Oh my. I am saddened to hear about the outcome.
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I have a question for those with FTD. Are any of you using homeopathic remedies for any symptoms/condition ? My nuerologist recommended I use OTC liquid B-12 drops which I have been taking since my diagnosis. I am not certain if any additional supplements are suggested.
Thank you in advance for your replies.
Hello Bill. Thank you for your reply and for sharing. I agree with you that a support group would be a benefit as there would be an understanding of the disease with the participants. I am currently participating in cognitive therapy sessions which is helping me to incorporate new routine behaviors.
Thank you for your encouragement.
Hello there. Thank you for your reply and suggestions. I feel like Alice in Wonderland in trying to advocate for myself and finding a local support group in the north Orange County region of California. I spoke with a respresentative from the AFTD and inquired about a group in my region and there is none. I am awaiting receipt of an information packet and curious to read the contents.
Hello Scott. Thank you for your post. It is encouraging to know you are knowledgeable of FTD and sad to hear that you MIL was also affected by the disease. I have a question, did your MIL have ear ringing and pressure headaches above the eyes? I have been experiencing these new symptoms this week.
Thank you for your time.