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ZLSJ
Regular Member


Date Joined Dec 2008
Total Posts : 263
   Posted 4/10/2009 9:18 AM (GMT -6)   
Is this common among us UCer's?
 
I'm beginning to show some pretty strong signs of this, I've lost about 10lbs in 3.5 mos which I know isn't a heck of a lot compared to many others.
 
Strong signs? Noticeable sunken cheeks, loss of muscle mass, people commenting on my weight loss, everything fitting bigger. I always tend to dismiss any stool signs towards my UP, so that can sometimes confuses the matter for me.
 
I have had Celiac screen which came back negative 2 mos ago.
 
Anyone experience this?

qsam6
Regular Member


Date Joined Nov 2008
Total Posts : 90
   Posted 4/10/2009 11:51 AM (GMT -6)   
You need to help your colon heal so that it can absorb. Take vitamin B-12 and folic acid. It also helps to eat foods that contain the two of these. If you have been bleeding a lot then your body needs these replaced so that the colon can function properly.

robray
Regular Member


Date Joined Mar 2005
Total Posts : 130
   Posted 4/10/2009 1:34 PM (GMT -6)   
I've read that malabsorption is more of a problem for Crohn's as vitamins are absorbed in the small bowel. However, I am thinking that it would be a problem for most UC sufferers too and here are my reasons.
I was complaining of my food not being fully digested before I discard it to my GI and his explanation was the GI tract is a continuous pipe and if the colon is contracting too quickly because you are in a flare then the small bowel is also contracting too quickly. This is the reason why foods comes out pretty much the same way it went in and I am thinking the small bowel would not be able to absorb all the nutrients it is supposed to.
Some more evidence of malabsorption in my case in particular is the fact that I have Osteoporosis at 35 years old. I have had some exposure to steroids, but I have only been on pred twice in 18 years of UC and the only other form of steroid use was entocort enemas which are not supposed to be systemic.
I haven't figured out how to fix this, but if you are having constant diarrhea like me then we need to slow it down. I believe this could be accomplished through supplementing with fibre. I plan on introducing some soluble fibre supplements in the next month after my condition is more stable.
UC (Pancolitis) diagnosed in 1992.
   Medications: Dipentum, Salofalk Enemas, prednisone (Stopped 2008), entocort enemas (Stopped 2008), Cortenema (Stopped), Asacol (Stopped 2003)
   Other therapies: Spinach & Sunflower Seeds, gluten free, dairy free (except for aged cheese and SCD yogurt), rice free, HPI (2008), SCD (Stopped, but still make yogurt), Vitamine E enema
Osteoporosis diagnosed in 2008.
   Medications: None yet, but they want me to take fosamax
GERD diagnosed 2008, but had it forever.
   Medicaitons: Parriet (Stopped)


doors12
Veteran Member


Date Joined Jul 2006
Total Posts : 723
   Posted 4/10/2009 8:11 PM (GMT -6)   
I want to know why the professional line is that there is no malabsorption with ulcerative colitis. I want to know why my teeth are so cavity prone, my hair so strange, and my fingernails so pitted. Not to mention the headaches. I want to know why no one is researching any of this. Why they don't issue simple surveys to UC hospital patients, GI offices etc. A Psychology 101 or anatomy 101 etc class could handle this. Blood tests, symptom surveys, genetics. Correlations.

What do you think about assembling personal health information (with personal identifiers stripped) and then having researchers mine the database. Maybe they would actually pull their heads out of the part of the body that GI's handle and realize some correlations - the point of my rant is, I believe there is some malabsorption. Maybe it is just due to bowel contents flying through at light speed...
Diagnosed with Ulcerative Colitis 6/2006 at age 26 after sudden E.R. visit
~Pancolitis (Mild to Moderate)
 ~I had Mono in 2000
On Colazal 3x3/day; Folic Acid 1mg; Calcium/Magnesium/Zinc combo
(Generic Balsalazide not as effective for me)
In remission about 2-3 months after E.R. but not back to normal!
I hate Ulcerative Colitis and can't wait till we eradicate it
 


ZLSJ
Regular Member


Date Joined Dec 2008
Total Posts : 263
   Posted 4/11/2009 11:36 AM (GMT -6)   
Forgot to add the "gross" smelling stools, and also are digestive enzymes something you'd stay away from until consulting with a doc.
 
