Archive for the ‘Treatment’ Category

What To Do When You Hit a Plateau In Treatment

https://globallymealliance.org/hit-plateau-treatment/?

By Kerry Heckman

My numbers won’t budge. Every month I go in for a blood test and every month I get an email from my doctor stating that my inflammatory markers are the same. The numbers are not so high to cause a panic, but they’re not low enough to signal any real improvement either. I’ve tried everything from meditation to medication, but nothing seems to work. Each month I pray the numbers will drop and I’m devastated when month after month they stay the same.

I’ve put in all the work; there’s been no stinting. I’ve been in treatment for three years. I’ve changed my lifestyle, my diet, and most difficult of all, my mindset. But I keep coming up short. There’s no doubt I’m better. My bedridden days are mostly in the past, and the pain that keeps me up at night (painsomnia, I call it) happens once or twice week instead of every day. Another marker of my improvement is after treatment my herxheimer reactions are greatly diminished. These are positive trends, but still I am not where I want to be. I want clinical proof that my recovery is real. I want to know unequivocally that I’m heading toward remission. I’ve  been at this dreaded plateau for months waiting to break free. I anxiously await the day when my inflammatory markers take a dramatic drop.

Your plateau may be different than mine. Maybe you, too, made big improvements in the beginning and now it’s tapering off, or maybe you’re stuck waiting for any minuscule improvement at all. Either way the lack of progress may be the hardest thing to bear.

All this was weighing heavily on me. Then one day I started thinking about actual plateaus in nature. Consider for a moment you are climbing up a mountain and reach a plateau. You’ve done the grueling work of going up the mountain and now you are walking on level ground. You are still moving forward, that hasn’t changed, but you’re not increasing your elevation. Maybe that’s what plateaus are in treatment—a leveling off that doesn’t feel like progress, because you aren’t climbing anymore. But you have achieved an incremental improvement in your recovery.

This bit of visualization changed the way I thought about my lack of headway, though  there were still some questions I needed to ask myself— questions you may need to  ask yourself as well:

Q: Have I really plateaued or is my progress just going slowly?

A: With Lyme disease the improvement can be slow . . . very slow. As they say, any progress is good progress. If you feel comfortable with your treatment protocol, you may need to practice patience and remember you are getting better. However, sometimes the progress is too slow and even if there is incremental improvement you may want talk to your doctor about exploring ways to speed up your treatment plan.

Q: Have you hit a plateau before? What helped jumpstart my healing?

A: If this has happened before, what was it that made the difference? Maybe it’s a new supplement or an increased dose of medication. Maybe your thyroid or adrenals are out of balance and need attention. Try to remember back to what helped you before and try it again. It may help to keep a journal about what you think is and isn’t working for you.

Q: Do I need to change my treatment or ride it out?

A: As I said, with Lyme getting better takes time. Ask yourself if you think your current treatment plan is sufficient to to get you better. This is a good place to use your intuition. If you feel skeptical every time you meet with your doctor that might be your body telling you something.

Q: If I plan to stay the course when will I know it’s time to adjust?

A: Give yourself a timeline—six months, nine months—for when you want to reevaluate. Verbalize your timeline to your doctor, so she or he knows what you’re thinking. Ask if there is a test that can be run at that time to compare where you were before to where you are now.

Q: Am I testing too often?

A: If you’re like me and your numbers aren’t budging, maybe it’s time to put more space between tests. This depends naturally on what is medically advisable. But I I did realize that the constant testing was causing me frequent disappointments, which weren’t good for my healing. I have since decided to go from once a month to once every other month for my bloodwork and focus on other things in the meantime.

Q: Is there something else I could do to move forward?

A: A plateau is the perfect time to reevaluate your habits. Perhaps it’s time to add more nutrients to your diet or increase detox. Have you always wanted to try a complementary therapy? Now may be the time. Or are there other options?

Q: Is this a good time for a healing pause?

A: Have no doubts, recovery from Lyme treatment is a full-time job. It seems like there’s always something else you can try, but is that the best thing for your body? This could be an indication that it’s time to take a break from all the intensity and let your body rest at the top of the mountain.

Take some time and ask yourself these questions. Get quiet and let your intuition speak. There are few doctors, medications, or therapies that can give us as much insight as our own common sense. Remember the image of the mountain and keep walking forward on the level ground of the plateau—the uphill slope may be only a few steps ahead.


kerry heckman

Opinions expressed by contributors are their own.

