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Lupron making me crazy? Lupron making me crazy?

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  #11  
Unread 08-29-2012, 05:44 PM
Re: Lupron making me crazy?

Hebynan, So glad you are starting to feel better and also get somewhere with your doctor. I know I have been lucky all around. Seeing everyone post and the difficulty others like you have had it almost makes me feel guilty. I had my 2nd Lupron shot. Having more hot flashes but that is about it. I am having trouble sleeping but I have for years anyway. They are worse during season changes so I figure it is probably just that. I hope things keep going well and moving along for you. One more shot for me and then a few days later my surgery. More Stressed about how training the person who will cover my job and how she is handling it then about the surgery. Big Hugs, Sister1209
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  #12  
Unread 01-28-2013, 02:54 PM
Re: Lupron making me crazy?

Just curious what happened here? Did you end up getting the next shot or was it sent back?
  #13  
Unread 01-28-2013, 02:56 PM
Lupron making me crazy?

  Quote:
Originally Posted by Fibrokitty View Post
Just curious what happened here? Did you end up getting the next shot or was it sent back?
It was sent back. I ended up having a TVH the end of November. I've never felt better! I'm the old me again. Gosh I've missed her!
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  #14  
Unread 01-28-2013, 04:06 PM
Re: Lupron making me crazy?

Glad to hear you are doing so much better finally! I know that is a huge relief. Thank you for sharing your story.
  #15  
Unread 01-29-2013, 08:49 AM
Re: Lupron making me crazy?

I had my first lupron shot 2 weeks ago and the headaches started a few days after I got the shot. I stayed home from work for 2 days due to the worst migraine ever! I haven't had any other side effects that I'm aware of yet.
  #16  
Unread 09-19-2013, 10:59 PM
Lupron making me crazy?

Hi I'm 38, had 3 children, have chronic kidney stones, and had an MRI for an episode I had. They found a large ovarian cyst in the process. I made an appointment with my OB and also found adenomyosis. I chose to have a partial hysterectomy because I was done having children and I couldn't deal with the pain any longer. After the surgery the endo was so extensive that Lupron was recommended. I have recently been given 3 out of 4 injections and I'm pretty sure that I'm losing my mind. My life just seems to be in such a downward spiral and the doctors are insisting that it is not the Lupron. They continue to put me on antidepressants and I'll take them for a short period of time but find that it just makes it worse. This situation I am in is burnt everything that surrounds me. If I could go back and do things over, I would have researched more natural options. The inside of my body feels like I'm melting, not to mention I'm still bleeding. Atrophic vaginitis is so severe that my doctor called his partner in to see because they have never seen anything like it! I don't sleep, I still cramp, I have headaches, and the hot flashes are tormenting. I'm at a loss and completely overwhelmed. My 3.8 GPA is suffering, my job is suffering, and most of all my relationships With everyone, including my husband and The Lord are suffering. I don't know what to do. Please do your research and/or have a few more opinions before having this procedure done. Good luck! I pray that no one ever goes through what I'm currently going through!
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