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Post Info TOPIC: Memory Loss


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RE: Memory Loss
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that's a big A-FIRM from me tigster! the trade off is well worth it. it keeps things simpler, eh?? thom and huey, I hear you. Math is crazy hard, even with the calculator. lol  - Have a simple kind of day!!

 



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HCV 1A 1980. Dual tx 2003 -UND at wk 11-discontinued due to severe depression

Started Triple 4/16/13 for 24 weeks

UND wk 4,6,8,12,17 & 24

E.O.T. 9/29/13

EOT + 12 weeks=SVR, and EOT +26 weeks=Cured!

Tig


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8 months post treatment and I've definitely noticed a change in my memory. I keep hoping I'll notice a return to days past, but so far all I remember is what it used to be like! I can relate Kellie, my ability to remember song lyrics, even the names of the songs, is sadly lacking. I used to fancy my ability to recall at moments notice,, quick witted I liked to say, but now I find myself searching for responses. I've tried some of the online brain games and exercises, but that ends up frustrating me, so I don't find any desire to beat myself up over it. That's when I tell myself that I have to accept the fact that some changes are evident and not stress over it quite as much as I was. I have to remind myself that I've achieved the coveted SVR and if doing so cost me my quick wit response time, so be it. I'll just keep my phone with me and thank God for Google! 

Tig



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Tig

67yo GT1A - 5 Mil - A2/F3 - (1996) Intron A - Non Responder, (2013) Peg/Riba/Vic SOT:05/23/13 EOT:12/04/13 SVR 9+ years!

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numbers, math i can do it but it is relay hard.



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  HCV Genotype 3a , now Psot-Tx was on S/riba. First VL was 5.8 mil on 7-5-13 then "und" at 3.8 weeks. 06/13/14 still und. off meds 3 days back on 7/29 Last pill 08/10/14 SVR+4

 



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My memory has always been marginal to begin with. I hope that I don't encounter any impairment of brain cells in this regard.

 

confuse

 

 



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62 years old. Probably became HCV positive in the early 70's. genotype 1. Started treatment August 15 2014 w/ pegasys, ribavarin, sovaldi.

Finished treatment on November 7th. Had no detectable viral load at week 6. Waiting until the fat lady sings.



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Yeppers, it's almost 11 months after tx eot and yes, i am having issues with my memory now. seems i can't remember words to songs i've known for decades and i'm quite the car singer and now i can't remember how they go, which i find disturbing. it may not seem like a big deal, but it is to me. i'm taking all my vitamins and eating right, exercising daily. hmmmm. wondering how much of this is left over pegasys. Good news is my thyroid tested aok this week. My t3,t4 and tsh are all very lovely. thanks for letting me chime in on this. have a nice weekend all!

 



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HCV 1A 1980. Dual tx 2003 -UND at wk 11-discontinued due to severe depression

Started Triple 4/16/13 for 24 weeks

UND wk 4,6,8,12,17 & 24

E.O.T. 9/29/13

EOT + 12 weeks=SVR, and EOT +26 weeks=Cured!



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I can't quite remember where I left my memory?   confuse  Yes it is sometimes embarrassing at work.  Major changes occurring with workload, and it is difficult to keep up.  What's that about an old dog and new tricks?  aww   I suppose stress, whether I will have insurance, and whether it will cover the next round of tx may contribute?  Hope all have a good weekend.



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1b  Int/Riba relapse @ 48 weeks.  Stop tx Peg Int/Riba 12 weeks ill. Relapse S/O 6/23/14 :(   Started Harvoni 11/12/14  EOT 4/28/15.  EOT+4 UND :)  SVR! 8/4/15  :)     Thankful for every morning.



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Wow...the toothpaste/prep H was a bomb...I don't know when I laughed so hard ...just what I needed...My hair is falling out like crazy...just call me PATCHES LOL...My memory is shot. I'm writing a personal statement for admission into grad school, and I'll know the word that I want to write, but it will escape me....And for the second time since I've been on treatment, I walked out of the house without putting on a hat, headband or other gear...PATCHES walked down the street about 6 blocks and then realized that my patchy hair was out in the open for the world to see.  Was I going to run back home and fix the situation, or keep moving and pray that I didn't run into anyone that I knew...that would certainly be a miracle, since I know so many people in the neighborhood and the storekeepers. Of course I saw people and tried to disappear...like I was invisible woman LOL. Anyhoo...I made it back home...me and my patches....