Kerry J. Heckman is a licensed therapist and author of the healing and wellness blog Words Heal. She was diagnosed with chronic Lyme disease in 2016.

 

 

______________________

**Comment**

Great article to begin meaningful dialogue.

  1.  Not sure what tests she keeps having done but I’ve heard mixed opinions about the CD-57 test which some docs swear by and others like my own say it’s a general, very basic indicator of immunity and unless you have the number before you were sick and then taken at regular intervals throughout treatment, it’s just a number. https://www.tiredoflyme.com/cd57.html
  2. Inflammation is a definite bad-boy.  One thing I discovered to eventually help me was MSM; however, I didn’t notice the help taking it while in treatment, only after treatment did it seem to really crush pain and inflammation:  https://madisonarealymesupportgroup.com/2018/03/02/dmso-msm-for-lyme-msids/.  This article also shows it’s good for the gut:  https://madisonarealymesupportgroup.com/2018/01/03/the-invisible-universe-of-the-human-microbiome-msm/
  3. Another thing that helped this inflammation/pain for me was systemic enzymes: https://madisonarealymesupportgroup.com/2016/04/22/systemic-enzymes/  There are many brands out there.  You might have to try a few to find one that works. I’ve tried different variations of Wobenzym as well as a brand my doctor sells. (I’m not affiliated with any companies)
  4. LDN was also a game changer:  https://madisonarealymesupportgroup.com/2016/12/18/ldn/ I use a compounded form with only olive oil as an additive.
  5. For many, Lyme/MSIDS causes imbalances and deficiencies in the body. Finding out what those are and supplementing can make all the difference.  For instance, most patients struggle with thyroid dysfunction (as well as other hormones) and magnesium deficiency (magnesium can help depression and 1,000 other things):  https://madisonarealymesupportgroup.com/2018/01/16/magnesium-an-invisible-deficiency/ (In the comment section I give the kind my LLMD sells in his office and it’s been particularly successful. Again – no monies are exchanging hands)  https://madisonarealymesupportgroup.com/2018/03/12/the-importance-of-vitamin-d-k-and-magnesium-for-lyme-msids-patients/ Most of us Northerners are deficient in vitamin D.
  6. I’ll never forget the ranger in the documentary, “Under Our Skin,” state that he never could have imagined that his greatest improvement would come AFTER three years of treatment.  This has been my experience and my husband’s as well.  I must add that after 4.5 years of treatment for us, and two relapses requiring 2-3 month stints of treatment, we got better EACH TIME we treated. This very well could be the “cycling” approached discussed by Dr. Burrascano here:  https://madisonarealymesupportgroup.com/2018/12/28/the-history-of-lyme-disease-dr-burrascano/  In brief:  he found that cycling 3-4 times typically worked for most patients. Ironically, the 3rd cycle yielded the worst herx.  Pam Weintraub wrote about this in, “Cure Unknown:  Inside the Lyme Disease Epidemic,” way back in the 90’s, yet few doctors do this. Cycling just means that after you are symptom-free for 2-3 months you quit ALL treatment.  If and when symptoms return, you hit hard with antibiotics until symptoms leave again. You do this 3-4 times.  Burrascano states his symptoms never returned and many of his patients had the same experience.
  7. Sometimes diet has made all the difference for some patients – like cutting out gluten or dairy or both. For some, herbs or treatments for inflammation made all the difference or help with sleep.  I’ve also known patients who got better only after they treated for worms/parasites: https://madisonarealymesupportgroup.com/2017/10/03/removing-parasites-to-fix-lyme-chronic-illnesses-dr-jay-davidson/
  8. When I hit a plateau after years of treatment yet still had symptoms, I called another LLMD I knew and asked if he’d be willing to do a phone consultation with me, not as a treating physician, but as a second ear to hear what I’ve done to give me ideas for any omissions he saw. That phone call was worth every penny as he carefully listened to what I’d done and gave me ideas for things to try.  Very helpful. I then took that knowledge to my LLMD and he was smart enough to implement them at my request based on another experienced practitioner’s wisdom.
  9. Lastly, I’ve found surrounding myself with experienced patients and doctors to be extremely helpful. You learn a lot by sharing your experiences and always come away with something you haven’t tried before.  Don’t let this information bog you down. Only try 1 thing at a time so you can track any changes. Support Group is a great place to do this.  Always run things by your practitioner as there might be drug interactions or things you need to consider or can’t try at all based on your specific issues/drug interactions.
I’ve learned the most from patients who are on the same journey. Don’t isolate yourself.

