pentasa assistance program

Procter & Gamble has a patient assistance program: http://www.pgpharma.com/patient_assistance.shtml if you can prove that you don't have insurance/$$ to cover the cost of medication, they allow you to get 270 days worth of free medication. it helped me out tremendously... i did it before and received asacol, not sure if asacol will even work for you, but i found it to be more effective than pentasa.

i believe that pentasa is more for management of colitis once it's under control from steroids like once the steroids bring down your flare up u will continue to take pentasa to maintain your colitis control so you could be on it for quite sometime i have never taken pentasa myself thought they have me on salofalk which i believe is for the same thing, just to keep uc under control. not sure if that helped at all but anyways good luck wishing you the best.

Ask them about baby clothing also.

http://www.bms.com/products/Pages/programs.aspx It took about a week and they have approved me to receive the medication and are shipping it to my home. If anyone is suffering financial hardship and needs medication, I encourage you to fill out the application and get it into them. Good luck and God bless.

Yes, I agree with you on Roche. After begging/borrowing $$$ from family for the first 2 shipments of Pegasys from private pharm & insurance. I applied to Roche assistance program and in 2 weeks my first no cost shipment was on it's way. The only complaint that I have is I have to be home to sign for it.

Japan has not done any drugs trials for this and prescribed oral pentasa to me, which let to an almighty flare. They prescibed pentasa liquid enemas, then steroids liquid enemas, then oral steroids all the while I am getting thinner, but puffier (thanks steroids!), my knees were very painful and my eyesight was blurry. I flew to the UK (nightmare 12 hour flight) + few hour transfer.

I am 56 year old male, diabetic type 2, have been diagnosed a year ago with ulcerative colitis, they prescribed pentasa as medication, now after one year I for rectal bleeding again, I took pentasa 2000 mg on my own , rectal bleeding stopped, watched my diet for a few days , then I went back to my bad eating habits drinking carrot juice , and tuna with little spices, diarreha came back and today I took 2000 mg pentasa orally, after but was eating sweets , now after a few hours at night bleeding

you have to be offered COBRA is you were covered while you were an employee. I would ask the HR department one last time and if the answer is still the same IMMEDIATELY contact your local MS chapter and ask for their assistance. They have specialists to help with these types of problems. There is a patient co-pay assistance program with Shared Solutions - be sure to talk to them about getting your drug covered.

Because she has sleeping issue and is late alot, and because she has ibs and has had to be dosed in the car or go in after an accident, she is being kicked off the program. She is on 120mg and will be detoxed in 30 days. I am not saying that she was not in the wrong about things but this is very sudden. She has no income--I have been trying to pay her insurance and methadone fees myself as she cannot work and has exhausted short term disability benefits.

Apparently, Acorda has both a co-pay assistance program and a patient assistance program for the uninsured and underinsured. There are some details at http://brassandivory.blogspot.com/2010/02/annual-price-for-ampyra-set-at-12850.html with more info in the comments. And yes, the base price for a 30-day supply is $1,056. The way the co-pay program works is that if your co-pay is more than $40, Acorda will pay the difference so the patient's max out-of-pocket is $40.

On another thread here, Mojogal has kindly posted the names of two resources that may be able to help financially with diagnosis/treatment of Lyme. Information is reposted below to highlight it. See the websites for full information. (Thanks, Mojo!

s different for everyone, but personally I find that, in addition to taking Pentasa, the lowest level non steroidal drug for Crohn's, diet and stress are key. In terms of diet- I avoid dairy, fatty and friend foods and super high fiber content foods (like flax meal or metamucil). I eat small meals, more often during the day and I drink a lot of water.

I personally have no experience with suboxone, but drug manufacters all have some kind of assistance program. You have to meet certain income parameters and all that, but it IS available. Check online or ask your pharmacist if they have an 800 number for the manufacturer. It won't hurt to make a phone call and see if they have an assistance program. Good luck!

And they even have other referral programs to help with the cost if you are on government insurance that keeps you from using their regular assistance program. Make the call and keep asking to speak to someone who can help if you get negative responses from the intial calls.

I have suffered from Crohns for 10+ years but only diagnosed last october. My doctor put me on pentasa that I am still on and I've tried numerous times to explain to him it doesn't work. I have daily pain and diarrhea 15+ times a day yet he still won't change my meds. The only test I have had done is a small bowel series which diagnosed it. No other tests to this day. He acts like he doesn't believe me when I say I have extreme pain every day.

They sent me a form to fill out. Once they received my form I was approved for their financial assistance program, which covers all costs for 1 year. After 1 year, I believe I need to reapply. I have a friend who is also on Gilenya and the Gilenya Go Progam is providing her with the same financial assistance that I have been offered. Try contacting the Gilenea Go Program about financial assistance. The seem to be very accommodating! I hope it all works out for you.

Pentasa assistance program

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