lumberjacket

no its an auto immun drug that messes with nuero transmitters, i think. because half of users get bad depression in use.

i have auto immune issues, it's an inferon drug. but in half the people who take it, it messes with their seratonin they think and they need to take ssris. i guess i shouldn't take it then?

Anybody tried l-serine? Amino acid so prob bad?

Is that going trip me? I did ghk-cu(petide) and for whatever reason falured me. Prolo/stem cells are ok surely?

Anybody done this peptide, need it for my kneck. Can't tell if it is making HPPD worse or not.

Hey Don. Thanks for the reply. I went off a cliff the last weeks after that vyvanse scare. My symptoms were much worse than at intial onset. Needless to say, I am staying away from Vyvanse and now even caffiene. Thanks for the reccomendations, I will try and start reading up on these drugs and consider them. I haven't told my doctor yet about HPPD, I see him on the 19th of this month. I'm not holding out hope he will know what I am talking about but I plan on discussing it with him. As far as the medications above, I think I might try Clonidine, although I am inattentive. Seems like as good a place to start as any with my new HPPD troubles! I am afraid to try any drug that messes with my brain, because I seem to be very fragile at the moment. I can't really do anything anymore that has an effect on my dopamine(and maybe other brain chemicals as well.) I will post back after I move forward!

Hi guys and gals, So I had some Quercetin laying around from before I got HPPD. I took some last night with my Magnesium supplement and my symptoms went way down. It was really, really nice. I did wake up this morning with increased visuals, which is strange for me. My symptoms go Vertigo->DA/DP->Visuals. It could have been related to the fact I didn't get to bed until late, maybe 2 A.M. This has increased symptoms in the past. I am going on my third month now, should I wait longer before trying to mess with my brain or is it safe to start testing things that make me feel better? A little background. Small amount of L, HPPD for about 2 weeks after. as far as I can remember I sobered up more or less, and stopped doing a lot of stuff that would agro it because l afterglow. I then did vyvanse, haven't really returned to baseline since then. that was two weeks ago. I also worked out VERY hard earlier this week which sent my symptoms off a cliff for 24 hours. it was fucking hell. they are much more managable now. Another quesiton I have. I have read on here that we should stop things that agro our symptoms. Because vertigo really ramps up my stuff, and vertigo is linked with my excersize(always has been, but used to be so minor) should I stop excersizing? I do hot yoga(which I am going to go back to normal yoga) and play 5v5 basketball. I was thinking maybe 1 or 2 games of bball a week and 1 or 2 lower stress yoga sessions and see how it goes, but I thought I would ask here as I don't want to "damage" myself any further. I have also given up all drugs including caffiene. I also can't seem to take a lot of my vitamins and supplemtns. I can't take my opti-men vitamin or omega-3 supplemtns. I have also given up video games and porn, because they both seem to agro symptoms as well. luckily I don't have a girlfriend at the moment, I am afraid I would need to give up sex as well. It seems that anything that messes with my dopamine is off limits for a while. This has been very difficult because I have Adult ADHD, another dopamine problem. just brain trouble for days it seems lately. Thanks for the advice, I'm having a hard time giving up so much right now. Please send good vibes : p

I recently got diagnosed with Adult ADD. It has been one of the most important moments of my life. I now had a reason for all of this stuff. Using the strategies I have read about in the last couple days, I had greatly improved my life. After trying Vyvanse today, It seemed like everything fit. I could finally be normal. Unfortunatley, as many of you already know, when I crashed I started ghosting worse than I have in 4 weeks. I also started getting bad visuals. My plan is try it one time a month until the 6 month point. At that point I will try and reavaluate my situation. Keppra(i think) as well as Vyvanse might be needed, but to that point I will not know until the day comes. My question is this. 0)Do you think that Vyvanse is permantly making my HPPD worse, or simply aggrivating it? I wonder about this because I feel like it is an incredible tool for me, one of which I would like to have access to if I deem the situation appropraite. 1)is 6 months enough time to move into the anti-seuzire/ CNS experiment or should I wait longer?(I developed HHPD Oct 12, 2015) 2)For people who have ADD, HPPD and are using CNS's and are taking anti-seuzire medication, do you notice a drop in ghosting? The visual increase is annoying as I work on a computer, but honestly the ghosting is what had me so upset. 3)Hold me Edit:Background, my HPPD is managable. By that it seems to go away sometimes, and sometimes it comes when I don't sleep, overexcersize, etc. It comes in waves.

Hi guys, Have had HPPD for 6 weeks. took 1/4 of a hit of L, but I was on Buspar and St. John's Wort. Assuming that helped brake my brain. In a HPPD slump at the moment, thought I would create an account. Best.