post concussion syndrome
 

hi there is anyone out there looking after someone who has pcs or has it thereself .My husband has been suffering from it for over a year after he was knocked unconscious in an attack over a year ago ,i am also carer to my partially sighted son so life is very hard all round ali

Hi and welcome to NeuroTalk! I'm so sorry for all that your family is going through. I've posted the link to the Post Concussion Syndrome forum in case you haven't found it......http://neurotalk.psychcentral.com/forum92.html. I'm sure someone there will be able to relate to your situation.

Sounds like you've had quite alot to deal with and I hope that this board will provide you with some hope and relief. I'm glad you found us. Please let us know if you have any questions. :hug:

Hi, Ali! :Wave-Hello: Welcome to NeuroTalk!

Wow, your hands are full, I'm sure. I hope you'll find our community here both supportive and informative. Please fee free to join in anywhere. :)

hi there yes you could say that my hands are full, i juggle a very heavy schedule and it is nice to chat to so many nice people online ali:)

Hello and welcome to NeuroTalk. Great to see you have come to be with us. Just let us know if we can be of any help.

Again welcome, looking forward to seeing you around.

Darlene :hug:

I see that you've found your way around the forums alisden, but I wanted to welcome you to NeuroTalk just the same.

I too suffered from PCS following a nasty head injury, but unlike your husband I was lucky enough to have mine ease over a period of around 6 months.

I wish him all the best and I hope his symptoms ease soon.

Hello Alisden and Welcome to NeuroTalk. I'm sorry for all the struggles you are having, but I hope you can find some comfort and advice here. I too, have a visually impaired son, but he is an adult now and on his own.

I know of the challenges that can bring to both child and parent. Please make yourself at home here and let us know if we can help in any way.

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hi ali
 

hi ali I have PCS our lives been changed in a similar way to yours see if you can get an appointment with a neurologist, if you have not seen one all ready there are things that can be done for him, also support groups for your husband and your self

I have PCS
 

I have PCS and luckily have a great neurologist who has seen me thru the worst. I have headaches pretty much under control. Poor memory, brain fog, confusion,
brain drain and slow processing. Basically, There is a new Lynda, not sure who she is, my kids want their old mother back. I think my grandson misses his old mommom who could pick him up and take him for the weekend and anywhere anytime. I have fatigue and brain fatigue. I have a phenominal neurophyscologist
who has helped me learn again. She has helped me rise from these ashes.
She tells me from the hip. I need that and appreciate it.

Nice to meet you!!
 

tbimommom,

:Wave-Hello: It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. Please, just let us know how we can help you out. You will find out we are supportive and relaxing place.

Check into the following forum for assistance.

Post Concussion Syndrome:
http://neurotalk.psychcentral.com/forum92.html

Please keep us up to date on your condition. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray:


:hug: