About Me – Medication


Since everyone tends to ask what kind of medication I am currently on I though I would post a section going over it. Now this may need to be updated often as I am always changing things up but more than likely I will explain that all to you if you message me or post a comment because I am not sure how often I will be able to update.

Anyways as you can see I am building up my own personal pharmacy here (lol) and this is after I got rid of a bunch of medication… What you can’t see in the picture are all the needles I no longer take… As much as I hate it, medication is part of my life. Prescription pills, pain killers, supplements, and needles. I have more pills on hand than most senior citizens I would imagine. I don’t take that all at once but I do take a lot… Although compared to others with MS it’s probably not that much because I am trying to cut out everything I can but still, for a 22 year old? Too much.

So let us go over my current cocktail,
I am not going to list the amounts because that changes way to often:


Citalopram – 40mg/Day
Nuvgil – 150mg

Baclofen – 30mg-40mg a Day
Temazepam – 30mg (As Needed)
Oxybutynin – 5mg (As Needed)

Acthar (For Flares) [No More Steroids]

Vitamin A – 8,000 IU
Vitamin B12 – 1mg
Vitamin C – 1,000mg
Vitamin D3 – 5,000 IU
Vitamin  E – 400 IU
Fish Oil (Omega 3) – 2,400mg
Magnesium – 1,200 mg (400 3x a Day)
Zinc – 45mg (15mg 3x a Day)
Lecithin – 1,200mg (400mg 3x a Day)
Calcium -1,200mg (600mg 2xa Day)

10 thoughts on “About Me – Medication

  • June 13, 2012 at 2:53 pm

    I'm not seeing any cannibis there… 🙂

  • June 15, 2012 at 8:08 pm


    What meds have you taken historically? I've read you were on and off Tysabri and LDN. It seems you've tried many but only for a short period of time. I think it's important that we stick with one long enough to know if it's working or not.


  • June 15, 2012 at 8:44 pm

    I have never been on Tysabri, Just Copaxone and now Rebif. Tried LDN for like a week but had a bad reaction to it I rhink… No other longer term therapies yet… Just a laundry list of medication for symptoms haha….

  • June 27, 2012 at 10:48 pm

    Hi Matt,

    Have you looked into the diet protocol promoted by Dr. Terry Wahls at all? I have been implementing her suggestions since April, and I have not experienced any symptoms since.

    Her suggestions also led me to get a food allergy test done – apparently I am allergic to pretty much anything pre-made due to corn and soy being in almost everything processed.

  • June 30, 2012 at 6:17 pm

    I have and have tried several others with no luck, ugh! I wanted diet to help so bad…. I still practice good diet but I see no symptom changes… BOO!

  • October 8, 2012 at 2:22 pm

    Hi matt

    I read that the milk is not good for ppl with ms ! Is that true

  • October 9, 2012 at 5:18 pm

    That is what I hear, I avoid it, look into leaky gut, do some reading, decide for yourself, but it has to do with Milk proteins being similar to Myelin proteins.

  • November 4, 2012 at 11:13 pm

    Matt why do you no longer take sterioids? How does Acthar work? I took solumedrol for a flare and quickly learned I am very allergic to it.

  • November 6, 2012 at 12:29 am

    I am going on Tysabri and you can't take imuno suppressive drugs on top. ACTH is a natural hormone produced that tells the adrenal glands to produce more cortisol, or, natural steroids.


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