advertisement
Reply
 
Thread Tools Display Modes
Old 04-24-2009, 08:35 PM #1
Coqui5 Coqui5 is offline
Junior Member
 
Join Date: Apr 2009
Posts: 6
15 yr Member
Coqui5 Coqui5 is offline
Junior Member
 
Join Date: Apr 2009
Posts: 6
15 yr Member
Cool Xcell Clinic Germany

Hi, I'm new to this site, please excuse any mishaps. I'm seriously considering going to Cologne, GE for the Stem Cell therapy for MS. Has anyone been there for stem cell therapy for MS, or knows anyone who has? I have Secondary Progressive MS and have all sorts of symptoms like; spasms, difficulty walking, footdrop, weakness, etc. It comews with the territory. Any feedback related to the XCELL Clinic will be greatly appreciated.
Coqui5 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Dejibo (04-25-2009), SallyC (04-24-2009), Twinkletoes (04-25-2009)

advertisement
Old 04-24-2009, 10:16 PM #2
MooseasaurusRex's Avatar
MooseasaurusRex MooseasaurusRex is offline
Member
 
Join Date: Jan 2008
Location: Standing right beside you. (Elizabethtown,NC)
Posts: 855
15 yr Member
MooseasaurusRex MooseasaurusRex is offline
Member
MooseasaurusRex's Avatar
 
Join Date: Jan 2008
Location: Standing right beside you. (Elizabethtown,NC)
Posts: 855
15 yr Member
Default

One big, warm, tight, hug, handshake and howdy, moose sized welcome to the site. This place is amazing!

I have MS as well and I was stationed in Germany for 4 years back in the 90s but I'm not familiar with the XCELL program you spoke of. I'm definitely interested in more info on this (and I bet others here are too) so please keep us posted on your progress.

You are not alone.
You are one of us.
And we are here to help.


I am the MonSter that MS fears.
__________________
You can't have everything. Where would you put it? -Steven Wright
Once you change your mind, you can change your life. -Della Reese

.
Always outnumbered...
Never outgunned
.

*I* am the MonSter that MS fears
MooseasaurusRex is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
SallyC (04-24-2009), Twinkletoes (04-25-2009)
Old 04-25-2009, 07:08 AM #3
Dejibo's Avatar
Dejibo Dejibo is offline
Elder
 
Join Date: Jan 2008
Location: New Hampshire
Posts: 7,332
15 yr Member
Dejibo Dejibo is offline
Elder
Dejibo's Avatar
 
Join Date: Jan 2008
Location: New Hampshire
Posts: 7,332
15 yr Member
Default

I just wanted to wave hello, and welcome
__________________
RRMS 3/26/07
.

Betaseron 5/18/07
.

Elevated LFTs Beta DC 7/07
Copaxone 8/7/07
.



.
Dejibo is offline   Reply With QuoteReply With Quote
Old 04-25-2009, 10:24 AM #4
azoyizes's Avatar
azoyizes azoyizes is offline
Magnate
 
Join Date: Sep 2006
Location: Salem, VA
Posts: 2,195
15 yr Member
azoyizes azoyizes is offline
Magnate
azoyizes's Avatar
 
Join Date: Sep 2006
Location: Salem, VA
Posts: 2,195
15 yr Member
Default



Hi Coqui, and welcome to NeuroTalk! I also have MS, and I think you will find this to be a great forum. Lots of very nice people hang out here.

I'm also interested in stem cell treatments. Please, do keep us informed.
__________________
Mair


.
azoyizes is offline   Reply With QuoteReply With Quote
Old 04-25-2009, 11:29 AM #5
SandyC's Avatar
SandyC SandyC is offline
Wise Elder
 
Join Date: Jan 2008
Location: Somewhere over the rainbow
Posts: 9,227
15 yr Member
SandyC SandyC is offline
Wise Elder
SandyC's Avatar
 
Join Date: Jan 2008
Location: Somewhere over the rainbow
Posts: 9,227
15 yr Member
Default

I don't know anyone who has had the treatment but I do know Germany is a great place for treatment of MS. Jim was dx'd by German doctors within 4-5 months. They were awesome! Let us know what you find out and does your insurance cover the treatment in Germany?
__________________
. . A woman is like a tea bag. You never know how strong she is until she's in hot water. Eleanor Roosevelt
SandyC is offline   Reply With QuoteReply With Quote
Old 04-25-2009, 12:24 PM #6
Coqui5 Coqui5 is offline
Junior Member
 