Am I totally "out there" with these thoughts???  

quincy
Elite Member


Date Joined May 2003
Total Posts : 30976
   Posted 4/11/2009 7:00 PM (GMT -6)   
Digestive enzymes would be helpful.

what do you mean "out there".?

gross smelling stools can definitely be from foods you eat, inflammation or IBS.

quincy
*Heather* Status: mild flare enemas tapered to every 2nd night
~diagnosed January 1989 UC (proctosigmoiditis)
~UC meds: Asacol (3 x2 daily); Salofalk enemas nightly for flares & taper to maintenance 
~Bentylol (dicyclomine) 20mg as needed; Ranitidine (reflux);  Effexor XR 75mg(depression);  Pulmicort/Airomir (asthma) 
~vitamins/minerals/supplementsProbiotics....(Natural Factors Protec, Primadophilus Reuteri Pearls, Natural Factors Ultimate). @ bedtime
~various digestive enzymes as needed; started Omega 3 
~URSO for PSC (or PBC) 500mg X 2 daily (LFTs back to NORMAL!!)
My doc's logic.. "TREAT (FROM)BOTH ENDS"  worth it !!!
 


ZLSJ
Regular Member


Date Joined Dec 2008
Total Posts : 263
   Posted 4/11/2009 8:09 PM (GMT -6)   
Hey Quincy,

Happy Easter!

What kind of digestive enzymes do you take?? Do you take them regularly?

By "out there", I just meant, am I just grasping at straws? I'm still trying to figure things out by myself. I can't see going to that idiot of a GP again. So now I'm feeling like I have nowhere to go. Doctor search doesn't happen overnight.

I'm getting to the point where I'm getting annoyed by my own behaviour ! Having a real tough time enjoying anything right now.

Sorry for the downer of a post at what should be a joyous time of year.

quincy
Elite Member


Date Joined May 2003
Total Posts : 30976
   Posted 4/12/2009 2:19 AM (GMT -6)   
Hi...Happy Easter to you as well!

No need to apologise....we all feel that way, sometimes more often than not.

Besides, this is your thread...lol!!

I use Gas Stop by Renew plus I use Bromelain by Natural Factors.

Digestive enzymes can give me gas sometimes...I pretty much take them only with supper. Have you given consideration to peppermint tea or fennel tea or chewing fennel seeds after eating...some options anyway.

I still think that anxiety and feeling distressed changes ones facial expression making it appear drawn.

If you are at your weight for your height and bone structure plus age, I dont think you need to focus much of your energies on that.



How is the Bentylol working out for you

quincy
*Heather* Status: mild flare enemas tapered to every 2nd night
~diagnosed January 1989 UC (proctosigmoiditis)
~UC meds: Asacol (3 x2 daily); Salofalk enemas nightly for flares & taper to maintenance 
~Bentylol (dicyclomine) 20mg as needed; Ranitidine (reflux);  Effexor XR 75mg(depression);  Pulmicort/Airomir (asthma) 
~vitamins/minerals/supplementsProbiotics....(Natural Factors Protec, Primadophilus Reuteri Pearls, Natural Factors Ultimate). @ bedtime
~various digestive enzymes as needed; started Omega 3 
~URSO for PSC (or PBC) 500mg X 2 daily (LFTs back to NORMAL!!)
My doc's logic.. "TREAT (FROM)BOTH ENDS"  worth it !!!
 


ZLSJ
Regular Member


Date Joined Dec 2008
Total Posts : 263
   Posted 4/12/2009 8:54 AM (GMT -6)   
I guess that's the great thing about a community like this. You can throw out an issue for discussion and if someone sees they can relate and post something that may help or even to say, " yeh, I know exactly what you're going through", it can certainly help a person get through whatever issues they're having.
 
Sorry for all the questions, but at what point was it that you decided to take the digestive enzymes? What issues were you having?
 
I'm just too hung up on the fact that I've seen these changes over a rather short period (or perhaps have only noticed them)
 
I know that my face has changed because I'm not smiling near as much as I used to, so I think my face is stuck! Need someone to slap me in the back of the head when I'm smiling and maybe it will stay that way. Wasn't there a movie like that, where a young girl couldn't change her expression after getting a blow to her head?
 
