Arachnoiditis: Looking to talk with others

Posted by arannek72 @arannek72, Jul 3, 2018

I just got diagnosed with arachnoiditis. The radiologist found it on my MRI. I have had 7 steroid injections and I fear that they have caused this chronic situation. My back is worse than it ever was.

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Currently getting workup to get confirmation of arachnoiditis Dx. I agree with everything that everybody says on these posts.. it’s comforting to hear that there are other people out there going through the same/ very similar things.
This is truly a hideous disease, not enough warnings are mentioned before you have epidurals, or even before back surgery. Warnings should be mentioned… nothing for me was EVER mentioned. Even when arachnoiditis was called in an MRI report and I asked my surgeons office about it .. I was told I did not have it . low and behold 4 months later with increasing pain , the exact same MRI is looked at by the same surgeon and I am asked if if arachnoiditis has ever been mentioned? Yeah!! Its in the report! Trying to stay positive but feel like I will be living the rest of my life very close to home. Pain makes it hard to do anything. Currently researching all I can to maintain whatever quality of life that I can and keep the pain at a tolerable level. I am fearful of progression. Does anyone know what or how that happens? There seems to be alot on management of pain which is of course a MUST but what about managing inflammation and nerve regeneration. Has anyone used any peptides?

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Profile picture for marcototti @marcototti

@mmata573085 your comment os so lovely it warmed my heart thank you God bless you, I'm still trying to learn and come to terms with the endless suffering and how to do it with grace and positivity I'm 34 been suffering for the last 10 years with nerve/back issues no one could figure it out. Is bitter sweet to get a diagnosis finally to find out its not fixable and could possibly progress even worst is a hard pill to swallow.

Guess I have to say goodbye to the old me who could climb mountains and had energy for days, my body is broken but my soul is still beaming with light.

It's 2am on the pain train once again oxycodone,morphine diazepam,pregablin and my final friend ketamine keeping me company, I just want to say I love you all this is a hard road but we must walk it in faith this test we have received I have to believe this is just the human experience and after this on to the next life 🙏 ❤️

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@marcototti Amen, an Absolute Truth... Something you may want to investigate? I have just found it recently. Having been brought to the unfortunate conclusion. That I may have Epidural Fibrosis or potentially arachnoiditis. but it appears most surgeons. Don't care to discuss or dismiss this topic in my experience because Surgery is contri-indicated with EF... And a procedure that came about in the late 90s that actually addresses the problem. Has been ran under ground or out of town. By the huge medical device entities. Epidural lysis of adhesions. Is only available in a few states. And I'm not even sure if they actually provide it or just list it as a hook for potential new patients. So I found this protocol and was fortunate enough to find a Dr. who was willing to give me the opportunity just 2 days ago. So anyways something you might consider... https://www.researchgate.net/publication/8233322_Resolution_of_symptomatic_epidural_fibrosis_following_treatment_with_combined_pentoxifylline-tocopherol

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Profile picture for smn1 @smn1

@marcototti Amen, an Absolute Truth... Something you may want to investigate? I have just found it recently. Having been brought to the unfortunate conclusion. That I may have Epidural Fibrosis or potentially arachnoiditis. but it appears most surgeons. Don't care to discuss or dismiss this topic in my experience because Surgery is contri-indicated with EF... And a procedure that came about in the late 90s that actually addresses the problem. Has been ran under ground or out of town. By the huge medical device entities. Epidural lysis of adhesions. Is only available in a few states. And I'm not even sure if they actually provide it or just list it as a hook for potential new patients. So I found this protocol and was fortunate enough to find a Dr. who was willing to give me the opportunity just 2 days ago. So anyways something you might consider... https://www.researchgate.net/publication/8233322_Resolution_of_symptomatic_epidural_fibrosis_following_treatment_with_combined_pentoxifylline-tocopherol

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@smn1
Thank you for this. I’ve bookmarked it and will read it.
I’ve done more research on this condition in the past week than I ever researched anything during my entire career as a medical Dosimetrist. I believe my arachnoiditis was caused by a nasty synovial cyst that was stuck to the Dura. I suffered multiple tears during the removal. .. and then for whatever reason that really doesn’t matter now multiple epidural injections were recommended to help with pain. After an entire year of suffering and questioning and reporting the same Pain, I’m now landing on this diagnosis. I do believe that the epidural injections that I had also probably made things much worse, but I don’t know if the problem was caused directly by them, I’m thinking no, but it certainly added to the scar tissue that’s there.
It helps to be on this forum to get information and Support.

