Anyone here used HIV/AIDS treatment for CFS?

Messages
38
Really happy for you! I am still trying to decide if I should try this or not due to potential bad reactions/worsened fatigue. Can I ask how severe you were and was your primary symptom fatigue?

I was never bed ridden. I would say I was at a 4 at my lowest. I never lost my job but I was becoming desperate and had to take vyvanse prescription amphetamine to just to navigate the world at one point. I have great vision but horrible eye issues. Bright light would drive me into the house like a vampire. Intestinal issues. I spent all my free time in bed. I don’t know what my CFS was. I had elevated EBV and CMV viral loads etc. I also thought this was PFS (post finasteride syndrome) after taking finasteride in my late 20s and early 30s. There is literally a whole other message board propeciahelp where PFS sufferers (which mimickes cfs) got better on truvada. I don’t know. I had classic CFS but classic CFS is very similar to classic PFS. I had one of the best CFS specialists in the world tell me I had CFS and I’ve had a really good endo tell me I had PFS.

All I can say is that in my case 4 things have lead to a huge change rapidly.

1.) diet. I do keto 50% of the year off and on. I eat pretty healthy. Rarely sugar and no processed foods. I cut alcohol out except on vacations and special occasions. (I was a drunk over the holidays on vaca). I eat/drink large amounts of probiotics. Keto started my journey.

2.) I started exercising religiously when this got bad. Obviously for some here excersise makes you worse but I treat exercise as a job I’m required to do at least 5-6x a week. I’m up every day before work or at lunch and I run or I’m in a bike or elípticle or weights at least 45m a day). I started doing this at my lowest point and probably only did 30m a day but it helped greatly with the fog. It made me worse at first but changed after 3 months or so. I looked at my tough grandfather who worked till he was 80 on a farm and made it through the depression and I decided he would tough this out. I couldn’t imagine him laying in bed even for the flu. Against the advice of my doctors (I had Dr Sundance Levine in NYC who is a specialist on this), I pushed myself every day. If this is an immune disorder I wanted my immune system healthy and exercise is a great way to do this. Again, I know some people are practically bed ridden so this is not an option but for me, no one was going to tell me resting in bed for years is going to fix this.

3. ) possibly truvada and antivirals. Can’t prove this helped but I wrote about this enough that it was significant to me in 2016. Literally in 3 or 4 months of taking truvada it’s like a cloud had lifted. This is about the time I also returned to the gym. This was also the time I changed my diet so it could be 100% diet (I don’t remember the order now). In this time something significant changed. I started truvada maybe 8 months before visiting Dr Levine. By the time I visited Dr Levine I had moved from a 3/4 to a 6. Levine started me on other antivirals and I progressively got better. Was it my diet? Was it truvada? Was it the additional anti virals? Who knows.

4.) when I got to about 85% about 11 months ago I decided to do TRT. Obviously this will not help women but any kind of HRT could help depending on age. I hit rock bottom at 36 and I’m 44 now. By this point I was active again and at the gym daily but still suffered lack of energy and foggyness. My hormones were not awful but my T was about 350-380. Technically not low enough for most Dr’s to prescribe testosterone but there are 20 online clinics that will which is 100% legal. If you are under 410 you can get prescribed testosterone. I decided that additional T would improve my immune system and made the jump. I just started maybe a year ago January 2018 so it’s something new but has turned me 18 again. It shot me from an 8-10 in 6 months. I don’t think everyone should mess with your hormones. It’s a tough decision but after dealing with this for 10 years I’d inject bleach if it made me better.

Obviosly this is my own journey and we are all different. I don’t think CFS is one single disease but many different diseases with the same symptoms.

I told someone I was 95% of where I was when this all started and they asked me what was the 5% I’m missing and I suddenly realized ... I got old during this process. The 5% I’ve lost is just me naturally being 44. I’ve seen people that have been active on here for 6+ years. If you have this for 10 years You are never going to feel like you did before this started.
 
Messages
38
Really happy for you! I am still trying to decide if I should try this or not due to potential bad reactions/worsened fatigue. Can I ask how severe you were and was your primary symptom fatigue?

FYI If you do try antivirals like truvada, there is a week of adjustment. I’m not sure why but it makes you feel rough the first week. This goes away quickly. I now can’t tell I’m on it and my multivitamin causes more issues than truvada.
 
Messages
36
I was never bed ridden. I would say I was at a 4 at my lowest. I never lost my job but I was becoming desperate and had to take vyvanse prescription amphetamine to just to navigate the world at one point. I have great vision but horrible eye issues. Bright light would drive me into the house like a vampire. Intestinal issues. I spent all my free time in bed. I don’t know what my CFS was. I had elevated EBV and CMV viral loads etc. I also thought this was PFS (post finasteride syndrome) after taking finasteride in my late 20s and early 30s. There is literally a whole other message board propeciahelp where PFS sufferers (which mimickes cfs) got better on truvada. I don’t know. I had classic CFS but classic CFS is very similar to classic PFS. I had one of the best CFS specialists in the world tell me I had CFS and I’ve had a really good endo tell me I had PFS.

All I can say is that in my case 4 things have lead to a huge change rapidly.

1.) diet. I do keto 50% of the year off and on. I eat pretty healthy. Rarely sugar and no processed foods. I cut alcohol out except on vacations and special occasions. (I was a drunk over the holidays on vaca). I eat/drink large amounts of probiotics. Keto started my journey.

