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» LymeNet Flash » Questions and Discussion » General Support » Cortizone Bad??

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Author Topic: Cortizone Bad??
Hikin Mike
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Are cortizone injections something to stay away from? My doctor wanted to do it, but I told him no way...mainly because I hate needles and it seems like a temporary fix.

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-Mike


Posts: 96 | From Atwater, Ca | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
Linda LD
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NO cortizone!!!

I don't understand the science but I know if you take it it will make everything MUCH worse--hopefully someone will be along that can explain the stuff.

L


Posts: 1171 | From Knoxville, TN US | Registered: Dec 2004  |  IP: Logged | Report this post to a Moderator
Lymetoo
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Good decision! No cortisone!

It suppresses the immune system, allowing the Lyme to get the upper hand. Go for prolotherapy instead.
http://www.prolodoc.com/faber4.htm http://www.prolodoc.com/zale.htm http://www.prolotherapy.com/ http://www.prolodoc.com/
Hear success stories: http://www.prolotherapy.com/proloaudio.htm

Rate prolotherapy: http://www.remedyfind.com/rm-715-Prolotherapy.asp

How do other treatments rate? http://www.remedyfind.com/hc-Osteoarthritis.asp

Articles on prolotherapy:
http://www.prolotherapy.com/documents.htm
http://www.prolotherapy.com/articles/banks.htm http://www.getprolo.com/
http://www.docbridges.com/prolo.htm

A great book on the topic:
Prolo Your Pain Away, by Dr. Ross Hauser


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oops!
Lymetutu

[This message has been edited by Lymetoo (edited 07 June 2005).]


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trailsgrl
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Dont EVER get a steroid shot.

I got one for a shoulder injury after completing a mini-triathlon while my lyme was in "remission" and it has caused me to relapse into FULL BLOWN LYME symptoms. Cant even THINK about triathlons, let alone walk around the block now. (6 months later)

Don't do it.
My opinion,
Trails


Posts: 196 | From Mesilla, NM USA | Registered: May 2005  |  IP: Logged | Report this post to a Moderator
Hikin Mike
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Thanks everyone!

I'm also taking Methotrexate, which I want off of. It also suppresses my already beat-up immune system.

------------------
-Mike


Posts: 96 | From Atwater, Ca | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
perplexed
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Just wondering. Does anyone know if this applies to hydrocortisone creams for rashes? My PCP gave me some yesterday for the wierdest rashes that I keep getting. The rashes usually itch and drive me nuts...for years now....OYE. Just curious.

Jean


Posts: 324 | From Lexington, KY, USA | Registered: Dec 2001  |  IP: Logged | Report this post to a Moderator
Lymetoo
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No, you're OK with the creams. This may be a Lyme-related rash.

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oops!
Lymetutu


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Linda LD
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perplexed,

I am also taking a topical steroid for my weird rash--I am convincd that it is babs. So you are o.k. with hydrocortozine cortizone topical cream--get that rash!

L


Posts: 1171 | From Knoxville, TN US | Registered: Dec 2004  |  IP: Logged | Report this post to a Moderator
trailsgrl
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Another vote for: Topicals are okay. Not much is actually absorbed into the body. Thank GAWD.
Trails

Posts: 196 | From Mesilla, NM USA | Registered: May 2005  |  IP: Logged | Report this post to a Moderator
Mo
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I disagree on safety of topicals.

The skin is the largest organ of the body and absorbs more than we think!

Some essential oils rubbed on the skin can be detected in breath minutes later.

I wouldn't risk it, IMO.

(except when someone needs oral or injected steroids in an emergency, of course)

Hey Hikin' Mike ..
if you can get of the methotrexate, I would sooner than later.

It is also very immune suppressive.

Mo


Posts: 8337 | From the other shore | Registered: Jul 2002  |  IP: Logged | Report this post to a Moderator
Hikin Mike
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Mo,

I agree. I go back to my doc on Thursday and I am going to tell him to take me off of the Meth and double my dose of Doxy, or get a new antibiodic. Zith worked well for a while. If he won't I think it's time for a new doc...

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-Mike


Posts: 96 | From Atwater, Ca | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
hatsnscarfs
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Just say NO and run for the door.

I had a cortisone injection in my hand for a strained ligament in 1993. The "hand specialists" said there were no risks or side effects and the worst that could happen was that it just wouldn't work.

The injection severely damaged my hand immediately and over the next year my hand closed up completely. I was in excruciating pain (worse than any Lyme pain I've had) and finally had surgery to remove the scar tissue. I have had 1 1/2 hours of massage on my hand every week for 10 years to regain range of motion and control pain. That comes to $36,000+ out of pocket for the only treatment that works for me. Can you afford the risk?

Timaca had a post about a similar experience. I think the injection invited the Lyme I didn't know I had to take over my hand.

hatsnscarfs


Posts: 956 | From MA | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
   

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