Before the visit to the hair stylist

Submitted by Michèle on Tue, 2008-10-07 07:33

Michele, you are looking so happy, who would be able to imagine the comparison with the early photos of the progressed alopecia?  Truely remarkable and certainly unheard of in my opinion.  It looks stylish as it is to me, can't wait until the reshaping photo is posted.  Thanks for sharing this progress as this is truely inspiring. 

This type of reversal is truely life changing as much as many of the other stories here.     Louise

  • CAP(TiniOnly): 06/07-02/09 for CFS
  • MethylationProtocolSupplements: Started08/08
  • Intermtnt CAP: 02/09-02/10
  • Full MethylProtocol & LDN 02/09
  • Off CAP: 02/10, cont LDN & MethlyProtocol support

Now I see where Elly gets her glow from..your're beautiful and so is your hair. i'm with louise, your hair looks very stylish.....and alot of it.

Mphs, TN. CFS, hypoT (Hashi), adrenal fatigue, hormonal inbalance. right arm neuropathy-getting better. cpn, myco, EBV, CMV, HHV-6. Cap began in 6/07. NAC 2400mg, mino 100mg bid, biaxin 500mg bid. cytomel, flagyl bid continuously.

Red

Truly amazing, Michele.   Antibiotics curing alopecia.   Who'd have thunk it? Wink

Red

P.S.  You look absolutely marvelous!

Treatment for Rosacea

  • CAP:  01/06-07/07
  • High-Dose Vit D3, NAC:  07/07-11/08
  • Intermtnt CAP, HDose Vit D3:  11/08-01/09
  • HDose Vit D3, Mg, Zn: 01/09-

What a great success story! Visuals are always good. Congratulations on getting your hair back! Ditto what everyone has said, You look BEAUTIFUL!
jodie

Wow, Michele... you look wonderful and healthy (even better than your pic of 2007!  I agree, too, your hair looks very attractive as it is :)

 

JeanneRoz ~ DX'd w/ CPN 4/2007; 6/07 -"officially" dx'd w/CFIDS/FM; also: HHV6, EBV, IBS-C, 100 Doxy:BID; 500 mg Biaxin BID; Tindamax Pulses, B12 shots, ERFA Dessicated Thyroid,Cortef, Iodoral 25 mg, Vit D-6,000 uni

Michele, Congratulations - it is truely amazing and you do look beautiful!

5oo mgs Ceftin 2 x/day, 500 mgs Zithromax, 500 mgs 2 x tini pulses,100 mg diflucan, 4.5 ldn; Wheldon protocol for MS April, 2006 to May 2008. 2008 MRI shows NO NEW DISEASE ACTIVITY, 2012 MRI no new disease activity.

Wow! Your hair is beautiful.

minocycline, azithromycine, metronidazole 2007-2009, chelation for lead poisoning, muscle pain, insomnia, interstitial cystitis (almost well), sinus, dry eyes, stiff neck, veins, hypothyroid, TMJ, hip joints (no longer hurt)

You are truly an inspiration!  And thanks for your very encouraging posts to others (like me)!

Mary Ann

SPMS. Dx 1991. EDSS 6.0, 6.5, 6.9; Weldon CAP. started 3/08.  All supps, NAC, Doxy, Azrith, 13 flagy pulses, 5th tini pulse 11/13/09, 19 total pulses, no improvements, worsening condition 

Michele, you look great!!

So happy for you!

Thanks for sharing.

Best Wishes from Maria

 

Cpn since sep 2006. Autoimmune thyroid,hypofunction.levaxin,b12+folic acid.All classic cpn,porphyria and toxinsymtoms.Not able to work.Selftreating cpninfection with AllicinMax(garlic), NAC, high vitamin D3. CAP for over 3 years. Back to work and life

Amazing transformation!  Michele, you truly are radiant these days.  How does it feel to have options on what to do with your hair?.....Perhaps the better question is "How does it feel to have so much hair?"  Good for you!

Joyce~caregiver-advocate in Dallas for Steve J (SPMS).  CAP since August 06, Cpn, Mpn, B. burgdorferi, systemic candidiasis, EBV, CMV & other herpes family viral infections, elevated heavy metals, gluten+casein sensitivity. 

I don't have anything original to say, but you do look good! Dare I say, younger, too?

 So far, the only additional hair is on my arms and chest, but it's become quite impressive (if that's the word.)