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DJ...dx 2005...geno 4c...twice interferon/riba failure....completed 24 weeks Sovaldi & Riba on 10/18/14....SOT VL 600,000 after 16 days VL <43. Day 45 <43 again. Day 59...8 weeks UNDETECTED.

Happy and grateful to God for new life....



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My heart goes out to everyone who is going through the memory and mental function pxs.  I've had to stop driving and other stuff.  My rx with interferon and ribaviran was in 2009.  I already had some trouble before that.  It is frustrating especially when I can't get answers from the medical community.  My doc referred me to an alzhiemers study, but they didn't accept me because I abused opiates in my youth.  So why aren't there studies about that stuff.  Where is the information?  Love you guys.  I've adjusted to this thing and have learned how to enjoy life anyway.  I have some trouble using his sight, but I'm getting better at it.



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alisa fillmore


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Thanks guys for all the extra insight you've offered on memory loss. 

It's good to hear all the different perspectives and experiences.   Caroline



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My husband had genotype 1a, 46yo, started triple therapy (peg/rib/vic) 23rd July 2012, VL prior to treatment 14 million, UNDET 12, 24 weeks, EOT 24th June 2013, EOT +1.5 weeks UNDET, EOT +12 weeks & EOT +27 weeks UNDET; SVR January 2014



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has anyone tried the online brain games to boost their memory?

also there are many books out there discussing this topic .

dan hurley, the science journalist recently published "smarter:the new science of building brain power" and it's getting decent reviews.

he will be discussing/reading passages of his book at an upcoming event in northern n.j. i believe it's this saturday afternoon.

finally i'm going to take the online iq test and see if there's been a change in my memory power.

sandy,ucbgal



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Hi Carolinemy memory is really horrible lately and I'm not even on treatment yet.  Fatigue also.  As I'm aging it appears these HCV symptoms are increasing.  I find lists are working for me.  Never used to keep them much before.

 

Good luck!



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Marcy

Long-term HCV, GT1a, IL28B C/T, T/G;  VL 2 mil.  Merck C-Edge Clinical trial  EOT 10/01/14. +24= UND



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hi caroline

the memory issues seem to be related to the tx for me.

it's getting better now. optimal nutrition and physical and mental exercises have made the biggest difference.

its like rebuilding a city after a huge earthquake. using better materials to form the foundation.

getting to know my body post tx.



__________________

HCV 1A 1980. Dual tx 2003 -UND at wk 11-discontinued due to severe depression

Started Triple 4/16/13 for 24 weeks

UND wk 4,6,8,12,17 & 24

E.O.T. 9/29/13

EOT + 12 weeks=SVR, and EOT +26 weeks=Cured!



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thank you for pouring out your heart to us -

my experience with tx was pretty bad. i started using a methyl folate supplement during week 8 for the severe depression and emotional problems created by the chemical imbalance caused by the interferon.

i have some genetic issues that made me more susceptible to it. not to say that you do though.

i did some posting on what happened to me if you want to take a look. let me know if you have any questions. i'm here to help.

i'm so sorry for all the troubles this tx has caused for you.

i hope life gets better for you soon.



__________________

HCV 1A 1980. Dual tx 2003 -UND at wk 11-discontinued due to severe depression

Started Triple 4/16/13 for 24 weeks

UND wk 4,6,8,12,17 & 24

E.O.T. 9/29/13

EOT + 12 weeks=SVR, and EOT +26 weeks=Cured!



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Jime,

Oh no not the weather too......wink. We, MJ and myself are considering moving to Long Island, her being a native from Belmore.  I always say I would go back to Antarctica in a heart beat, but I was there 34 years ago. And besides being older, it would not be the the same. There, at S.Pole we made our own roads, no traffic lights, no worries of millions of people going in different directions.   



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Timothy

GT3a Baseline VL 514,000, Week 4 VL 130, Week 12 UND and have been UND ever since.  

Completed 48 week of Pegasys & Copegus. EOT VL UND.   Achieved SVR after 48 weeks of treatment.                                                   



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Thanks everybody,

And I see that this problem is not rare, scarier than anything I been faced with before.  I stay away from this sight, not because I don't appreciate all the wisdom, strength and input.