The height/weight thing is a tough one for me. I was 193 or so for a long time prior to a few months ago, have dropped to about 185 and could drop another 30 lbs and I'd be closer to the "medical normals". I'm a stockier build, used to weight lift lots, so when I was fit, being 5'6" or so and 165-70 or so, though seemingly heavy for a normal person according to the charts, was a comfortable weight because of the extra muscle I was carrying. I'm feeling very thin even though I weigh at least 30 lbs more than I should (according to the charts)
 
The bentylol seems to be able to stop some of that twisting/turning for me, I've only taken it two days actually, the first day I wasn't really having thissues and yesterday I was so I took it and it seemed to help.
 
Kids will be getting up soon for the hunt...there will be no shortage of chocolate around our house today, the Easter Bunny overspent...again!! 

quincy
Elite Member


Date Joined May 2003
Total Posts : 30976
   Posted 4/12/2009 1:41 PM (GMT -6)   
Well, no Easter bunny here this year....I've requested no visit..lol!

I decided to take the enzymes about 3 years ago...maybe more, can't remember. I mentioned to the doc I was taking them...but he didn't say anything negative about it. I think I was wanting to try them to help  get food  cleared out of my stomach faster because I do have reflux.

I was taking Zymactive for a while and the intent was to lose a bit of weight as well as to help with my sore body at that time. It did help and I did notice some weightloss. I've since stopped taking them.

I do think the Bromelain is helping with some of the body/joint pain....it's not on my mind a lot...but I haven't been taking them consistently.

Worth a try, regardless. The other one to take would be beano...I have that as well, and come to think of it, I'll take it tonight at supper (yum, turkey dinner).

Smiling will definitely help.....

I think the weight issue is more psychological. Many of us who have been extremely underweight don't want to be that again. I'm liking the extra weight, but it's not toned...I have control over that, however...no excuses.
I'm afraid to become a rail again, but I'm not sick like I was. So, the 109 pounds on a 5'8" frame wasn't nice, but 145 at age 54 feels more solid and secure.

Regarding your worry about weightloss...from your perspective, maybe the weight represents a comfort....or a time of being fit...losing the weight represents losing fitness...?

Some of us become our moment of focus...losing some weight of your height seems a good thing....so if you can turn it around to a plan rather than a worry, that might be a good thing?

I hope you're able to enjoy the day. I don't think one needs to have the 100% yahoo day....just enjoy the positives and make a big deal out of them....Try not to make the negatives bad, but try to keep them in perspective that they're there but not becoming the final judgement of the day.

As always....hang tough.

quincy.


*Heather* Status: mild flare enemas tapered to every 2nd night
~diagnosed January 1989 UC (proctosigmoiditis)
~UC meds: Asacol (3 x2 daily); Salofalk enemas nightly for flares & taper to maintenance 
~Bentylol (dicyclomine) 20mg as needed; Ranitidine (reflux);  Effexor XR 75mg(depression);  Pulmicort/Airomir (asthma) 
~vitamins/minerals/supplementsProbiotics....(Natural Factors Protec, Primadophilus Reuteri Pearls, Natural Factors Ultimate). @ bedtime
~various digestive enzymes as needed; started Omega 3 
~URSO for PSC (or PBC) 500mg X 2 daily (LFTs back to NORMAL!!)
My doc's logic.. "TREAT (FROM)BOTH ENDS"  worth it !!!
 

Post Edited (quincy) : 4/12/2009 12:44:53 PM (GMT-6)


fruitgirl
Veteran Member


Date Joined Feb 2009
Total Posts : 7150
   Posted 4/12/2009 3:17 PM (GMT -6)   
I think that I had to have been suffering from malabsorption/lack of nutrition when I was flaring badly. I'd eat something, and see traces of it in my poop less than 8 hours later at times. There's no way there's time for the body to get all it needs out of the food if it's moving through that quickly. I also lost a lot of weight really fast, too.
Symptoms began in November 2008, ~4 weeks after giving birth to my son.
Eased for ~3 weeks in December, possibly b/c of probiotic use?
Returned in January 2009 (with a vengeance), diagnosed with pancolitis on January 30.
Currently taking Asacol (400mg 4 pills 3x daily), Rowasa nightly, 40mg 30mg 20mg 15mg 10mg of Prednisone (quick taper), Culturelle probiotic, and Zoloft (25 mg).


ZLSJ
Regular Member


Date Joined Dec 2008
Total Posts : 263
   Posted 4/13/2009 8:11 PM (GMT -6)   
I guess I'll check into the digestive enzymes a bit more.
 