 Really, congratulations!

 

Ron

On CAP for CFS starting 01/06 (NE Ohio, USA)

Began rifampin trial 1/14/09

Currently: on intermittent

The best bit about the hair is that you can see it as a sign of recovery.   Many people have to wait for a long time to see significant recovery.   My daughter is a case in point, it would be so good if she could see signs of recovery which are really visual.

Although my hair is spectacularly better than it was, other symptoms are only just beginning to improve, but having a daily reminder that this treatment works keeps me going.

Thanks for all the comments, I really appreciate the encouragement and I'll have Norman Parkinson (aka Hamish) take another picture of my new look on Thursday.

Michèle (UK) GFA: Wheldon CAP 1st May 2006. Daily Doxy, Azi MWF, metro pulse.

Michele, it is interesting to me from an Oriental Medicine perspective that  correspondences of the Lung and the Large Intestine (a pair of yin and the yang organs expressioning the metal element) are the skin, (sometimes referred to as the third lung) and the hair.

I find this all quite interesting from a theoretical point of view since CPn is a respiratory bacterial infection in it's transmission and onset. 

Personally my element is wood.  Which is expresses by the Liver and the Gall Bladder. My continued moderate liver enzyme elevations may be indicative of a primary site of CPn in my situation (particularly since all the viruses that take up residence there have been ruled out) and to note also that I do have resident Gall Stones, have known this for 30 years.  For me hair has been easy, I have been able to grow hair to the bottom of my torso, even into my 50's. 

I could go on about the other elements it is just another way of looking at the body. 

Yes I agree, it certainly is a sign of recovery and quite a remarkable sign for sure.  To regrow lost hair is no easy task, almost impossible.

  • CAP(TiniOnly): 06/07-02/09 for CFS
  • MethylationProtocolSupplements: Started08/08
  • Intermtnt CAP: 02/09-02/10
  • Full MethylProtocol & LDN 02/09
  • Off CAP: 02/10, cont LDN & MethlyProtocol support

Michele,

I have pics of myself that date back thru the MP.  My hair started out very thin and scrawny looking (so did I at one point) and then as I began to feel weller, my hair (and skin) and the rest of me looked much more radiant.  My hair looked vibrant and thicker and my haidresser commented.  

Since I began CAP and have had stronger reactions, my hair has been falling out more again, getting thinner and lifeless.  I think the hair is indicative of your state of wellness.  I believe my hair (and skin) have both worsened now as I am eradicating the infection, hence, increase in cortisol activity and instability in the hormones.  

Glad to see you!  You look mahvelous!!! Kiss

NAC 2.4g, Zith 250mg/MWF, mino 200mg, Tini 5day/1g/5 pulses, Valcyte
Supplements, CFIDS/FMS, Hashimoto's, Psoriasis, PA, IBS, Sec Addisons

Don't believe everything you think!  

Michele- you do look healthier too! This is an amazing visual record. Thanks for continuing to post your progress this way.

Reenie- I think Michele reported a period of hair loss prior to regrowth. The thought being apoptosis or necrosis of previously infected cells, the hair falling out, then regeneration with fresh uninfected cells, especially after flagyl pulses. Maybe Michele will remind us.

 

CAP for Cpn 11/04. Dx: 25+yrs CFS & FMS. Currently: 250 aithromycin mwf, doxycycline 100mg BID, restarted Tini pulses; Vit D2000 units, T4 & T3, 6mg Iodoral

holy moly, you look marlevous!! absolutely radiant!

congrats!

peace

r

 

CFIDS/ME, FMS, MCS, IBS, EBV, CMV, Cpn, H1, chronic insomnia, Chronic Lyme, HME, Babesia, Natural HRT-menopause, NAC 2.4 gm,Full CAP 6-2-07, all supplements+Iodorol, Inositol-depression, ultra Chitosan, L lysine Pulse#27 04-19-10 1gm Flagyl/day-5 days<

Couldn't be happier for you, Michèle...you SO deserve this!!! You, who work so hard taking care of your loved ones, and supporting all of us, too. It's a wonder that you've had any time or energy left to take care of you and achieve such a remarkable accomplishment!