Not All Headaches Are Alike: What’s Causing Your’s?

https://globallymealliance.org/lyme-disease-symptoms-headaches/

Headaches are a common symptom of tick-borne illness. Now that I’m in remission, I rarely get headaches. When I do, I’ve become adept at recognizing why I have them. Knowing the nuances of my headaches helps me determine whether my pain is Lymeor babesia related—or from something else entirely—and how to treat it. In short, I now know my own head as well as I know my own body.

I trained myself to recognize gradations and causes of headaches in part as a defense against people who thought they knew my head and body better than I did. In my worst days of battling tick-borne diseases, when I would complain to an acquaintance of a smashing migraine, they might say “It could be the weather.”

I wanted to scream. A headache that severe does not result from a shift in barometric pressure. Sometimes on muggy days with impending rain, I felt fine. My head was clear. I had no brain fog or pain. Other days, it would be beautiful and sunny outside, and I felt my head might explode. Healthy people were outside playing, encouraging me to enjoy the weather—“it’ll be good for you!”—when all I really needed was to take some migraine medication and sleep.

My headaches were caused by tick-borne illnesses, not by the weather. They also weren’t stress-related (though stress could aggravate them), or caffeine withdrawal. If you are bedridden with Lyme, wishing you could just take your head off and put it on the nightstand because it hurts so much, I am here to remind you that your pain is likely caused by a bug in your brain, not by any of these more typical causes.

It’s important to talk to your Lyme Literate Medical Doctor (LLMD) and perhaps get a scan of your brain to make sure nothing else—outside of the scope of tick-borne illness—is going on. It also helps to recognize different headache symptoms, so you can be as specific as possible when talking with your doctor. In my case, headaches related to Lyme took over my whole skull with a throbbing pressure, sometimes making me feel like my brain was getting too big for my skull. Pain caused by babesia was different; that tended to be a migraine, focused on the left side of my head. It was more searing, like someone sawing into the left side of my skull. Babesia headaches caused nausea and light sensitivity, while Lyme headaches caused a more generalized, tolerable pain.

Your own headache symptoms might be different. You might be suffering from co-infections I did not have, and suffer relapsing fevers that can cause their own species of headaches. Do you tend to get migraines for a few days in a row? Are your headaches local or generalized? Do they come on during Herxheimer reactions, or when you are pulsing antibiotics? If you’re female, are your headaches specific to a certain time of the month? Figuring out these nuances can help your LLMD treat you. I recommend keeping a written log, and marking any external factors (like stress or certain foods) that you think might be worsening your symptoms.

These days when I do get a migraine, it’s usually because I’ve pushed myself way too hard neurologically or physically. If they persist, I know my babesia is flaring. But the headaches I usually get now are the “normal” headaches healthy people thought I was suffering from years ago.

I’ve learned to differentiate between these headaches, too. Weather-related headaches mean slight pressure at the base of my skull, across both sides of my head. These I can’t do anything about until the storm passes, but the pain is minimal. Stress-related headaches cause inflammation only on the left side of the base of my skull, creating a knot that I can actually feel with my hand. It helps to rub the knot or get cranial-sacral therapy and sleep. Hormonal headaches feel like a buzzing across my temples, and are relieved with over-the-counter painkillers. Dehydration headaches are a tightening on the top of my head, signaling that I need to drink electrolyte-enhanced water.

All of these headaches are bearable. Getting these typical, that is, non tick-borne disease related headaches reminds me how very, very different they are than the agonizing headaches I suffered years ago. Learn the nuances of your own headaches, talk to your LLMD about them, and don’t let anyone but your trusted medical providers tell you what the cause of pain is in your own body.


jennifer crystalOpinions expressed by contributors are their own.

Jennifer Crystal is a writer and educator in Boston. She has written a memoir, One Tick Stopped the Clock, for which she is seeking representation. Contact her at: lymewarriorjennifercrystal@gmail.com. 

 

 

________________________

**Comment**

This article takes me back to when I wondered if there would EVER be a day without an excruciating, all encompassing headache. Thankfully, these headaches are a thing of the past due to appropriate treatment. One of the most effective drugs for me was minocycline due to its ability to cross the blood/brain barrier:  https://madisonarealymesupportgroup.com/2017/06/04/minocycline-for-ms-and-much-more/

Appropriate Babesia treatment was also crucial:  https://madisonarealymesupportgroup.com/2016/01/16/babesia-treatment/

For me initially, the headaches were in the meninges (the layer encompassing the entire brain). The inflammation and pain were beyond anything I’d ever experienced. Then they became occipital (base of where head meets neck).  Since I met numerous patients that had a Lyme diagnosis as well as Chiari, I had a MRI to rule that out:  https://madisonarealymesupportgroup.com/2016/04/02/chiari/  The MRI for me was normal – showing nothing that should cause the type of pain I was experiencing.

