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JohnS

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Posts posted by JohnS

  1. Originally posted by Eman:

    Anybody experience this? Just herniated L5/SI and cannot seem to find much online, just people suffering and no clear cut solutions. Of course do not want surgery (already had two epidurals), so wanted to get any of this community's help.

     

    It hurts most in the morning getting out of bed. Getting in and out of cars is torture. Sitting down hurts, but sitting is ok, but then getting back up from hurts.

     

    Anyone? Any neurosurgeons on here?

     

    Been through all this before, tried a lot of stuff. The epidurals should really help a lot, they did for me. I once had 6 done before it resolved.

     

    The best supplements I have found to help were Zyflamend and Cosamin DS. The Zyflamend is a very potent herbal Cox-2 inhibitor that will reduce the inflammation over time. Also begin using the Cosamin DS, this will help rebuild the disc, there even was a study done a few years ago showing its benefits. It will take time, but it works.

     

    Once you heal enough to go to the gym begin using the lower back machine religiously. I start off each workout with it.

  2. Originally posted by Flavio:

    Laser combs are useless. Have you considered Avodart (dutasteride)? There could be, however, some serious side effects - like Bill said, consult with your doctor first. Good luck!

     

    I would have to agree, use of dutasteride is a very tricky situation, there may be possible long term issues in its use, namely neurological implications. There is no long term model as with finasteride. Best to play it safe and avoid it.

  3. Originally posted by wantego:

    Azza I'm hoping you do not mind me adding my own question to your thread. If you do let me know and I will delete it. icon_smile.gif

     

    My doctors paperwork suggest we use Rogaine on our transplants for 12 months. I think this may be to "jump start" the grafts. What will happen if we stop Rogaine after 12 months? Will we lose our growth to our grafts?

     

     

    The transplanted hairs will not regress when stopping minoxidil applications, since they are not prone to miniaturization, though the surrounding hairs might regress to their former state if they were prone to miniaturize.

     

    In a small study, minoxidil used within 48-72 hours following a transplant avoided the normal shedding of transplanted hairs in a number of participants and in others that did shed, growth began earlier than normal, using within a month or so. IMO, there really is no downside in early minoxidil applications.

  4. Originally posted by wantego:

    What do you guys find is the best way to get the foam directly to the scalp instead of all over your hair?

     

    Maybe you should try melting the foam before applying it. In small studies with the macaque, the foam was melted before application and worked. Put it into the cap and let it melt by using a small amount of heat from a blow dryer, then apply it will a dropper. This will get it directly to your scalp and it dries just as quick as in the foam state.

  5. Originally posted by alexjohnson:

    thanks guys, sore nipple or bald?? hmmm id rather suffer with my nipple lol, anyway thanks john but this sup will in no way interupt with my prop regime right? thanks again

     

    Absolutely no problem, infact it will help against hair loss by binding to the androgen receptors making it harder for the existing DHT to do so.

  6. Originally posted by alexjohnson:

    hey, been takain prop for about 9 weeks now and had no side effects untill now, my left nipple has become tendr and inflamed.... it is uncomfortable and does not look good!!! so was wondering if there was any supplements out there to counteract this? the word gyno, or geno nipple come to mind??? thanks for any help .

     

    I suggest you look into the supplement, Diindolylmethane, commonly called DIM. Dim is a phytonutrient derived from cruciferous vegetables such as broccoli and cabbage. Testing has found that is a potent hormone disrupter, being both a androgen receptor and estrogen agonist.

     

    In basic terms DIM competes with DHT for the androgen receptor (good for hair and prostate) and also rebalances estrogen metabolism by converting estradiol to the more harmless estrone (good for estrogen dependent growths, ie gyno).

     

    From my experience one of the most potent brands on the market is by Source Naturals. It is definitely worth a try in lieu of the more common anti-aromatase drugs commonly prescribed. Hope this helps.