Been noticing a bit more undigested food in my semi-formed stools and after reading the extensive "float or no float" post can't really make up my mind whether having floaters is a good thing or bad thing (appears like it's different for many)
 
The weight thing is funny because I keep checking and my weight is not dropping out of the sky, yet I feel like I'm looking thinner (did I mention my sunken cheeks...lol) Like I said, I could still lose another 30 lbs before I'd be considered to be my ideal body weight.
 
Yet to try the Effexor for the way I've been feeling, I'm so nervous about it. Though I think my wife would love to jam the pills down my throat. She is not handling the way I've been too well lately and it's beginning to really have an effect on us. I know, it's not just her, but support is not what I'd call what she has been giving me for the past while. We'll get through it I guess, but telling me to quit feeling sorry for myself constantly is starting to grate on me. Just as my constant concern for my health grates on her.
 
Were you working today?
 
We had family in town so I was off today as well, which was kind of nice. Weather could have been a bit nicer. 

Got2Believe
Regular Member


Date Joined Feb 2007
Total Posts : 436
   Posted 4/14/2009 9:49 AM (GMT -6)   
I think there may be some sort of malabsorption with UCers but the colons main function is to absorb water and the main nutritional absorbtion is done in the small intestine.
The things i would want to attribute to malabsorption for me are weight loss and hair loss. But the only time i have weight loss is during hard flares where my appetite goes down. I need at least 3 meals and snacks per day. Anything less my body goes for the reserves in my body and pounds drop fast. The hair loss really had me worried b/c i would see it all over my pillow and when i showered but i don't take prescriptions any more and don't have hair loss anymore so i have to assume it was one or a combination of drugs causing that.
As for traces of food passing through your system i would suggest chewing more. When i was diagnosed with UC 4 years ago I had just started my career and began to inhale my meals really fast and would notice chunks of food but I don't see anything like that anymore. Of course if you eat jalapenos and salsa like I do or any other things with seeds or nuts these are not going to break down with enzymes even in a healthy digestive system unless you chew them until they are mush.
                                                                                         
28/M/TX single parent of gorgeous 3yo girl (revised 12/12/08)
Severe Colitis (pancolitis) since January 9, 2005
currently:  Mildly Flaring 
RX/day: none! Tapered off Prednisone 9/20/08. Lost job and insurance 10/2007 and stopped taking asacol and Imuran cold turkey
OTC: enzymes everyday, turmeric, seldom use probiotics, vitamins & other natural treatments
Diet: SCD helps tremendously, but am not strictly on it.
Other: Prayer, food combos, good posture, chewing more, etc.


ZLSJ
Regular Member


Date Joined Dec 2008
Total Posts : 263
   Posted 4/15/2009 6:30 AM (GMT -6)   
Hair loss is something I have not paid any attention to, because as I get older mine is starting to recede, so I just
suck it up and don't pay a lot of attention to it.
 
I don't have a lot of chunks of food...it may be the fgact that my stools are finally beginning to have some form and that is why I'm noticing.
 
Thanks!

princesa
Veteran Member


Date Joined Aug 2007
Total Posts : 2204
   Posted 4/15/2009 8:58 AM (GMT -6)   
I'm a big fan of listening to your body which may be telling you something different than what your doctor tells you or what you've read. The symptoms you've listed do indicate you're not digesting at optimal levels and/or you have some type of food reactions. In my experience, a careful diet and supplements that reduce inflammation and promote gut healing will help improve digestion. Also, just because you've tested negative for celiac disease doesn't mean you aren't sensitive to gluten. I've had allergy tests and the celiac blood test (as well as an endoscope) come back all negative, but trial and error and keeping a food journal tells me I feel better when I don't consume certain foods - including gluten. Ultimately, your body will tell you what it needs.
Diagnosed with ulcerative colitis spring 1999.
 
Maintenance dose sulfasalazine. Probiotics, l-glutamine, vitamin D and fish oil caps. George's aloe vera juice. Oregano oil antibiotic, antiviral, antifungal. Mostly grain-free and dairy-free diet. Long-term remission with only minor blips.
 
 


quincy
Elite Member


Date Joined May 2003
Total Posts : 30976
   Posted 4/15/2009 2:38 PM (GMT -6)   
Hi ZLSJ....what dosage of Effexor XR is the doc starting you at?