At this point, I tried MSM for pain/inflammation with good success & have been taking daily since:  https://madisonarealymesupportgroup.com/2018/03/02/dmso-msm-for-lyme-msids/

I also added in systemic enzymes for the same reasons, although both MSM & enzymes do 1,000 beneficial things:  https://madisonarealymesupportgroup.com/2016/04/22/systemic-enzymes/

https://madisonarealymesupportgroup.com/2018/03/05/how-proteolytic-enzymes-may-help-lyme-msids/

https://madisonarealymesupportgroup.com/2018/01/03/the-invisible-universe-of-the-human-microbiome-msm/

I recommend you discuss these options with your practitioner IF you’ve had sufficient antimicrobial treatment but are left with a lot of pain. These substances did not work for me while in treatment for active infection. It wasn’t until after stopping treatment that they worked for me; however, you may be different.

I do feel one mistake people make is quitting treatment too soon.  ILADS recommends being symptom-free for 2-3 months before stopping any treatment.  As you see from the article on Babesia, Dr. Horowitz recommends 9 months to a year of steady 3 weeks on, one week off treatment. Many quit this too soon.  It’s important to overlap treatment as well with numerous things hitting all the various angles.  It’s also important to switch meds when you reach plateaus.  My husband and I were treated with 4.5 years and have relapsed twice requiring 2-3 month stints of treatment. Make sure you see your practitioner if symptoms return.  Read the following articles for examples to discuss with your practitioner:

https://madisonarealymesupportgroup.com/2016/02/13/lyme-disease-treatment/

https://madisonarealymesupportgroup.com/2016/01/16/babesia-treatment/

https://madisonarealymesupportgroup.com/2016/01/03/bartonella-treatment/

https://madisonarealymesupportgroup.com/2016/02/07/mycoplasma-treatment/

https://madisonarealymesupportgroup.com/2016/03/28/combating-viruses/

https://madisonarealymesupportgroup.com/2017/10/03/removing-parasites-to-fix-lyme-chronic-illnesses-dr-jay-davidson/

Ticks: A Ticking Lyme Bomb

https://torontosun.com/health/diet-fitness/ticks-a-ticking-lyme-bomb

Ticks: A ticking Lyme bomb

A Lyme disease infected tick is pictured crawling on wood in this undated file photo. (Getty Images)

Nice weather is here and you’re out and about? Be on the lookout for eight-legged menaces on the march. Tick populations armed with the Borrelia bacteria are increasingly creeping into Canada, expanding and growing – and so too the number of tick-borne diseases, predominantly Lyme.

It’s a ticking Lyme bomb, and vastly under-detected across Canada. Dr. Vett Lloyd, a researcher and biology professor at Mount Allison University in New Brunswick, says eight out of 10 cases are being missed – along the coast, the number is higher.

The majority of Canadians who have Lyme disease are slipping through the cracks.

“Diagnosis is missed when Lyme disease is not considered as a diagnosis by the physician or patient and when the standard blood testing procedure is fault,” says Lloyd, a member of the new Lyme Disease and Tick-Borne Illnesses Task Force.

Decades-old testing protocols are a failure. Patients and advocacy groups report access-to-care a nightmare. If the disease is treated promptly with antibiotics, people get better. No treatment, and the illness becomes chronic and debilitating. Even deadly.

“It’s a serious and growing epidemic,” says Sue Faber, co-founder of the advocacy group LymeHope. She believes that because of so many missed cases of Lyme disease, “instead of 2,025 annual cases reported by Public Health of Canada, we are actually dealing with approximately 56,000 cases every year in Canada.”

Lyme-disease-carrying ticks are deposited randomly by our friendly migratory birds, such as wrens and robins. Lloyd actually got bit by a tick in her backyard – she describes her Lyme disease battle as “hell.” That’s how many would also describe navigating the health care system for diagnosis and treatment.

Many Canadians are being alienated by the conventional health-care system and seek costly private health care, even beyond the country’s borders, at their own expense, says Lloyd. Others follow home remedies obtained from Dr. Google and either natural products or antibiotics purchased from the black or grey market.