  7. Actually Retin-A alone will promote hair growth in 58% of participants, through reversal of perifollicular fibrosis and vascular proliferation. Some speculation exists that a stem cell influence may also exist. Undoubtally most subjects employ it's use in combination with minoxidil. One other point, using Retin-A separately would be advisable since some data exists that the two may react when combined over long term, also using it separately allows users control on customizing its application to regulate individual reactions to the drug. Just wanted to clarify the point.

     

    Bazzano GS, Terezakis N, and Galen W: Topical tretinoin for hair growth promotion. J Am Acad Dermatol 15:880-883, 1986

  8. Unfortunately once daily is not equal to twice daily. A crossover study was conducted comparing subjects who switched from twice daily to once daily, all subjects lost hair. If you wish to utilize a once daily regimen, consider also adding Retin-A to your routine. A study has proven that this is equivalent to twice daily applications.

  9. Originally posted by Bill - Associate Publisher:

     

    I too would like to see some clinical evidence that propylene glycol itself is a hair growth agent. This is news to me.

     

     

    Bill

     

    I am rather surprised that you would not be aware of this, but I am more than happy to provide you with several references.

     

    I hope this information can enable members to make a more informed decision in their determination of the appropriate treatments. One should research hair loss protocols with the same fervor as one does hair transplant surgeons. Those that do reap the benefits, those that don't accept the dissapointment.

     

     

     

    Mitchell AJ, Douglass MC. Topical photochemotherapy for alopecia areata. J Am Acad Dermatol. 1985 Apr;12(4):644-9.

     

    Lassus A, Kianto U, Johansson E, Juvakoski T. PUVA treatment for alopecia areata. Dermatologica. 1980;161(5):298-304.

     

    Li LF, Fiedler VC, Kumar R.The potential role of skin protein kinase C isoforms alpha and delta in mouse hair growth induced by contact dermatitis. J Dermatol. 1999 Feb;26(2):98-105.

     

    van der Steen PH, Boezeman JB, Happle R. Topical immunotherapy for alopecia areata: re-evaluation of 139 cases after an additional follow-up period of 19 months. Dermatology. 1992;184(3):198-201.

     

    Rokhsar CK, Shupack JL, Vafai JJ, Washenik K. Efficacy of topical sensitizers in the treatment of alopecia areata. J Am Acad Dermatol. 1998 Nov;39(5 Pt 1):751-61.

     

    Shapiro J. Topical immunotherapy in the treatment of chronic severe alopecia areata. Dermatol Clin. 1993 Jul;11(3):611-7.

     

    Rauch H. The effects of topical applications of chemical agents on hair development. Physiol Zool. 1952; 25: 268-272.

     

    Chase HB, Montagna W. Relation of hair proliferation to damage induced in the mouse skin. Proc Soc Exptl Biol Med 1951; 76: 35-37.

     

    LI L.-F.; FIEDLER V. C. ; KUMAR R.; Department of Dermatology, University of Illinois; Induction of hair growth by skin irritants and its relation to skin protein kinase C isoforms; British Society for Investigative Dermatology Annual Meeting, Cardiff , ROYAUME-UNI (07/04/1999)

    1999, pp. 783-810 (26 ref.)

  10. Originally posted by Stimpson:

    Okay John, do you have evidence supporting your claim the prolyene glycol increases growth?

     

    All it ever did was make my scalp irritated to the point it peeled.

     

    Regards - Stimpy

     

    You just said the magic word, "irritated". PPG is a known irritant, something that everyone who has used it finds out at one point or another. Skin irritants can cause hair growth. This has been proven time and time again in trials with Alopecia Areata. In fact dinitrochlorobenzene, one the most potent skin irritants, is used to treat it. Another skin irritant, retinoic acid, aka Retin-A, works in a similar manner.

  11. Originally posted by Ceasar08:

    There's a doctor named Peter Proctor who is very well known for being extremely well versed on the subject of hair loss. He has long made the claim that the propylene glycol actually enhances growth quite a bit.

     

    Again... I really would like to hear more on this topic. I'd like to know if I should switch back to the liquid.

     

     

    Exactly! You hit the nail right on the head! Good!

