HPV - Cervicitis And A Relapse Of EBV
Feb 25, 2015
Just found out I have hpv...cervicitis...and just had a relapse of ebv. Been 3 months of hell what could be causing my body to all of a sudden be reactivating viruses? Hpv is new but I'm sure I was exposed 10 years ago and I got ebv when I was 15. My blood work was mostly normal I have high ALT (SGPT) Levels at 40
I have high platelets 534
A high count for EBV which is mono. ENT wasn't concerned about anything else besides the mono. But that it's not active anymore. Still have awful symptoms my throat hurts feeling sharp pains in my abdomen. I have a low risk strain of hpv everything came back normal with my biopsy and colposcopy except that i have an inflamed cervix. my symptoms won't stop! !! Feels like even more is going on since it just seems like my body is pulsating diseases through my veins. It's awful. It hurts and it's uncomfortable.
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Has anybody ever had a VN relapse as it seems i have after a year is it possible or have i just picked up another virus?
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I have been using oxycodone 30's for 2 1/2 years. The dose I was using was up to 9 a day I finally reached a breaking point and decided to get clean I started out with suboxone 8/2 3x a day then I stepped down to gabapentin 400mg 3x a day, clonidine 0.1 mg a day and baclofen 20mg 3x a day. I have been on these meds for 2 months and as much as I don't like it I relapsed 3 weeks ago now I went back on my meds but I'm still getting detox symptoms when I'm off of them. I get headaches runny nose over heating aches and pains but not as bad as if I was coming start off Roxie's. now my question is how long does it take for me to go back to normal or even if ,
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I have just found out that my father who has finished his 12 weeks treatment (Sofosbuvir + Daclatasvir) about a month ago has had the virus relapse. It was undetectable in all previous tests, but the recent test showed it. I was wondering if anyone can point me to the right sources, perhaps specialists and experts we could contact as in Poland (where we live) there doesn't seem to be enough information. We are not sure what to do next... He has had this horrible virus for more than 10 years, we were so happy to have cured it! But refuse to lose hope and want to keep fighting!
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I recovered from stg 3 Sarc (in lungs, lymph, joints, sinus) 13yrs ago, after 5yrs of illness and 2yrs of steroids.
I now have Erythema Nodosum (sp?) - red painful bumps on lower legs.
Research suggests that 'EN' is associated with a specific version of Sarc, Lofgren syndrome, which is usually resolves quickly and without treatment.
I'm scared to go to the Dr, as I don't want to face the tension & round of tests to exclude a Sarc relapse. It's not something I want to go through again...
I wonder if it's very likely for a relapse to come with a whole new presentation of the Sarc? Or is it unlikely to be sarc, as I never had EN the last time?
Does anyone have any experience or advice which may help me decide what to do?
Best wishes to all who are currently battling with their Sarc, I truly understand your pain and your exhaustion. I was not expected to recover last time - but I did.
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About 4 years or so ago I had a relapse in the left upper leg and thigh. Recently I have been under quite a bit of stress... since this.morning I woke up with more severe pain in left that is now going down my whole leg into my little toe and the toe next to it... I have been taking 7.5mg vicodin twice daily since the last relapse that helped me out alot to function.... I was transferred to a pain specialist who said that is was not my ms cause this problem ( I have had 3 docs) tell me it was due to my ms relapse previously now I am scared and am lost as to what to do. As the day has progressed on I can barely even walk or put weight on my left leg?
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Does anyone know what the possibility of relapse is if you are und at 4 weeks post treatment?
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I was diagnosed with PMR July 2012, with ESR 62, put on 15 mg Pred, 11 days passed before I was free of pain. 1 month later Doc reduced me to 10 mg. ESR than 10. Then later to 7.5mg and finally to 2mg by Oct 2013. Relapse started Dec 2013. Doc started to increase Pred. to 6mg.but pain persisted so Doc increased me in stages to 15 mg, (pain persisted) so Doc said go to 20mg or even 30 mg if pain still persists. Pain is persisting. Meanwhile, a full blood test was done and all came back normal, ESR now 12. Just to complicate matters, there was a moment 12 days ago when for 4 days I mixed up my tabs and was taking only 4 x 1mg, when I should have been taking 4 x 5mg. I am now on 3rd.day at 30mg. but pain still persists.Does anyone have any comments please?
The only other query on my mind is the fact that I was given a Pneumonia jab 3 weeks ago, could this play a part.?
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I'm looking for advice. My 60 year old father (who has had HCV for more than 10 years; previously treated with Interferon but bad side effects) finished his 12 week Sofosbuvir+Daclatasvir (considered same as Harvoni) treatment a month ago. Already first tests after 2 weeks showed virus was Undetected, but yesterday he received his most recent results and he has a relapse of the virus. He is genotype 1, fibroscan result 4 (close to final stage). He is based in Poland and I'm not sure if our doctors are fully informed of the new generation medications and HCV itself.
Is anyone able to give us any advice? We are pretty desperate and my dad is just so depressed as he thought he finally got rid of the virus (he got infected while on an operation in a public hospital) and now it is back...
Are there any specialists that you are aware of I could possibly get in contact with?
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Does anyone here relapse after harvoni treatment?
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