This Is MS Multiple Sclerosis Community: Knowledge & Support

Just read B's last post in the Tysabri section. Hope that it is another one of his jokes, as he states he is going to stop posting, after the "Harry Z' fiasco.

I find Bromley's posts to be very informative, and I think this site will be diminished by his absence. Take a while to lick your wounds Bromley, and to get over your misinterpreted attempt at humor, but don't give up on the site. Your posts indeed carry much value...

Well said

_________________
John was diagnosed Jan 2005. On lipitor 20mg .On Copaxone since July 4,2005. Vitamin D3 2000iu-4000iu (depending on sunshine months)June 10 2005(RX::Dr. O'Connor) Omega 3 as well Turmeric since April 2005. Q10 60mg. 1500mg liquid Glucosamine Nov 2005.

I also agree with marcstck!

I would like Bromley to stay.

Ian--

I'd like you to stay as well. Your posts are valuable and informative.

Most importantly, you're a valuable person to the community, your wife and family too.

Sharon

IAN:

Please come back. You were an asset to this board.

_________________
Karen
Age 50


Sinus Symptoms dizziness/MRI shows multiple lesions 2002,
"Wait and See."
Dx 3/05
Rebif 4/05
David Wheldon Protocol 1/06

IAN:

Please come back. You were an asset to this board.

_________________
Karen
Age 50


Sinus Symptoms dizziness/MRI shows multiple lesions 2002,
"Wait and See."
Dx 3/05
Rebif 4/05
David Wheldon Protocol 1/06

I also hope you stay Ian. You and Dignan are the reason I was drawn to this board. The research info that you both provide is outstanding. You are definitely an asset to this board. So what if your joke didn't go over well-we have MS! There are much more important things to worry about Please come back.

I second that. Please can we revert to normal?

Ian this site needs you. Please have a re-think and come back.

J.

I miss you too Ian. I really like your posts they're very informative. The only thing that gets to me is when you attach something cynical / negative to them. Im all for discussion but when you berate the drug or say something along the lines of 'we've all heard that before..' (paraphrasing) it gets to me. Aside from that your posts have always been great and id hate to be without them.

I'm sure that many of you who have read the recent message by Ian to me were quite surprised to say the least. I know that I certainly was!

Since that original post, Ian and I have exchanged numerous private messages about the content of the post and the intent behind it. We have been able to clear up a lot of the misperception that existed between us and just why this happened.

One definite fact we discussed was the problems that MS can cause someone when it slices and takes away from its victim many of the things that one can cherish....everything from every day living tasks to the loss of family enjoyment. The resulting fear, anxiety and frustration
can effect how a person thinks and communicates. Believe me, I have seen this very problem happen to my wife who has suffered from this dreaded disease for 35 years and I can understand what Ian was describing to me.

Ian and I have decided to put this episode in the past and move on. I know that he stated that he would stop posting on ThisIsMs but Ian has contributed far too much so far to take this step. I am going to strongly suggest that he continue to offer his messages of insight into what is
going on in the world of MS and ask him to please continue to participate in this forum.

Harry

I think, we all need help, every one of us feels fear most of the times. We all are in the same ship, a ship that goes to an uncertain trip and we need to be strong all together not to succumb by this MonSter, so Ian please come were you belong, come home, we all loves you even if sometimes we express different opinions, this is even good for all.

love from

Rita

Harry, Ian

I am glad you have resolved this.

This thing does get to us, as you say Harry, and sometimes it's hard to understand the effect it has, let alone accept it.

Looking forward to seeing both your posts soon.



J.