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prof
Veteran Member


Date Joined Feb 2003
Total Posts : 1195
   Posted 2/6/2008 9:49 AM (GMT -7)   
How soon after you start 6mp can a blood test be given to see the levels in your blood stream?
I know if can take a while to work but i was told the levels can be dedected before.


meshice
Veteran Member


Date Joined Jan 2003
Total Posts : 734
   Posted 2/6/2008 1:49 PM (GMT -7)   
My bloodwork was done three months after I started and has been done every three months since. I have been on 6MP for over 4 years now - it has been my wonder drug.
The first itme they did bloodwork they could tell it was in my system because of the lowered WBC. Now they just watch to make sure it doesn't get too low or in a danger zone.
My liver enzymes are checked yearly.
"We can't beat this disease, YET, but we can't let it beat us!"
Mandy

"Do not worry about tomorrow, for tomorrow will worry about itself. Each day has enough trouble of its own." Matthew 6:34


chroniemomx2
Veteran Member


Date Joined Apr 2005
Total Posts : 2346
   Posted 2/6/2008 2:15 PM (GMT -7)   
When I was on imuran, they waited 6 weeks after a dosage change to check.

Sharann
Veteran Member


Date Joined Sep 2005
Total Posts : 778
   Posted 2/6/2008 5:47 PM (GMT -7)   
My white count is almost 10,000 on 6MP for only 4 weeks. Not low at all. Upped my dose to75mg, hope it kicks in soon!
I am a Certified Doxie Lover(Weinerdogs)


kgirlie
Regular Member


Date Joined Jan 2008
Total Posts : 101
   Posted 2/6/2008 6:38 PM (GMT -7)   

Can I ask what mp stands for? I should probably know, but I have been lucky to survive on pentasa and I just started on prednisone.

Thanks,

Kgirlie


Kgirlie
 
27 year old female dx with CD in 2001. Pentasa 4 g/day, Prednisone 30 mg/day, Amytripaline 25mg/day, Lexapro 20 mg/day, Maxalt 10 mg as needed. Mother of son, 3, and daughter, 6 months.  


Ides
Forum Moderator


Date Joined Nov 2003
Total Posts : 7077
   Posted 2/6/2008 9:00 PM (GMT -7)   
mp = mercaptopurine
Moderator Crohn's Disease Forum
CD, Ankylosing Spondylitis, small fiber peripheral neuropathy, avascular necrosis, diffuse connective tissue disease, Sjogren's Syndrome ?
 


mj8dokken
Regular Member


Date Joined Dec 2006
Total Posts : 149
   Posted 2/8/2008 1:24 PM (GMT -7)   
I was just put on 6mp two days ago and was told it would take 6 months to kick in.

Bad flare May '06 resulted in CD diagnosis-symptoms for 10 yrs prior.
Asacol: 2400 mg/day
Now off Prednisone!


heavly
Regular Member


Date Joined Nov 2007
Total Posts : 83
   Posted 2/8/2008 1:41 PM (GMT -7)   
he told me to come in every 2 - 3 weeks. the first 3 weeks i did well - he increased to 75mg and then i felt nauseous all the time - more blood work and dropped back to 50mg and then hives.
25 yrs - female : diagnosed with Crohn's 11/29/07

"i believe - you can keep going long after you can't"


br4d
Regular Member


Date Joined Feb 2008
Total Posts : 71
   Posted 2/8/2008 1:53 PM (GMT -7)   
mj8dokken said...
I was just put on 6mp two days ago and was told it would take 6 months to kick in.


that's correct. it usually takes a while to actually notice any changes in your symptoms, but the drug will have an impact on your body before that. i've been on 6mp for 6 years and i've been doing well with it, aside from the recent bloody stool that is worrying me a bit, but i just noticed that a few weeks ago.
-brad
"you can't fax glitter!"


Doc2007
Regular Member


Date Joined Oct 2007
Total Posts : 294
   Posted 2/8/2008 2:05 PM (GMT -7)   

Been on 6MP since November...I am feeling 100% better but dont know if its the 6mp kicking in as it has only been two months or if I am just finally going into remission. I did have nausea a bit at first but that wore off after about three weeks, and not sure  if it was the 6 mp or the pred which I am tapering off of. Now on 5 mg every other day.

I have heard really great things about 6 mp. I was very scared to take it. But as my Doc explained that the fears that have concerned the medical world over using 6mp for crohns and colitis have been unofounded over the long term use of the drug and patients. And whats most reasurring is that any side affects that take place are reversed by merly stopping the drug.

I havent been sick or anything or had any colds since starting and I have been around my 3 yo who has a cold every week and my partner who just got over the flu. As well as friends and coworkers who have all been down this season...I seem to be going up!

 

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