Adds Lloyd: “When Canadians are obtaining health care from the internet and antibiotics from their local drug dealers, I think it is safe to say that the current situation is both dangerous and cruel.”

Dr. Vett Lloyd. (Supplied photo)

Climate change is empowering ticks to grow in numbers. places and pathogens, says Mary Beth Pfeiffer, investigative journalist and author of Lyme: The First Epidemic of Climate Change. “By virtue of the developed world’s lifestyle and influence… we have paved the way for the first global epidemic abetted by climate change. Warming may not have caused this scourge, but it most certainly is enabling it.”

Winnipeg resident Joanne Seiff describes Lyme as “insidious. Being sick with Lyme is awful, and it creeps along – you feel worse and worse but it’s hard to get anyone to believe you.”

She got sick in May, 2016 with what felt like the flu.

“I had recurring fevers, swelling and fatigue that progressed to swollen joints, lymph nodes, and other Lyme symptoms.”

She saw multiple physicians, including specialists, and was dismissed in every case.

“Canadian health systems are unprepared for this. Doctors aren’t well-trained, labs don’t test for all the strains, cases are under-reported and there’s a real sense of disbelief that Lyme – and other tick-borne illnesses – exist here,” says Seiff, author and knitwear designer at joanneseiff.com.

Doctors need to become better educated and responsive, says Seiff, and “follow the protocol that suggests an immediate, prophylactic dose of doxycycline if Lyme disease is at all suspected.”

She also believes laboratory testing needs major updating and tick research proper funding.

Adds Lloyd: “The cost to individual Canadians ill with Lyme disease, and their families and communities, is already appalling in terms of personal suffering. At some point that will translate into a societal cost and change will have to happen.”

It’s a polarizing issue, and what’s more, Faber, a nurse, wants the public to know that

“human to human maternal transmission has been demonstrated in peer-reviewed medical and scientific literature. Lyme disease can be transmitted from mother-to-baby in utero causing miscarriage, death and/or newborn infection.”

Both Faber and LymeHope (lymehope.ca) co-founder/lawyer Jennifer Kravis believe they unknowingly transmitted Lyme disease to their children while pregnant. The medical world isn’t convinced, including the Health Canada website, that says “there is not enough evidence to confirm that Lyme disease during pregnancy has adverse effects for the fetus…”

Meanwhile, if you suspect you have Lyme disease, Jim Wilson, of Canadian Lyme Disease Foundation, advises “asking your doctor for the standard Lyme test with the full understanding that if the results comes back negative that in no way rules out Lyme disease.” More guidance is available at canlyme.com, including prevention and safe tick removal.

Protect yourself with tips from microbiologist and author Jason Tetro:

  •  Take a look at the Government of Canada’s tick surveillance webpage to find out if your area is at risk.
  • When outside, wear long, light-coloured protective clothing and tuck in pant legs into socks or boots.
  • Always use a product containing DEET such as Off! Deep Woods Tick.
  • After being outdoors, check your entire body for ticks including under the arms, inside the belly button and in and around the hair. Check your clothing, gear and pets for ticks.
  • Shower within two hours of coming indoors and throw clothing in a dryer on high heat for 10 minutes.

Yolanda Hadid Opens Up About Her Battle With Lyme Disease

**Comment**
Once again, an independent Canadian tick researcher has proven that climate change has ZIPPO to do with this, despite what a journalist selling a book with that title states.
I find it highly interesting that groups will promote Pffeifer’s book but not actual research showing how ticks proliferate. To state that climate change is “empowering ticks,” shows a real lack of understanding of ticks. They are extremely ecoadaptive and will be the last species on the planet besides the IRS.
It’s important we do not fall prey as Science has to populism and schticks in efforts of obtaining grant money for research.  Lyme/MSIDS has been driven by politics and power since inception.  
We should know better and refuse to climb into bed with the devil.
Climate data never has and never will help extremely sick patients.  So much research on practical issues is screaming to be done that will actually make a difference.

Septic Shock Caused by RMSF in Suburban Texas Patient With Pet Dog Exposure: A Case Report

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6091339/

. 2018; 19: 917–919.
Published online 2018 Aug 4. doi: 10.12659/AJCR.909636
PMCID: PMC6091339
PMID: 30076285

Septic Shock Caused by Rocky Mountain Spotted Fever in a Suburban Texas Patient with Pet Dog Exposure: A Case Report

Abstract

Patient: Female, 45

Final Diagnosis: Rocky mountain spotted fever

Symptoms: Altered mental state • ataxia • dyspnea • fever • headache

Objective:

Unusual clinical course

Background:

Rocky Mountain spotted fever (RMSF) is associated with high mortality and requires prompt identification and treatment to ensure better outcomes.

