Chiari Malformation Community
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Avatar universal

Weight lifting and sports after surgery?

Im a 21 year old male athelte in college, who was diagnosed with pots and dysautonomia along with pretty intense headaches, i weight lift and play soccer and other sports. I was found to have a 7 mm chiari malformation during an mri because of my dizzines and my changes in vision. As ive seen cardiologist, endocrinologists, internists ect they ruled out any of these symptoms beign another organic problem. I currently dropped out this semester since my symptoms are a little worst( im on beta blockers, but dont seem to help much). I know that surgery is tough and is prob going to be inevitable, i feel worst every day and tired of all these symptoms. I wanted to ask, have any of you know of someone that recovered from this surgery as was able to play sports and weight lift again? I know everyone is different but i just want to find a little bit of light these days as i want to be my normal self again. Than you very much.
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Avatar universal
I also wanted to add that ive heard of people coming back to sports and their cerebellum going down even further, this makes me want to stay with pots and dysautonomia, surfing, soccer, and the gym are my life, well not recently as i had to cut those down because of my unexplained fast heart rate, which a couple of months ago before symptoms was 54 at rest since i did a lot of cardio
620923 tn?1452919248

  Hi and welcome to the Chiari forum.

As you already mentioned, we are all different.....and yes, some that have had surgery did go back to sports and some have had a recurrence of symptoms. as a result....some have not....

It is possible post op that you will feel up to doing the  things you love, but it is best to give your body time to heal and it will take longer then most allow or want to wait until....''

I had surgery in May of '09 and each yr since I found new changes to me and my symptoms....I know had I tried to do more yrs ago after surgery I may have had set backs....and I have seen others try to get back to their "normal" suffer set backs as well....

I am lucky as to date I have only required one surgery.....but some others have not been as lucky....and I can only say, that you can decide for yourself what you will or will not do if you have surgery....only we can live our life with our own rules...I suggest you listen to your body....and enjoy feeling better.....you could do the sports you enjoy and it could lead to having continued symptoms....no one can know for sure....

My life has changes drastically ...I am on a different path but on this path I am doing things I never thought I could.....or might have tried ....so, there are positives even if we can no longer so some of the things we did b4....Chiari is life altering....that I know for certain.
9432311 tn?1432828685
Hello. I read your post and have felt very similar feelings. I was a figure skater when I was younger and I played soccer and ran cross country in college, so I have been athletic my whole life. Four years ago, I started training for a half marathon. I ran two and thought I would continue. I have always had symptoms of chiari, but largely pushed through them. However, about two years ago, the pain in my head and neck greatly increased, along with lots of nausea. This led me to start searching for answers. In short, I had a decompression surgery in July and I am having a craniocervical fusion soon.

Running is something I had to stop, which makes me very sad. It was something I did with my best friend and really made me feel wonderful. Over the past month, after getting the chiari diagnosis and having the surgery, I started walking and I am slowly going to build up to some time doing long distance walk racing. It is not running, but, as Selma says above, but has brought its own rewards. Chiari is life-changing and it also forces you to sort through your priorities. I struggle with this, but keeping current with this community really does help me put things into perspective. Being an athlete has always been my life; now, I just change my focus and concentrate on a different sport. I hope you can sort through your feelings about this and come to feel a little better. You are young enough to have a very real chance at resuming your life - after giving your body the necessary time to heal from surgery if you should choose to have it. Keep us posted so that we can help you.
Avatar universal
Thank you very much on your response, i know many people are different but hopefully we will recover enough to resume a normal life. Im currently in mayo clinic with a cardiologist appoinment, traveled to jacksonville last night. But ive already seen cardiologist before and told me everything was okay after an echo and stress test, that my fast heart rate and symptoms of pots were caused by something else. I wanted to ask if you know of someone who experienced fast heart rate and dysautonomia like pots. Im pretty sure its chiari related, since ive done all the possible tests. Also it is very hard for me to gain weight, ive lost a couple of punds and they dont seem to come back any time soon. Thankyou for everything and for welcoming me, honestly i dont feel as alone as i felt before knowing theres people who has gone through things way worse or similar. I hope with time eveything ends up perfect and symptom free for you guys, wish you the best and ill kep you guys posted if anything, and again thank you have a great day.
620923 tn?1452919248

  A true Chiari specialist should be able to help you with your POTS and Dysautonomia issues....

AS I mentioned I also would get periods where my heart would race, I called them heart palps....and since I have had surgery I have not had them....so, it is possible that it is Chiari related ....I too went and had my heart checked out to make sure all was ok there....better safe then sorry.

Have you been to any Chiari specialists? I know there is one in the Jacksonville area and one in Miami.....
Avatar universal
Hey selma thank you for answering, ive actually not gone to a chiari speciallist, because i live in miami and i think the only one around here is dr green and its pretty hard to find an appoinment, if you know of any recomended doctors that treat this chiari issue around miami or close by would be awesome.
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