caret icon Back to all discussions

help me help her

My cousin has MS and graves. The bad news is she doesn't eat and when she does its some kind of sugar or garbage. she doesn't exercise. But, this is also optimistic because it means there's alot shes not doing for her self that she can.

ive done some reading about supplements and such. I could go on for hours doing this, but thought I would save some time and ask you guys for the ground floor.

I want to start getting her to eat, even if its small amounst, like i combine stuff like broccoli sprouts, kale, spinch, blueberries, flax, just whatever-into ice cube trays as servings. was going to go with this and also something like "athletic greens".

im getting mixed info about dairy and calcium and not sure what to make of it. calcium interacts with iodine preventing hormone production but then youll read somewhere else about the bone loss and need for calcium. I thought greek yogurt would be a good base for the supplements.

ive read about Vit.D, E,C, B12 omega-3 Yingliu mixture, coenzyme1Q10, selenium, L-carnitine.

medical marijhuana, seems like a daunting task with so many combinations and strains, how the hell can anyone ever get to knowing what works for what.

i am open to whatever anyone has to say, but I have to do this for her, no one else will and she sure wont. shes given up a long time ago. Enough crap medicare doctors who dont care will do this to you.

  1. Hi, !


    First off, I think it's awesome that you are wanting to help your cousin improve her health. I think your passion and determination show how much you care about her.


    That said (and I am sure you know this), you can't make her want to take a proactive approach to improving her health. You can do everything possible (make healthy, appealing meals, act as a personal trainer, etc) and she still may not be interested.


    Some of our members have had some levels of success with various diet protocols, but, like every treatment for MS, what works for one person may not work as well for another. Since you specifically brought up supplements, I thought you might appreciate this info -- https://multiplesclerosis.net/natural-remedies/vitamins-supplements and -- https://multiplesclerosis.net/mental-health/coping-complementary-alternative-therapies. There are supplements and minerals that can help!


    Also, you didn't mention fermented foods, but I thought you might find this article on health gut biome and mental health interesting -- https://multiplesclerosis.net/living-with-ms/fermented-foods-mental-health.


    I haven't heard much about calcium being an issue for folks with MS, but maybe that's more of an issue with Grave's? But, greek yogurt is almost always a good option in almost any healthy eating plan.


    I wish you the best of luck and I hope your cousin starts seeing improvements in her health.


    Best, Erin, MultipleSclerosis.net Team Member.

    1. Also Erin, I am a bit discouraged that you are the only one to answer me. Is there a reddit or facebook group , or discord, etc, you know to be particularly active and full of the intelligent go getter types I am looking for? I will read your links now, thank you for answering

  2. thank you for your time. I know you can lead a horse to water but cant make it drink. I am just hoping the horse was too tired and beat up to look for water. The state of "the best" medical care in the world applies to those with money. Its so disgusting and beyond belief the ineptitude. She has Graves because of their negligence. the most recent was a switch to a different thyroid med that gave her heartburn, to which they prescribed her heartburn medication. Until she reached out to a retired provider who was kind of enough to let her know that generic wouldn't due in this circumstance and she needed a particular drug. she got it, heartburn gone. this is what she has been up against her whole life and I do not blame her not for a second for her learned helplessness. many people just dont understand, they think "MD" and "god" are the same and getting through to people they are fallible and wrong is hard, even harder to get through you must take action yourself.

    1. , I agree that the state of healthcare in America (and many other places around the world) is . . . less than stellar, to say the least. Our Facebook page is pretty active -- https://www.facebook.com/MultipleSclerosisDotNet. I bet there are some pretty active communities out there, but you might have to try TikTok or Instagram to find really busy communities and I know both of those platforms have their drawbacks. Younger people are on TikTok and Instagram while older folks (like myself) are still on Facebook. There are specific support groups that cater to different communities via the National Multiple Sclerosis Society -- https://www.nationalmssociety.org/Resources-Support/Calendar-of-Programs-and-Events. I know these aren't necessarily what you're looking for, but it's a start.


      Best, Erin, MultipleSclerosis.net Team Member.

  3. First, you rock! In all the years I’ve been involved in ms stuff I’ve never heard someone ask such a detailed caring question. She may not care, may get angry or maybe, just maybe with baby steps, she will start to improve. I’ve had ms since 95’. I have great difficulty eating because I’m not hungry and only eat when I am. Weight 107-143lbs depending on the day. There are so many groups, websites, well meaning people, societies, blogs, podcasts, etc.. Overwhelming. Does she want to feel better? Does she have any interests? A lot of us get sucked into tv/games and isolate. So true about medical care, or lack of. Being on disability is a full time job. Has she tried marijuana yet? It’s worth the hassle. I wouldn’t sleep or deal with occasional anxiety without medical marijuana. It takes biggest chunk of SSDI money but literally couldn’t function without it. I’d be in a facility. That’s enough for now, too long already. Pretty please let us know how you are doing and thank you for caring. Hoping today is a good day! 🫧✌🏻🌎

    1. thank you for taking the time to share such a thoughtful message. Its wonderful to hear that this post came through with such care and authenticity. It sounds like you've been managing MS for a number of years now, almost 20!, and dealt with a lot in that timeframe. You clearly have developed a lot of resilience through it all, and have learned what works best for you to get through the day to day.
      Thanks again for being part of this community and the conversation.
      Best
      Alene, Moderator

      1. I wish there was a love reaction because I love that you are stoking that empathy fire! Such a beautiful thing to do! Thanks for being in this community with us and sharing the love! 🧡 Kayleigh, MultipleSclerosis.net team

      2. sharing this kind of support and encouragement is exactly what we need as a community. Thanks for being a great example. <3
        Best
        Alene, Moderator

    Please read our rules before posting.