New here? Some Best Practices

Newcomer introductions, personal anecdotes, caregiver issues, lab results, and n=1 experimentation.
Resilientk
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Re: New here? Some Best Practices

Post by Resilientk »

All: Thank you for your kind and thoughtful replies. I am so overwhelmed.
Renlets: Your words about seeing me and my pain made me cry. Thank you so much!!! That should be what doctors tell patients all the time. I bet that would make a huge difference. And thank you for the resources, I will look through everything.
Tincup: The resources on breathing were quite interesting, thank you so much. Sometimes we forget simple things in the search of a solution.
NF52: You are wonderful, thank you for your feedback. And I commend you on turning your focus on yourself and your family. You can try helping someone, but you cannot do it for them. I had a similar situation with my sibling, but some time ago I sat down, analyzed our whole relationship and realized there is nothing I should feel guilty about, that was a big relief.
I have been upset about the gene finding the last few days, testing my memory, trying to give myself new tasks at work, etc. but decided to give myself a break for now. I have enough reasons for minor memory gaps for now: my mind frequently goes in circles due to anxiety and pain, I have a four year old full of energy, and I have been very uncomfortable with my rigid diet—that’s not forever, I can survive without flavor for a few months :).
I have a Lyme test coming up. If it’s negative, I should stop searching and focus on all the good information you have shared.
Thank you again.
Best,
K
maritimemaid
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Re: New here? Some Best Practices

Post by maritimemaid »

Thanks for outlining the lifestyle changes and dietary advice. I recently learned of a ApoE4- one copy result in my blood work. I believe that knowledge is power so became pro-active about cognitive decline which led me to the Bredesen ReCode program.
This is a wonderful resource here, and I hope to be able to contribute with my limited knowledge of fatty fish and seafood in general. My husband and I have been commercial fishermen (35-50 yrs) and now run a mom&pop oyster farm.
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lgoring
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Re: New here? Some Best Practices

Post by lgoring »

maritimemaid wrote:I believe that knowledge is power so became pro-active about cognitive decline which led me to the Bredesen ReCode program.
This is a wonderful resource here, and I hope to be able to contribute with my limited knowledge of fatty fish and seafood in general. My husband and I have been commercial fishermen (35-50 yrs) and now run a mom&pop oyster farm.
Welcome and Happy New Year’s Eve maritimemaid,

I wanted to take a moment to welcome you to the APOE4 community and quickly introduce you to the site.

Some helpful tips and tricks to navigate the site include the How-To Guide. This guide is a great resource I found helpful when I started posting. It includes topics such as navigating the forum, private messaging, and searching. One great tip is using the quote button (") when replying to a post. Using this button will automatically alert the member of your response. It really helps keep the conversation rolling.

The Primer also gives a nice intro about the ApoE4 gene and was written by a physician member of the ApoE4.info community. I’m happy you found the forum and look forward to your contributions about fish and seafood!

If you would like any other tips for navigating the site, feel free to reach out!

All the best,

lgoring
ApoE4/4
Certified Health Education Specialist
Functional Medicine Certified Health Coach
jblake
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Re: New here? Some Best Practices

Post by jblake »

I am new here. I have not been tested yet. Need to find reputable source. Also one I van afford. I read testing APOF4 genes was $300 but lowered to $99. Where can I find for $99? I am 76 and had very severe head injury in 1983. I have had minor ones since. I have always feared Alzheimer’s. I have had more and more memory confusion. I live in Los Angeles area.
NF52
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Re: New here? Some Best Practices

Post by NF52 »

jblake wrote:I am new here. I have not been tested yet. Need to find reputable source. Also one I van afford. I read testing APOF4 genes was $300 but lowered to $99. Where can I find for $99? I am 76 and had very severe head injury in 1983. I have had minor ones since. I have always feared Alzheimer’s. I have had more and more memory confusion. I live in Los Angeles area.
Welcome, jblake!

We're so glad you found this community and have reached out with a great question. I want to first apologize for taking the liberty of removing your zip code and email from your post. As a Moderator and member of the Admin. Support Team, we want to support the privacy of all of our members, and having your email on a post would make it visible to anyone who read it.

You don't mention why you want to get tested, but might want to read this information on Thinking About Testing [Click on the blue to go to that page.]

If you have an Amazon Prime membership, you can order a 23andme Health and Ancestry test that includes ApoE for $99. ONLY through tomorrow (6/22/21. Here's a link: Amazon Prime: 23&me DNA test

Life Extension also offers a sale on an ApoE test for $ 111.75 here: Life Extension: ApoE Genetic Test.

