Comments on: Another Bad Actor In MS

By: David Gladstone

David Gladstone — Thu, 15 Dec 2011 23:19:57 +0000

Interesting and disturbing information on iron being a “bad actor” in MS. How does one limit iron consumption, given it being widely used as a nutritionl supplement?

By: Susan Russo

Susan Russo — Mon, 28 Nov 2011 23:42:12 +0000

About two weeks ago, while in physical therapy, I noticed a pressure in my left shoulder, mid-back and left chest. I assumed I had overdone and pulled a muscle. Several doctors later and stress test, echo, Cat scan to rule out CAD revealed 2 blocked arteries. Are there any special precautions or steps to take prior to the angiogram? I am concerned about
possible overnight hospitalization and exposure to germs. Any suggestions?

By: Theresa Norton

Theresa Norton — Wed, 23 Nov 2011 17:15:42 +0000

I did leave a comment it is my daughter h who has MS She works 5 days a week does TiChi 2 times a week they have a house to look after and normal family duties. Thank you
Theresa Norton

By: Theresa Norton

Theresa Norton — Wed, 23 Nov 2011 17:13:44 +0000

My Daughter has MS for the past 3 years. I will mention the article of Iron to her.
She works with her Husband 5 days a week in their TWO STORES
She is doing Ti Chi Exercise two times a week looks after their house etc. Plays Bridge (Cards) two times a week and also belongs to a BOOK CLUB. She is very active and has no serious signs yet.
Thank You Theresa Norton

By: Sue Auld

Sue Auld — Wed, 23 Nov 2011 02:08:09 +0000

I have had MS for 15 yrs. The first 10 yrs it was like an invisible disease.
The course of my MS has changed to SPMS. I broke my right hip in 2009 and found out I have osteop. The doctor wants me to take calcium for my bones. They also want me to take Forteo a daily inj. to rebuild my bones.
Dr. Cartwright should I continue the calcium? Are you familar with Forteo? Right now I am on Reclast a yearly invusion for my Osteop.
I was on Fosamax which bothered my stomach. I have heard bad things about this drug. I have the involuntary jerking of my legs that seems worse. I do go to the pool 3 days a week.
Let me know if you have any suggestions for this symptom?
I appreciate your valuable knowlege and help!

Sue

By: Pat

Pat — Mon, 21 Nov 2011 01:42:37 +0000

Would like to see some information on Primary Progressive M.S.

By: Dave Laudin

Dave Laudin — Sun, 20 Nov 2011 05:26:26 +0000

Note I neglected to say that it was up to 500milligrams per time of injestion, that the body can absorb. So don’t think that taking any supplement amounting to greater that 500 mg. at any one time, will allow a greater absorption of the calcium at any one time. This in why it is suggested that it be taken as 500mg. in A.M. and P.M. for the 1000mg. that should be the minimul amount taken each day for M.S. Patients. Don’t let your levels drop, or you could require a greater amount, later. Good Luck.

By: Dave Laudin

Dave Laudin — Sun, 20 Nov 2011 05:20:31 +0000

Great to see a source of adding helpful and precise information for us M.S. patients. Well, as my M.D. felt that the 5000I.U of vitamin D/day was not as adquate nor showing the positive improvement in my lab values except with 7500 I.U. per day. I would consider conferring with your own M.D. before taking any of this advise, however. Please note that Calcium cannot be absorbed by your bloodstream without the presence of adequate quality Vitamin D3. Also, your body can only absorb 500 mg. at any one time, so I have to take mine both A.M. & P.M. If I needed more, I would alter. Note: recent research confirms that Vitamin D3 cannot be absorbed by the body without the presence of fat. The best recommended types are Unsaturated fats, especially Omega-3 fish Oil (Mercury free) and /or Flaxseed Oil. Taking Calcium, Vitamin D3 and Omega3 Fatty fish oil capsules is your goal. Prevent Osteo-demineralization complications. Good Luck. Regards, Dave

By: viv peck

viv peck — Sat, 19 Nov 2011 08:25:07 +0000

what are the newest treatmenhts for ms with intrAvenouds treatments

By: Eunice Nafziger

Eunice Nafziger — Sat, 19 Nov 2011 03:57:49 +0000

Now testing for CCSVI, says md, ask to be on waiting list in AB