This will be short, not because I don't wish to speak. There is so much going on that I would want to remove anyone's hope, but as I write this I am in my local library.... I made here with my laptopsmile.

In truth the last two days I have, and better still those that were my friends before starting treatment, say I look so much better than even a week ago.  I actually do feel better, was able to get out do a little yard work this morning, racked up the front lawn.biggrin

I too have started taking a low dose of sequel 100 mg, then I too have 50 mg tabs if I feel myself going over the edge.confuse

After reading about others experiencing the same thing..... I believe age has less to with it than I would like to claim.hmm

I truly am grateful for those who have not had to suffer this delima, and I have to catch myself from discounting those who have had no side effects, which troubles me too because that means I don't believe some things I read cynic.gif. Forgive me, for being so distrusting.

 

 

 



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Timothy

GT3a Baseline VL 514,000, Week 4 VL 130, Week 12 UND and have been UND ever since.  

Completed 48 week of Pegasys & Copegus. EOT VL UND.   Achieved SVR after 48 weeks of treatment.                                                   



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i'm almost 1 month eot of tx for 6mo. about 2 months into tx i started noticing memory loss to my dismay. coming from the educational field you always need to be sharp & one step ahead. thus it really took me by surprise especially when friends and ex started noticing it.

i found that the more lists i made ,fish oil, b12 and getting my hemoglobin up to be a huge improvement. right now my hemo is at 9  and memory loss seems to be nonexistant. thus i'm chalking it up to low cbcs caused by the meds & insomnia due to riboviron.

sandy,ucbgal



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Since I am on a clinical trial without interferon, with ribavirin, I had felt there would be few side effects.  In fact the trial data released said there were few side effects. 

I just found my riding lawn mower key --on my desk???  I have trouble remembering bills.  And I forget to file things where I can find them.  It has gotten worse the last 5 weeks.  Most only did 12 weeks on this trial, so maybe it was not so difficult for them.  Right side pain and stomach pain have become a daily event.  Just have a week to go and I am hoping that  pain and memory get better when I am off the meds.  

I live alone in a rural area so I really need to depend on myself.  Although my memory loss is not great, it is very frustrating.  And my lack of energy is really a challenge.  If I don't do it, then no one does.  And it is so annoying to drive 8 miles into town and not remember why I went there. 

I feel sure it will be better once I am off the meds.  Guess the meds have not affected my optimism.

Jim--  It was 70 here on Saturday and 14 here last night.  I plan to return to my supplements as soon as I am through with treatment.  At my age, I need all the help I can get.  If my virus remains UND, then it is time to start helping the liver to heal--at least that is my belief.

SuziQ 



-- Edited by suziq on Monday 6th of January 2014 02:54:06 PM



-- Edited by suziq on Monday 6th of January 2014 03:02:48 PM

__________________

Geno 1A  Age 82 Treatment naive Cirrhotic Told I had liver disease in 1966. Diagnosed as Hep C 1999.Started Merck clinical trial with Riba on 9/9/2013 Week 1 and 2 <25  Weeks 4, 8, 12,16,18 UND.  EOT Jan 14,2014  EOT +12 UND   JULY 1 2014 EOT+24= SVR



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I must admit I do put a lot of my memory loss and poor concentration down to my age, at 64, although Malcolm is living proof that it`s not necessarily so!   Although actually it was just as bad, if not worse, before my tx, and at least I`m able to do a lot more over the course of a day now than I could before tx, so all in all I can`t really complain, although I still do!  Very happy to have achieved SVR though.

Yes, Jim, let`s blame the weather!  wink

 



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Jill 

(71 yo, lives in UK)

Was Gen 3a, 

24wks Peg Ifn/Riba, Sep 2010 - Mch 2011

UND @ Wk.4, UND @ EOT, 

SVR Nov 2011 --> Still UND @ EOT + 4 yrs.

 

 



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I had something to say about this memory loss topic but I forgot what my point was...:(

Seriously, we all can't be experiencing it because of age. There is definitely something going on with me too. Thought process is a little off for sure. I haven't been taking any supplements for about a year now. Does anybody see any improvement with them? ( Fish oil, multi vit., e, d, b, folic acid. Any others that people are using that seem to help? )

Almost 60 degrees here in NJ today. Going down to 5 tomorrow. Weather patterns are insane, can I blame them for my lack of mental clarity?

