Where are you now, #1RiskyRich - My MSAA Community

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Where are you now, #1RiskyRich

CalfeeChick profile image
CalfeeChickCommunityAmbassador
β€’8 Replies

We were chatting about stem cell treatment. Didn't you go to Mexico for treatment?

Lynn

#Calfeechick

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CalfeeChick profile image
CalfeeChick
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8 Replies
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swb83 profile image
swb83

No, sorry my brain does not work like it used to!

CalfeeChick profile image
CalfeeChickCommunityAmbassadorβ€’ in reply toswb83

:-)

1RiskyRich profile image
1RiskyRich

Yes. I went to Mexico. I will be 6 months post in November 8th. Saw a lot of improvements the first 2 months and everything else is coming little by little. I was told I would see a lot of relief at the beginning because there will be nothing to creat anymore inflammation and what's there will start to go down. He also said that I will be seeing improvements for up to 2 years. I am already happy with the results.

CalfeeChick profile image
CalfeeChickCommunityAmbassadorβ€’ in reply to1RiskyRich

Thanks for your reply. Hope you continue to see improvements! Keep us posted. Lynn

Amore55 profile image
Amore55

Kelly Morgan here. Don't want to intrude in your personal conversation, but what are your thoughts on stem cell treatment? I am very interested in it. Thanks so much!

CalfeeChick profile image
CalfeeChickCommunityAmbassadorβ€’ in reply toAmore55

I was just diagnosed in August. No treatment yet. What I have found out through research is that stem cell is not legal in the United States. However if you read Richie Rich above,he went to Mexico and is doing well. I would definitely consider it sounds very expensive not within my means.

Amore55 profile image
Amore55β€’ in reply toCalfeeChick

Hi Calfee Chick! Thanks for responding so quickly. I know that treatment is beyond my means too. My husband and I thought about a go fund me set up. But it is a lot to raise. It would be nice to be rich for something like this. I am so sorry you just got diagnosed, it can be really scary the first little while. If I can be of any help, please let me know. By the way, my name is Kelly. Stay in touch.

CalfeeChick profile image
CalfeeChickCommunityAmbassadorβ€’ in reply toAmore55

Thanks Kelly, i'm really trying to remain optimistic. I've started with a Neuro at UCSF and have confidence that I'm going to receive really good treatment. I'm also open to research and have already okayed them to use my blood and spinal fluid for research so maybe I'll get considered for some stem cell research. πŸ‘πŸ˜Š

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