Living In Ignorance How I Didn't Realize I Was Disabled

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Ketovore Kandi

Ketovore Kandi

Місяць тому

I was almost 47 years old when I discovered that I had Spinal Muscular Atrophy. I had suffered from weakness my entire life and didn't have any answers.
Link to my first video: • Unlocking My Optimal H...
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КОМЕНТАРІ: 38
@dixiemerchant1052
@dixiemerchant1052 Місяць тому
It’s very encouraging to hear something so mysterious finally got figured out. It’s like you found the needle in a haystack! It gives hope:-)
@ketovorekandi
@ketovorekandi Місяць тому
I am very grateful to find out! It really helps me to be able to move forward!
@rochellethundercloud346
@rochellethundercloud346 Місяць тому
It's horrible when you know something is very wrong,but nobody will listen to you.
@ketovorekandi
@ketovorekandi Місяць тому
Yes it sure is!
@JaneNorthrop
@JaneNorthrop Місяць тому
I am so sorry for your experience....I had tears in my eyes... recalling my daughter's childhood when I knew something was wrong with her and I kept being dismissed and told I was paranoid, over-protective etc because she was perfectly healthy. I finally got her primary pediatrician to listen to me and he referred her to a cardiologist and at 15 years old we found out she had been born with congenital heart defects and because they weren't diagnosed she has a heart/lung disease that has no cure. She is on oxygen and takes medication one is a IV medication through a central line. It is so sad that doctors do not listen and just brush you off... it still happens to this day with my daughter. You have to be so aggressive. Thank you for sharing your story.
@ketovorekandi
@ketovorekandi Місяць тому
I’m so sorry to hear about your daughter! It really does suck when we are just brushed off and people think it’s all in our heads.
@fwebster6226
@fwebster6226 21 годину тому
Wow! I can’t believe the attitude of your first neurologist! This is important information that needs to be passed on to your children whatever the outcomes were.
@ketovorekandi
@ketovorekandi 20 годин тому
I totally agree!
@heatherfling7820
@heatherfling7820 17 днів тому
I had similar experience
@heatherfling7820
@heatherfling7820 17 днів тому
I am so sorry. I empathize with you and I can tell you that I can understand and relate with you. I had been going through that too myself. This was so me. But, I was diagnosed with mild several palsy and and depth perception. I am so sorry you had to go through all of that.
@ketovorekandi
@ketovorekandi 17 днів тому
I’m sorry to hear of your experiences as well. How long did it take for you to get diagnosed?
@heatherfling7820
@heatherfling7820 16 днів тому
@@ketovorekandi I was diagnosed in my early adulthood. No one ever told me what I had but. I’ve always had to wear glasses and had weakness through out my body and had an hearing loss in both my ears and couldn’t ever run full speed or jump and jump off of things. When I would run I couldn’t run fast or my legs would give out on me and would be painful to get up.
@ketovorekandi
@ketovorekandi 16 днів тому
I can definitely relate to the running part!
@canbenchecocat9729
@canbenchecocat9729 Місяць тому
You come off as such a sweet person. You definitely have a wonderful attitude. I've subscribed, hoping to get good news about your condition in the future. Much love until then.
@ketovorekandi
@ketovorekandi Місяць тому
Thank you so much!
@melissadollxoxo
@melissadollxoxo Місяць тому
I love this! thank you for sharing
@ketovorekandi
@ketovorekandi Місяць тому
Thank you 🤜❤️
@user-sh6um1ns6k
@user-sh6um1ns6k 4 дні тому
God bless you hun x
@ketovorekandi
@ketovorekandi 4 дні тому
Ty, Maureen ❤️
@user-dm6nq4rr2d
@user-dm6nq4rr2d Місяць тому
I love you Kandi. 💝
@ketovorekandi
@ketovorekandi Місяць тому
I love you too! ❤️😘
@canadianhotbod1
@canadianhotbod1 Місяць тому
God bless ❤🫂✝
@ketovorekandi
@ketovorekandi Місяць тому
Thank you 💕
@babsk4071
@babsk4071 Місяць тому
❤GOOD ON YOU💐
@ketovorekandi
@ketovorekandi Місяць тому
Many many thanks
@liswoods9
@liswoods9 Місяць тому
Wow, what a story! I thought I was diagnosed late at 23. I’m type 3 and 56 now. Very similar stories. I also am keto/carnivore. Thanks for sharing ❤
@ketovorekandi
@ketovorekandi Місяць тому
I am so glad meet another SMA warrior that is doing ketovore! How long have you been at it?
@liswoods9
@liswoods9 Місяць тому
@@ketovorekandi started keto 6 years ago but been mostly carnivore for the last year. I’ll never go back to the SAD way of eating. I wish I had known about it earlier.
@ketovorekandi
@ketovorekandi Місяць тому
@@liswoods9 I totally understand. I wish I had LISTENED to it earlier as well.
@xxxyyy1880
@xxxyyy1880 Місяць тому
Doesnt carnivore diet cause having less energy because lack of carbohydrates? In normal healthy person this is easily measured and common effect that is well know. For someone with musclular disease the effect might be even bigger since body has less strenght. Of course carnivore is good if youre trying to lose weight but being constantly in it might not be that great...
@liswoods9
@liswoods9 Місяць тому
@@xxxyyy1880 the carnivore diet gives me more energy! Because I don’t eat carbs, I don’t use glucose for energy, I produce and use ketones for energy. It’s a beautiful thing. I never knew there was another energy source available. I also make sure I keep up on electrolytes. You can’t just do carnivore without understanding the science behind it. I may also add, it may not be for everyone, but I know it is for me.
@rochellethundercloud346
@rochellethundercloud346 Місяць тому
I had gallbladder disease,and changed my eating habits, because of debilitating pain when I ate. Finally had it removed and still kept the same eating habits because I know from trial and error,some food is fine,but some makes me really sick.
@ketovorekandi
@ketovorekandi Місяць тому
Does eating a lot of fat make you sick?
@myaccount9498
@myaccount9498 17 днів тому
What kinds of food make u sick?
@YeshuaKingMessiah
@YeshuaKingMessiah Місяць тому
I am so sry Our society is such a failure, esp with sick women. They are dismissed far more often than not and FAR more often than men. I am not asking u for this test. I’m telling u to get it for me! Ur MY dr. I’m not UR patient. U work for ME. That’s how I have to be.
@ketovorekandi
@ketovorekandi Місяць тому
You’re so right!
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