Have a great day everybody.

FYI, I was only on Interferon for 2 months. Riba, a total of 8 months over a 10 month period. And I was on 7977 ( Sofosbuvir ) for 6 months w/ the riba.



-- Edited by JIme on Monday 6th of January 2014 02:31:12 PM

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jim

GT1a, St2 Lv2 last biopsy 2002, VL  11.4m,  start triple tx 9/30/11

VL 470 @4wks.....VL 22,000 @8wks  stopped tx

Round 2-  Started 3/16/12   PSI-7977, BMS-790052, Riba Undetectable day 14

Did 24 weeks Still UND 12 weeks post tx, SVR24!!!!!!! 2/14/13

 

 

 

 

 



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JoAnneh wrote:

All and all I feel great! I am Hep C free
And feel better than when I started tx.
Bill, hope to see you Hep C Free soon.
Xxoo


 I also have memory loss, but i am 58 also. Gets aggravating at times. But i too went through a grueling 48 weeks and am now HepC free..So i will take it..



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58 yo..Relapsed in 99 and again in 2004. Started triple therapy with Victrelis July 22,2012.  genotype 1a. week 8,12,16,24 VL Undetectable..E.O.T -- 6-22-2013,,,EOT + 24., UND. 

SVR !!!

 

~Bob~



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I enjoy this forum! I am 8 months post tx.
Energy level is good:)
Memory not as sharp as I would like it.
I have trouble with spelling words I always
Knew how to spell!
I use to be in mid sentence and forget
my point of conversation. That was scary
But has greatly improved.
I can still cut a great haircut:) and do about
Anything else. I also have some joint issues.
I was on a brutal 48 weeks tx w/Invicek.
I hope everyone on the forum memory will continue
To improve as it can be scary!
Malcolm, you are so BRILLITANT you wouldn't
Notice a little memory loss!
All and all I feel great! I am Hep C free
And feel better than when I started tx.
Bill, hope to see you Hep C Free soon.
Xxoo



-- Edited by JoAnneh on Monday 6th of January 2014 01:07:29 PM

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JoAnne

Genotype 1a, Triple therapy w/Invicek started May 19, 2012

DET 4 wk. UND 2,6,12,24 48 treatment. Achieved SVR 2013!



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Hello Tim,

For actually going through treatment and completing it successfully, i applaud you!

My heart goes out to you,terribly sorry for your loss and i pray that this is the eve of your great comeback. This journey we are on is NOT easy. All that you are feeling is valid and real. Am sure it takes time to shake all this treatment madness off. It seems life has handed you some tough situations lately. But hang in there. Going through this treatment alone, you come away a warrior. For smacking the life out of this pesky Hep C, you are a victor! That counts for something. Everything this virus threatened to take from you, you got it back. Life!! The real you was not smoked up with the virus. Your old self is still in you. Only that its not old anymore. Its a new you! No one can take our spirit,our zest for life. We have to willingly give it away ourselves. Take heart, be strong and hold on.Your dawn is near. You can find encouragement and support from all the people here.

The very best wishes.



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Diagnosis:2012. Tests Results: GenoType 1/ Viral Load 51,000/ Liver Normal.

Rx started: 10.06.2013 Copegus (Ribavirin) 200mg + Peg Interferon 180mcg . Down to

Peg Interferon 135mcg 3 months later. No Virus Detected (NVD) result to date. Rx duration: 48wks.



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newmex wrote:

I am still on treatment but memory and focus is getting pretty sketchy. Cant count the times I have gone into a room to do some thing and forget what I went for, or have my meds in my hand and when I get water to wash them down they are already gone. So did I take them? throw them away? put them back in bottle? Try to keep them straight in pill container, but some times that's just too long to focus, from popping the container to swallowing, its amazing how many ways there are to get side tracked. Looked for my glass of water I just poured the other day for ten minutes, until my wife noticed I had the glass in my hand as I looked for it. She thinks its all pretty funny so far, but im gonna wipe that smile off her face. Next time she has a mouth full of tooth paste, im gonna tell her "Oh crap, don't use that tube, I thought that was Preparation H last night," haha that will get her attention.


I can totally relate to this. It was like someone flicked the light switch off. I was only on Victrelis for 30 days and a lot of it cleared up pretty fa

That being said, my cognitive skills have noticably slowed down. I havent gone back to work yet; kind of scared. I feel stupid at times.