Case Report:

We describe an advanced case of RMSF in a 45-year-old female patient with pet dog exposure who presented with altered mental status, dyspnea, and ataxia progressing to septic shock and acute hypoxic respiratory failure requiring intubation and mechanical ventilation.

Conclusions:

This case illustrates the importance of keeping RMSF in the differential diagnosis in patient populations outside of the usual geographic areas of incidence in the appropriate clinical setting.

___________________

**Comment**

This is what can happen when diagnosis is delayed.

This woman that lived in the suburbs had a 7-day history of fevers associated with headache, arthralgias, nausea, fatigue, and neck pain, but did NOT have the tell-tale blotchy RMSF rash.

Two days later, she worsened with confusion, combativeness, dyspnea, and ataxia. She got multiple recent bug bites from her pet dogs sleeping in her bed. The dogs were not up to date on flea and tick medication but were healthy and showed no sign of illness.
  • Rule #1:  Do NOT sleep with pets.  The risk is too great.
  • Rule #2:  If you choose to have pets, make sure you treat them if they go outdoors.  The risk is too great.
  • Rule #3:  Doctors need to start treating this plague with the respect it deserves and frankly should keep it in the back of their minds AT ALL TIMES.
Positive findings were R. typhi IgM 1: 1024 (normal <1: 64), R. Rickettsii IgM 1: 1024 (normal <1: 64), IgG 1: 128 (normal <1: 64), and echovirus Ab 1: 80 titer (normal <1: 80). The Rickettsial titers were repeated for possible cross-reactivity and R. typhi antibodies were noted to be negative (<1: 64).
Although R.typhi was ruled out due to cross-reactivity, I believe we will start seeing more of this strain in the future.
The patient improved on doxycycline, the drug of choice for RMSF and was discharged.
Why isn’t there a full-out media blitz on this like there was on Zika?

Woman Wakes up With Black Eye & Swollen Face After Cat Scratch That Left Her on IV Drip For Four Days

https://www.dailymail.co.uk/health/article-7053027/Woman-42-wakes-BLACK-EYE-swollen-face-scratched-cat.html

Woman, 42, wakes up with a BLACK EYE and swollen face after being scratched by her cat that left her on an IV drip for four days

  • Heidi Plamping had been trying to calm down her cat, Storm, who was scared
  • The cat scratched her on the face and arm, but Ms Plamping wasn’t worried
  • Three days later she woke up with a mild reaction she thought was due to dust
  • But her face was soon covered in a rash, and she needed to visit the hospital 

A woman woke up with a black eye and swollen face after being scratched by her pet cat.

Heidi Plamping, from Canada, had been trying to calm down her cat, Storm, who had been freaked by a large dog.

As three-year-old Storm clambered on to her head for refuge, her claws caught Ms Plamping’s skin, drawing blood.

When the 42-year-old’s eyes and hands started to swell three days later, she thought dust mites were to blame.

But her face worsened over the next few days, to the point where it was covered in a rash.  She was given pills by her doctor and sent home.

However, they did not work and she needed to go to the hospital every day for four days to receive a drip of antibiotics to fight her swelling.

Doctors warned her cat scratches can be very serious – cats carry and can transfer bacteria, which, in very rare cases, can lead to life-threatening complications such as sepsis.

Heidi Plamping, 42, of Cochrane, Alberta, Canada, had been trying to calm down her cat, Storm, who scratched her face and arm as she clambered onto her head for safety
Heidi Plamping, 42, of Cochrane, Alberta, Canada, had been trying to calm down her cat, Storm, who scratched her face and arm as she clambered onto her head for safety

Ms Plamping's face swelled and became covered in a rash that worsened over the course of a few days. Pictured, on May 8, six days after being scratched

Ms Plamping had to go to hospital every day to receive a drip of antibiotics. Pictured on May 10

As three-year-old Storm clambered onto Ms Plamping's her head for refuge, her claws caught Ms Plamping's skin ten times. Pictured, cuts to her face
As three-year-old Storm clambered onto Ms Plamping’s head for refuge, her claws caught Ms Plamping’s skin ten times.  Pictured, cuts to her face.

Ms Plamping, a digital marketing consultant who lives in Cochrane, Alberta, had travelled to British Columbia at the start of May with Storm to stay and work with friends for the summer.

