What happened to life? I made some poor decisions during the past 2 years.
I used Finasteride, a generic version from mid Nov. 2008 to January 2009. I don’t even want to say how foolish my ‘logic’ was that led me to buy and use Finasteride.
I noticed fat accumulation on my neck and belly, poor sleep, and some cognitive problems during those days on Fin. When I finally shaved my neck in January and saw the fat on my neck for the first time, I stopped taking Fin and panicked a little. 5 days later, I found this forum and couldn’t bear to read much beyond, "irreversible, " “long-term” and “genetic” along with a quick scan of speculative theories on why people have these side effects long-term. I remember seeing someone’s post about “years” of side effects. I don’t think re-opened this forum’s site until about one week later or more.
I also noticed the information about the typical 2 weeks following FIN use and a discussion of whether to quit suddenly vs. gradually… I had already stopped 5 days prior to entering this forum the first time.
During those final two weeks of January, I did not notice a hormonal rush or a change as described on this web forum. I think that I already had too much dread.
I’ve never done blood tests. My thought on the matter was that no one knows how to treat these side-effects and that it would take my own willpower and good habits to defeat this problem I walked into.
Unfortunately, any ‘plan’ to defeat these side effects for me needed to be delayed because:
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I’ve been hit by a taxi and had foot and ankle problems since May 2007. I have had two surgeries on my foot and ankle this year. 2009.
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I decided to have nasal surgery twice since March 2008 and my nose is now worse
My entire year (2009) has been nothing but social isolation, inability to express myself vocally, emotionally, or facially (because of my nose), poor sleep (post-FIN), and a gradual decay of pleasure or joy.
After learning about the post-FIN, I remained somewhat optimistic that I would find a way to defeat this condition. However, my nasal surgery at the end of March nearly destroyed all my remaining hope and willpower.
I’ve just survived another surgery on my foot whereby bones were successfully fused together. I just started walking yesterday.
While I don’t take my foot doctor and successful surgery for granted, I can say that I correctly assumed that all would go as well as it could with my foot. My orthopedic surgeon is excellent, IMO.
However, I am finding that weeks are now becoming a little more difficult to endure and my fits of crying and calling myself an “idiot” for not dealing with one problem at a time, for not researching Finasteride beforehand, for not delaying further surgery on my nose, for not changing my geographic location (and thus climate and air quality) back in January or February of 2008, prior to nasal surgery (for some perspective)… And, of course, I have no one to “help” me and there’s no way to help these problems until later.
Anxiety has prevailed in my life since post-FIN and since my nasal surgery in March. For those reading this, I can tell you that the reason for this is that the nose doctors I’ve seen since March have given me very little hope.
I think that it’s important for anyone here to consider the role of anxiety, depression, and poor sleep when coping with your symptoms. I actually began having softer and less-sustained erections last year, before using FIN because I was having a lot of anxiety while living in Bangkok and getting far too little sleep, exercise, or calories. Every single day since then (and probably since my nasal surgery in 2008), I’ve been dealing with anxiety, not enough exercise, and having a poor diet or eating routine/habits on a daily basis (I know some of you might like Thai food, but when you live there you don’t feel the same way, plus there’s MSG on almost everything).
Actually, I want add one other detail to my story: during the first month on FIN, I returned to America and my appetite was better than it had been since my nasal surgery in 2008. It wasn’t my “true” self appetite, or my healthy self’s appetite, but it was a little better and I remember being able to breathe better when I came back to cold, brisk air (Pennsylvania, November, December 2008). During December or January, this changed. Also, it’s obvious to me now that as I spent more time indoors during the winter, my nose was always closed down on one side, thus causing me more anxiety and less interest in food.
I still really want to believe that there is a way for all of us here to use exercise, diet, and good sleep to overcome post-FIN life. Every day of my life now I struggle to believe that, but I struggle even more with anxiety about my nose TBH.
I wonder about many of the proposed and tried recovery methods used on this forum. The story about myelin sheaths being damaged is interesting… so, I wonder about Omega 3 and magnesium sulfate. I once used chelation therapy to help me recover from something and magnesium sulfate is used for chelation therapy.
I just want to say to any of you on here that I am on the web daily, wasting time or reading some stuff. I can be reached through pm and I will chat or link with you on facebook as I am not embarassed to talk about anything to anyone or anywhere.
October 2nd is my first appt. with an endocrinologist. I am going to UPMC in Pittsburgh. I cannot see Dr. Shippen at this time, but may attempt to move near Philadelphia in order to see him (and a top rhinoplasty surgeon) and attend school. I plan to update or ask questions on this forum regarding my test results.
what a disaster.