 



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Geno 1A, since 1981. SOT 1/2013   TX stopped 11/2013 in week 45/48 due to Myositis & Interstitial Lung Disease. Completed 94% of Peg-Inter dbl TX, UND since week 4.  SVR 4/2014!  Still SVR after 4+ yrs!

"Day by day, step by step, breath by breath"



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It seems that on and after treatment our world becomes very small. Tim, you are not alone here. You are surrounded by kindness, compassion, love and understanding.



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Geno 1A, since 1981. SOT 1/2013   TX stopped 11/2013 in week 45/48 due to Myositis & Interstitial Lung Disease. Completed 94% of Peg-Inter dbl TX, UND since week 4.  SVR 4/2014!  Still SVR after 4+ yrs!

"Day by day, step by step, breath by breath"



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Memory loss?

Absolutely and pretty scarey. I have real short term memory and my biggest fear is the drug companies won't admit it and use age, family hist as a scape goat

My last TX lasted 74 weeks ( yup 74 not a typo ) I just coming up on a year post TX and as you know Virus came back so I've got to do something again soon. So sofosbuvir will be better but with what? No Interferon or riba for me, no use in touching them again in my case or by my choice. I am waiting to see what happens wit Intf free TX

  My wife see's it, i know it and don't know if its going to stop or get worse. I guess brain fog mem loss is better than liver failure X plant etc so I'm just sitting.

Bill S



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Bills

Harvoni started 12-12-14 for 24 wks PrevTX Geno 1 stage 3 cirrhosis - non resp Int/ ribv. Started Trial  in Aug 2011 -July 2012 into Incivek relapsed  Feb 2013 Had 72 weeks on interferon & Riba.

Tig


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Hey John,

Not to worry Friend, there certainly was no offense taken. Often times it's humor that lifts a saddened spirit and brings a smile to the face of all affected and concerned. For me you did both and I encourage you to keep lifting our spirits! Be well and I hope you all keep a smile in your heart and on your face!

 



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Tig

67yo GT1A - 5 Mil - A2/F3 - (1996) Intron A - Non Responder, (2013) Peg/Riba/Vic SOT:05/23/13 EOT:12/04/13 SVR 9+ years!

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rotting to the core wrote:

This is such a personal topic. I finished a 48 week treatment plan, easy one I know.....dual therapy. ( peg and copeg ). But I too find the mental side effects are so troubling I have begun to wonder whether or not I destroyed any hope of any quality of life. I spent two days in the cardiac unit, New Years Eve and New Years day. Just to find out my physical side is recouping great, but my brain chemistry is wack. I spoke to my PCP yesterday and she too is unclear if I will return to normal.

At the moment there is no way I can even go to the store by myself without fear of not finding what I was sent for or  my way home. Sounds ridicules but that is now my life... for the moment.

I hope I am just being stupid, but I am understanding why my step son took his life on Nov. 4th. 4 days after I completed treatment He had been treating with topomax for 8 weeks. But he said he felt as if brain was melting and could not be a burden  to those who love him.

I was a Quality Engineer at Northrop Grumman for gods sakes and now even basic algebra sends over the edge. Now I can't trust myself to drive.

So I am understanding I am a rare case.         

I have spoken to two Psychs with Phd's and they questioned the wisdom of my treating in the first place at my age. I too wonder why my Dr.s pushed for me to clear the virus if the possibility of such an outcome was possible. I hate to sound negative, and yet I miss being the person I once was, always with the ability to speak with others and having hope and given others hope.

Now I am afraid I have too become a burden to those I love and who love me.

Please pray that this too shall end. 



-- Edited by rotting to the core on Saturday 4th of January 2014 09:08:53 PM



-- Edited by rotting to the core on Saturday 4th of January 2014 09:10:56 PM



-- Edited by rotting to the core on Saturday 4th of January 2014 09:12:24 PM



-- Edited by rotting to the core on Saturday 4th of January 2014 09:13:23 PM


Timothy,

So sorry to hear about your step son and sorry,didnt mean to make light of a subject so personal to you. Some days I cant remember something I did 2 minutes ago, next day can remember leaving my glasses somewhere a week ago. Just kinda comes and goes. Was worse last time I was on and  treatment, and this time am taking anti depressants and they help me all the way around. Lessens my anxiety, raises my mood, which in turn seems to lessen my side effects. All I can do now is try to finish the treatment, and I try to use some humor sometimes, and I hope I don't offend any one. Just wanted to let you know, wasn't my intent to bring up any hurtful feelings. Hope every thing gets better with you, if there is ever any thing I can do for you, let me know. Some times, there is nothing we can do, and some times a little time is all it needs. Hang in there, if you ever need to talk, send me a line,     



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John


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Timothy, Tig said it well - we are here for you.  If you have to open up and get some encouragement you have come to the right place where people care.

