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Anyone know where to get Compression socks? Do tube socks with extra elastic do the same?
One thing I've been very confused about is who exactly is in charge of determining what mix of stem cells is best for CFS patients. My initial impression was that Cheney was mostly dictating this, but I've done a lot of digging and it turns out that it's more of a collaborative effort between Dr. Cheney and the owner of the clinic, and actually it seems that most if not all of the alteration happens within the clinic and later becomes reported to Cheney.
I think this is opposite from what most of us assumed was going on.
Regarding specifics, I've been informed that the clinic's owner and medical director currently thinks the threshold is at around 30mil expanded cord cells for clinical benefit. (Expanded means they have been previously expanded under culture conditions and frozen) In addition are "fresh" unexpanded cord cells which he thinks to have the potential to multiply once they're injected, so although the unexpanded cord cell count going into both the IV and intrathecal is about 500,000-1mil each, this can quickly become tens of millions. It is not clear just how much they replicate.
So with that said, this is the exact protocol that the clinic is quoting as the current "standard CFS protocol that all cheney patients are receiving":
3 infusions of 3 mil, 4.5 CD34 cord cells (all expanded)
1 infusion of 3 mil mesenchymal + 1 fresh cord of CD34 (~1 million unexpanded)
1 intrathecal injection of 3 mil mesenchymal + 1 fresh cord of CD34 (~1 million unexpanded)
So if you add it up, the technical grand total of stem cells we'll be getting is 30.5 million, but ~2 million are unexpanded so it has the potential to become far more.
Please understand that the protocols may change as the clinic learns what's best for us. Autism and MS patients have been getting intrathecals as well. Cheney is telling his patients it is optional for now because the long-term risks are too unknown, but since it is being recommended by the clinic to all the CFS patients applying now, the clinic must believe it is pretty safe.
Originally Posted by Mr.Kite
I'm also wary of these reports of the cheney patients showing either no results, or results only lasting for 6 months before some relapse.
Anyone know where to get Compression socks? Do tube socks with extra elastic do the same?
I love these knee socks--they are mostly cotton, imported from Italy and make a huge difference for me if I need to be standing or walking for any length of time. They are so comfortable I forget I am wearing them. I found the sizing chart wrong though--needed a larger size--but the company happily sent a new pair and told me to keep the old ones. http://www.brightlifedirect.com/BRA...-Sock-20-25mmHg---Item#-113/product_info.html
Sushi
So with that said, this is the exact protocol that the clinic is quoting as the current "standard CFS protocol that all cheney patients are receiving":
3 infusions of 3 mil, 4.5 CD34 cord cells (all expanded)
1 infusion of 3 mil mesenchymal + 1 fresh cord of CD34 (~1 million unexpanded)
1 intrathecal injection of 3 mil mesenchymal + 1 fresh cord of CD34 (~1 million unexpanded)
Yes there are multiple groups going. One is going for sure at the end of August. I'm planning on going in September.
This hasn't been discussed yet, but for all those that are thinking about going or planning on going, this is the org through which patients can organize fund-raising with tax-deductible donations: http://www.ntafund.org/
It doesn't work if you are paying for it yourself, but does if you have family members of friends contribute. For every $5000 you raise, then match with a $500 grant, and for every $10k they match with $1k, equaling a total of $1500 grant if you get the full 10k contribution. The funds raised can be used to cover not only treatment expenses but also transportation, housing, and other treatment-related expenses.
m0joey
Do you guys have enough people yet that are committed to the trip to actually do it? I'm deeeeeeeply interested!
If you are deeeeeeeeeply interested in going (and deeeeeeeeeply is good!)--then you should PM Molly29 as she's coordinating the non-Cheney groups headed for Panama.
And btw, for all y'all interested, I can confirm that for her generous efforts, Molly's referral fee has her walking with a suitcase filled with $98,000 in Monopoly money per patient. Plus a shiny promotional thermos of hot jack Sh*t.
And you are "confirming" that how?
Not that it really matters. As long as the treatment is legitimate, I personally wouldn't care if they gave the whole 10 grand to a referrer. With Cheney it would be a slightly different story, as in that case there obviously would be a more formal, or professional/ethical conflict of interest. But with a "private"/non-medical provider individual, the only question in that case would be to what degree the necessity of paying a middleman (as it were - or middlewoman) was adding to the final cost that could instead be passed on to us. I just find it a little amusing that someone would claim to be "confirming" something for which they actually haven't confirmed anything. :Retro tongue:
For anyone wondering, I'm confirming that I actually ran a 10k today, after 20 laps in my friend's olympic pool before breakfast.
I can confirm because
1. Saw the multicolored monopoly bills spilling out of the suitcase.
2. I got the thermos and it's monogramed "Mr. Kite" -- do you want it?
But as long as your asking, here's the full story:
--------------------------------------------------------
• MOLLY'S PAYMENT -- CYNICISM, NAME CALLING, QUESTIONED MOTIVES, AND FAR TOO FEW “THANK YOU’S”
To set the record straight:
I was present during the two phone calls as Molly negotiated your excellent group rate (~40% discount) with the heads of the Clinic.
Never on a board have I seen so many intelligent, helpful and well researched posts juxtaposed with so
much cynicism, ingratitude and entitlement (from a vocal few anyway).
For the countless hours Molly has spent fielding our phone calls (questions, tragic stories, requests), negotiating a dream price,
dealing with the clinic....I've watched my respected new friend exert maximum effort simply because she wants to help.
And what's more, she can. She's a savvy businesswoman and wouldn't need kickbacks even if they existed.
And they don't. Call the clinic and ask Melisa about referral fees. She (and her colleagues) will laugh.
Melisa Cristaldi
Patient Relationship Coordinator
Stem Cell Institute
Panama City, Panama
International Phone (507) 301-0210
International Phone Fax (507) 204-8531
US Toll Free 1-954-636-1126
US or Canada 1-954-636-5117
www.cellmedicine.com
OR if you're going to Panama, ask the Medical Director Dr. Paz about referral fees.
If this is how we treat healthies, no wonder most of them leave the boards.
But Molly chose to stay, cultivate and offer us an amazing gift even though every step
of the way we kick the tires, say "it's too good to be true, " question her motives, call her "a shill."
No wonder she doesn't come round her much.
I am SO LUCKY that out of sheer kindness Molly busted her backside to organize a group
and negotiate a price from something that would be totally out of my range to something
that I can somehow beg and borrow to make happen.
For the final time. MOLLY SHILLS FOR NO ONE -- BUT YOU. With no reward except our
gratitude and in my opinion there has been far to little.
THANK YOU MOLLY.
(and I'm done with this banter. Goodnight.)