MrPauljd's channel

Good point, Judy. Yes, you had a good result first time round, however briefly. I never did, which makes me think they should have used a balloon bigger than 12mm- the surgeon didnt want to cause more scar tissue. Anyway, the result's the same. Good luck, hope you find a way past this.

I did very well for 2 years on Tysabri, then stopped for same reasons as you. Then after 6 months I had a bad relapse ( apparently its the MS resuming its normal activity with nothing to damp it down). I had a 5 day course of steroids, felt better, will probably start another drug after I try the...

Hi Andrea. The last time I spoke to Dr Tom Gilhooly in Glasgow he said they were working on "alignment" or head and neck position, with a physiotherapist. Its their new thing. Even suggested it might be an alternative to venoplasty. Am still going back to Belgium for that tho. Are you satisfied w...

Hello again Angela. I am revisiting your videos because I see my neurologist today, who will want me to go back on Tysabri after my latest relapse of ms. I will DEFINITELY say NO. I hope to try my 3rd veinous angioplasty soon. Got to keep hoping. Best wishes and good health to you.

Paul x

Hi Andrea. I just stopped taking Tysabri, after 2 years on it ( a difficult decision, made easier for me because of testing positive for JC virus). I was thinking of trying LDN if need be. Have you tried it? I hope you keep this channel going. Dont know the answer to your question, but do you thi...

Superb! Totally spot on speech. This will give us all inspiration to carry this fight forward, even in the face of unbelievable hostility from the "experts" in MS.

Thanks Kerri.

Paul.

Hi Vern. Glad you're doing well. When I first decided to go on Tysabri it was your vids that made my mind up. According to my MS nurse the risk of PML goes down a bit if you get past the 2-3 year mark, which must be good news for you. I'm fast approaching 2 years now, so am not entirely confident...

Hello. Thanks for putting your thoughts forward. I'm also on Tysabri- just had no.25. Also had venoplasty (which was incomplete and therefore failed) I'm going elsewhere to spend even more money to have it done properly. I still believe, like you, that ccsvi is the main cause of MS. I'm seriously...

Angela. Just to add my voice to all the cheers from around the world, thank you and welcome back amongst us on youtube. You DO give us hope!

Love,

Paul

Hello again Judy. Sorry about that message getting deleted. Just got paranoid about it not sounding right. I was realy impressed with your video. I had my procedure done here in Edinburgh on sat 8th jan, also hope for gradual improvements. Good luck to us all!