A Big Thank You To Everyone. Cerebral Amyloid Angiopathy

I have been blown away with all the comments and to all of the wonderful people who have subscribed to this channel, I thank you.
I am not alone. There is strength in numbers.
A big thank you to everyone for being there for me.
Cerebral Amyloid Angiopathy

[@larissagibbs4837]

Sound plan. Keep your chin up. 👍 ❤

[@mycerebralamyloidangiopath4710]

I keep trying. Thanks

[@a_diamond]

❤❤❤

[@mycerebralamyloidangiopath4710]

Stay strong

[@inmyhead_sharon421]

💜

[@mycerebralamyloidangiopath4710]

Take care

[@loriann3896]

Good job!! You're not alone. We're all here and on your side!

[@mycerebralamyloidangiopath4710]

Thank you

[@Sarahthompson2237]

You are not alone ❤!

[@mycerebralamyloidangiopath4710]

Thanks so much

[@Sarahthompson2237]

@@mycerebralamyloidangiopath4710 : I hope you have a good day!💓

[@rosemaryeveleigh3562]

You are special so stand up for yourself

[@mycerebralamyloidangiopath4710]

Thank you Rosemary. I am trying. Take care

[@susankelland638]

Well done and good luck! Let us know how you get on won't you. XOXO

[@mycerebralamyloidangiopath4710]

Yes I will

[@mandan28]

Hello Jean, I hope you are doing well, I'm wanting to get in contact with you if I may, or could you point me to the CAA forum you have discussed in previous videos ? I am also in Australia (Qld) Thankyou.

[@mycerebralamyloidangiopath4710]

There are two that I am on. 1.. facebook.com/groups/775736939275525/ Amyloidosis-CAA- Cerebral Amyloid Angiopathy 2.. facebook.com/groups/443042499391499/ Cerebral Amyloid Angiopathy Support Group and Chat If the links do not work just search for their names. I believe they are for any country and not just Australia

[@mycerebralamyloidangiopath4710]

Is it yourself who has CAA or a carer/family member? How are you finding the Doctors are with giving you information?

[@mandan28]

@@mycerebralamyloidangiopath4710 Thankyou Jean have requested to join, It is a family member only just been diagnosed but shown symptoms for the last 2yrs +, the neurologist seems great so far, he admits he doesn't know a lot about it but he was the one that suspected it after months in hospital.