Thanks also to everyone for their feedback.  I did think that the 48 weeks of treatment is so gruelling that it's going to take another 48 weeks to get over it.  My hubby had also worked right through the 48 weeks and plodded the whole time - I think he's exhausted still and I guess this wouldn't be great for your memory.  So I'm believing time will be the healer.  Thanks again guys.



__________________

My husband had genotype 1a, 46yo, started triple therapy (peg/rib/vic) 23rd July 2012, VL prior to treatment 14 million, UNDET 12, 24 weeks, EOT 24th June 2013, EOT +1.5 weeks UNDET, EOT +12 weeks & EOT +27 weeks UNDET; SVR January 2014

Tig


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Hi Timothy,

I'm sorry Brother for all the memory problems. I'm certain that must be quite a concern of yours and rightly so. What a tragedy to have lost your step son to suicide, I'm very sorry for his loss and your family. That's an awfully rough thing for any family to handle and I hope you all find peace in your hearts and minds soon.

What happened that placed you in the Cardiac ICU, if I may ask? You've had a mighty tough period in your life lately and I'm praying for things to get back to the normal you're searching so hard to find. 

When did you finish treatment? I've been done with triple therapy for 4 weeks and the memory is slowly clearing up, but there are still moments when like you I find myself wondering what I'm doing and why am I there. Sometimes with something in my hand and wondering what I'm holding onto that for. But it's coming around and I hope things improve for you soon.

Please trust that things will turn in your favor. You seem very eager to have the life you had and that's the right attitude to have. Don't ever think that you're a burden to anyone. You're obviously a very bright individual with the desire to succeed and if I may say, you've likely got a family that loves you very much and would agree with me that you are not a burden, but a valuable part of their lives. Keep the door of communication open with them and your health care doctors. Let them know how you're feeling now and talk about it. Okay? Hang in there buddy! We care for you here, that goes without saying!

Tig



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Tig

67yo GT1A - 5 Mil - A2/F3 - (1996) Intron A - Non Responder, (2013) Peg/Riba/Vic SOT:05/23/13 EOT:12/04/13 SVR 9+ years!

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This is such a personal topic. I finished a 48 week treatment plan, easy one I know.....dual therapy. ( peg and copeg ). But I too find the mental side effects are so troubling I have begun to wonder whether or not I destroyed any hope of any quality of life. I spent two days in the cardiac unit, New Years Eve and New Years day. Just to find out my physical side is recouping great, but my brain chemistry is wack. I spoke to my PCP yesterday and she too is unclear if I will return to normal.

At the moment there is no way I can even go to the store by myself without fear of not finding what I was sent for or  my way home. Sounds ridicules but that is now my life... for the moment.

I hope I am just being stupid, but I am understanding why my step son took his life on Nov. 4th. 4 days after I completed treatment He had been treating with topomax for 8 weeks. But he said he felt as if brain was melting and could not be a burden  to those who love him.

I was a Quality Engineer at Northrop Grumman for gods sakes and now even basic algebra sends over the edge. Now I can't trust myself to drive.

So I am understanding I am a rare case.         

I have spoken to two Psychs with Phd's and they questioned the wisdom of my treating in the first place at my age. I too wonder why my Dr.s pushed for me to clear the virus if the possibility of such an outcome was possible. I hate to sound negative, and yet I miss being the person I once was, always with the ability to speak with others and having hope and given others hope.

Now I am afraid I have too become a burden to those I love and who love me.

Please pray that this too shall end. 