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Dear old Ferry Rd,
I am so glad the Lyrica is helping you with the pain. Problem “stitching “ your words together is an excellent way to describe the side effect! I didn’t have any problem with Lyrica at first - it was a great pain reliever . My dose is small 25mg 3 times a day.
Suddenly at the 6 month mark, I couldn’t talk, couldn’t string words into a thoughtful sentence. Couldn’t remember something 15 minutes later. I brought my hubby another sandwich when I had made him one 15 minutes earlier . I stared at the bread, mustard etc trying to remember what I did. Once, I took my meds twice because I didn’t remember having just took them.
We have come up with a particular way to lay out one day of meds and I can tell due to the pattern what I have already taken and what is left. But taking my meds twice really scared me. I took 2 Oxycodone, 4 muscle relaxers and 2 gabapentin within 1 hour! We called my daughter who is a nurse, and she told my hubby what he could get OTC to make me throw up. I spent the next couple of hours throwing up!! Not easy! My daughter helped me wean off Lyrica, and things went back to normal.
But now it’s spring, and with it comes extra chores. Weeding, planting, clearing - all leave me in extra pain, and I am back taking the Lyrica. Only now - I warn my family I took it and they keep a closer eye on me. As soon as I take some, I’m back to speech and memory issues. It’s sad and frustrating that something that gives such good pain relief, makes me unable to communicate well and makes me scary forgetful. And it is a small dose!

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Profile picture for toiolinger @toiolinger

Hi Rachel, I am so sorry what that doctor did to you. What an idiot. I don’t know what caused all this pain. I have several steroid injections, three back surgeries, and cat scans. I am making an appointment tomorrow to an neurologist to
confirm that I have Arachnoiditis. People don’t understand how much pain this disease causes.
They would say but “you look good”. I read about the hormone imbalance from Dr. Forrest Tennant’s article. I contacted my
Primary Physician and she said the hormones are NOT recommended for someone over 65. The side affects are too risky. Thank you.

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@toiolinger My husband and I have been on hormone replacement therapy for about ten years+ .
For the first time EVER I balanced my thyroid hormones.
The FDA just recently took the black box warning off of hormone replacement therapy . They know now, it actually helps, not hurts.
I am 65, my hubby will be 70. We feel much better on our hormones and plan to continue.Good luck!

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Profile picture for smtaylor @smtaylor

@toiolinger My husband and I have been on hormone replacement therapy for about ten years+ .
For the first time EVER I balanced my thyroid hormones.
The FDA just recently took the black box warning off of hormone replacement therapy . They know now, it actually helps, not hurts.
I am 65, my hubby will be 70. We feel much better on our hormones and plan to continue.Good luck!

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@smtaylor
Can I ask what hormones you take? I am a female , and which doctor has prescribed them??
Thx!!

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I take estrodial , testosterone , and progesterone. I moved from Utah to Tennessee and my primary care provider was comfortable just refilling current perscriptions. I am tested ever 6 months, and stay pretty steady. I have been on my current dose for several years now. It took a long time in Utah to dial in my dose, but once we did, we had our sweet spot. I take Naturethroid, and cytomel for my thyroid. After thyroid cancer, it took a few months to dial in my dose, but we hit the sweet spot and I have been very steady.
We retired to a small community in Tn and have a lake cottage we now call home. There are not many specialists here, and it is a 30 min drive to go to the doctor, or an hour if you need a specialist in Knoxville. We have a small grocery store 15 min away, but otherwise you are driving way more than I am used to!
As I mentioned before, the black box labels from hormone replacement drugs have been removed. Dr.s know better now. I could have told them years ago that I could not dial in my thyroid meds until I got my female hormones where they needed to be. But who listens to patients, right??

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Profile picture for sherij @sherij

Currently getting workup to get confirmation of arachnoiditis Dx. I agree with everything that everybody says on these posts.. it’s comforting to hear that there are other people out there going through the same/ very similar things.
This is truly a hideous disease, not enough warnings are mentioned before you have epidurals, or even before back surgery. Warnings should be mentioned… nothing for me was EVER mentioned. Even when arachnoiditis was called in an MRI report and I asked my surgeons office about it .. I was told I did not have it . low and behold 4 months later with increasing pain , the exact same MRI is looked at by the same surgeon and I am asked if if arachnoiditis has ever been mentioned? Yeah!! Its in the report! Trying to stay positive but feel like I will be living the rest of my life very close to home. Pain makes it hard to do anything. Currently researching all I can to maintain whatever quality of life that I can and keep the pain at a tolerable level. I am fearful of progression. Does anyone know what or how that happens? There seems to be alot on management of pain which is of course a MUST but what about managing inflammation and nerve regeneration. Has anyone used any peptides?

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@sherij - do you now have confirmation from the doctor on a diagnosis of arachnoiditis?

How is your pain today?

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Profile picture for Lisa Lucier, Moderator @lisalucier

@sherij - do you now have confirmation from the doctor on a diagnosis of arachnoiditis?

How is your pain today?

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@lisalucier
Recent Mri and lumbar puncture indicate arachnoiditis .
In addition , to complicate matters a dural leak is noted on both LP and MRI. I had multiple dural tears during my surgery a year ago. Possibly not fully repaired?
Pain is always present. Usually quite severe. Sometimes it is just unmanageable!!

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