Re: having exacerbation need help/ME kind of TOO

[Guest guest]

Hi dear,

I'd like encourage you very much in your determination to heal.

Like you, I too am not able to simply avoid the doctors and all the " standard "

treatments, because when I'm worst and picture myself severely disabled in a

wheelchair, I always tell myself I have to do and try EVERYTHING to get better,

INCLUDING mainstream medicine, no matter how much I am aware of it's dangers and

potential harm of vaccines etc. I am determined to never ever get a single

vaccine and I'm careful about what I put in my body.

I'm now having my 5th (and hugest) relapse, which is lasting since 21st October

2010, with only few days of improvement every now and then.

I am on the BBD since september 2009, and on Avonex precisely since then as

well. Now tell me which of these actually work (ed) :-))) Well, I am a huge

believer of the diet thing... And also avoiding chemicals plus drinking pure

water helps a lot. In the past three months, I have had three sessions of

IV/oral steroids with no steady improvement.

I always eventually get better, but when I try to go back to the normal life,

i.e. work or attending a whole-day seminar, I always get worse, presently my

whole left arm is significantly disabled, my balance is affected and I am

generally very weak. Trying to stay spiritually and mentally strong though.

I have developed a new way how to look at it all. Perhaps it's not that I am so

bad with it, maybe all that I have done to heal has contributed much positively

to my present state, and without all this effort, I could have been much worse?

Who knows.

And now the hard part. I know most members of this group won't approve of this,

but I am going to meet up with my neurologist tomorrow and agree to switch

medicines. Avonex might have done the good job for 13 months when I had been ok,

and now the doc wants to switch either to Rebif or Tysabri. I have denied

Tysabri coz of the lumbar puncture need to be done yearly, and I just hate this

part. And as I have not found a way how to get LEGALLY and officially LDN or

CCSVI, I will just have to go for Rebif. And try to do my best.

To me, diet is crucial. And strict listening to any allergic reaction... Then

it's sleep, stress-free lifestyle, psychic enhancement, walking in the forest,

creative activity and strong determination and belief.

Plus supplements of course :-)

I'm presently suffering from numbness, too, and cold. So I have begun taking

colloidal silver today. Half of a teaspoon 4 times a day of a 15mg/liter

liquid... What do you think?

Good luck and strong effort to get healed.

>

> Hello all,

> I am currently having my 2nd exacerbation and would like to know some tips

anyone might have on recovering faster. I did have IV steroids for 1 week and my

symptoms have gotten worse. Numbness was just on my left side but now has taken

over my entire body. My hands and feet feel like they are frostbitten. I'm

having headaches and now have a cold. The numbness is what I would love to hae

go away...please help.

> Thanks

>