← Return to Brachial plexus injury

Discussion
Daniel avatar

Brachial plexus injury

Brain & Nervous System | Last Active: Jul 17, 2025 | Replies (16)

Comment receiving replies
Profile picture for jenn5423 @jenn5423

Wanted to find out other people's opinion's on there situations regarding the brachial plexus injury.

Jump to this post


Replies to "Wanted to find out other people's opinion's on there situations regarding the brachial plexus injury."

Hi @jenn5423. I'd like to invite @bionicwoman, @seathink, and @dleeowen to this discussion who have discussed their experiences with a brachial plexus injury on Connect. Each member has a different route to what caused their injury, but may be able to share some of their experiences with you.

@jenn5423, if you are comfortable sharing, would you be willing to tell a bit more about what caused your injury and how you have currently been managing it?

Hi Jenn, I had/have radiation induced brachial plexus neuropathy so my experience may differ from yours, but happy to share.

Symptoms came on very fast, extreme weakness, volume of arm reduced by 15% over a couple months, total numbness/pins & needles, loss of finger sensation and ability to write or do any fine motor skills.

Brain/shoulder MRI and EMG showed the damage, a now very rare side effect from chest radiation (35 rounds the year before).

Luckily I was still seeing my cancer team and my radiologist at UCLA took point, basically throwing everything at it. I took steroids, Trental and high dose Vitamin E, Vitamin B, Occupational Therapy, and I was still doing PT for my surgeries,and my PT had had a patient once with my type of case.

We were also able to oxygen therapy at the Hyperbaric Chamber at UCLA. It took finessing for the insurance company and a denial, but since it was linked to the radiation my radiologist and the docs at the chamber got me in for 40 rounds. That was a long shot but worked for me. Today I can lift/write/do fine motor skills, and some feeling has returned to my fingers. Some of my arm still feels numb/tingling but it's nothing like it was.

The one thing I don't know about is if the reversal is permanent or not, but it's been a year and a half so far.

Hope this is helpful.

Mine came on through a winding path of surgeries. I fell twice (once broke my clavicle and one broke my humerous bone). I wound up in an emergency room in St. Paul, waited for a week for treatment. The first surgeon put a plate and screws in my clavicle to help it heal correctly, the second surgeon, after a 7 day wait in the emergency ward of the same hospital, did a reverse shoulder surgery. I went back to a local nursing home for a month. Following that was several months of physical therapy, The only clue I was injured somehow came when the sling came off in a session of physical therapy. A lightning bolt went up my right arm (at least that is how it felt). I found out in post-surgery checkups by my shoulder surgeon that I had a damaged axillary nerve. A neurologist ran a EMG test. Axillary Palsy. I went to Mayo Clinic; and I was send home with brachial plexus disorder. Currently have had an MRI that I wanted a long time ago, it seems. Unfortunately, the implant for the shoulder made it almost impossible to read throughly, So I am getting another opinion next Monday on where I am. This is the back story to date. Lee

No information follow-up. Sorry to report that my shoulder is weaker and uglier than I could have imagined. PT didn't do it for me. I am still super TIGHT and feel ugly. If it were strong enough to walk my dogs, I would be happy, but that is not going to happen. I am stuck with this for the rest of my life, I guess.