2.) I started exercising religiously when this got bad. Obviously for some here excersise makes you worse but I treat exercise as a job I’m required to do at least 5-6x a week. I’m up every day before work or at lunch and I run or I’m in a bike or elípticle or weights at least 45m a day). I started doing this at my lowest point and probably only did 30m a day but it helped greatly with the fog. It made me worse at first but changed after 3 months or so. I looked at my tough grandfather who worked till he was 80 on a farm and made it through the depression and I decided he would tough this out. I couldn’t imagine him laying in bed even for the flu. Against the advice of my doctors (I had Dr Sundance Levine in NYC who is a specialist on this), I pushed myself every day. If this is an immune disorder I wanted my immune system healthy and exercise is a great way to do this. Again, I know some people are practically bed ridden so this is not an option but for me, no one was going to tell me resting in bed for years is going to fix this.

3. ) possibly truvada and antivirals. Can’t prove this helped but I wrote about this enough that it was significant to me in 2016. Literally in 3 or 4 months of taking truvada it’s like a cloud had lifted. This is about the time I also returned to the gym. This was also the time I changed my diet so it could be 100% diet (I don’t remember the order now). In this time something significant changed. I started truvada maybe 8 months before visiting Dr Levine. By the time I visited Dr Levine I had moved from a 3/4 to a 6. Levine started me on other antivirals and I progressively got better. Was it my diet? Was it truvada? Was it the additional anti virals? Who knows.

4.) when I got to about 85% about 11 months ago I decided to do TRT. Obviously this will not help women but any kind of HRT could help depending on age. I hit rock bottom at 36 and I’m 44 now. By this point I was active again and at the gym daily but still suffered lack of energy and foggyness. My hormones were not awful but my T was about 350-380. Technically not low enough for most Dr’s to prescribe testosterone but there are 20 online clinics that will which is 100% legal. If you are under 410 you can get prescribed testosterone. I decided that additional T would improve my immune system and made the jump. I just started maybe a year ago January 2018 so it’s something new but has turned me 18 again. It shot me from an 8-10 in 6 months. I don’t think everyone should mess with your hormones. It’s a tough decision but after dealing with this for 10 years I’d inject bleach if it made me better.

Obviosly this is my own journey and we are all different. I don’t think CFS is one single disease but many different diseases with the same symptoms.

I told someone I was 95% of where I was when this all started and they asked me what was the 5% I’m missing and I suddenly realized ... I got old during this process. The 5% I’ve lost is just me naturally being 44. I’ve seen people that have been active on here for 6+ years. If you have this for 10 years You are never going to feel like you did before this started.

Thank you so much for your detailed response and story. I certainly have a lot to think about, but I may go ahead with truvada soon and see if it helps.
Thanks again
 

xcell

Always looking for new knowledge and options!
Messages
94
Location
Germany
Messages
73
Hello all!

Is anyone here (HIV negative) that used HIV treatment for CFS?
If yes, please provide what specific medicament(s) you took, what dosage, for how long.
How you felt during the treatment, and what was the result?

Thank you
Sorin


I had mNGS Metagenomic sequencing and found HERV-K in my blood. This is new in my this time mNGS results. In 2018. 2019I had 3 times mNGS for diagnostic parasites and fungus but no retrovirus during those results.

I confirm I was infected from a lady by a kiss with her.

mmexport1590633570096.jpg
 
Messages
73
Hello everyone

I set up a petition for ME/CFS patients with HERV on We the people.

There is evidence shows HERV is infectious disease now. Very dangerous.

Here is the link

https://petitions.whitehouse.gov/pe...nts-infected-human-endogenous-retrovirus-herv

Pls sign your voice.

I got infected with 2 kinds of HERV, there's theory says EBV could transactive HERV but I have 2. At least one of them is infected by other people because I have only 1 genome.

-71c2fbced6b551bd.png


Here is the mNGS sequencing results shows I infected with 2 HERV.
 

YippeeKi YOW !!

Senior Member
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16,075
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Second star to the right ...
FYI If you do try antivirals like truvada, there is a week of adjustment. I’m not sure why but it makes you feel rough the first week. This goes away quickly.
It sounds like it could be rapid viral die-off, a form of Jarisch-Herxheimer reaction that corrects itself once the viral overload has been reduced, yes?


Great posts @cornwellsb ... informative and well-written. Thank you !!!

HEllo, everyone! Is the group started here about cfs being caused by a hiv-like virus still active?
I'm new to this thread, but my experience is that all threads wander slightly (or more than slightly) off-topic. Feel free to post your questions or issues re HIV/ME here, you're in the right place, and there are some terrifically savvy posters here who can probably help you.


Unfortunately, I'm not one of them :( :wide-eyed:.....
 
Messages
38
I’ve been doing pretty good for years. On Truvada for 4 or 5 years. I recently switched to the new version descovy. Lately I noticed some fuzzy blurry eye issues and minor tiredness which I can’t correlate to changing to descovy. I’m able to run 4 miles daily so nothing extreme. I had some old valtrex and I added it in after experiencing eye issues for 6 months and amazingly it went away in days
 
Messages
5
I’ve been doing pretty good for years. On Truvada for 4 or 5 years. I recently switched to the new version descovy. Lately I noticed some fuzzy blurry eye issues and minor tiredness which I can’t correlate to changing to descovy. I’m able to run 4 miles daily so nothing extreme. I had some old valtrex and I added it in after experiencing eye issues for 6 months and amazingly it went away in days

How can you get ARVs??
 
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