Need advice/encouragement!!

[Guest guest]

Jen, you could add Copaxone as an adjunct to LDN. They are considered compatible treatments. From: jen <tritherz@...>low dose naltrexone Sent: Wed, February 17, 2010 8:17:07 AMSubject: [low dose naltrexone] Need advice/encouragement!!

Hi All,

I've been using LDN (4.5mg) since receiving my diagnosis of RRMS last June. After a brief stint with the Inclined Bed Therapy last December, both feet went numb. At first, I thought it may be yeast related, so I changed my diet dramatically. Now 4 days ago, some new symptoms surfaced, causing me to reevaluate my course of treatment. Both feet now have a pulsing like (constant) sensation that my Neuro says is Transverse Myelitis and is a sign of disease activity. He advised me that it indicates the LDN isn't working for me (he really didn't have much faith in it from the get-go), and that I need to consider an alternative (CRAB). Argh!! Now what? I have felt sooo much better since starting LDN, and really have NO desire to start injecting myself with that stuff. I've been following the CCSVI research and am already signed up for the next phase of the trial. But what do I do in the meantime? If there's disease activity, does it make sense to start the

injections? I'm at such a loss and was so hopeful LDN would be my answer....

Jen

[Guest guest]

go to the forum of brenda.she will help you.

http://ldn.proboards.com/index.cgi?