could anyone give me ideas as to where or who i would contact to get some patient assistance for acute hep c treatment? I am not working, cannot wait on s.s. disability. I try to do some construction work when available, but it is really rough.
20 hours from the encounter i started up PEP( kaletra+ truvada), with the usual side effects + blood in the spitting ( a consequence of the deep throat or of the kaletra ? i noticed the blood only 1/2 days after the 1th assumption)
tomorrow morning the male of the couple promised me he's gonna test and show the result.
in case of negativity should i interrupt the treatment ? or i need both of them to be tested ?
Is combivir an appropriate HIV nPEP regimen for one time unprotected encounter with CSW of unknown status in Kenya? I'm a 24 yr male from UK. Insertive vaginal and oral. Asked about Kaletra and doc said it's low risk doesn't recommend, but I am still very worried. Started within 12 hours, but still within 72 if kaletra should be added. I feel terrible of course but appreciate any advice.
30am and 8:30pm along with Kaletra, is it ok to change this to say 6am and 6pm or will the moving around times effect their effectiveness at least on the day I changed the time of taking them?
Also will taking PEP have any long term side effects. It just that with all the sport I do I need to stay muscular, would PEP have any effect on this?
I'm currently taking Kaletra and Combivir.
s viral load was undetectable and was last tested in Aug 2012
6) unrelated (the patient was tested for Hep C last month and was - )
7) probably is just an assumption as to how safe the patient is but the patient is in a married relationship
8) I followed protocol of rinsing with soap and water for 3 minutes
Now the physician told me that without those factors listed above and without any medication, that I had a 0.
1 Truvada and 2 Kaletra at 7am while 2 Kaletra at 7pm. Yesterday, I took 1 Truvada at 7am but since I was in a hurry after dinner, I accidentally took one more Truvada last night. I tried to vomit it up but I was able to vomit only a part (dissolved part) of it. Because of panic, I forgot to take Kaletra last night. I rushed to the A&E and asked the doctor's advice on what to do.
Since the chances a quite low Can I stop taking pep or can I stop kaletra and remain with truvada take it upto 28days.coz kaletra gives me diarrhea.
My sister-in-law is just above 10 years old. She takes Viread and Kaletra every day. My mother-in-law takes Videx EC and Ziagen. My mother-in-law is currently in Africa, and I've searched on the pills my sister-in-law is taking, and I found out that it was HIV treatment :'( I couldn't hold my tears, because I love her so much, and she is so young. I want to know what it means. Please tell me.
Started PEP at roughly 56 hours, was prescribed Truvada and Kaletra (those orange ones). However in such panic I took the one Truvada and stupidly only one Kaletra (I was meant to take two), the second tablet I took at roughly 68 hours. I then realised my stupidity and the next day (about 80 hours) I began to take the correct dosage (one truvada and two Kaletra twice daily).
Tested negative for all other STD's inc. HIV on roughly 12th Jan.
I also commenced Truvada that evening ( approx 4 hrs post exposure) . Is this adequate . I have now been on it for a week . I was considering commencing kaletra as well . Is my risk high ? would you recommend anything else?
thanks for advice
worried !!
This is my understanding of the patient assistance programs for Incivek. The list price, which no patient will have to end up paying, is $49,200 for 12 weeks. HOWEVER, the patient assistance programs, are more than generous. Typical Co-pay for the three prescriptions that will be needed will be between $50 and $250 each.
In the morning of Thursday I took 1 Kaletra. In the evening of Thursday I realized I misread the label and took 2 Kaletra though I forgot to take the Truvada because I was used to taking the other medicine in the morning (I’ve also not been thinking straight and been very stressed, I made a mistake). On Friday morning I came to my senses and took 2 Kaletra and 1 Truvada and set a plan so I wouldn’t mess it up and that’s the regiment I will stick too.
Without the patient assistance program I probably wouldn't be SVR - when my insurance refused to let me extend, they coudln't have made it easier and didn't even make me feel bad about needing them to help.
I am also on Copaxone - can I suggest that you talk with them again at Shared Solutions and ask what criteria they use for patient assistance? They fund for people without insurance or underinsured through NORD - national organization of rare disease. Unfortunately it sometimes takes more than one phone call to connect with the right people at SS to get help.
If you can't work it out with SS you might talk to your neurologist about other options.
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