This Is MS Multiple Sclerosis Knowledge & Support Community

Hi Sarah, Long time,no see, but I'm still alive! I read you're doing well, thats good! I've been diagnosed with auto-immune hepatitis january 2009 besides the MS. I wrote to David,got a message back of his retirement and decided to go on the Marshall Protocol,which I started january 2009. I believe ...

I started LDN february 2006. First I was on 3 mg,now 3,5. Last january I had a relapse(still recovering) When I first started the LDN I noticed an improvement in my bladderfunction and my head fealt much clearer. My MS dx is from 1997,first relapsing/remitting,now for about a year secundary progress...

I do,Sarah

But at the time i am well enough to start the antibiotics!

My GP is willing to cooperate and I just contacted the hospital in Bedford for a first consultation.

I will keep writing about how it is going to work out.


Many regards!

Annemarie

Thank's for all of your helping and encouraging words,I'm gratefull... At the time I still am willing to go for antibiotics.....my neurologist won't cooperate anymore. Also the news about the newly discovered virus (cryptovirus) is only an affirmation that gives me the feeling that the direction I'm...

Hi everybody here!

The news also came trough in Holland,lots of people with and without MS are exited..

Let's hope this brings a cure or at least a profylaxe!

We cross our fingers!

Thank´s for your (again) beautiful painting,Sarah,and i´m so glad about your further improvement on antibiotics! Already printed both sites....looks good and promising! Hello Rica,nice to meet you,i´ve already read about you and your great improvement,congratulations! When i have news i´ll be back h...

Hi Sarah and others, After a long time I am back on stage...... :wink: Still having MS....meanwhile even secundary-progressive.. I started one week ago with LDN,my GP was so kind to prescribe it... I am waiting for a call-up to go to Nijmegen in The Netherlands,to Professor De Jong,I´ll tell and giv...

:) Sarah, You are so right by saying if MS was infectious would we not be treated with antibiotics? After two awfull months I feel almost my old (MS) self again,becoming new hope,also from your last reply and getting a bit impatient. I drink all the water I can get,eat everything thats eatable,have ...

Hi Sarah, A -for the time being- last message from me,I had a toxic hepatitis,caused by avonex,wich I used for six years. I can't take interferon anymore for the rest of my live and my blood has to be controlled always when I have to take medicins. I don't know if antibiotics in this case is still a...

Hi Sarah, Thank you for your kind answer,when the time is right I will ask my GP to contact your husband. It will take some time now,last week I have become very ill,new bloodtests show that my liver is infected,i also have an icterus,but no stones. Maybe its a hepatitis, a toxic(avonex?) or viral o...

Hi Sarah, I believe you are a very modest person,too modest,if I look again at your tulips. And yes,I've read what you wrote to James,I already was aware of these things,but it seems that none of the people I've seen in my neighbourhood ,know much about long-term effects,and are afraid of prescribin...

Hi Sarah, Thank you for answering,yesterday I went to see my GP and handed him lots of information about Cpn and the antibiotic treatment.He has a lot of reading to do before he can come to his point of view. In Holland I here mostly that long-term treatment with antibiotics will affect your health ...

:) Hi, I once read a book,written by Cari Loder in 1997,title:"Standing in the light",about ms. Cari Loder found a medicine she developed herself,thinking it was the solution for ms. Unfortunately,it wasnt. Is there anyone who ever heard of Cari Loder,I wonder very much how she is doing. A...

Hi all, Today I went to see my GP today.I have a gastritis after the prednisolon last month. So again medication....... :cry: I also asked him about the treatment with antibiotics and gave him several prints from this forum and more. He promised me to read it all,but preferes to leave any kind of tr...

Hi Sarah and Daunted, That might be a step forward again,the interest of your neurologist,Sarah. That is my greatest fear also;that the MS is getting so bad,it makes it unable for me to do much with all the time i have. At this time i can still walk,talk and think clear,so now is the time,my last re...