What are your biggest fears about it?
q
*Heather* Status: mild flare enemas tapered to every 2nd night
~diagnosed January 1989 UC (proctosigmoiditis)
~UC meds: Asacol (3 x2 daily); Salofalk enemas nightly for flares & taper to maintenance 
~Bentylol (dicyclomine) 20mg as needed; Ranitidine (reflux);  Effexor XR 75mg(depression);  Pulmicort/Airomir (asthma) 
~vitamins/minerals/supplementsProbiotics....(Natural Factors Protec, Primadophilus Reuteri Pearls, Natural Factors Ultimate). @ bedtime
~various digestive enzymes as needed; started Omega 3 
~URSO for PSC (or PBC) 500mg X 2 daily (LFTs back to NORMAL!!)
My doc's logic.. "TREAT (FROM)BOTH ENDS"  worth it !!!
 

Post Edited (quincy) : 4/15/2009 4:12:09 PM (GMT-6)


ZLSJ
Regular Member


Date Joined Dec 2008
Total Posts : 263
   Posted 4/15/2009 2:50 PM (GMT -6)   
37.5mg a day for 2 weeks, then doubling that for 2 weeks and see where I'm at after that. I'm just scared of what I've read about side effects and withdrawal effects.

Dr-A
Veteran Member


Date Joined Jul 2006
Total Posts : 2105
   Posted 4/15/2009 3:21 PM (GMT -6)   
I know with my UC it always sounds like a party in my intestines. With all the increased mobility I imagine things do not get absorbed as well compared to normal bowel activity. This would definately affect absorption in UC patients. I've also read (www.med.unc.edu/medicine/fgidc/gastrointestinal_motility_disorders.pdf) that the dysfunctional mobility of the intestine can cause bacterial overgrowth in the upper small intestines that lead to alot of the symptoms I get sometimes after eating, and contribute to malabsorption. Just a way of seeing that the large intestines will affect the rest of the plumbing too. Add the extra anxiety and stress onto the digestive process and I really start to struggle.
Proctitis DX 1999, Pancolitis DX 2008
Lialda 1 day
Immuran
Golimumab study (100mg every 4 weeks)
Vitamin E Enemas as needed
Probiotis/GreenTea/VitD3+Ca/SuperDHA


ZLSJ
Regular Member


Date Joined Dec 2008
Total Posts : 263
   Posted 4/15/2009 4:50 PM (GMT -6)   

Party in the intestines...like that one! The party in there rarely stops for me. Doc figures that I have IBS as well as my diagnosed Ulcerative Proctitis so it's a nice combination that many of the folks on this board have. Like Princesa says; listen to your body, I am doing that and it continues to tell me something different all the time. I just drive myself crazy so often with the constant need to pinpoint what ails me.

Malabsorption is what I'm trying to pinpoint as the cause of some of my current issues , something does not seem quite right yet the doc says I have nothing to be concerned about. Perhaps I should start believing someone. It is easier said than done!


princesa
Veteran Member


Date Joined Aug 2007
Total Posts : 2204
   Posted 4/15/2009 5:11 PM (GMT -6)   
ZLSJ said...

 Like Princesa says; listen to your body, I am doing that and it continues to tell me something different all the time. I just drive myself crazy so often with the constant need to pinpoint what ails me.

Unfortunately, our the condition/health of our body and digestive system isn't a static thing; it's a moving target requiring we constantly monitor and adjust. When you're flaring badly, you may feel everything bothers you. When you're in remission, you may feel nothing bothers you. During allergy season, you may find you have alot more trouble than other times of the year. It can be frustrating, but with time, you'll get better at "interpreting" your body's messages and responding appropriately.

Diagnosed with ulcerative colitis spring 1999.
 
Maintenance dose sulfasalazine. Probiotics, l-glutamine, vitamin D and fish oil caps. George's aloe vera juice. Oregano oil antibiotic, antiviral, antifungal. Mostly grain-free and dairy-free diet. Long-term remission with only minor blips.
 
 


quincy
Elite Member


Date Joined May 2003
Total Posts : 30976
   Posted 4/15/2009 5:17 PM (GMT -6)   
and in order to get there, there has to be an understanding that our minds can contribute/exacerbate the process.

It takes time...yes.

And unless one is willing to adhere to something strict in order to cross it off the list, then don't worry about it until one is ready to do so.

