Cerebellar stroke experience, treatment, recovery - want to dialogue
I suffered a Cerebellar Stroke in Dec 2015 in my 40s and am interested in connecting with other cerebellar stroke survivors to share our experiences, testing/therapy options, struggles on the path to recovery.
Interested in more discussions like this? Go to the Stroke & Cerebrovascular Diseases Support Group.
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@iam7811
I help folks cuz so many people helped me. And it's who I am.
I am 68 years old, I have had 19 surgeries in my life. Diagnosed with multiple sclerosis 35 years ago.
I am sick to death of doctors. I used to be on 16 medicines, 6 of which were sedating...I am off every single one of them.
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When the doctors were in charge, I spent years in bed. Been there, didn't like it, don't wanna do it again. Now I can only speak for myself here.
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I decided to take charge of my life. I got to know enlightened people, people with gifts of healing. I listened. I asked questions. I did reflexology, Accupuncture, chiropractic, kinesiology.
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Ask at your local health food store. Talk to an Herbalist there...and ask for suggestions. Trust your gut...it will tell you if something someone says will help you.
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Someone told me about CBD last summer. I started taking it and realized it helped my multiple sclerosis...I stopped falling down. It took care of my nausea and my tremors.
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I take 25 mg 3 times a day. But don't start out at that...start out with 25 mg and let your body tell you when you need more...there is a group here in Mayo Clinic Connect for CBD. Go there and read your little heart out. You will be glad you did.
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I remember you are in Scotland? I don't know if its legal there, but I will take this wonderful healing plant medicine until the day I die.
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I also was told about a product that is bringing my brain back to life. It is called Ultra Colloidal Gold. Company name, Source Naturals. Cost $9.59
I receive no compensation from the company.
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What it does is wake up unused portions of your brain and repair it.
My MS is so much better. I feel better. My balance is much better...I will take this until I die also.
The third product I use us called Wild Shiaga. Company name, American Dream Nutrition. I receive no compensation. It gives me energy and repairs my immune system. Again, I will take this until I die.
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BTW, I went camping last weekend and am going camping again this weekend. I expect 50 to 75 of my friends to show up also.
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I took my life back...AND IT TAKES AN ACTION TO FEEL BETTER.
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So what does your gut tell you to do.
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I have a bunch of mottos that keep me going...
I am the Energizer Bunny...I keep going and going and going...
One foot I front of the other gets you a long long way. ..
Take an action to change your life...
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Ian, I hope this helps...and on those really difficult days...my best friend motto...FAKE IT TILL YOU MAKE IT.
I also studied how to give myself endorphins...and how to avoid negative chemical dumps...changed my life...that put me in control of how I felt...
I wish you well, Ian...Bright Wings, who is really flying now!
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1 ReactionYour are welcome, best of luck with your recovery. It does get better.
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1 ReactionDear Narciso, thank you too, the family doctor thought it might be damage but the stroke people never commented. I wish you all the very best in your recovery. It sounds like a big improvement with the change to a cane and I hope you can soon move on from that too. My goodness, there’s great positivity on this site, it’s all very uplifting.
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1 ReactionThank you for your advice, I’ll ask to trial that one next time Im at the Doctors. Best wishes Ian.
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1 ReactionI had a Cerebellar Stroke about 3 months ago. I can tell you that if the doctors and therapist say that the Vertigo is due to damage, there really isn’t anything you can do about it. My Vertigo lasted about two months, but no one ever told me that the Vertigo was due to a damage.
I only threw up several times in the emergency room and then a few days due to the tubes in my mouth. Once they took the tubes off, I haven’t thrown up or feel nauseas ever since.
I also lost my balance and for most of the rehab I have been on a walker. It was only last week when I transitioned to a cane.
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1 ReactionHi, fortunately , my vertigo / nausea has in the main has gone. The medication I was given that seemed to work for me was cyclizine, I believe its an antihistamine. Importantly - Speak to your doctor before taking it though, as too much can make you high and stop your bladder from emptying properly amongst other things.
May I just ask if anyone with a cerebellar stroke has any advice about relieving persisting nausea. Medical staff say it’s just resulting damage and medication won’t help but maybe someone has knowledge of prescribed medication that worked for them or perhaps even a home remedy. I’ve tried stematil but no luck. Thank you, Ian.
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1 ReactionThank you so much for your reply, you’ve shown great resolve and I hope I can push myself in the way you did and continue to do. Best wishes for the future jmjlove and brightwings, I like to read this site because of the inspirational stories which you both shared with others and myself. Well done to everyone who share their personal experiences, it so uplifting to read about the challenges faced by so many and yet people still take a few minutes out of their lives to help with a few kinds words. Ian.
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2 Reactions@ian7811 ....thank you for your story. I love reading testimonials. Cerebellar stroke here, neurologist said it's large, not massive, but sure caused me a lot of issues. Got TPA, but I guess most of the damage was done though received it within the window for effectiveness. I do believe it provided a speedy recovery for my vision.
I was a mess when I came home. Not even stable enough for a walker.
Hubby was a great help. He ran out and cut a wide walking path around our 5 acre farm. I'd hang on for dear life while he dragged me around the path. I was like a drunken sailor, but within 6 weeks I was making my way around while he watched.Occasionally he'd lose sight of me and he'd have to pull me out of the cornfield. I'd done many faceplants, but in time gained control of left leg. Then it was the grandkids cheering me on. Received 8 months of therapy, but I swear that path did more for me than any therapist could, sweet as they were!
Glad you had great home support. I had 3 kids living at home still, so I was rarely alone.
Unlike you, dizziness and nausea cleared up, but balance is a big problem.
Like brightwings, I was very motivated and life was not going to pass me by. My whole left side had what is called ataxia, where you have strength, but little control. Hard as I'd try, I could not touch my own nose with finger.
Later, I developed a tremor in left hand which really frustrates me. It is only activated when I try to do something, like my hair, buttoning shirt, tying shoes, clipping nails, etc, so hubby has to help. After 3 years, I've probably done as much recovery as I can.
Unlike you, stroke does not run in my family. Never figured out the why of it, but now I don't really care. Vascular studies are great. Now, I still fall a lot, still have a limp and tremors up and down left side, but I don't think people would ever suspect that I have brain damage. I do a lot less than I did, but more than most who've never had a stroke!
Hoping your nausea and dizziness clears up for you, Ian. God bless!
Oh, by the way, I am not the same. I hardly know myself, even though physically, I'm ok. I know how you feel. We may not be the same, but we've seen we can rise above and move on, instead of wallowing in self pity and taking on a bleak outlook on life. As long as I'm not pushing up daisies, I'm gonna laugh, work, and enjoy my family. Like Brightwings, i will not only exist, but be active, take charge and enjoy life! I wish the same for all!
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2 ReactionsThank you for your kind reply. Ian.
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