  12. Originally posted by Stimpson:

    One additional thing that is getting lost in the shuffle here...

     

    The foam and the liquid are merely CARRIERS.

     

    The MINOXIDIL is the active ingrediant.

     

    As long as both carriers are safe and effective (they are), the minoxodil is still just the minoxidil.

     

    It is just a matter of preference. They are the same thing. Most agree the foam delivers better and irritates the scalp less.

     

    Stimpy

     

     

    Well...yes and no. PPG is a very important carrier, but serves many other purposes also, something the glycerin, the carrier of choice in the foam, cannot approach.

     

    One important note, many people may not realize it but PPG should be considered as an active ingredient, as is minoxidil, since it contributes to hair growth also.

  13. Originally posted by Stimpson:

    With all due respect, John, unless I am missing something (a possiblity), your data is not straight across comparable. The first study evaluates the foam. The second study evaluates the liquid at various strenghts.

     

    The studies are not comparable AT LEAST because the first study (TMF) does NOT specify a 1 inch diameter area on the scalp for the TAHC, whereas the second study clearly does. If the TAHC areas were not directly comparable across studies, and it is unlikely that they would be, since the studies were NOT made for comparison with one another, than you CANNOT use the TAHC as a basis for comparison between the studies. That is undisputable fact.

     

    Additonally, the first study indicates it was carried out on men of Norwood III, IIIv, or V. The second study is silent as to the subjects MPB patters.

     

    What would be useful is a study evaluating the foam versus the liquid, carried out under EQUALLY CONTROLLED CIRCUMSTANCES (i.e. patients in similar control conditions, etc.).

     

    Bottom line - Comparing two different studies with different control circumstances is a fruitless and meaningless endeavor.

     

    Stimpy

     

     

    As a matter of fact, the target area in both studies was exactly the same, one inch. You have to understand these are abstracts, not the full study, so they include only certain excerpts. My employer has a subcription to various online services so I was able to view these for further evaluation. You are free to do the same to satisfy your inquisitiveness.

     

    As far as a study pitting Rogaine Foam to Rogaine Liquid, that would never happen, since it would be financial suicide to Johnson and Johnson if it appeared their new product was relatively ineffectual as compared to their older product. They had good reason to release this product, but that is a whole different thread.

  14. Originally posted by Ceasar08:

    John---

    Thanks... but this is super confusing. According to the foam study, there was a 40% placebo effect. That's pretty crazy.

     

     

    That is easily explained. The foam acts as a thickening agent, this I am sure you noticed when using it. It simply makes your hair look thicker, quite in contrast to the liquid when makes it look worse, at least until it dries. But as you can see, the hair count increase averaged only 4 hairs in the specified area, definitely not enough to notice.

  15. This is the 5% Rogaine Foam study abstract submitted to the FDA for its approval.

     

    A Multicenter, Randomized, Placebo-

    Controlled Double-Blind Clinical Trial of a

    Novel Formulation of 5% Topical Minoxidil

    Foam vs. Placebo in the Treatment of

    Androgenetic Alopecia in Men

     

    Olsen, Elise;1 Funicella, Toni;2 Roberts, Janet;3 Kempers, Steven;4

    Piacquadio, Dan;5 Wanser, Rita;6 Zhang, Paul;6 Kohut, Bruce;6

    1. Duke University Medical Center, Durham, Northe

    CArolina, USA; 2. DermResearch, Inc., Austin, TX, USA;

    3. Northwest Cutaneous Research Specialists, Portland, OR,

    USA; 4. Minnesota Clinical Study Center, Fridley, MN, USA;

    5. Therapeutics, Inc., Lajolla, CA, USA; 6. McNeil Consumer

    Healthcare, Morris Plains, NJ, USA

     

    Although 5% topical minoxidil solution is safe and effective,

    a vehicle that does not contain propylene glycol and is more

    aesthetically pleasing to the consumer, would be a distinct

    advantage to consumers for use in androgenetic alopecia

    (AGA).