It's like rolling downhill with no brakes and watching the scenery change from all positions and speeds.

Impossible to function.....something has to give.

q
*Heather* Status: mild flare enemas tapered to every 2nd night
~diagnosed January 1989 UC (proctosigmoiditis)
~UC meds: Asacol (3 x2 daily); Salofalk enemas nightly for flares & taper to maintenance 
~Bentylol (dicyclomine) 20mg as needed; Ranitidine (reflux);  Effexor XR 75mg(depression);  Pulmicort/Airomir (asthma) 
~vitamins/minerals/supplementsProbiotics....(Natural Factors Protec, Primadophilus Reuteri Pearls, Natural Factors Ultimate). @ bedtime
~various digestive enzymes as needed; started Omega 3 
~URSO for PSC (or PBC) 500mg X 2 daily (LFTs back to NORMAL!!)
My doc's logic.. "TREAT (FROM)BOTH ENDS"  worth it !!!
 


quincy
Elite Member


Date Joined May 2003
Total Posts : 30976
   Posted 4/15/2009 5:19 PM (GMT -6)   
Regarding the Effexor....I guess you'll figure a time when you'll feel it's worth it.

q
*Heather* Status: mild flare enemas tapered to every 2nd night
~diagnosed January 1989 UC (proctosigmoiditis)
~UC meds: Asacol (3 x2 daily); Salofalk enemas nightly for flares & taper to maintenance 
~Bentylol (dicyclomine) 20mg as needed; Ranitidine (reflux);  Effexor XR 75mg(depression);  Pulmicort/Airomir (asthma) 
~vitamins/minerals/supplementsProbiotics....(Natural Factors Protec, Primadophilus Reuteri Pearls, Natural Factors Ultimate). @ bedtime
~various digestive enzymes as needed; started Omega 3 
~URSO for PSC (or PBC) 500mg X 2 daily (LFTs back to NORMAL!!)
My doc's logic.. "TREAT (FROM)BOTH ENDS"  worth it !!!
 


quincy
Elite Member


Date Joined May 2003
Total Posts : 30976
   Posted 4/16/2009 11:30 AM (GMT -6)   
I just want to add that the first time I was on Effexor XR....I did the 37.5mg for about 6 months. Went off it, then started it again about 6 months afterward, but that time I had to up it to 75mg. (bad thoughts)....but it did help a lot!

The first time on it, I had more feelings of "elation" and it took the edge off of my feeling down,.

I do hope you consider it if you get feeling any worse.

q
*Heather* Status: mild flare enemas tapered to every 2nd night
~diagnosed January 1989 UC (proctosigmoiditis)
~UC meds: Asacol (3 x2 daily); Salofalk enemas nightly for flares & taper to maintenance 
~Bentylol (dicyclomine) 20mg as needed; Ranitidine (reflux);  Effexor XR 75mg(depression);  Pulmicort/Airomir (asthma) 
~vitamins/minerals/supplementsProbiotics....(Natural Factors Protec, Primadophilus Reuteri Pearls, Natural Factors Ultimate). @ bedtime
~various digestive enzymes as needed; started Omega 3 
~URSO for PSC (or PBC) 500mg X 2 daily (LFTs back to NORMAL!!)
My doc's logic.. "TREAT (FROM)BOTH ENDS"  worth it !!!
 


Miss Green
New Member


Date Joined Apr 2009
Total Posts : 4
   Posted 4/16/2009 11:57 AM (GMT -6)   
Hi everyone,
I have recently been studying Ulcerative Colitis. I wanted to note that once food is digested in the small intestine and all that is left is fiber, water, bile, cells from the lining of the intestine, and bacteria. Once it reaches the large intestine because this material cannot be digested, digestion does not accure in the colon/ large intestine.
 
:D
 
No worries about digesting properly
..
I know I probably didn't answer many questions but I hope this information has some value to you
~Miss Green

Miss Green
New Member


Date Joined Apr 2009
Total Posts : 4
   Posted 4/16/2009 12:14 PM (GMT -6)   
Okay well I'm in Medical school right now and need to go. I'm messing around and need to focus on my research now. I will check in later and see if anyone responds.

~Bye all
Life is too short to wake up with regrets. So love the people who treat you right and forget the one's who don't. Believe everything happens for a reason. If you get a second chance, grab it with both hands. If it changes your life, let it. Nobody promised life would be easy, just that it would be worth it.

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