Did Trauma during Childbirth set off her YOPD?

I met Lisa Boyd in boxing classes several months ago.  She is in her late 40’s, and it was sad to see her come in to class with a walker.  After a few weeks of exercise, she left the walker behind and began using only a cane.  Like many with Young Onset PD, it took a while for her doctors to finally make the diagnosis. In the meantime, her health deteriorated quickly. Her grit and her spirit to work through her physical disabilities, always with a smile,  is inspiring to us all.

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Lisa Boyd and Gail Buckley
Lisa’s story is very different from many others in our group of Inspired Women with Parkinson’s.   She was pregnant with her second child at age 41.  The pregnancy went well, but there was a mishap during the delivery and she never recovered.  She began noticing things almost immediately afterwards. She would drop her baby, she started losing her balance.  The doctors told her she was just depressed, there was nothing wrong. She insisted there is something wrong going on.  For 2 years they kept telling her she was crazy.  Then they said she had AIDS (she didn’t), asked if she was a drug user, etc.   She did not have a tremor for two years, so people couldn’t see what was wrong.   She was stumbling over her feet, choking on her food and water.  She was a new mom who could not take care of her child.

She moved to Atlanta about two years later and eventually went to the Neurology Department at Emory.  They found she had all 10 symptoms of PD.   She finally got her diagnosis 2 1/2 years after her son was born.  Lisa said she had to advocate for herself to get anything.   Prior to going to Emory no one thought she had PD because she was so young.  In addition, because she is African-American woman, she had to fight to get good health care.  She had to demand that Emory see her as a patient. The doctors now say that the trauma from the birth most likely triggered the symptoms of Parkinson’s Disease, which was probably there all along.

She has changed her diet, which made a big difference in her life.  She tries to eat as clean as possible, with no processed foods.  She takes turmeric, blueberries, strawberries and flaxseed for inflammation.  All of these have helped.

She was very depressed for a while, but eventually decided not to let it get to her.  She does self-affirmations and tries to be around positive people whenever possible.

Her advice to the newly diagnosed:  try to spend time with other women with Parkinson’s.  Being around people who understand what you are going through helps.  There are not a lot of women with Parkinson’s and even fewer African-American women with PD, so she wants to get into support groups to meet others.  Another woman in our group said that the one of the best things about having PD is meeting other women who understand and you can talk to about your problems.  She has made some great new friends as a result.

In response to a question about how her children respond to a mother with PD, Lisa says her son, who is 7, has never known her any other way.  But her 23 year old daughter knows how active Lisa was and wants her to get back to the way she used to be.  She used to be Superwoman. Cheer Mom, PTA, active in her church, but she can’t do those things anymore.  Her daughter is supportive, but now that Lisa can’t do everything for everyone anymore, the whole dynamic of the family has changed.  It also affected her relationship with her husband whom she had been with since she was young.

She now knows what she has to do to modify her activities so that she can get out of the house.  She has extremely supportive friends, but some have disappeared, a common problem with many of the room.  She is now going through a divorce and the stress has made her worse, but she is looking forward to getting back to boxing and exercise very soon.

 

6 thoughts on “Did Trauma during Childbirth set off her YOPD?

  1. cindybittker

    Most people I know with PD, (and I have met hundreds over the past 11 years since i was dx, had some sort of trauma, emotionsl truma, physical trauma, or had surgery, or had recent hysterectomt, menopause, death or illness of a loved one, relationship oroblems or ending. My own little theory is that the disease process has been mounting slowly for decades, and for some reason, the flood gates are opened with stress and the disease process moves faster. Maybe if we did not have the stressful event the disease would not manufest until much later in life. PD in some ways is advanced aging. No science behing any of this..?.jusr my impression!,

    Liked by 1 person

    1. Cindy, Thanks for the response! I agree that for many, including me, a traumatic event set things in motion. I broke my leg and my opposite foot starting twitching a few weeks later. But the signs had been there for quite a while. I just didn’t know what they were. For some, it just appears as they age, with no obvious trigger. We need to get the science to help with earlier diagnoses, before symptoms becomes severe.

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  2. Roger A. Jenkins

    Lisa and Cindy, my heartfelt compassion goes out to both of you!
    It’s unfortunate, but the doctors did not know that the symptoms perfectly pointed to Parkinson’s.
    The biggest detriment I see with a slow (several years for unfortunate individuals) is the delay in an agreesive exercise program! It is vital to exercise early and to do it faithfully.
    Exercise is more important than medicine. I absolutely stand by my last statement.
    I have had PD for 11 years and was DX’d at 47.
    Exercise, good support groups, and a good MDS trained Neurologist are the THREE most vital elements of successfully living with Parkinsons Disease. 🙂 🙂 🙂

    Liked by 1 person

  3. Pingback: Odds & Ends – Twitchy woman

  4. Celeste

    Hello. You all left wonderful posts/suggestions, but no specific names of support groups etc. My 68 year old mom has been diagnosed. Her doctor isn’t very helpful, simply referring her to pamphlets. We live in the south suburbs of Illinois. Any specific help/info you could provide Re. doctors, therapy, management, diet, exercise, would be appreciated.
    Thanks.

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    1. Celeste, You did not say where in Illinois you live. However, the best recommendation I can give you is to get on the internet and look for local Parkinson’s resources. A Movement Disorders Specialist, rather than a general Neurologist is recommended, if there is one in your area. Check the Michael J Fox Foundation, Parkinson’s Foundation and APDA websites for the information you are looking for about management, diet,exercise, etc. They all offer webinars, which are recorded, so you can access them at any time. I hope this helps. Sharon

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