    Objective: To assess the efficacy and safety of 5% topical

    minoxidil when formulated in a new foam vehicle (TMF)

    for men with AGA.

    Method: Two-phase study:

    "?? Sixteen week double-blind placebo-controlled phase

    to evaluate the efficacy and safety of the 5% TMF.

    This phase was conducted on 352 men ages 20-49 with

    patterns IIIv, IV or V Hamilton Norwood with the primary

    efficacy endpoints of change between Baseline and Week

    16 target area hair counts (TAHC) and Week 16 subject

    assessment of change in hair loss condition from Baseline.

     

    "?? Open-label extension phase to collect 52 weeks of

    safety data with 5% TMF. One hundred forty-three

    subjects continued on this phase of the study. Safety

    was monitored by taking intercurrent history, vital signs

    and scalp irritation assessment by both investigator

    and subject.

     

    Results:

    "?? Statistically significant increase at Week 16 compared to

    Baseline in TAHC with the 5% TMF group (170.8 to 190.8

    hairs) compared to placebo (168.9 to 174.4) (p<0.0001).

     

    "?? Statistically significant subjective assessment of hair loss

    condition (p<0.0001) on 5% TMF (70.6% noted increased

    hair growth, including 47.8% moderate or marked hair

    growth) compared to placebo (42.4% noted increased

    hair growth, including 21.5% moderate or marked hair

    growth).

     

     

    "?? No significant safety concerns were raised and the 5%

    TMF was well tolerated over a one year use period.

    Conclusions: The 5% topical minoxidil product, formulated

    without propylene glycol and in a foam vehicle, is a safe and

    effective treatment for men with AGA.

     

    Only 20 hairs grew in 16 weeks...

     

    "Statistically significant increase at Week 16 compared to

    Baseline in TAHC with the 5% TMF group (170.8 to 190.8

    hairs) compared to placebo (168.9 to 174.4) (p<0.0001)"

     

     

    Due to the fact that all the 5% minoxidil studies were evaluate beyond a 16 week trial, and it would be unfair to use them as comparison, I have submitted a sample 2-3% minoxidil liquid trial using the same 16 week time period...

     

    Use of topical minoxidil in the treatment of male pattern baldness.

    Savin RC.

     

    This 12-month, double-blind, randomized study evaluated the safety and efficacy of topical minoxidil in the treatment of male pattern baldness. Three formulations were compared: 2% minoxidil solution, 3% minoxidil solution, and placebo. After 4 months all placebo patients crossed over to treatment with the 3% solution. Of the 96 patients randomized into the study, 79 were evaluable at month 12; 25 of these were in the 2% minoxidil group, 24 were in the 3% minoxidil group, and 29 were in the placebo-to-3% solution switchover group. At monthly intervals a hair count was obtained within a 1-inch diameter area on the scalp vertex. In addition, a gross visual estimate of the degree of new hair growth over the entire balding area was made independently by the investigator and the patient. At the end of 4 months there was significant regrowth of nonvellus (terminal and indeterminate) hairs in the patients using the 2% and 3% solutions (p = 0.0001). The mean nonvellus hair count at month 4 was 162.8 in the 2% minoxidil group, 155.4 in the 3% minoxidil group, and 107.1 in the placebo group. The mean increase in the 2% and 3% treatment groups was 58.2 and 48.8, respectively, whereas the mean increase in the placebo group was 4.0. Total hair counts at month 4 demonstrated significantly more growth of hair in the 2% minoxidil group than in the placebo group (p = 0.013), with no significant difference between the 3% minoxidil group and the other two treatment groups.(ABSTRACT TRUNCATED AT 250 WORDS)

     

    Bottom line..... 2-3% minoxidil liquid grew 48.8 to 58.2 hairs as opposed to 5% minoxidil foam's 20 hairs, that amounts of 2.5-3.0 times as much hairs, clearly the superior of the two.

     

    Please also note the in head to head trials, 5% minoxidil was clearly superior to 2-3% minxoidil at all data points.

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