In both cases, you will be sent a kit with a cheek swab or "spit tube", with instructions on how to take the sample and send it back. Results are usually returned in a few weeks.

Unfortunately, Medicare does not pay for genetic testing like ApoE.

If you have concerns about your memory, language, hearing, balance or other skills, Medicare would probably pay for an evaluation at UCLA Memory Health UCLA also has what looks like great online program for "healthy living" for seniors in the UCLA Longevity Center They include a Memory Training program, Brain Boot Camp and Sharper Mind Series.

Happy Summer from someone who's a few years behind you in age and aware of how much hard work you've put into recovering from a severe TBI years ago. Enjoy having a brain (and a spirit) that doesn't give up!
4/4 and still an optimist!
NoNotMe
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Re: New here? Some Best Practices

Post by NoNotMe »

Hi Jblake,

Welcome to APOE4. We're very happy you found us. I see you have a thoughtful response from Nancy. She is so knowledgeable and a real expert! As she said, recovering from a severe TBI is quite an accomplishment. I'm very happy for your recovery.

As you gather information I thought you might find the following pages on the site helpful. Here is the Primer which was written by a doctor who is also a member of our community. This is a link to the WIKI page which also has a search function. There is such a huge amount of content here.

Please explore, discover and share your story. We all learn from each other here.

In Best Health!
Erin
Functional Medicine Health Coach
Integrative Nutritionalist
bellavend
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Re: New here? Some Best Practices

Post by bellavend »

Hello,

I'm new to the forum and a 4/4 and from Australia. I'm looking forward to delving around this forum and discovering new things.

Cheers, Bella
Keto306
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Frightened a little but hopeful

Post by Keto306 »

I am reading Dr Bredesen’s survivor’s book and will read his program book next. I am so thankful to this forum as it will answer so many questions and help me to do what I can. I have one variant of the ApoE4 gene. While reading the survivor stories I recognize me in a few ways. Well … here I go … to learn all I can.
JeniO
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Re: Frightened a little but hopeful

Post by JeniO »

Keto306 wrote: Wed Jan 26, 2022 4:34 pm I am reading Dr Bredesen’s survivor’s book and will read his program book next. I am so thankful to this forum as it will answer so many questions and help me to do what I can. I have one variant of the ApoE4 gene. While reading the survivor stories I recognize me in a few ways. Well … here I go … to learn all I can.
Welcome to APOE4.info, Keto306! Glad to see you in the forum!

It sounds like you love to learn, care about your health, and are digging in to figure out how to apply this information.

As you look around the forum, here are some pages that may be helpful to begin:

Here is a link to the primer and our How to Guide.

As you may have already seen, there is a helpful search tool available in the top right-hand corner of the site that you can use by clicking the three dots next to your log-in id. You can use that to search for topics in the various forums.

If you'd like to tell us more about yourself and how you found us, check out the Our Stories Forum

We are glad you found us and hope that this site will continue to be useful to you in your journey.
Be well,
Jeni
Functional Medicine Certified Health Coach
National Board Certified Health & Wellness Coach
"Don't judge each day by the harvest that you reap but by the seeds that you plant." - Robert Louis Stevenson
Tim@1009
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Re: New here? Some Best Practices

Post by Tim@1009 »

Hi - My name is Tim. I joined in November 2019 but have not been to this site in a couple of years.

I wanted to share an experience I just went through. I found out in 2019 through 23 and Me that I have two copies of the APOE4 gene. I recently became involved in a Clinical Trial call the AHEAD Study. My father passed with Alzheimer's in 2008 (86) and my sister has Alzheimer's (74). My dad was diagnosed with Alz in his late 70's. My sister was 68 when diagnosed. She has one copy of the APOE4 gene. The Ahead Study is looking for people with a family history of Alz similar to mine that currently do not have cognitive/memory issues. They are trying to reduce or remove Amyloid plaque from the brain before there are cognitive/memory issues with an experimental drug, Lacanemab.

I met with the AHEAD Study team and did extensive cognitive/memory testing which confirmed at this time I do not have cognitive/memory issues. I had blood tests done. One test was to confirm my APOE4 status. I then had a PET scan of my brain to determine the amount of Amyloid plaque in/on my brain. It was revealed that I have no Amyloid plaque in/on my brain. This means I can no longer be part of the AHEAD Study. The doctor heading this study said I am a anomaly of sorts because of my APOE4 status and my age (64).

I am on this site to see about folks with similar APOE4 status as me. Thanks.
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