-- Edited by rotting to the core on Saturday 4th of January 2014 09:08:53 PM



-- Edited by rotting to the core on Saturday 4th of January 2014 09:10:56 PM



-- Edited by rotting to the core on Saturday 4th of January 2014 09:12:24 PM



-- Edited by rotting to the core on Saturday 4th of January 2014 09:13:23 PM

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Timothy

GT3a Baseline VL 514,000, Week 4 VL 130, Week 12 UND and have been UND ever since.  

Completed 48 week of Pegasys & Copegus. EOT VL UND.   Achieved SVR after 48 weeks of treatment.                                                   

Tig


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Hi Caroline,

I also had memory problems through Tx. There were times it was unnerving, because I would lose entire days. Like Bill, I wrote myself notes and relied on my wife for direction and reminders at times. I even went so far as to send myself emails and not delete them for a period of time! It has improved greatly but I do think it's going to be another one of those SFX that has to run itself out and who knows how long that might be. Tell him to be positive that it will correct itself eventually and buy an industrial pack of Post-It note pads! Good luck!

Tig



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Tig

67yo GT1A - 5 Mil - A2/F3 - (1996) Intron A - Non Responder, (2013) Peg/Riba/Vic SOT:05/23/13 EOT:12/04/13 SVR 9+ years!

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I am still on treatment but memory and focus is getting pretty sketchy. Cant count the times I have gone into a room to do some thing and forget what I went for, or have my meds in my hand and when I get water to wash them down they are already gone. So did I take them? throw them away? put them back in bottle? Try to keep them straight in pill container, but some times that's just too long to focus, from popping the container to swallowing, its amazing how many ways there are to get side tracked. Looked for my glass of water I just poured the other day for ten minutes, until my wife noticed I had the glass in my hand as I looked for it. She thinks its all pretty funny so far, but im gonna wipe that smile off her face. Next time she has a mouth full of tooth paste, im gonna tell her "Oh crap, don't use that tube, I thought that was Preparation H last night," haha that will get her attention.



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John


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I can't remember if I used to remember more than I remember now.  Maybe I remember less. Oh, what a mess.

I did find my cell phone yesterday after having "misplaced" it for 10 days. 

Couldn't remember what I did with it.



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1a, 35+ years; liver cancer survivor 7-2012 surgery; triple therapy 12-2012 (Interferon, riba, victrelis) - end 48-week treatment Nov. 29, 2013 - post tx 24 weeks undetected - SVR.



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I experienced memory loss and in fact don't remember a lot about treatment, was worried about Altimerz as mother had died with it, use to right notes to remember and then a note to remember where I put the note ! today after some council ling memory back to normal seems treatment fear of not clearing virus, divorce, financial fear, etc was main factor, I agree with Malani and it will be over come like in my case, time and healthy eating and getting back into physical shape has improved my memory, hope this helps

Bill emma and raven



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Geno type 1  rib and peg September 2012 , 5 weeks tripple and viral down to < 15 und april Aug 25 finished stay at peg 3 rib and eprex + blood transfussion finished treatment Aug 25 2013



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Hi Caroline,

We all worry so much about post-Rx issues that we tend to focus on what's wrong with us.  The 48 weekers go through an extreme length of anxiety-producing, physically demanding punishment. It takes a long time to get over, and some symptoms are worrying. Time will heal most problems so lets hope it's only temporary.  Personally I did not have any problems with memory loss. Best of luck to you both. Cheers.



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Geno 1b, IL28B CT,  x3 prior relapser,  ex-cirrhotic, 75 yo, did 48 weeks with Victrelis/Peg./Riba.  VL 1.28m at start, UNDET. at 8 ,12 ,16 ,24 ,30  and 48 weeks.  EOT 15 Feb 2013 , UNDET. at EOT + 28 weeks. SVR!  Still Undet. at EOT +5 years

Malcolm



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Hi everyone, I just have a question - my husband was on triple therapy with Victrelis and is 6 months post now.  He is getting worried about his memory not being what it used to be.  I can tell he is clearly concerned.  We are seeing the specialist in early February so will take it up with her then, but wondered if any others have experienced this and did it improve and is it in fact a side effect from the meds?  Any feedback will be appreciated.  Caroline.



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My husband had genotype 1a, 46yo, started triple therapy (peg/rib/vic) 23rd July 2012, VL prior to treatment 14 million, UNDET 12, 24 weeks, EOT 24th June 2013, EOT +1.5 weeks UNDET, EOT +12 weeks & EOT +27 weeks UNDET; SVR January 2014

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