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Tell us what you are using to treat your MS-- and how you are doing.


Do prosthetics really work for those with Multiple Sclerosis.
Read more : Prosthetics | Views : 1213 | Replies : 3

Have not started yet.

I am currently taking 50,000 IU of D 2 x/week. B complex, and Fish oil 3, 6, 9.

My JCV test came back borderline positive. I am eligible for Tsyabri, and I am considering Plegerdy. Is there anything else I should consider. I will of course check with the Doc at my appointment in a couple of weeks. I also live with a nurse.
Read more : Have not started yet. | Views : 1927 | Replies : 10

Multiple Sclerosis desatascador

MS should be renamed Magnetite Supersufficiency. As children, we have had a bout of iron overload and not realised. The excess iron has been oxidised, chiefly as hematite and magnetite and stored because the bodies own chelation mechanism is insufficient. This you can read about on the net. What you can't read is lateral thinking in that the storage sites are in the head and feet at the ends of the arterial network. The reason ...
Read more : Multiple Sclerosis desatascador | Views : 1379 | Replies : 0

Aubagio - side effects

hi and help

after taking aubagio for only 5 weeks my hair has been falling out for the last 3 months and shows no signs of stopping.

I really dont know whats going on - ive refused any additional medication until this stops. Neither of my doctors both men even
mentioned this as a side effect and to be honest if they had i probably would not have opted for this. I am feeling a ...
Read more : Aubagio - side effects | Views : 1871 | Replies : 4

Starting treatment...before diagnosis?

Hey there everyone, thanks for reading. I'm a 28 year old female; I've been followed by a neurologist for almost 4 years now. I have NOT been officially diagnosed with MS, but I have had textbook symptoms and family history.
3 years ago I developed optic neuritis in one eye (likely postpartum, my first child was 8 weeks old) -- this is the ONLY diagnosable MS symptom I have had in almost 4 years (June ...
Read more : Starting treatment...before diagnosis? | Views : 1726 | Replies : 2


HI FRIENDS Please read

AXIM Moving Ahead with Testing of Cannabinoid Products, Including Chewing Gum for MS Patients ... 56e2954-71

On IVIG for 12 years, now Tecfidera or Copaxone?

I have been on IVIG for over 12 years now. MRIs and other health issues are causing that to change. I am JCV+, so no option for other infusion med.

Had a terrible reaction to Avonex when tried years ago.

Looks like my choices are Tecfidera or Copaxone...

Tried Copaxone years ago, young and single and scared. Stopped pretty quickly due to emotions. Reading here reactions to Tecfidera can be pretty strong.

I am employed ...
Read more : On IVIG for 12 years, now Tecfidera or Copaxone? | Views : 1664 | Replies : 4

Modafinil, Ritalin

I use occasionally modafinil to make something against my fatigue and weakness. I also feel some effect in terms of concentration while walking. Now I have heard that the effect can be increased if you grind a tablet and snuff in the nose.
- Who has done this already?

Read more : Modafinil, Ritalin | Views : 1824 | Replies : 1

Try plant based diet: new study

I am reading that a study from the University of Oregon Mendical School says plant based diet benefits MS. Is anyone vegan or vegetarian here? If yes, how is it working for you?

Here is the reference.
Read more : Try plant based diet: new study | Views : 4406 | Replies : 24

MS and Spinal fusions?

Hi everyone, this is my very first post. I'm not new to auto immune diseases. I've had rheumatoid arthritis for 36 years. I've had most of my joints replaced and in the last five years I've had C1-T2 fused completely with 14 inch rods on each side of my spine from the base of my skull into my ribs. This past March I had lower lumbar fusion with 6 inch rods on the sides of ...
Read more : MS and Spinal fusions? | Views : 2326 | Replies : 10


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