ones that you take. I’m very keen and heard the benefits on Vitamin D, can you name others. Thank you for the advice and stay strong.
I have a autoimmune condition pls do a video on how do you manage stress and anxiety.
Thank you for your story! Are you on meds currently? Also, have you seen any improvements or changes in your spinal/brain MRI's? (Lesions, demylination)
Can you share how you eat liver/recipes? I know I need to add it to my diet, I’m just struggling with it.
I am 1 mon into the Wahls protocol. For those who are following this lifestyle/diet how long before you noticed a difference in how you felt? I have been dealing with numbness and tingling down both arms and left leg. Also burning/cooling sensation across my shoulders. Fatigue, aches and skin sensitivity (even the lightest touch on my skin is painful).
👍♥️🙂
U r gorgeous❤️
I have a similar early story to yours. When I was diagnosed in my early 20s I refused treatment and changed my lifestyle (quit smoking, non more alcohol, diet and exercise). I have been relapse free and feeling great for 8 years, until MS struck again... Unfortunately MS is not caused by what we eat (wouldn't that be wonderful?), but our lifestyle can definitely influence our level of inflammation which is what makes us feel bad and what makes this disease worse. I know the story and work of doc Whals and is right to point out that when she was diagnosed the treatment options were very few and undoubtedly not very effective. Doctor Whals said in an interview a couple of years ago that she is now not against disease modifying therapies anymore.
I don't want to convince you to start a therapy, I know it won't work because I was exactly like you. Definitely medicines alone don't work, if one keeps smoking or eating very badly, but in the same way only lifestyle changes won't work either, at least not in the long run.
I don't think your story is outrageous, I think it's human nature to avoid a life of medication with side effects. Hoping you'll keep staying strong and healthy!
what's ur age now
Another Note: Your story gave me pause. .. Now that I think about it., I realized something. I'm thinking to myself: .. She's mentioning the way the problem comes back and hits you like a ton of bricks, the moment One experiences a stressful low point in life. Hmm..., that reminds me of the way I almost always end up getting sick with a cold, flu, or that same cold sore I got back in 2004 from some girl I once dated. It comes back every spring, and right on schedule. For this reason, this tells me.., is telling me, that this disease is very much and somehow connected to the Family of Viruses That Typically Cause Epstein Barr, Herpes Simplex Viruses, and the like. Wahl's Protocol seems to have some degree of efficacy, as it works to make the body stronger, so as to keep those very viruses from going from [Dormant] to [Active]. Hmmm.... Thanks for posting. My Best, MDM JD Candidate. \\//
Hey!!
I was also just 15 Years old when multiple sclerosis diagnosed and everyone was making me feel scared by telling it's so dangerous disease. After every 3 months i was getting one eye blind. Some people says me to not go school stay home you can't study and everyone was making me feel that I'm not of any work but i never feel like a loser. I fight with multiple sclerosis with help of doctors. Now I'm 18 years old and feeling like a normal person how i was before 4 years. My story is same as yours..
where are you from bro?? india?
Rohtak, Haryana, India
WHAT TREATMENT ARE YOU TAKING NOW?
SCLETERI 14MG
GINKOCER PLUS
Tablets
@@sahilphougat Did you take any steroids ?? this past three years?