When they arrived on May 2, Ms Plamping let Storm out on her lead as she had done countless times before when they’ve visited the unidentified friend.

However, since their last visit, Ms Plamping’s friend had got two Great Danes who were very friendly and excited to meet Storm.

The large dogs scared her and she started to get tangled in her lead as she panicked to get away.

Ms Plamping said: ‘Their dogs are very friendly, but my cat hasn’t met a dog before so when one of them showed up she freaked out.’

Ms Plamping rushed to Storm’s rescue and started to untangle her beloved cat as she climbed up her face to the safety of her head.

Ms Plamping said: ‘Eventually I picked her up so I could bring her inside. She was so scared she climbed my face to my head while I screamed murder and put her inside.’

As a result, Ms Plamping had seven scratches on her face and three more on her hand and arm.

When she woke up the next day with a black eye, Ms Plamping thought nothing more of her injuries.

But by May 5, Ms Plamping had a swollen hand and eyes. Due to having sensitive skin, she thought that she could possibly be having a reaction to any dust that could have been present in her new surroundings.

Storm, pictured, was freaked by a Great Dane dog at Ms Plamping's friend's houseStorm, pictured, was freaked by a Great Dane dog at Ms Plamping’s friend’s house

When Ms Plamping woke up the day after the scratches with a black eye (pictured), but didn't think much of her injuries
When Ms Plamping woke up the day after the scratches with a black eye (pictured), but didn’t think much of her injuries
But by May 5, Ms Plamping had a swollen hand and eyes (pictured). Due to having sensitive skin, she thought that she could possibly be having a reaction to dust mites
But by May 5, Ms Plamping had a swollen hand and eyes (pictured). Due to having sensitive skin, she thought that she could possibly be having a reaction to dust mites
On May 7, pictured, Ms Plamping's face was significantly more swollen and covered in rashes so she went back to the doctor she had seen the day before

On May 7, pictured, Ms Plamping’s face was significantly more swollen and covered in rashes so she went back to the doctor she had seen the day before

Ms Plamping said: 'When they had to order antibiotics that had to go into me through an IV, I knew it was serious'. Pictured, an IV line to administer the drugs

Ms Plamping said: ‘When they had to order antibiotics that had to go into me through an IV, I knew it was serious’. Pictured, an IV line to administer the drugs

Ms Plamping, a digital marketing consultant, said it wasn't the first week in British Columbia she had been hoping for. Pictured, on May 13 when the swelling and rashes had almost gone

Ms Plamping, a digital marketing consultant, said it wasn’t the first week in British Columbia she had been hoping for. Pictured, on May 13 when the swelling and rashes had almost gone

Ms Plamping, pictured before the drama, said if she had to rescue Storm again, she would
Ms Plamping, pictured before the drama, said if she had to rescue Storm again, she would
Ms Plamping has had Storm ever since she was four months old and said that this incident hasn't changed their relationship. Pictured together
Ms Plamping has had Storm ever since she was four months old and said that this incident hasn’t changed their relationship. Pictured together 
Ms Plamping was put on an IV and had to return every day for four days to get a new dose of antibiotics administered.

She said: ‘They said it is common for cat scratches or bites to cause infection. When they had to order antibiotics that had to go into me through an IV, I knew it was serious but was just thankful that we were heading in the right direction to make me better.

‘The next day, the swelling was going down but a rash was spreading on my arm. 

‘The doctor outlined my arm where the rash was and told me to go to the emergency room if it spread any further that night. Thankfully it didn’t and once the hand swelling went down they finally gave me prednisone [a medication to calm the immune system] to help with the swelling and rash in my face.’

The medication made Ms Plamping nauseous and sleepy, and she said: ‘I started getting upset when my face was so tight and itchy.

‘I knew it would get better, but I was growing impatient. So, it wasn’t exactly the first week in British Columbia that I had pictured for myself.’

Following her ordeal, animal lover Ms Plamping said that Storm looked at her funny for a few days whilst the swelling went down.

But the two forgave each other instantly and Ms Plamping said she wouldn’t hesitate to rescue Storm again if the situation arose.

Ms Plamping has had Storm ever since she was four months old and said that this incident hasn’t changed their relationship, but Storm is now more wary of going outside.

‘Storm is very hesitant to leave the cabin. Back home in Alberta she freely goes outside. Here she is nervous about the dog,’ said Ms Plamping.

‘If I had to protect her again and pick her up, I would. I don’t have kids. She is my baby. My fur baby.

