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Protracted withdrawal syndrome


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Posted

Hi,

 

I was rapidly withdrawn from lorazepam, over three months, in 1991, after 16 years of taking them. I have had post-withdrawal syndrome ever since and still suffer greatly from head pressure and severe migraines and  find it difficult to lead a normal life, as my health is so unpredictable. Are there any other members with protracted withdrawal syndrome?

Posted

Welcome to the forum! We're glad to have you as a new member.  I'm sorry you're still suffering after such a long time.

 

You'll find lots of information and support here.  Our members have been through all aspects of withdrawal, and you're likely to find  people who understand what you're going through.

 

For those who are starting a new taper, we suggest reducing no faster than 5-10% every 10-14 days at first, and then adjusting the taper rate to suit your own needs.  One exception: very short-term users of a few weeks or less may be able to taper faster.  Having some withdrawal symptoms is normal, especially near the end of a taper and for a few months after discontinuing the medication.  First/only withdrawals after a slow taper tend to be easier than multiple reinstatements/withdrawals over time, which may make symptoms worse and longer lasting. The most common symptoms are anxiety and insomnia, but there are many others.

 

Here are a few links you may find useful:

 

Protracted Withdrawal Support Board

 

The Ashton Manual is an authoritative source on what to expect in withdrawal and recovery.  Dr. Ashton is an expert in the field. Section III explains and describes symptoms, and there is also a section with suggested taper schedules.

 

Please take the time to Create a Signature.  This will allow others to see where you are in the process so they can better support you.

 

Again, welcome!

 

 

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