I just talked to my LLMD about this today. He recommends the Jiroffa brand at no more than 3,000-4000mg/day.
He says "Jiroffa nutritional products carry a guarantee of satisfaction. The best ingredients known on planet earth are what go into Jiroffa supplements."
I fully trust him!
I just placed my order today, so I haven't started taking it yet, but will, just as soon as I get it.
It's $14 for 60 pills. That's all the information I have right now.
If you google the brand, you should be able to purchase some. If you want to, that is.
-------------------- My Lyme dx:11/05. My Mom's Lyme dx:5/16. ISO ASAP-Lyme Literate Dr & Neurologist-Prefer IL, IN, KY, MO, OH, TN. Can travel farther. Finances limited. Prefer Drs take Medicare or Payments. Need great list to find best fit. Tyvm. Posts: 701 | From Owensboro, KY | Registered: Sep 2005
| IP: Logged |
heiwalove
Frequent Contributor (1K+ posts)
Member # 6467
2 members with active lyme 1 member in remission for the last 5 years (symptoms and abx's free) 1 member in denial of having lyme but taking all the supplements including MAg Tab !
I was wondering even thoug we, lymies, need more Magnesium than healthy people, if there is any side effects or damage that can potentially be caused in the future by long term extra Magnesium intake...... I think marnie might have the explanation.....!
Posts: 983 | From The sky | Registered: Feb 2005
| IP: Logged |
posted
I am really struggling to work magnesium supps into both my daughter's daily regimen and my own. We both take abx morning and dinnertime and probiotics at bedtime. My LLMD says just take abx first thing in the morning, wait an hour and take supplements, but that's easier said than done when you're heading out to school and work. We both take Neurontin, which I know cannot be taken with magnesium.
My biggest question is what magnesium can and cannot be taken with. For example, can I take it at bedtime along with my theralac probiotics? Can it be taken along with DHA and alpha lipoic acid? Milk thistle?
I'd love to hear what others do or know about this?
Posts: 164 | From USA | Registered: Jul 2005
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/
UBBFriend: Email this page to someone!
![[Smile]](smile.gif)
Printer-friendly view of this topic