‘I wasn’t aware that cat scratches were so infectious. If you get a cat scratch or bite, go to your doctor right away.’

CAN YOU GET AN INFECTION FROM A CAT SCRATCH?

Cat-scratch disease (CSD) is a bacterial infection spread by cats. The disease spreads when an infected cat licks a person’s open wound, or bites or scratches a person hard enough to break the surface of the skin. 

About three to 14 days after the skin is broken, a mild infection can occur at the site of the scratch or bite.

The infected area may appear swollen and red with round, raised lesions and can have pus. The infection can feel warm or painful. A person with CSD may also have a fever, headache, poor appetite, and exhaustion.

Later, the person’s lymph nodes closest to the original scratch or bite can become swollen, tender, or painful.

CSD is caused by a bacterium called Bartonella henselae. About 40% of cats carry B. henselae at some time in their lives, and it is more common in kittens. 

Although rare, CSD can cause people to have serious complications. CSD can affect the brain, eyes, heart, or other internal organs.

These rare complications, which may require intensive treatment, are more likely to occur in children younger than five years and people with weakened immune systems.

WHAT SHOULD YOU DO IF YOU’RE BITTEN BY AN ANIMAL? 

  • Clean the wound immediately by running warm tap water over it for a couple of minutes, even if the skin does not appear broken.
  • Remove any dirt or foreign objects from the wound.
  • Encourage the wound to bleed slightly by gentle squeezing (unless already bleeding freely).
  • If there is heavy bleeding, place a clean pad or sterile dressing over wound and apply pressure.
  • Dry the wound and cover with a clean dressing or plaster.
  • Seek medical advice unless the wound is very minor.
  • For severe wounds, go to A&E. 

___________________

**Comment**

Bartonella with cat scratch and fairly immediate & severe symptoms, while scary, is fairly straight forward.  Bartonella, without cat exposure that smolders over years, along with potential tick bites and other pathogen involvement can be devastating, fly under the radar, and remain undiagnosed for years.  This is what many Lyme/MSIDS patients struggle with.  

For more:  https://madisonarealymesupportgroup.com/2018/05/07/fox-news-bartonella-is-the-new-lyme-disease/

https://madisonarealymesupportgroup.com/2019/03/24/cat-scratch-disease-caused-teens-schizophrenia-like-symptoms-report-says/

https://madisonarealymesupportgroup.com/2019/03/02/skin-inflammation-nodules-letting-the-cat-out-of-the-bag/  Cases of Bartonella with NO cat exposure listed in comment section.

https://madisonarealymesupportgroup.com/2019/04/24/human-bartonellosis-an-underappreciated-public-health-problem/

https://madisonarealymesupportgroup.com/2019/05/09/bartonella-transmitted-to-children-at-birth-causing-chronic-infections/

More about Bartonella & Treatments: https://madisonarealymesupportgroup.com/2016/01/03/bartonella-treatment/

https://madisonarealymesupportgroup.com/2019/05/05/good-news-for-bartonella-patients-identification-of-fda-approved-drugs-with-higher-activity-than-current-front-line-drugs/

Pets can also bring ticks into the house to infect you:  https://madisonarealymesupportgroup.com/2017/08/12/pet-owners-have-nearly-2-times-the-risk-of-finding-ticks/

 https://madisonarealymesupportgroup.com/2019/01/29/woman-links-lyme-disease-diagnosis-to-pet-cat-sleeping-in-bed/

https://madisonarealymesupportgroup.com/2019/05/28/septic-shock-caused-by-rmsf-in-suburban-texas-patient-with-pet-dog-exposure-a-case-report/

https://madisonarealymesupportgroup.com/2018/09/20/tick-infestations-of-wildlife-companion-animals-in-ontario-canada-with-detection-of-human-pathogens-in-ixodes-scapularis-ticks/

https://madisonarealymesupportgroup.com/2019/04/16/april-lyme-prevention-month-for-dogs-a-pet-owners-guide/

https://madisonarealymesupportgroup.com/2019/05/14/tick-population-soaring-as-local-vets-see-lyme-disease-cases-in-dogs-quadruple/

https://madisonarealymesupportgroup.com/2018/10/02/fda-flea-tick-meds-for-pets-causing-seizures-neurological-issues/

If you are currently treating your fur baby with Bravecto, Nexgard or Simparica you need to be careful. According to the FDA, some animals treated with these medications

“have experienced adverse events such as muscle tremors, ataxia, and seizure.”1 There is also another product in that class of drugs called, Credelio (it recently received FDA approval).