Join Date: Apr 2009
Posts: 6
15 yr Member
Coqui5 Coqui5 is offline
Junior Member
 
Join Date: Apr 2009
Posts: 6
15 yr Member
Default

Hi! I can't post links here yet. Google xcel in Germany. I'm currenyly on rearch mode. Apparently there has been a few patients that have gone for treatment in Costa Rica that attest to some remarkable improvement in balance spasticity, etc. Have a great day!
Coqui5 is offline   Reply With QuoteReply With Quote
Old 04-25-2009, 11:01 PM #7
Judy2's Avatar
Judy2 Judy2 is offline
Senior Member
 
Join Date: Sep 2006
Location: PA
Posts: 1,236
15 yr Member
Judy2 Judy2 is offline
Senior Member
Judy2's Avatar
 
Join Date: Sep 2006
Location: PA
Posts: 1,236
15 yr Member
Default

Just wanted to say Hi! and Welcome to the group! I too will be watching your progress if you go with the xcel treatment since I'm also spms. Please keep us posted and the best of luck to you in your ms journey!
__________________
_____________________________________________

.....Judy
SPMS -- FIBROMYALGIA -- Ouch! and Ouch!
.
Judy2 is offline   Reply With QuoteReply With Quote
Old 04-26-2009, 12:59 AM #8
RedPenguins's Avatar
RedPenguins RedPenguins is offline
Member
 
Join Date: Jan 2008
Location: Southern California
Posts: 308
15 yr Member
RedPenguins RedPenguins is offline
Member
RedPenguins's Avatar
 
Join Date: Jan 2008
Location: Southern California
Posts: 308
15 yr Member
Default

I looked into this in Feb 2008. It costs a lot of money and there really isn't much data to support it. Not to mention, insurance won't pay a lick for it.

Have you looked into HiCy at Hopkins (Baltimore) or at Rush (Chicago)? Basically the treatment is the precursor to a bone marrow treatment where they kill of your immune system and then reboot it...hopking to kill the MS in the mix.

Check out www.thisisms.com - they have info on lots of different treatments - all on different boards, so easy to find.

I did HiCy at Hopkins and insurance covered it, fyi.

~Keri
RedPenguins is offline   Reply With QuoteReply With Quote
Old 04-27-2009, 09:48 PM #9
Coqui5 Coqui5 is offline
Junior Member
 
Join Date: Apr 2009
Posts: 6
15 yr Member
Coqui5 Coqui5 is offline
Junior Member
 
Join Date: Apr 2009
Posts: 6
15 yr Member
Smile

Quote:
Originally Posted by MooseasaurusRex View Post
One big, warm, tight, hug, handshake and howdy, moose sized welcome to the site. This place is amazing!

I have MS as well and I was stationed in Germany for 4 years back in the 90s but I'm not familiar with the XCELL program you spoke of. I'm definitely interested in more info on this (and I bet others here are too) so please keep us posted on your progress.

You are not alone.
You are one of us.
And we are here to help.


I am the MonSter that MS fears.
I will keep you informed. I also lived in Landtuhl for 3.5 years in the early 90's, when I was walking straight. Ha!
Coqui5 is offline   Reply With QuoteReply With Quote
Old 04-27-2009, 09:56 PM #10
Coqui5 Coqui5 is offline
Junior Member
 
Join Date: Apr 2009
Posts: 6
15 yr Member
Coqui5 Coqui5 is offline
Junior Member
 
Join Date: Apr 2009
Posts: 6
15 yr Member
Default

Quote:
Originally Posted by SandyC View Post
I don't know anyone who has had the treatment but I do know Germany is a great place for treatment of MS. Jim was dx'd by German doctors within 4-5 months. They were awesome! Let us know what you find out and does your insurance cover the treatment in Germany?
Hi! As for the insurance, no, it will not cover it. The average cost for tx is approx 10,000 USD. Their site is under Xcel. There are other places like; Costa Rica, China, Panama, etc.
Coqui5 is offline   Reply With QuoteReply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
XCell Center - Cologne, Germany Shake 'Em Up Parkinson's Disease 73 05-12-2011 06:37 AM
Xcell - Germany - post your experiences hirak1977 Parkinson's Disease 0 01-21-2009 11:10 AM
Did one of us travelled to Germany last year pdinfo Parkinson's Disease 5 09-06-2007 09:10 AM


All times are GMT -5. The time now is 07:25 PM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.