 

It was you, and your story that recently helped me with a recent episode of hair loss--due to weight loss/protein deficiency. Whenever I was scared or felt sorry for myself, I had only to think of youWink

 

You look so beautiful in that picture...am looking forward to seeing more!Laughing

 

 --Minai

 

RRMS, diagnosed 2/04. NAC 4/06. Started Wheldon/Stratton regime 8/30/06. Doxycycline, 8/06, Azith, 10/06. Switched to Roxithromycin 11/06. Psuedo relapse/die-off with hospitalization 1/07. GAD-enhanced MRI of brain and spine shows NO NEW DISEASE ACTIVITY. LDN 4/07. 1st Tinidazole Pulse, 8/11/07. Keflex 2/08. IV Rocephin 3/08. IV Clindamycin 5/08. USA

 

Jim is right, initially there was a marked regrowth of hair and from that point the amount of hair never returned to the previously thin covering I had when I started the cap, but the process is still two steps forward and one step back, so after a pulse (not necessarily every pulse as some of us have noticed that the pulse affects different areas of the body at different times) I will get the tell tale signs of impending hair loss: a bruised feeling, some itchiness and then about 10 to 15 days later the hair falls out.   It then takes about 3 to 4 months for signs of new hair growth. 

The process is ongoing, there are still small (smaller and smaller) patches of hair falling out at different times, but the balance is on the side of regrowth and staying put... not falling out.    Possibly when I no longer have hair loss in this way it will be time for me to go on intermittent protocol.   I hope by then that the rest of my body will have caught up, I'm still having skin problems: an incredible number of small blind spots on chest and legs, some IBS pain (not as much as in the past), some joint pain (not as much as in the past), numbness in my feet, (not worse but not better), although the pain in my legs and feet is no longer constant; but I think it was Dr Stratton who said that Cpn may be affected by gravity, in which case the feet will be the last thing to recover.

It might be worth mentioning that in the two and a half years I have been doing this treatment I have done 43 flagyl pulses.   I start a new pulse every 21 days, so if people are doing one a month it might well take longer for them to see results.   This regime was pretty tough and for 9 months it was really unpleasant and on a number of occasions I had to cut the pulse short.   I still find it practically impossible to do more that 5 days, but I have upped the dose to four 350mg tablets a day for 5 days.   My urine is mostly a normal colour now, so that indicates that the Cpn load has been reduced considerably, as it always used to be a very dark brown colour during pulses.

I would like to say that I very much appreciate the nice comments people have made about my glowing appearance.   There are days when I look at myself in the mirror and wonder what has happened to me in the past two years, but maybe from a distance that does not show up so much.   Norman Parkinson (aka Hamish) took a good picture....   Even I think I look good in it, and I must be the worst critic of my appearance....

In the future I will write a part two to my story and include some other photographs to chart the progress of the treatment.   I feel so lucky that I have a condition that lends itself to this kind of charting, visual evidence is always so convincing.

Michèle (UK) GFA: Wheldon CAP 1st May 2006. Daily Doxy, Azi MWF, metro pulse.

Michèle, please don't have too much done to your new hair because it is so lovely and natural as it is..............Sarah

An Itinerary in Light and Shadow

Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.

Michele, how many people would love to have hair like yours - it looks wonderful without much time-consuming care. You look stunning!

3/9 Symptoms returning. Began 5 abx protocol 5/9 Rifampin 600, Amox 1000, Doxy 200, MWF Azith 250, flagyl 1000 daily. Began Sept 04 PPMS EDSS 6.7 Now good days EDSS 1 Mind, like parachute, work only when open. Charlie Chan  In for the duration.&am

What a stunning difference, Michele. No one can deny the effect of abx in your case. Remarkable!

The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi

You look great in that pink top!  I think pink is really a good color for you.  I hope you don't color your hair.  It looks so pretty.  And you look so happy.

FMS/CFS 1995. tinnitus, ibs, sinusitis, EBV, NAC 2400mg, valtrex, cortef, armour, doxy, biaxin, tini, vita c 5 - 10,000 daily 

I thought I would show you the state of my hair before I visit the hair stylist on Thursday.   I'll show you an after too....   Hamish took this picture whilst I was sitting on Eastbourne seafront yesterday.   I was on my way to have a consultation with the hair stylist and make the appointment.   A red letter day for me.

For those who don't know when I started the protocol I had very little hair and what was there was white, now it is a steel grey (for the time being) which means that a lot of my dark hair has grown back.   If you want to see what it was like when I started take a look at my story the patient's stories.